Nucleotide Sequences Encoding Insecticidal Proteins

Abstract

The present invention provides nucleotide sequences encoding an insecticidal protein exhibiting lepidopteran inhibitory activity, as well as a novel insecticidal protein referred to herein as a Cry1A.105 insecticide, transgenic plants expressing the insecticide, and methods for detecting the presence of the nucleotide sequences or the insecticide in a biological sample.

Description

BACKGROUND OF THE INVENTION

[0001] The present invention provides novel coding sequences for use in plants. The coding sequences encode a chimeric insecticidal protein toxic to a wide range of lepidopteran species crop pests.

[0002] Commercial formulations of naturally occurring B. thuringiensis isolates have long been used for the biological control of agricultural insect pests. Bt spores and crystals obtained from fermentation of Bacillus thuringiensis species are concentrated and formulated for foliar application according to conventional agricultural practices.

[0003] Members of the family of Cry1 crystal proteins are known to exhibit bioactivity against lepidopteran insect larvae and are useful as agents for controlling lepidopteran insect pests. The precursor form of Cry1 .delta.-endotoxins consist of two approximately equal sized segments. The carboxy-terminal portion of the precursor protein, or pro-toxin segment, stabilizes crystal formation and exhibits no insecticidal activity. The amino-terminal half of the precursor protein comprises the toxin segment of the Cry1 protein and, based on alignment of conserved or substantially conserved sequences within Cry1 family members, can be further sub-divided into three structural domains. These three sub-domains are based on a three dimensional crystallographic structural model of a Cry1A .delta.-endotoxin in which the three sub-domains were referred to as Domain I, Domain II, and Domain III, respectively as measured from the amino terminus of the protein toxin segment. Domain I comprises about the first third of the active toxin segment and has been shown to be essential for channel formation (Thompson et al., 1995). Domains II and III respectively comprise about the central and carboxy-terminal segments of the active toxin portion. Domains II and III have both been implicated in receptor binding and insect species specificity, depending on the insect and .delta.-endotoxin being examined (Thompson et al., 1995).

[0004] The likelihood of arbitrarily creating a chimeric protein with enhanced properties from the reassortment of the domain structures of the numerous native insecticidal crystal proteins known in the art is remote. This is a result of the complex nature of protein structure, folding, oligomerization, and activation including correct proteolytic processing of the chimeric precursor, if expressed in such form, to release an insecticidal toxin segment. Only by careful selection of specific target regions within each parental protein for inclusion into a chimeric structure can functional insecticidal toxins be constructed that exhibit improved insecticidal activity in comparison to the parental proteins from which the chimeras are derived. Experience has shown that reassembly of the toxin domains, i.e., assembly of a chimeric toxin consisting of domain I, II, and III of any two or more toxins that are different from each other, results in the construction of a protein that exhibits faulty crystal formation and/or the complete lack of any detectable insecticidal activity directed to a preferred target insect pest species. In some instances, a chimeric toxin will exhibit good crystal formation properties, yet exhibit no detectable insecticidal activity. Only by trial and error are effective insecticidal chimeras formulated, and even then, the skilled artisan is not certain to end up with a chimera that exhibits insecticidal activity that is equivalent to or improved in comparison to any single parental toxin protein from which the constituents of the chimera may have been derived.

[0005] The literature reports examples of the construction or assembly of chimeric proteins from two or more Bt insecticidal crystal protein precursors, yet not all exhibited insecticidal or crystal forming properties that were equivalent to or improved in comparison to the precursor proteins from which the chimeras were derived. (Bosch et al. (WO95/06730); Thompson et al. (WO95/30753); Thompson et al. (WO95/30752); Malvar et al. (WO98/22595); Gilroy et al. (U.S. Pat. No. 5,128,130); Gilroy (U.S. Pat. No. 5,055,294); Lee et al. (1992) Gene 267:3115-3121; Honee et al. (1991) Mol. Microbiol. 5:2799-2806; Schnepf et al. (1990) J. Biol. Chem. 265:20923-20930; Perlak et al. (1990) Bio/Technol. 8:939-9943; Perlak et al (1993) Plant Mol. Biol. 22:313-321).

[0006] Expression of B. thuringiensis .delta.-endotoxins in transgenic corn plants has proven to be an effective means of controlling agriculturally important insect pests (Perlak et al. 1990; 1993). Transgenic crops expressing B. thuringiensis .delta.-endotoxins enable growers to significantly reduce the time and costs associated with applications of topically applied chemical insecticides. Use of transgenes encoding B. thuringiensis .delta.-endotoxins is particularly advantageous. Crop plants expressing B. thuringiensis .delta.-endotoxins in areas under heavy insect pressure exhibit improved yields that are better than otherwise similar non-transgenic commercial plant varieties. However, it is anticipated that insects may evolve resistance to B. thuringiensis .delta.-endotoxins expressed in transgenic plants. Such resistance, should it become widespread, would clearly limit the commercial value of germplasm containing genes encoding such B. thuringiensis .delta.-endotoxins. One possible way of increasing the effectiveness of the transgenic insecticides against target pests and contemporaneously reducing the development of insecticide-resistant pests would be to ensure that transgenic crops express high levels of B. thuringiensis .delta.-endotoxins (McGaughey and Whalon 1993; Roush 1994). In addition, having a repository of insecticidal genes that are effective against groups of insect pests and which manifest their effects through different modes of action can safeguard against any development of resistance. Expression in a plant of two or more insecticidal compositions toxic to the same insect species, each insecticide being expressed at levels high enough to effectively delay the onset of resistance, would be another way to achieve control of the development of resistance. Examples of such insecticides useful in such combinations include but are not limited to Bt toxins, Xenorhabdus sp. or Photorhabdus sp. insecticidal proteins, deallergenized and de-glycosylated patatin proteins and/or permuteins, plant lectins, and the like. Achieving co-expression of multiple insecticidally active proteins in the same plant, and/or high expression levels of those insecticidal proteins without causing undesirable plant morphological effects has been elusive.

[0007] Only a handful of the more than two-hundred and fifty individual insecticidal proteins that have been identified from Bacillus thuringiensis species have been tested for expression in plants. Several Cry1's, Cry3's, Cry2Aa and Cry2Ab, binary toxins Cry33/34 and Cry23/37, and a Cry9 have been successfully expressed in plants. Cry1 proteins represent the largest class of proteins that have been expressed in plants, but none have been expressed at high levels. It was necessary to target the Cry2Ab to the chloroplast to avoid undesirable phytotoxic effects. The majority of acres planted in recombinant plants express Cry1A proteins. The likelihood of the onset of resistance to Cry1A proteins by targeted insect pest species is substantially higher than it would be if a resistance management allele was also expressed along with the cry1 allele, or if the cry1 allele was expressed at high levels. Therefore it is desirable that alternative toxin genes be developed for expression in plants as supplements and replacements for those being used presently in the first and second generations of transgenic insect resistant plants.

SUMMARY OF THE INVENTION

[0008] The invention provides isolated nucleotide sequences for expression in plants encoding an insecticidal protein exhibiting lepidopteran insect inhibitory properties. SEQ ID NO:1 is an example of such nucleotide sequences consisting of a cry1A.105 gene and encodes an insect inhibitory Cry1A.105 protein. SEQ ID NO:1 is similar to SEQ ID NO:3, both encoding a Cry1A.105 protein. SEQ ID NO:1 is preferred for use in a dicotyledonous cells, while SEQ ID NO:3 is preferred for use in monocotyledonous cells. SEQ ID NO:4 is encoded from SEQ ID NO:3 and is identical in amino acid sequence to SEQ ID NO:2. The isolated nucleotide sequence is intended to include sequences that exhibit at least from about 88% to about 90% or greater nucleotide sequence identity to the sequence as set forth at SEQ ID NO:1, or that hybridize to SEQ ID NO:1 under stringent hybridization conditions. The isolated nucleotide sequence is also intended to include sequences that exhibit at least about 90% nucleotide sequence identity to the sequence as set forth at SEQ ID NO:3, or that hybridize to SEQ ID NO:3 under stringent hybridization conditions.

[0009] The invention also provides an isolated and purified insecticidal protein exhibiting inhibitory activity directed to lepidopteran insect species. The insecticidal protein is designated herein at least as the toxin portion of Cry1A.105 and exhibits an amino acid sequence as set forth in SEQ ID NO:2. The full length precursor protein consisting of about 1177 amino acids as set forth in SEQ ID NO:2 is also referred to as an insecticidal Cry1A.105 protein, however any fragment of the precursor protein that exhibits insecticidal bioactivity is intended to be referred to as an insecticidal Cry1A.105 protein, and includes at least a Cry1A.105 insecticidal protein corresponding to an amino acid sequence segment from about amino acid 1 through about amino acid 612 as set forth in SEQ ID NO:2, and may also include a segment from about amino acid 2 through about amino acid 610. Any composition consisting of an insecticidally effective amount of the insecticidal protein is intended to be within the scope of the invention.

[0010] The invention also provides an expression cassette for use in expressing an insecticidal protein as set forth in SEQ ID NO:2 in a host cell. The expression cassette preferably contains a promoter functional in the intended host cell which is linked to and regulates the expression of a nucleotide sequence encoding an insecticidal segment of a Cry1A.105 protein. Exemplary expression cassettes are provided herein as set forth at SEQ ID NO:5 and SEQ ID NO:7, intended for use in a dicot plant cell or a monocot plant cell, respectively. The promoter and the coding sequence are operably linked and function together in the host cell. The expression cassette can be intended for use in any host cell, but is preferably for use in a bacterial cell, a fungal cell, a mammalian cell, or a plant cell. Bacterial cells are preferably selected from the group consisting of a Bacillus species cell, a Enterobacteriacae species cell, a Pseudomonas species cell, a Clostridium species cell, and a Rhizobium species cell, and a Agrobacterium species cell. If the host cell is a plant cell, it is preferable that it is a cell chosen from a crop species of plant cell, preferably either a dicotyledonous plant or a monocotyledonous plant cell. Examples of dicotyledonous plant cells are alfalfa, apple, apricot, asparagus, bean, berry, blackberry, blueberry, canola, carrot, cauliflower, celery, cherry, chickpea, citrus tree, cotton, cowpea, cranberry, cucumber, cucurbit, egg plant, fruit tree, grape, lemon, lettuce, linseed, melon, mustard, nut bearing tree, okra, orange, pea, peach, peanut, pear, plum, potato, soybeans, squash, strawberry, sugar beet, sunflower, sweet potato, tobacco, tomato, turnip, and vegetable. Monocotyledonous plant cells examples are corn, wheat, oat, rice, sorghum, milo, buckwheat, rye, grass (fescue, timothy, brome, orchard, St. Augustine, Bermuda, bentgrass), and barley. Expression cassettes intended for use in a plant cell typically contain in operable linkage sequences that regulate the levels and efficiencies of expression of an intended substance, such as a Cry1A.105 insecticidal protein. Such sequences may be an expression enhancer sequence, an untranslated leader sequence, an intron sequence, a chloroplast targeting peptide encoding sequence, and a transcription termination and polyadenylation sequence.

[0011] The expression cassette is preferably incorporated into a vector for use in stabilizing the maintenance of the Cry1A.105 coding sequence within the host cell. A vector can be any number of structures known in the art, but is typically a plasmid or replicon into which the expression cassette is constructed or inserted prior to incorporation into the host cell. A vector is intended to include but not be limited to a plasmid, a cosmid, a bacmid, a phagemid, a YAC, a BAC, a suicide vector, an insertion sequence, a transposon, or even a linear nucleotide sequence to which the expression cassette is linked or in which the expression cassette is embedded.

[0012] Transgenic plants resistant to lepidopteran insect infestation are an embodiment of the present invention. Such plants contain a nucleotide sequence that encodes a Cry1A.105 insecticidal protein as set forth in SEQ ID NO:2 at least from about amino acid 2 to about amino acid 612. The transgenic plant is effective in controlling lepidopteran insect infestations brought about by insects such as leaf rollers, cutworms, armyworms, borers, bagworms, and any forage feeder. Preferred pests are fall armyworms, European corn borers, corn earworms (cotton bollworms), southwestern corn borers, and black cutworms. The present invention is intended to include the progeny and seed or fruits or product yielded from the transgenic plant of the present invention, so long as the nucleotide sequence of the present invention encoding a Cry1A.105 insecticidal segment is maintained within the heritable and/or plastid genome of the cells of the plant, its progeny, seed, and the like.

[0013] The present invention also provides one or more methods for controlling lepidopteran insect infestation of a plant by providing in the diet of an insect pest a composition that contains an insecticidally effective amount of an insecticidal Cry1A.105 protein. One such composition would be plant cells that have been or are descended from a plant cell transformed with a nucleic acid sequence that encodes an insecticidal segment of a Cry1A.105 amino acid sequence as set forth in SEQ ID NO:2. A transgenic plant generated from a plant cell transformed to contain an expression cassette, exemplified as set forth at SEQ ID NO:5 and SEQ ID NO:7, which contains a sequence encoding a Cry1A.105 insecticidal amino acid sequence, would be one means for providing an insecticidal composition in the diet of the insect. Another means would be to produce an insecticidally effective amount of a Cry1A.105 protein in a bacterial or fungal cell and provide the bacterial cell or fungal cell or a purified amount of the Cry1A.105 protein in the diet of one or more target insect pests susceptible to the Cry1A.105 protein.

[0014] A method of identifying a nucleotide sequence encoding a Cry1A.105 amino acid sequence in a biological sample is provided. The method consists of contacting a sample being tested for the presence of the Cry1A.105 coding sequence with a polynucleotide probe that binds with specificity to the Cry1A.105 coding sequence. In particular, the probe sequence binds, or hybridizes to, a Cry1A.105 coding sequence under stringent hybridization conditions. Detecting binding in a reaction mix is diagnostic for the presence of the Cry1A.105 coding sequence.

[0015] A method of identifying an insecticidal fragment of a Cry1A.105 protein in a sample is also provided. The method consists of contacting a sample being tested for the presence of a Cry1A.105 insecticidal fragment with an antibody that binds specifically to the insecticidal fragment. Detecting the binding in a reaction mix is diagnostic for the presence of the Cry1A.105 protein in the sample.

[0016] Chimeric or hybrid insecticidal proteins are also provided. Such hybrids are composed of two or more different insecticidal proteins, each of which exhibits insecticidal activity directed to at least one member of the same insect species. The hybrid insecticidal protein is made up of parts of each of the different insecticidal proteins. Segments of insecticidal proteins used in constructing the hybrid consist of from at least about 50 to at least about 200 contiguous amino acids selected from the contiguous amino acids making up any one of the different insecticidal proteins. A Cry1A.105 insecticidal protein as set forth in SEQ ID NO:2 from about amino acid position 2 through about amino acid position 612 is intended to be included within the group of the different insecticidal proteins from which a segment may be selected for constructing a hybrid insecticidal protein.

[0017] Various advantages and features of the present invention being apparent, the nature of the invention may be more clearly understood by reference to the following detailed description, the examples, and to the appended claims.

BRIEF DESCRIPTION OF THE SEQUENCES

[0018] SEQ ID NO:1 is a synthetic sequence for expression of a Cry1A.105 insecticidal protein, preferably in a dicot cell.

[0019] SEQ ID NO:2 is a Cry1A.105 protein encoded from the nucleotide sequence as set forth at SEQ ID NO:1.

[0020] SEQ ID NO:3 is a synthetic sequence for expression of a Cry1A.105 insecticidal protein, preferably in a monocot cell.

[0021] SEQ ID NO:4 is a Cry1A.105 protein encoded from the nucleotide sequence as set forth at SEQ ID NO:3.

[0022] SEQ ID NO:5 represents a nucleotide sequence consisting of an expression cassette that functions in a plant cell, and preferably in a dicot plant cell, for expressing a Cry1A.105 insecticidal protein.

[0023] SEQ ID NO:6 represents a Cry1A.105 insecticidal protein encoded by a segment within the expression cassette as set forth in SEQ ID NO:5.

[0024] SEQ ID NO:7 represents a nucleotide sequence consisting of an expression cassette that functions in a plant cell, and preferably in a monocot plant cell, for expressing a Cry1A.105 insecticidal protein.

[0025] SEQ ID NO:8 represents a Cry1A.105 insecticidal protein encoded by a segment within the expression cassette as set forth in SEQ ID NO:7.

DETAILED DESCRIPTION OF THE INVENTION

[0026] In accordance with the present invention, the inventors have constructed nucleotide sequences that encode a novel insecticidal protein identified herein as a Cry1A.105 protein. It has been identified that the Cry1A.105 amino acid sequence, set forth in SEQ ID NO:2, exhibits properties that provide advantages over naturally occurring Bt insecticidal proteins that are toxic to lepidopteran insect species. In particular, the Cry1A.105 protein can be expressed at high levels in both monocot and dicot plants without most transgenic events exhibiting phytotoxic effects as a result of the increased levels of expression compared to effects observed when naturally occurring Cry1 proteins are expressed in plants. In addition, the Cry1A.105 protein form stable crystals when expressed in Bacillus thuringiensis, likely because of the stabilizing effect of the Cry1Ac protoxin segment linked to the toxin moiety of the chimeric Cry1A.105 protein. In addition, the Cry1A.105 insecticidal protein exhibits a range of insecticidal bioactivity directed to lepidopteran species that is not observed with other naturally occurring Cry1 proteins that have been identified to date. Therefore, expression of the Cry1A.105 protein in transgenic plants results in increased numbers of morphologically normal transgenic events expressing higher levels of an analogue of a Cry1 toxin that exhibits a broad range of control of lepidopteran insect pest species for any event that is selected for commercial development. Such events should result in the advantage of delaying the onset of resistance to the Cry1A toxin analogue, and when combined with a second toxin that is toxic to one or more of the insect pest species to which the Cry1A analogue is also toxic and that exerts its mode of action in a way that is different from that of the Cry1A analogue, any likelihood of the development of resistance to either toxin is anticipated to be extremely remote.

[0027] The inventors have constructed at least two different nucleotide sequences for use in plants, each nucleotide sequence encoding the same Cry1A.105 insecticidal protein. The first (or amino terminal) about two thirds of the insecticidal portion of the Cry1A.105 protein consists of amino acid sequences derived from a Cry1Ab amino acid sequence. This sequence is linked to the carboxy-terminus of the toxin portion and a part of the protoxin domain of an amino acid sequence derived from an insecticidal Cry1 protein obtained from an Ecogen Bt aizawai strain EG6346 (Chambers et al., 1991, J. Bacteriol. 173:3966-3976). The Cry1A.105 toxin segment is linked then to a segment that is substantially a Cry1Ac protoxin peptide sequence. The inventors demonstrated that this construction provides a unique amino acid sequence that exhibits surprisingly improved insecticidal properties when compared to the properties exhibited by the protein from which the chimera is derived. Furthermore, the Cry1A.105 precursor protein exhibits excellent crystal forming properties and is efficiently solubilized and processed to the active toxin form in the gut of specific targeted lepidopteran insect pests.

[0028] The nucleotide sequences embodied herein have been constructed using methods set forth in U.S. Pat. Nos. 5,500,365, and 5,689,052, in particular by avoiding certain inimical sequences in the coding sequence that have been observed to be problematic for expression of heterologous gene sequences in plant cells. The segment encoding the toxin portion of the Cry1A.105 protein consists of nucleotides as set forth in SEQ ID NO:1 and SEQ ID NO:3 from about position 1 through about position 1830, more or less. The sequence as set forth at SEQ ID NO:1 was constructed for use in dicotyledonous plant species, and in particular, in cotton plants. The sequence as set forth at SEQ ID NO:3 was constructed for expression in monocotyledonous plants, and in particular, in maize or corn plant species.

[0029] Nucleotide sequences of the present invention exhibit an overall identity of about 94.3% to each other and are identical from about nucleotide position 1330 through about nucleotide position 3534. The segment of each of these nucleotide sequences encoding the toxin portion of the Cry1A.105 protein exhibits, from about nucleotide position 1 through about nucleotide position 1830, about 88.9% identity to each other. The segment of these nucleotide sequences encoding the first two domain structures of the Cry1A.105 protein is substantially more diverse and exhibits only about 84.7% identity to each other.

[0030] The inventors have constructed transgenic plant events using these sequences.

[0031] SEQ ID NO:1 was introduced into a plasmid vector containing an expression cassette consisting of a enhanced Figwort Mosaic Virus promoter (eFMV) sequence operably linked to a Petunia hybrida Hsp70 untranslated leader sequence (Ph.Hsp70, a.k.a., DnaK), an Arabidopsis thaliana ribulose bis phosphate carboxylase small subunit chloroplast targeting peptide coding sequence, and a Pisuin sativum E9 ribulose bis phosphate carboxylase small subunit gene transcription termination and polyadenylation sequence. The Cry1A.105 coding sequence as set forth at SEQ ID NO:1 was inserted into this expression cassette in frame with and immediately adjacent to the 3' end coding sequence of the targeting peptide coding sequence, and upstream of the E9 termination sequence. The nucleotide sequence of the resulting expression cassette is set forth at SEQ ID NO:5. A segment of the vector containing the Cry1A.105 expression cassette linked to a second expression cassette containing a plant expressible GUS marker was excised and used to generate transgenic cotton events using biolistic methods. Transgenic events were tested in bioassay for insecticidal activity against several different lepidopteran pest species and were determined to exhibit significantly better insect controlling properties than previously existing insect resistant cotton plants containing only Cry1Ac or a combination of Cry1Ac and Cry2Ab proteins. In addition, some of the Cry1A.105 transgenic cotton events exhibited levels of Cry1A.105 protein accumulation exceeding 10 to 20 parts per million throughout the growing season, even in cotton bolls, and without exhibiting any phytotoxic effects on the plant or reproductive tissues. This is in contrast to other Cry1 proteins that have been tested previously, which generally were only capable of levels of accumulation to less than about 10 parts per million, whether or not targeted to the chloroplast. Phytotoxic effects were observed when other Cry1 type proteins were tested in cotton, especially when levels of Cry1 accumulation approached or exceeded about 10 ppm.

[0032] SEQ ID NO:3 was introduced into a plasmid vector containing an expression cassette consisting of a enhanced Cauliflower Mosaic Virus promoter (eCaMV) sequence operably linked to a Triticum aestivum major chlorophyll a/b binding protein gene untranslated leader sequence and an Oryza sativa actin intron sequence, and a Triticum aestivum hsp17 gene transcription termination and polyadenylation sequence. The Cry1A.105 coding sequence as set forth at SEQ ID NO:3 was inserted into this expression cassette immediately adjacent to and 3' of the intron sequence and upstream of the termination sequence. The nucleotide sequence of the resulting expression cassette is set forth at SEQ ID NO:7. The vector also contains a glyphosate herbicide selectable marker that was used to select events transformed with the Cry1A.105 expression cassette. Maize events selected after transformation with the Cry1A.105 expression cassette were tested in bioassays against several lepidopteran pest species and determined to exhibit a wide range of insecticidal activity that was not prevalent with events transformed with other Bt insecticidal proteins such as Cry1Ab. The fall armyworm and black cutworm activities exhibited by events expressing insecticidal levels of Cry1A.105 coupled with the Cry1A.105 insecticidal activity directed to corn earworm and corn borer equivalent to or greater than that of events expressing Cry1Ab, provides a broader spectrum of insecticidal activity for Cry1A.105 events.

[0033] The nucleotide sequences of the present invention are exemplary. Other nucleotide sequences are capable of expressing a Cry1A.105 insecticidal protein fragment in a plant cell, and still other nucleotide sequences are capable of being designed that express well in other types of host cells. Without limiting the scope of the disclosure, it is intended that a nucleotide sequence for use in expression of a Cry1A.105 insecticidal fragment exhibit at least about 85%, or at least about 90%, or at least about 95%, or at least about 99% or greater nucleotide sequence identity to the nucleotide sequences exemplified herein. Other nucleotide sequences intended for expression of a Cry1A.105 insecticidal fragment in a host cell other than a plant cell can be of any percentage identity or similarity to the exemplified nucleotide sequences. Nucleotide sequences can vary because of the redundancy of the genetic code, and so it is possible to synthesize any number of nucleic acid sequences that encode any part of the amino acid sequence set forth in SEQ ID NO:2, and all of these sequences are intended to be within the scope of the present invention. Any isolated and purified nucleic acid sequence encoding at least an insecticidal fragment of a Cry1.105 protein is intended to be within the scope of the disclosure, as well as any composition in which the nucleic acid can be detected by antibody, by nucleic acid probe, or by one or more pairs of primers designed to produce an amplicon consisting of such sequence.

[0034] The nucleic acid sequence exemplified herein and expressed in maize consists only of a Cry1A.105 precursor protein coding sequence, while the sequence expressed in cotton consists of a chloroplast targeted Cry1A.105 precursor protein coding sequence. The expression of Cry1 proteins in plants has proven to be problematic. It is not known whether or if any particular Cry1 protein will be expressed well in any particular plant, and so trial and error experimentation is required. Some Cry1 proteins expressed in corn will result in phytotoxic effects, and so targeting the protein to the chloroplast sometimes alleviates such effects. Similar circumstances are observed with cotton plant expression of Cry1 proteins. The examples herein are not intended to teach that Cry1A.105 expression is only possible in maize if localized to the cytoplasmic space, and similarly, are not intended to teach that Cry1A.105 expression is only possible in cotton if localized to the plastid. The examples are intended to teach that either method of protein localization functions with this protein to achieve morphologically normal plants that exhibit high levels of Cry1A.105 protein expression and accumulation, and that exhibit commercial levels of resistance to a broad range of Lepidopteran insect plant pests in the genus' selected from the groups consisting of Anticarsia, Pseudoplusia, Rachiplusia, Helicoverpa, Heliothis, Spodoptera, Epinotia, and Armigera. It is believed that any plastid targeting peptide coding sequence would function effectively for directing the precursor Cry1A.105 protein to the plastid/chloroplast.

[0035] Untranslated leader sequences, introns and 3' transcription termination and polyadenylation sequences are known in the art, and the skilled artisan would understand that in certain circumstances, expression can be enhanced or stabilized by incorporating these sequences into the expression cassettes. A number of such sequences are known in the art and are intended to be included within the scope of the present disclosure. Similarly, promoters that function to achieve the regulated expression of a linked sequence are known in the art and are also intended to be included within the scope of the present disclosure. Promoters can be selected for use to drive expression of a linked sequence in any number of combinations of parameters, including but not limited to temporal control of expression, spatial or tissue specific control of expression, and to control the amount of a particular gene product desired to be accumulated within a particular plant cell or tissue.

[0036] The isolated and purified protein comprising an insecticidal fragment of the Cry1A.105 amino acid sequence is also intended to be within the scope of the present invention. Variants are also intended to be within the scope of the invention so long as the amino acid substitution or substitutions effecting the variation are generally conservative with respect to the substituted amino acid(s), and the substitution(s) does not result in a reduction of insecticidal bioactivity or range of species specificity. It is intended that an insecticidal fragment of a Cry1A.105 protein is a segment of the amino acid sequence as set forth in SEQ ID NO:2 from about amino acid position 1 through about amino acid position 650, or from about amino acid position 2 through about amino acid position 612, or from about amino acid position 5 through about amino acid position 610, or from about amino acid position 10 through about amino acid position 600. Alternatively, it is intended that an insecticidal fragment of a Cry1A.105 protein consist of from about 550 to about 650 contiguous amino acids selected from the group consisting of amino acid residues 1 through about 650 as set forth at SEQ ID NO:2. The full length precursor protein, consisting of amino acid residue 1 through about residue 3534, exhibits excellent crystal formation properties and is tolerated well by both monocot and dicot plant species. The precursor protein also exhibits excellent stability when in crystalline form, and also exhibits excellent solubility at alkaline pH, in particular alkaline pH within a range of from about 8.0 to about 12.0, or from about 8.5 to about 11.5, or from about pH 9.0 to about pH 11.0.

[0037] The protein of the present invention can be purified and used alone in an insecticidally effective amount in any number of compositions intended for use as a lepidopteran pest control agent, or can be combined in an insecticidally effective amount with any number of other pesticidal agents that are different from the Cry1A.105 protein. Such other pesticidal agents are intended to include but not to be limited to other Bt Cry or other insecticidal compositions whether or not toxic to a lepidopteran species including chemical insecticides, fungicidal or fungistatic agents, antibiotics, antibacterial agents, bacteriostatic agents, and nematicidal or nematostatic agents. Such pesticidal combinations including a Cry1A.105 along with any number of other pesticidal agents can be produced by a transgenic cell, or formulated using purified or substantially purified pesticidal agents into a pesticide composition in a form consisting of a dust, a granular material, an oil suspension, a water suspension, a mixture of oil and water emulsion, or a wettable powder, and then provided in a an agriculturally acceptable carrier for foliar applications. The compositions can be formulated into a seed treatment as well, either together with a Cry1A.105 in the composition intended for inclusion in the seed treatment, or as a composition applied to a seed that is derived from a trans genic plant transformed to express insecticidally effective amounts of a Cry1A.105, so that the seed treatment composition containing pesticidal agents is provided to a target lepidopteran pest along with cells of a plant grown from the seed that are producing pesticidally effective amounts of a Cry1A.105 protein. A combination of insecticidal proteins the each are toxic to the same insect species and yet manifest their toxicity effects through different modes of action would be a particularly useful combination of pesticidal agents for controlling lepidopteran species or delaying the onset of resistance to any single pesticidal agent otherwise effective against a particular lepidopteran species. An exemplary combination of such proteins would be a Cry1A.105 protein of the present invention, i.e., a first insecticidal protein, coupled with at least a second insecticidal protein different from the first. Such different insecticidal proteins include but are not limited to other lepidopteran Bt. crystalline proteins (other Cry1's, Cry2's, Cry5's, Cry9's), VIP proteins, lepidopteran insecticidal proteins referred to as TIC proteins, and insecticidal proteins produced by Xenorhabdus and Photorhabdus species of bacteria. Providing in the diet of an insect pest a combination of one or more insecticidal proteins along with an agent designed for achieving dsRNA mediated gene suppression of one or more genes essential for insect survival is a particularly useful combination of pesticidal agents for controlling lepidopteran species or delaying the onset of resistance to any single pesticidal agent otherwise effective against a particular lepidopteran species.

[0038] Plants transformed with the nucleotide sequences of the present invention are provided as another embodiment of the present invention. Methods for stably introducing DNA into plant cells is known in the art, and includes but is not limited to vacuum infiltration, Agrobacterium or Rhizobium mediated transformation, electroporation, and various ballistic methods. DNA introduced into plants is generally targeted for insertion into the nuclear chromosome, although insertion into the chloroplast or plastid DNA can be achieved. DNA introduced into plants is generally linked to or associated with a sequence that provides a means for identifying or selecting the cell or cells that have been stably transformed with the DNA of interest, including but not limited to scoreable markers such as fluorescence or light emitting genes and genes encoding pigments or enzymes that, in the presence of the appropriate substrate, impart a colorimetric feature to the transformed cell or cells, or by including selectable markers that allow a positive selection of transformed cells and tissue, providing a growth advantage to the transformed cells and essentially causing the non-transformed cells or tissue to become static or to die. Such selectable markers include but are not limited to genes encoding basta, bar, methotrexate resistance, neomycin phosphotransferase, glyphosate insensitive EPSPS enzymes, glyphosate oxidoreductase (GOX) enzymes, E. coli phnO or its equivalent, and the like.

[0039] Vectors and other types of sequences designed for maintaining, manipulating, and/or shepherding the exemplified nucleotide sequences while being manipulated in the laboratory or for introduction into a host cell are also included within the scope of the invention, and are intended to include but not be limited to phages, plasmids, bacmids, yacmids, cosmids, and the like.

[0040] Transformed plants are also within the scope of the present invention. Plants transformed to contain a nucleotide sequence encoding at least an insecticidal fragment of a Cry1A.105 protein are specifically enabled by the present disclosure. Both monocot and dicot plants are envisioned to be within the scope of the present invention. Monocots are intended to include but not be limited to corn, wheat, oat, rice, sorghum, milo, buckwheat, rye, grass (fescue, timothy, brome, orchard, St. Augustine, Bermuda, bentgrass), and barley, and dicot plants are intended to include at least alfalfa, apple, apricot, asparagus, bean, berry, blackberry, blueberry, canola, carrot, cauliflower, celery, cherry, chickpea, citrus tree, cotton, cowpea, cranberry, cucumber, cucurbit, egg plant, fruit tree, grape, lemon, lettuce, linseed, melon, mustard, nut bearing tree, okra, orange, pea, peach, peanut, pear, plum, potato, soybeans, squash, strawberry, sugar beet, sunflower, sweet potato, tobacco, tomato, turnip, and vegetable. Produce from these plants as well as seeds and tissues produced from these plants are specifically included within the present invention, so long as the seed, tissue, or produce contains a transgene encoding an insecticidal fragment of a Cry1A.105 protein.

[0041] Methods for detecting, in a biological sample, a Cry1A.105 protein or a nucleotide sequence encoding an insecticidal fragment of a Cry1A.105 protein are provided by the present invention. Cry1A.105 can be used to immunize animals to produce antibodies specific for Cry1A.105 epitopes. Cry1A.105 specific antibodies can be used to detect the presence of Cry1A.105 in a biological sample. Methods for detecting the binding of an antibody to an antigen are known in the art. Detecting the binding of an antibody to a Cry1A.105 epitope in a biological sample is diagnostic for the presence of the protein in the sample.

[0042] Nucleotide sequences encoding a Cry1A.105 insecticidal fragment can be detected as well. Synthetic nucleotide probes can be used to bind to a target sequence, i.e., a nucleotide sequence encoding a Cry1A.105 insecticidal fragment. Methods for detecting the binding of a probe to a target sequence are known in the art. Detecting the binding of a probe to the target Cry1A.105 coding sequence is diagnostic for the presence of the coding sequence in the sample.

[0043] Synthetic nucleotide primers can be used in thermal amplification reactions to produce an amplicon from a biological sample suspected of containing a nucleotide sequence encoding an insecticidal fragment of a Cry1A.105 protein. The presence of an amplicon produced in such a thermal amplification reaction is diagnostic for the presence of the nucleotide sequence in the sample. Particularly useful sequences as probes which are diagnostic for detecting the presence of the Cry1A.105 coding sequences of the present invention in a biological sample are sequences that correspond to or are perfectly complementary to (1) nucleotide position 1401-1420 as set forth at SEQ ID NO:1 or SEQ ID NO:3, or (2) nucleotide position 1821-1840 as set forth at SEQ ID NO:1 or SEQ ID NO:3. These sequences correspond to (1) the 20 nucleotides spanning the sequence encoding the junction between Domain II and Domain III of the segments of different insecticidal proteins used for constructing the insecticidal portion of the proteins of the present invention, and (2) the 20 nucleotides spanning the sequence encoding the junction between Domain III and the protoxin coding segment of the different protein coding segments used for constructing the coding sequence of the pre-pro-toxin Cry1Ab.105 protein. Nucleotide sequences that are, or are complementary to, either of these segments of DNA (1401-1420 or 1821-1840) can be used as probes for detecting the presence of these coding sequences in biological samples. The detecting of such binding is diagnostic for the presence of such coding sequences in a biological sample. Other sequences as will be recognized by the skilled artisan that flank either side of these segments of DNA can be used as primers for amplifying various sized amplicon segments from such biological samples, and such amplicons are diagnostic for the presence of such coding sequences in the sample. For example, a first primer sequence corresponding to the nucleotide sequence set forth at SEQ ID NO:1 from position 1201-1220 could be used as a forward primer in a thermal amplification reaction with a second primer sequence corresponding to the reverse complement of the nucleotide sequence as set forth at SEQ ID NO:1 from position 1581-1600. Such primers when used together in a thermal amplification reaction with a biological sample containing SEQ ID NO:1 would result in the synthesis of an amplicon corresponding to SEQ ID NO:1 from nucleotide position 1201 through 1600, i.e., a 400 nucleotide amplicon, which would contain the 20 nucleotide segment from nucleotide position 1401-1420 as set forth in SEQ ID NO:1, and would therefore be diagnostic for the presence of the Cry1A.105 coding sequence in such sample.

[0044] A kit for detecting the presence of a Cry1A.105 or detecting the presence of a nucleotide sequence encoding a Cry1A.105 in a sample is provided. The kit is provided along with all reagents and control samples necessary for carrying out a method for detecting the intended agent, as well as instructions for use.

[0045] The following examples describe preferred embodiments of the invention. Other embodiments within the scope of the claims will be apparent to one skilled in the art from consideration of the specification or practice of the invention as disclosed herein. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit of the invention being indicated by the claims which follow the examples.

EXAMPLES

Example 1

[0046] This example illustrates synthetic nucleotide sequences encoding an insecticidal Cry1A.105 protein.

[0047] A nucleotide sequence as set forth at SEQ ID NO:1 encoding a Cry1A.105 insecticidal protein was constructed for use in dicotyledonous plants. The amino acid sequence translation is set forth at SEQ ID NO:2. The toxin encoding segment consists of nucleotides from about position 1 through about position 1830, more or less.

[0048] A nucleotide sequence as set forth at SEQ ID NO:3 encoding a Cry1A.105 amino acid sequence was constructed for expression in monocotyledonous plants. The amino acid sequence translation is set forth at SEQ ID NO:4. The toxin encoding segment consists of nucleotide from about position 1 through about position 1830, more or less.

[0049] The nucleotide sequences as set forth at SEQ ID NO:1 and SEQ ID NO:3 are substantial equivalents of each other. SEQ ID NO:1 and SEQ ID NO:3 exhibit an overall identity of about 94.3%. The two coding sequences are identical from about nucleotide position 1330 through the nucleotide position 3534. The toxin encoding portion of each sequence consists of from about nucleotide position 1 through nucleotide position 1830, and these segments exhibit about 88.9% identity to each other. The substantial differences between the two sequences lie within from about nucleotide position 1 through about nucleotide position 1329, or about the first two thirds of the segment encoding the toxin portion of the Cry1A.105 protein. The two sequences exhibit about 84.7% identity throughout this segment.

[0050] An E. coli strain (TOP10, Invitrogen, Inc.) transformed with a plasmid designated as pMON70522 containing a beta-lactamase selectable marker and a sequence as set forth at SEQ ID NO:3 encoding a Cry1A.105 was deposited on Aug. 31, 2005, with the Agriculture Research Culture Collection (NRRL) International Depository Authority at 1815 North University Street, in Peoria, Ill. 61604 U.S.A., according to the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purpose of Patent Procedures and was designated as NRRL B-30873.

Example 2

[0051] This example illustrates transgenic cotton plants expressing a Cry1A.105 protein.

[0052] Delta and Pineland DP50 cotton seeds were surface sterilized and germinated overnight. Meristem explants were isolated and the primary leaves were removed by micro dissection. Dissected explants were placed in a targeting medium such that the meristems were oriented perpendicular to the direction of the particle delivery. The transformation vector, pMON47740, comprises an expression cassette having a nucleotide sequence set forth in SEQ ID NO:9. A KpnI fragment containing a GUS marker gene under the control of an e35S promoter and a chloroplast targeted Cry1A.105 coding sequence under the control of an eFMV promoter was excised from this plasmid and isolated by HPLC and used for gun transformation of the cotton meristem explants. Purified DNA containing both the Cry1A.105 expression cassette and the GUS marker was precipitated onto microscopic gold beads and coated in a thin layer onto a Mylar sheet. The DNA was accelerated into the meristem tissue by electric discharge particle delivery under a partial vacuum. Following bombardment, explants were de-targeted onto hormone-free media without a selective agent. Leaf tissues from regenerated plantlets were sampled and assayed for expression of the GUS marker. Transgenic plants exhibiting a high level of GUS expression were sent to the greenhouse for further screens. These plants were again tested for expression of GUS and negative portions of the plants were pruned off. This cycle of sampling and pruning of GUS-negative tissues was repeated until all sectors of from each plant were positive for the GUS marker. The plants were then maintained under standard greenhouse conditions until seed harvest.

[0053] Tissues obtained from F1 GUS positive transgenic cotton plants were tested in bioassays for insecticidal activity against cotton bollworm (CBW) and fall armyworm (FAW). Previously generated isogenic cotton plants expressing insecticidal levels of Cry1Ac or a combination of Cry1Ac and Cry2Ab were used as positive controls and a non-transgenic isoline was used as the negative control.

[0054] CBW square assays were used as one means for determining insecticidal activity of the transgenic cotton plants. (Adamczyck et al., (2001) J. Econ. Entomol. 94:284-290; Kranthi et al (2005) Current Science 89:291-298). Squares of leaf tissue (match head size or larger) were collected and placed individually in assay wells. Each square was infested with a single third-instar CBW larva. The number of surviving insects was recorded five days after infestation.

[0055] CBW boll assays were also used to determine the insecticidal activity of boll tissue collected from the transgenic plants. 8 hard green bolls (post bloom) from each event were collected and placed in individual cups and infested with third instar CBW larvae. The number of surviving insects was recorded five days after infestation.

[0056] Leaf assays were conducted to determine the insecticidal activity of transgenic leaf tissue against FAW. New leaves were taken from terminals of cotton plants. 2 leaf punches, each about 3/4'' in diameter, were collected and placed in each of 16 individual assay wells. Each well was infested with a single second or third instar FAW larva. The number of surviving insects was recorded five days after infestation.

[0057] Bioassay results are shown in Table 1. The results show that transgenic cotton events expressing Cry1A.105 exhibited greater insecticidal activity than transgenic events expressing either Cry1Ac or a combination of Cry1Ac and Cry2Ab against both FAW and CBW.

TABLE-US-00001 TABLE 1 Bioassay results of FAW and CBW using the transgenic cotton plant tissue. FAW CBW CBW (% survival) (% survival) (% survival) Plant (leaf tissue) (Square tissue) (Boll tissue) Cry1Ac/ 74.5 32.0 35.8 Cry2Ab Cry1Ac 92.7 35.5 35.8 Isoline 99.6 96.8 54 17238 10.9 9.4 25 17567 0 12.5 12.5 17774 1.6 1.2 0 17875 3.1 4.2 0 18026 1.6 18.8 12.5 18122 7.8 22.9 0

[0058] Tobacco budworm and corn earworms were also tested in similar bioassays. In each case, the Cry1A.105 plants exhibited insecticidal activity against these pests as well.

Example 3

[0059] This example illustrates transgenic corn plants expressing a Cry1A.105 protein. Transgenic corn plants were regenerated from cells transformed with the vector pMON40232. pMON40232 contains an expression cassette having a nucleotide sequence as set forth in SEQ ID NO:7 that contains, in operable linkage, an enhanced CAMV 35S promoter, a wheat CAB leader sequence, a rice actin 1 intron, a Cry1A.105 coding sequence and a wheat hsp17 gene 3' transcription termination and polyadenylation sequence. A nucleotide sequence encoding an Arabidopsis thaliana EPSPS chloroplast targeting sequence (At.EPSES-CTP2) is positioned upstream of and in frame with the Cry1A.105 coding sequence. pMON40232 contains a recombinant gene encoding an EPSPS that is insensitive to the herbicide glyphosate, for use in selection of transgenic events. Transgenic events arising from tissue transformed with pMON40232 were designated as LAJ 105. Transgenic events were screened for the absence of any vector backbone, for the presence of a single simple inserted sequence, and for the intactness of the expression cassette containing the nucleotide sequence encoding the Cry1A.105 protein.

[0060] Bioassays were conducted with events that met the limitations of the event screen. LAJ105 transgenic corn plants were compared in the bioassay to an isogenic LH198 negative control and a positive control MON810 variety expressing the insecticidal portion of a Cry1Ab protein. Five leaf disks, each about one centimeter in diameter, were obtained from each of 10 individual Cry1A.105 transgenic events and from the controls. Leaf disks were placed on agar filled wells to keep the plant material turgid. Discs were then subjected to feeding by FAW, black cutworm (BCW), European corn borer (ECB), corn ear worm (CEW), and Southwestern corn borer (SWCB) neonate larvae. A single neonate FAW larvae, a single CEW larvae, two neonate BCW, two neonate SWCB larvae, or four neonate ECB larvae were applied to each well. Feeding damage was evaluated after four days, using a leaf damage rating (LDR) scale from 0-11, 0 indicating no visible feeding damage, 11 indicating at least 50% of the disc was eaten, and each point on the scale between 0 and 11 indicating a 5% increase in observed feeding damage to the leaf disc under observation.

[0061] Bioassay results indicated that events expressing Cry1A.105 protein exhibited greater insecticidal activity toward FAW, ECB and CEW than the LDR's exhibited by the Cry1Ab control against the same pest larvae. LDR's for these three pests on the Cry1A.105 events was less than 1 while the Cry1Ab control exhibited LDR's ranging from about 8 to about 10. The LDR was consistently between 1 and 2 both for the Cry1A.105 events and for the Cry1Ab control when tested for activity against SWCB, indicating that the Cry1A.105 protein was no more toxic to SWCB than was Cry1Ab. The results of this bioassay supported previous results that indicated that Cry1Ab is ineffective in controlling BCW. The Cry1A.105 events were no more effective against BCW than was the Cry1Ab control. Thus, at the levels of expression of the Cry1A.105 protein in planta, these plants would be effective in controlling other lepidopteran genus plant pests including but not limited to those in the genus Anticarsia, Pseudoplusia, Rachiplusia, Heliothis, Helicoverpa, Spodoptera, Epinotia, and Armigera.

Sequence CWU 1

1

813534DNAartificialsynthetic nucleotide sequence encoding Cry1A.105 amino acid sequence 1atg gac aac aac cca aac atc aac gaa tgc att cca tac aac tgc ttg 48Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu 1 5 10 15 agt aac cca gaa gtt gaa gta ctt ggt gga gaa cgc att gaa acc ggt 96Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly 20 25 30 tac act ccc atc gac atc tcc ttg tcc ttg aca cag ttt ctg ctc agc 144Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser 35 40 45 gag ttc gtg cca ggt gct ggg ttc gtt ctc gga cta gtt gac atc atc 192Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile 50 55 60 tgg ggt atc ttt ggt cca tct caa tgg gat gca ttc ctg gtg caa att 240Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile 65 70 75 80 gag cag ttg atc aac cag agg atc gaa gag ttc gcc agg aac cag gcc 288Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala 85 90 95 atc tct agg ttg gaa gga ttg agc aat ctc tac caa atc tat gca gag 336Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu 100 105 110 agc ttc aga gag tgg gaa gcc gat cct act aac cca gct ctc cgc gag 384Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu 115 120 125 gaa atg cgt att caa ttc aac gac atg aac agc gcc ttg acc aca gct 432Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala 130 135 140 atc cca ttg ttc gca gtc cag aac tac caa gtt cct ctc ttg tcc gtg 480Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val 145 150 155 160 tac gtt caa gca gct aat ctt cac ctc agc gtg ctt cga gac gtt agc 528Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser 165 170 175 gtg ttt ggg caa agg tgg gga ttc gat gct gca acc atc aat agc cgt 576Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg 180 185 190 tac aac gac ctt act agg ctg att gga aac tac acc gac cac gct gtt 624Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val 195 200 205 cgt tgg tac aac act ggc ttg gag cgt gtc tgg ggt cct gat tct aga 672Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg 210 215 220 gat tgg att aga tac aac cag ttc agg aga gaa ttg acc ctc aca gtt 720Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val 225 230 235 240 ttg gac att gtg tct ctc ttc ccg aac tat gac tcc aga acc tac cct 768Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro 245 250 255 atc cgt aca gtg tcc caa ctt acc aga gaa atc tat act aac cca gtt 816Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val 260 265 270 ctt gag aac ttc gac ggt agc ttc cgt ggt tct gcc caa ggt atc gaa 864Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu 275 280 285 ggc tcc atc agg agc cca cac ttg atg gac atc ttg aac agc ata act 912Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr 290 295 300 atc tac acc gat gct cac aga gga gag tat tac tgg tct gga cac cag 960Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln 305 310 315 320 atc atg gcc tct cca gtt gga ttc agc ggg ccc gag ttt acc ttt cct 1008Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro 325 330 335 ctc tat gga act atg gga aac gcc gct cca caa caa cgt atc gtt gct 1056Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala 340 345 350 caa cta ggt cag ggt gtc tac aga acc ttg tct tcc acc ttg tac aga 1104Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg 355 360 365 aga ccc ttc aat atc ggt atc aac aac cag caa ctt tcc gtt ctt gac 1152Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp 370 375 380 gga aca gag ttc gcc tat gga acc tct tct aac ttg cca tcc gct gtt 1200Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val 385 390 395 400 tac aga aag agc gga acc gtt gat tcc ttg gac gaa atc cca cca cag 1248Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln 405 410 415 aac aac aat gtg cca ccc agg caa gga ttc tcc cac agg ttg agc cac 1296Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His 420 425 430 gtg tcc atg ttc cgt tcc gga ttc agc aac agt tcc gtg agc atc atc 1344Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile 435 440 445 aga gct cct atg ttc tct tgg ata cac cgt agt gct gag ttc aac aac 1392Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn 450 455 460 atc att gca tcc gac agc att act caa ata ccc ttg gtg aaa gca cat 1440Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His 465 470 475 480 aca ctt cag tca ggt act act gtt gtc aga ggt cca ggg ttt aca gga 1488Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly 485 490 495 gga gac att ctt cgt cgc aca agt gga gga ccc ttt gct tac act att 1536Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile 500 505 510 gtt aac atc aat ggc caa ttg ccc caa agg tat cgt gca aga atc cgc 1584Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg 515 520 525 tat gcc tct act aca aat ctc agg atc tac gtg act gtt gca ggt gaa 1632Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu 530 535 540 agg atc ttt gct ggt cag ttc aac aag act atg gat acc ggt gac cct 1680Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro 545 550 555 560 ttg aca ttc caa tct ttt agc tac gca act atc aac aca gct ttt aca 1728Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr 565 570 575 ttc cca atg agc cag agt agc ttc aca gta ggt gct gac act ttc agc 1776Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser 580 585 590 tca ggg aat gaa gtt tac atc gac agg ttt gaa ttg att cca gtt act 1824Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr 595 600 605 gca acc ctc gag gct gag tac aac ctt gag aga gcc cag aag gct gtg 1872Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val 610 615 620 aac gcc ctc ttt acc tcc acc aat cag ctt ggc ttg aaa act aac gtt 1920Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val 625 630 635 640 act gac tat cac att gac caa gtg tcc aac ttg gtc acc tac ctt agc 1968Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser 645 650 655 gat gag ttc tgc ctc gac gag aag cgt gaa ctc tcc gag aaa gtt aaa 2016Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys 660 665 670 cac gcc aag cgt ctc agc gac gag agg aat ctc ttg caa gac tcc aac 2064His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn 675 680 685 ttc aaa gac atc aac agg cag cca gaa cgt ggt tgg ggt gga agc acc 2112Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr 690 695 700 ggg atc acc atc caa gga ggc gac gat gtg ttc aag gag aac tac gtc 2160Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val 705 710 715 720 acc ctc tcc gga act ttc gac gag tgc tac cct acc tac ttg tac cag 2208Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln 725 730 735 aag atc gat gag tcc aaa ctc aaa gcc ttc acc agg tat caa ctt aga 2256Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg 740 745 750 ggc tac atc gaa gac agc caa gac ctt gaa atc tac tcg atc agg tac 2304Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr 755 760 765 aat gcc aag cac gag acc gtg aat gtc cca ggt act ggt tcc ctc tgg 2352Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp 770 775 780 cca ctt tct gcc caa tct ccc att ggg aag tgt gga gag cct aac aga 2400Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg 785 790 795 800 tgc gct cca cac ctt gag tgg aat cct gac ttg gac tgc tcc tgc agg 2448Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg 805 810 815 gat ggc gag aag tgt gcc cac cat tct cat cac ttc tcc ttg gac atc 2496Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile 820 825 830 gat gtg gga tgt act gac ctg aat gag gac ctc gga gtc tgg gtc atc 2544Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile 835 840 845 ttc aag atc aag acc caa gac gga cac gca aga ctt ggc aac ctt gag 2592Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu 850 855 860 ttt ctc gaa gag aaa cca ttg gtc ggt gaa gct ctc gct cgt gtg aag 2640Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys 865 870 875 880 aga gca gag aag aag tgg agg gac aaa cgt gag aaa ctc gaa tgg gaa 2688Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu 885 890 895 act aac atc gtt tac aag gag gcc aaa gag tcc gtg gat gct ttg ttc 2736Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe 900 905 910 gtg aac tcc caa tat gat cag ttg caa gcc gac acc aac atc gcc atg 2784Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met 915 920 925 atc cac gcc gca gac aaa cgt gtg cac agc att cgt gag gct tac ttg 2832Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu 930 935 940 cct gag ttg tcc gtg atc cct ggt gtg aac gct gcc atc ttc gag gaa 2880Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu 945 950 955 960 ctt gag gga cgt atc ttt acc gca ttc tcc ttg tac gat gcc aga aac 2928Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn 965 970 975 gtc atc aag aac ggt gac ttc aac aat ggc ctc agc tgc tgg aat gtg 2976Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val 980 985 990 aaa ggt cat gtg gac gtg gag gaa cag aac aat cag cgt tcc gtc ctg 3024Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu 995 1000 1005 gtt gtg cct gag tgg gaa gct gaa gtg tcc caa gag gtt aga gtc 3069Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val 1010 1015 1020 tgt cca ggt aga ggc tac att ctc cgt gtg acc gct tac aag gag 3114Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu 1025 1030 1035 gga tac ggt gag ggt tgc gtg acc atc cac gag atc gag aac aac 3159Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn 1040 1045 1050 acc gac gag ctt aag ttc tcc aac tgc gtc gag gaa gaa atc tat 3204Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr 1055 1060 1065 ccc aac aac acc gtt act tgc aac gac tac act gtg aat cag gaa 3249Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu 1070 1075 1080 gag tac gga ggt gcc tac act agc cgt aac aga ggt tac aac gaa 3294Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu 1085 1090 1095 gct cct tcc gtt cct gct gac tat gcc tcc gtg tac gag gag aaa 3339Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys 1100 1105 1110 tcc tac aca gat ggc aga cgt gag aac cct tgc gag ttc aac aga 3384Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg 1115 1120 1125 ggt tac agg gac tac aca cca ctt cca gtt ggc tat gtt acc aag 3429Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys 1130 1135 1140 gag ctt gag tac ttt cct gag acc gac aaa gtg tgg atc gag atc 3474Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile 1145 1150 1155 ggt gaa acc gag gga acc ttc atc gtg gac agc gtg gag ctt ctc 3519Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu 1160 1165 1170 ttg atg gag gaa taa 3534Leu Met Glu Glu 1175 21177PRTartificialSynthetic Construct 2Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu 1 5 10 15 Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly 20 25 30 Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser 35 40 45 Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile 50 55 60 Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile 65 70 75 80 Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala 85 90 95 Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu 100 105 110 Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu 115 120 125 Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala 130 135 140 Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val 145 150 155 160 Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser 165 170 175 Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg 180 185 190 Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val 195 200 205 Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg 210 215 220

Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val 225 230 235 240 Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro 245 250 255 Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val 260 265 270 Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu 275 280 285 Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr 290 295 300 Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln 305 310 315 320 Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro 325 330 335 Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala 340 345 350 Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg 355 360 365 Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp 370 375 380 Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val 385 390 395 400 Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln 405 410 415 Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His 420 425 430 Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile 435 440 445 Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn 450 455 460 Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His 465 470 475 480 Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly 485 490 495 Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile 500 505 510 Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg 515 520 525 Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu 530 535 540 Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro 545 550 555 560 Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr 565 570 575 Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser 580 585 590 Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr 595 600 605 Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val 610 615 620 Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val 625 630 635 640 Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser 645 650 655 Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys 660 665 670 His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn 675 680 685 Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr 690 695 700 Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val 705 710 715 720 Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln 725 730 735 Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg 740 745 750 Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr 755 760 765 Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp 770 775 780 Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg 785 790 795 800 Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg 805 810 815 Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile 820 825 830 Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile 835 840 845 Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu 850 855 860 Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys 865 870 875 880 Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu 885 890 895 Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe 900 905 910 Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met 915 920 925 Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu 930 935 940 Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu 945 950 955 960 Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn 965 970 975 Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val 980 985 990 Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu 995 1000 1005 Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val 1010 1015 1020 Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu 1025 1030 1035 Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn 1040 1045 1050 Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr 1055 1060 1065 Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu 1070 1075 1080 Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu 1085 1090 1095 Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys 1100 1105 1110 Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg 1115 1120 1125 Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys 1130 1135 1140 Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile 1145 1150 1155 Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu 1160 1165 1170 Leu Met Glu Glu 1175 33534DNAartificialsynthetic nucleotide sequence encoding Cry1A.105 amino acid sequence 3atg gac aac aac cca aac atc aac gag tgc atc ccg tac aac tgc ctc 48Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu 1 5 10 15 agc aac cct gag gtc gag gtg ctc ggc ggt gag cgc atc gag acc ggt 96Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly 20 25 30 tac acc ccc atc gac atc tcc ctc tcc ctc acg cag ttc ctg ctc agc 144Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser 35 40 45 gag ttc gtg cca ggc gct ggc ttc gtc ctg ggc ctc gtg gac atc atc 192Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile 50 55 60 tgg ggc atc ttt ggc ccc tcc cag tgg gac gcc ttc ctg gtg caa atc 240Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile 65 70 75 80 gag cag ctc atc aac cag agg atc gag gag ttc gcc agg aac cag gcc 288Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala 85 90 95 atc agc cgc ctg gag ggc ctc agc aac ctc tac caa atc tac gct gag 336Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu 100 105 110 agc ttc cgc gag tgg gag gcc gac ccc act aac cca gct ctc cgc gag 384Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu 115 120 125 gag atg cgc atc cag ttc aac gac atg aac agc gcc ctg acc acc gcc 432Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala 130 135 140 atc cca ctc ttc gcc gtc cag aac tac caa gtc ccg ctc ctg tcc gtg 480Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val 145 150 155 160 tac gtc cag gcc gcc aac ctg cac ctc agc gtg ctg agg gac gtc agc 528Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser 165 170 175 gtg ttt ggc cag agg tgg ggc ttc gac gcc gcc acc atc aac agc cgc 576Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg 180 185 190 tac aac gac ctc acc agg ctg atc ggc aac tac acc gac cac gct gtc 624Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val 195 200 205 cgc tgg tac aac act ggc ctg gag cgc gtc tgg ggc cct gat tct aga 672Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg 210 215 220 gac tgg att cgc tac aac cag ttc agg cgc gag ctg acc ctc acc gtc 720Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val 225 230 235 240 ctg gac att gtg tcc ctc ttc ccg aac tac gac tcc cgc acc tac ccg 768Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro 245 250 255 atc cgc acc gtg tcc caa ctg acc cgc gaa atc tac acc aac ccc gtc 816Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val 260 265 270 ctg gag aac ttc gac ggt agc ttc agg ggc agc gcc cag ggc atc gag 864Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu 275 280 285 ggc tcc atc agg agc cca cac ctg atg gac atc ctc aac agc atc act 912Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr 290 295 300 atc tac acc gat gcc cac cgc ggc gag tac tac tgg tcc ggc cac cag 960Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln 305 310 315 320 atc atg gcc tcc ccg gtc ggc ttc agc ggc ccc gag ttt acc ttt cct 1008Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro 325 330 335 ctc tac ggc acg atg ggc aac gcc gct cca caa caa cgc atc gtc gct 1056Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala 340 345 350 cag ctg ggc cag ggc gtc tac cgc acc ctg agc tcc acc ctg tac cgc 1104Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg 355 360 365 agg ccc ttc aac atc ggt atc aac aac cag cag ctg tcc gtc ctg gat 1152Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp 370 375 380 ggc act gag ttc gcc tac ggc acc tcc tcc aac ctg ccc tcc gct gtc 1200Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val 385 390 395 400 tac cgc aag agc ggc acg gtg gat tcc ctg gac gag atc cca cca cag 1248Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln 405 410 415 aac aac aat gtg ccc ccc agg cag ggt ttt tcc cac agg ctc agc cac 1296Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His 420 425 430 gtg tcc atg ttc cgc tcc ggc ttc agc aac tcg tcc gtg agc atc atc 1344Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile 435 440 445 aga gct cct atg ttc tct tgg ata cac cgt agt gct gag ttc aac aac 1392Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn 450 455 460 atc att gca tcc gac agc att act caa ata ccc ttg gtg aaa gca cat 1440Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His 465 470 475 480 aca ctt cag tca ggt act act gtt gtc aga ggt cca ggg ttt aca gga 1488Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly 485 490 495 gga gac att ctt cgt cgc aca agt gga gga ccc ttt gct tac act att 1536Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile 500 505 510 gtt aac atc aat ggc caa ttg ccc caa agg tat cgt gca aga atc cgc 1584Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg 515 520 525 tat gcc tct act aca aat ctc agg atc tac gtg act gtt gca ggt gaa 1632Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu 530 535 540 agg atc ttt gct ggt cag ttc aac aag act atg gat acc ggt gac cct 1680Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro 545 550 555 560 ttg aca ttc caa tct ttt agc tac gca act atc aac aca gct ttt aca 1728Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr 565 570 575 ttc cca atg agc cag agt agc ttc aca gta ggt gct gac act ttc agc 1776Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser 580 585 590 tca ggg aat gaa gtt tac atc gac agg ttt gaa ttg att cca gtt act 1824Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr 595 600 605 gca acc ctc gag gct gag tac aac ctt gag aga gcc cag aag gct gtg 1872Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val 610 615 620 aac gcc ctc ttt acc tcc acc aat cag ctt ggc ttg aaa act aac gtt 1920Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val 625 630 635 640 act gac tat cac att gac caa gtg tcc aac ttg gtc acc tac ctt agc 1968Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser 645 650 655 gat gag ttc tgc ctc gac gag aag cgt gaa ctc tcc gag aaa gtt aaa 2016Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys 660 665 670 cac gcc aag cgt ctc agc gac gag agg aat ctc ttg caa gac tcc aac 2064His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn 675 680 685 ttc aaa gac atc aac agg cag cca gaa cgt ggt tgg ggt gga agc acc 2112Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr 690 695 700 ggg atc acc atc caa gga ggc gac gat gtg ttc aag gag aac tac gtc 2160Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val 705 710 715 720 acc ctc tcc gga act ttc gac gag tgc tac cct acc tac ttg tac cag 2208Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln 725 730 735 aag atc gat gag tcc aaa ctc aaa gcc ttc acc agg tat caa ctt aga 2256Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg 740 745 750 ggc tac atc gaa gac agc caa gac ctt gaa atc tac tcg atc agg tac 2304Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr 755 760 765 aat gcc aag cac gag acc gtg aat gtc cca ggt act ggt tcc ctc tgg

2352Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp 770 775 780 cca ctt tct gcc caa tct ccc att ggg aag tgt gga gag cct aac aga 2400Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg 785 790 795 800 tgc gct cca cac ctt gag tgg aat cct gac ttg gac tgc tcc tgc agg 2448Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg 805 810 815 gat ggc gag aag tgt gcc cac cat tct cat cac ttc tcc ttg gac atc 2496Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile 820 825 830 gat gtg gga tgt act gac ctg aat gag gac ctc gga gtc tgg gtc atc 2544Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile 835 840 845 ttc aag atc aag acc caa gac gga cac gca aga ctt ggc aac ctt gag 2592Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu 850 855 860 ttt ctc gaa gag aaa cca ttg gtc ggt gaa gct ctc gct cgt gtg aag 2640Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys 865 870 875 880 aga gca gag aag aag tgg agg gac aaa cgt gag aaa ctc gaa tgg gaa 2688Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu 885 890 895 act aac atc gtt tac aag gag gcc aaa gag tcc gtg gat gct ttg ttc 2736Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe 900 905 910 gtg aac tcc caa tat gat cag ttg caa gcc gac acc aac atc gcc atg 2784Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met 915 920 925 atc cac gcc gca gac aaa cgt gtg cac agc att cgt gag gct tac ttg 2832Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu 930 935 940 cct gag ttg tcc gtg atc cct ggt gtg aac gct gcc atc ttc gag gaa 2880Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu 945 950 955 960 ctt gag gga cgt atc ttt acc gca ttc tcc ttg tac gat gcc aga aac 2928Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn 965 970 975 gtc atc aag aac ggt gac ttc aac aat ggc ctc agc tgc tgg aat gtg 2976Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val 980 985 990 aaa ggt cat gtg gac gtg gag gaa cag aac aat cag cgt tcc gtc ctg 3024Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu 995 1000 1005 gtt gtg cct gag tgg gaa gct gaa gtg tcc caa gag gtt aga gtc 3069Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val 1010 1015 1020 tgt cca ggt aga ggc tac att ctc cgt gtg acc gct tac aag gag 3114Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu 1025 1030 1035 gga tac ggt gag ggt tgc gtg acc atc cac gag atc gag aac aac 3159Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn 1040 1045 1050 acc gac gag ctt aag ttc tcc aac tgc gtc gag gaa gaa atc tat 3204Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr 1055 1060 1065 ccc aac aac acc gtt act tgc aac gac tac act gtg aat cag gaa 3249Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu 1070 1075 1080 gag tac gga ggt gcc tac act agc cgt aac aga ggt tac aac gaa 3294Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu 1085 1090 1095 gct cct tcc gtt cct gct gac tat gcc tcc gtg tac gag gag aaa 3339Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys 1100 1105 1110 tcc tac aca gat ggc aga cgt gag aac cct tgc gag ttc aac aga 3384Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg 1115 1120 1125 ggt tac agg gac tac aca cca ctt cca gtt ggc tat gtt acc aag 3429Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys 1130 1135 1140 gag ctt gag tac ttt cct gag acc gac aaa gtg tgg atc gag atc 3474Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile 1145 1150 1155 ggt gaa acc gag gga acc ttc atc gtg gac agc gtg gag ctt ctc 3519Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu 1160 1165 1170 ttg atg gag gaa taa 3534Leu Met Glu Glu 1175 41177PRTartificialSynthetic Construct 4Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu 1 5 10 15 Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly 20 25 30 Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser 35 40 45 Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile 50 55 60 Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile 65 70 75 80 Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala 85 90 95 Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu 100 105 110 Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu 115 120 125 Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala 130 135 140 Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val 145 150 155 160 Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser 165 170 175 Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg 180 185 190 Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val 195 200 205 Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg 210 215 220 Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val 225 230 235 240 Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro 245 250 255 Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val 260 265 270 Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu 275 280 285 Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr 290 295 300 Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln 305 310 315 320 Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro 325 330 335 Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala 340 345 350 Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg 355 360 365 Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp 370 375 380 Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val 385 390 395 400 Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln 405 410 415 Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His 420 425 430 Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile 435 440 445 Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn 450 455 460 Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His 465 470 475 480 Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly 485 490 495 Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile 500 505 510 Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg 515 520 525 Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu 530 535 540 Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro 545 550 555 560 Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr 565 570 575 Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser 580 585 590 Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr 595 600 605 Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val 610 615 620 Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val 625 630 635 640 Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser 645 650 655 Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys 660 665 670 His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn 675 680 685 Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr 690 695 700 Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val 705 710 715 720 Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln 725 730 735 Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg 740 745 750 Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr 755 760 765 Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp 770 775 780 Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg 785 790 795 800 Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg 805 810 815 Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile 820 825 830 Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile 835 840 845 Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu 850 855 860 Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys 865 870 875 880 Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu 885 890 895 Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe 900 905 910 Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met 915 920 925 Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu 930 935 940 Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu 945 950 955 960 Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn 965 970 975 Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val 980 985 990 Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu 995 1000 1005 Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val 1010 1015 1020 Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu 1025 1030 1035 Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn 1040 1045 1050 Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr 1055 1060 1065 Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu 1070 1075 1080 Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu 1085 1090 1095 Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys 1100 1105 1110 Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg 1115 1120 1125 Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys 1130 1135 1140 Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile 1145 1150 1155 Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu 1160 1165 1170 Leu Met Glu Glu 1175 55480DNAartificialexpression cassette encoding Cry1A.105 amino acid sequence 5aattctcagt ccaaagcctc aacaaggtca gggtacagag tctccaaacc attagccaaa 60agctacagga gatcaatgaa gaatcttcaa tcaaagtaaa ctactgttcc agcacatgca 120tcatggtcag taagtttcag aaaaagacat ccaccgaaga cttaaagtta gtgggcatct 180ttgaaagtaa tcttgtcaac atcgagcagc tggcttgtgg ggaccagaca aaaaaggaat 240ggtgcagaat tgttaggcgc acctaccaaa agcatctttg cctttattgc aaagataaag 300cagattcctc tagtacaagt ggggaacaaa ataacgtgga aaagagctgt cctgacagcc 360cactcactaa tgcgtatgac gaacgcagtg acgaccacaa aagaattagc ttgagctcag 420gatttagcag cattccagat tgggttcaat caacaaggta cgagccatat cactttattc 480aaattggtat cgccaaaacc aagaaggaac tcccatcctc aaaggtttgt aaggaagaat 540tctcagtcca aagcctcaac aaggtcaggg tacagagtct ccaaaccatt agccaaaagc 600tacaggagat caatgaagaa tcttcaatca aagtaaacta ctgttccagc acatgcatca 660tggtcagtaa gtttcagaaa aagacatcca ccgaagactt aaagttagtg ggcatctttg 720aaagtaatct tgtcaacatc gagcagctgg cttgtgggga ccagacaaaa aaggaatggt 780gcagaattgt taggcgcacc taccaaaagc atctttgcct ttattgcaaa gataaagcag 840attcctctag tacaagtggg gaacaaaata acgtggaaaa gagctgtcct gacagcccac 900tcactaatgc gtatgacgaa cgcagtgacg accacaaaag aattccctct atataagaag 960gcattcattc ccatttgaag gacacagaaa aatttgctac attgtttcac aaacttcaaa 1020tattattcat ttatttgtca gctttcaaac tctttgtttc ttgtttgttg attgagaata 1080tttaaaacaa tggcttcctc tatgctctct tccgctacta tggttgcctc tccggctcag 1140gccactatgg tcgctccttt caacggactt aagtcctccg ctgccttccc agccacccgc 1200aaggctaaca acgacattac ttccatcaca agcaacggcg gaagagttaa ctgcatgcag 1260gccatg gac aac aac cca aac atc aac gaa tgc att cca tac aac tgc 1308 Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys 1 5 10 ttg agt aac cca gaa gtt gaa gta ctt ggt gga gaa cgc att gaa acc 1356Leu Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr 15 20 25 30 ggt tac act ccc atc gac atc tcc ttg tcc ttg aca cag ttt ctg ctc 1404Gly Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu 35 40 45 agc gag ttc gtg cca ggt gct ggg ttc gtt ctc gga cta gtt gac atc 1452Ser Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile 50 55 60 atc tgg ggt atc ttt ggt cca tct caa tgg gat gca ttc ctg gtg caa 1500Ile Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln 65 70 75 att gag cag ttg atc aac cag agg atc gaa gag ttc gcc agg aac cag 1548Ile Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln 80 85 90 gcc atc tct agg ttg gaa gga ttg agc aat ctc tac caa atc tat gca

1596Ala Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala 95 100 105 110 gag agc ttc aga gag tgg gaa gcc gat cct act aac cca gct ctc cgc 1644Glu Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg 115 120 125 gag gaa atg cgt att caa ttc aac gac atg aac agc gcc ttg acc aca 1692Glu Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr 130 135 140 gct atc cca ttg ttc gca gtc cag aac tac caa gtt cct ctc ttg tcc 1740Ala Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser 145 150 155 gtg tac gtt caa gca gct aat ctt cac ctc agc gtg ctt cga gac gtt 1788Val Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val 160 165 170 agc gtg ttt ggg caa agg tgg gga ttc gat gct gca acc atc aat agc 1836Ser Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser 175 180 185 190 cgt tac aac gac ctt act agg ctg att gga aac tac acc gac cac gct 1884Arg Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala 195 200 205 gtt cgt tgg tac aac act ggc ttg gag cgt gtc tgg ggt cct gat tct 1932Val Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser 210 215 220 aga gat tgg att aga tac aac cag ttc agg aga gaa ttg acc ctc aca 1980Arg Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr 225 230 235 gtt ttg gac att gtg tct ctc ttc ccg aac tat gac tcc aga acc tac 2028Val Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr 240 245 250 cct atc cgt aca gtg tcc caa ctt acc aga gaa atc tat act aac cca 2076Pro Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro 255 260 265 270 gtt ctt gag aac ttc gac ggt agc ttc cgt ggt tct gcc caa ggt atc 2124Val Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile 275 280 285 gaa ggc tcc atc agg agc cca cac ttg atg gac atc ttg aac agc ata 2172Glu Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile 290 295 300 act atc tac acc gat gct cac aga gga gag tat tac tgg tct gga cac 2220Thr Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His 305 310 315 cag atc atg gcc tct cca gtt gga ttc agc ggg ccc gag ttt acc ttt 2268Gln Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe 320 325 330 cct ctc tat gga act atg gga aac gcc gct cca caa caa cgt atc gtt 2316Pro Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val 335 340 345 350 gct caa cta ggt cag ggt gtc tac aga acc ttg tct tcc acc ttg tac 2364Ala Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr 355 360 365 aga aga ccc ttc aat atc ggt atc aac aac cag caa ctt tcc gtt ctt 2412Arg Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu 370 375 380 gac gga aca gag ttc gcc tat gga acc tct tct aac ttg cca tcc gct 2460Asp Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala 385 390 395 gtt tac aga aag agc gga acc gtt gat tcc ttg gac gaa atc cca cca 2508Val Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro 400 405 410 cag aac aac aat gtg cca ccc agg caa gga ttc tcc cac agg ttg agc 2556Gln Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser 415 420 425 430 cac gtg tcc atg ttc cgt tcc gga ttc agc aac agt tcc gtg agc atc 2604His Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile 435 440 445 atc aga gct cct atg ttc tct tgg ata cac cgt agt gct gag ttc aac 2652Ile Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn 450 455 460 aac atc att gca tcc gac agc att act caa ata ccc ttg gtg aaa gca 2700Asn Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala 465 470 475 cat aca ctt cag tca ggt act act gtt gtc aga ggt cca ggg ttt aca 2748His Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr 480 485 490 gga gga gac att ctt cgt cgc aca agt gga gga ccc ttt gct tac act 2796Gly Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr 495 500 505 510 att gtt aac atc aat ggc caa ttg ccc caa agg tat cgt gca aga atc 2844Ile Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile 515 520 525 cgc tat gcc tct act aca aat ctc agg atc tac gtg act gtt gca ggt 2892Arg Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly 530 535 540 gaa agg atc ttt gct ggt cag ttc aac aag act atg gat acc ggt gac 2940Glu Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp 545 550 555 cct ttg aca ttc caa tct ttt agc tac gca act atc aac aca gct ttt 2988Pro Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe 560 565 570 aca ttc cca atg agc cag agt agc ttc aca gta ggt gct gac act ttc 3036Thr Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe 575 580 585 590 agc tca ggg aat gaa gtt tac atc gac agg ttt gaa ttg att cca gtt 3084Ser Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val 595 600 605 act gca acc ctc gag gct gag tac aac ctt gag aga gcc cag aag gct 3132Thr Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala 610 615 620 gtg aac gcc ctc ttt acc tcc acc aat cag ctt ggc ttg aaa act aac 3180Val Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn 625 630 635 gtt act gac tat cac att gac caa gtg tcc aac ttg gtc acc tac ctt 3228Val Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu 640 645 650 agc gat gag ttc tgc ctc gac gag aag cgt gaa ctc tcc gag aaa gtt 3276Ser Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val 655 660 665 670 aaa cac gcc aag cgt ctc agc gac gag agg aat ctc ttg caa gac tcc 3324Lys His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser 675 680 685 aac ttc aaa gac atc aac agg cag cca gaa cgt ggt tgg ggt gga agc 3372Asn Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser 690 695 700 acc ggg atc acc atc caa gga ggc gac gat gtg ttc aag gag aac tac 3420Thr Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr 705 710 715 gtc acc ctc tcc gga act ttc gac gag tgc tac cct acc tac ttg tac 3468Val Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr 720 725 730 cag aag atc gat gag tcc aaa ctc aaa gcc ttc acc agg tat caa ctt 3516Gln Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu 735 740 745 750 aga ggc tac atc gaa gac agc caa gac ctt gaa atc tac tcg atc agg 3564Arg Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg 755 760 765 tac aat gcc aag cac gag acc gtg aat gtc cca ggt act ggt tcc ctc 3612Tyr Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu 770 775 780 tgg cca ctt tct gcc caa tct ccc att ggg aag tgt gga gag cct aac 3660Trp Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn 785 790 795 aga tgc gct cca cac ctt gag tgg aat cct gac ttg gac tgc tcc tgc 3708Arg Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys 800 805 810 agg gat ggc gag aag tgt gcc cac cat tct cat cac ttc tcc ttg gac 3756Arg Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp 815 820 825 830 atc gat gtg gga tgt act gac ctg aat gag gac ctc gga gtc tgg gtc 3804Ile Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val 835 840 845 atc ttc aag atc aag acc caa gac gga cac gca aga ctt ggc aac ctt 3852Ile Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu 850 855 860 gag ttt ctc gaa gag aaa cca ttg gtc ggt gaa gct ctc gct cgt gtg 3900Glu Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val 865 870 875 aag aga gca gag aag aag tgg agg gac aaa cgt gag aaa ctc gaa tgg 3948Lys Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp 880 885 890 gaa act aac atc gtt tac aag gag gcc aaa gag tcc gtg gat gct ttg 3996Glu Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu 895 900 905 910 ttc gtg aac tcc caa tat gat cag ttg caa gcc gac acc aac atc gcc 4044Phe Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala 915 920 925 atg atc cac gcc gca gac aaa cgt gtg cac agc att cgt gag gct tac 4092Met Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr 930 935 940 ttg cct gag ttg tcc gtg atc cct ggt gtg aac gct gcc atc ttc gag 4140Leu Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu 945 950 955 gaa ctt gag gga cgt atc ttt acc gca ttc tcc ttg tac gat gcc aga 4188Glu Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg 960 965 970 aac gtc atc aag aac ggt gac ttc aac aat ggc ctc agc tgc tgg aat 4236Asn Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn 975 980 985 990 gtg aaa ggt cat gtg gac gtg gag gaa cag aac aat cag cgt tcc gtc 4284Val Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val 995 1000 1005 ctg gtt gtg cct gag tgg gaa gct gaa gtg tcc caa gag gtt aga 4329Leu Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg 1010 1015 1020 gtc tgt cca ggt aga ggc tac att ctc cgt gtg acc gct tac aag 4374Val Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys 1025 1030 1035 gag gga tac ggt gag ggt tgc gtg acc atc cac gag atc gag aac 4419Glu Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn 1040 1045 1050 aac acc gac gag ctt aag ttc tcc aac tgc gtc gag gaa gaa atc 4464Asn Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile 1055 1060 1065 tat ccc aac aac acc gtt act tgc aac gac tac act gtg aat cag 4509Tyr Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln 1070 1075 1080 gaa gag tac gga ggt gcc tac act agc cgt aac aga ggt tac aac 4554Glu Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn 1085 1090 1095 gaa gct cct tcc gtt cct gct gac tat gcc tcc gtg tac gag gag 4599Glu Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu 1100 1105 1110 aaa tcc tac aca gat ggc aga cgt gag aac cct tgc gag ttc aac 4644Lys Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn 1115 1120 1125 aga ggt tac agg gac tac aca cca ctt cca gtt ggc tat gtt acc 4689Arg Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr 1130 1135 1140 aag gag ctt gag tac ttt cct gag acc gac aaa gtg tgg atc gag 4734Lys Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu 1145 1150 1155 atc ggt gaa acc gag gga acc ttc atc gtg gac agc gtg gag ctt 4779Ile Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu 1160 1165 1170 ctc ttg atg gag gaa taa tgagatccac gatatcctgc aggaattggc 4827Leu Leu Met Glu Glu 1175 cggccagctt tcgttcgtat catcggtttc gacaacgttc gtcaagttca atgcatcagt 4887ttcattgcgc acacaccaga atcctactga gtttgagtat tatggcattg ggaaaactgt 4947ttttcttgta ccatttgttg tgcttgtaat ttactgtgtt ttttattcgg ttttcgctat 5007cgaactgtga aatggaaatg gatggagaag agttaatgaa tgatatggtc cttttgttca 5067ttctcaaatt aatattattt gttttttctc ttatttgttg tgtgttgaat ttgaaattat 5127aagagatatg caaacatttt gttttgagta aaaatgtgtc aaatcgtggc ctctaatgac 5187cgaagttaat atgaggagta aaacacttgt agttgtacca ttatgcttat tcactaggca 5247acaaatatat tttcagacct agaaaagctg caaatgttac tgaatacaag tatgtcctct 5307tgtgttttag acatttatgg actttccttt atgtaatttt ccagaatcct tgtcagattc 5367taatcattgc tttataatta tagttatact catggatttg tagttgagta tgaaaatatt 5427ttttaatgca ttttatgact tgccaattga ttgacaacat gcatcaatcg acc 548061176PRTartificialSynthetic Construct 6Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu Ser 1 5 10 15 Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly Tyr 20 25 30 Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser Glu 35 40 45 Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile Trp 50 55 60 Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile Glu 65 70 75 80 Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala Ile 85 90 95 Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu Ser 100 105 110 Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu Glu 115 120 125 Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala Ile 130 135 140 Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val Tyr 145 150 155 160 Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser Val 165 170 175 Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg Tyr 180 185 190 Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val Arg 195 200 205 Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg Asp 210 215 220 Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val Leu 225 230 235 240 Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro Ile 245 250 255 Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val Leu 260 265 270 Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu Gly 275 280 285 Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr Ile 290 295 300 Tyr Thr Asp Ala His

Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln Ile 305 310 315 320 Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro Leu 325 330 335 Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala Gln 340 345 350 Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg Arg 355 360 365 Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp Gly 370 375 380 Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val Tyr 385 390 395 400 Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln Asn 405 410 415 Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His Val 420 425 430 Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile Arg 435 440 445 Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn Ile 450 455 460 Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His Thr 465 470 475 480 Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly Gly 485 490 495 Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile Val 500 505 510 Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg Tyr 515 520 525 Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu Arg 530 535 540 Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro Leu 545 550 555 560 Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr Phe 565 570 575 Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser Ser 580 585 590 Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr Ala 595 600 605 Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val Asn 610 615 620 Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val Thr 625 630 635 640 Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser Asp 645 650 655 Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys His 660 665 670 Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn Phe 675 680 685 Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr Gly 690 695 700 Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val Thr 705 710 715 720 Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln Lys 725 730 735 Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg Gly 740 745 750 Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr Asn 755 760 765 Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp Pro 770 775 780 Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg Cys 785 790 795 800 Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg Asp 805 810 815 Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile Asp 820 825 830 Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile Phe 835 840 845 Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu Phe 850 855 860 Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys Arg 865 870 875 880 Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu Thr 885 890 895 Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe Val 900 905 910 Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met Ile 915 920 925 His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu Pro 930 935 940 Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu Leu 945 950 955 960 Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn Val 965 970 975 Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val Lys 980 985 990 Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu Val 995 1000 1005 Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val Cys 1010 1015 1020 Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu Gly 1025 1030 1035 Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn Thr 1040 1045 1050 Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr Pro 1055 1060 1065 Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu Glu 1070 1075 1080 Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu Ala 1085 1090 1095 Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys Ser 1100 1105 1110 Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg Gly 1115 1120 1125 Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys Glu 1130 1135 1140 Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile Gly 1145 1150 1155 Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu Leu 1160 1165 1170 Met Glu Glu 1175 74990DNAartificialexpression cassette encoding Cry1A.105 amino acid sequence 7ggtccgatgt gagacttttc aacaaagggt aatatccgga aacctcctcg gattccattg 60cccagctatc tgtcacttta ttgtgaagat agtggaaaag gaaggtggct cctacaaatg 120ccatcattgc gataaaggaa aggccatcgt tgaagatgcc tctgccgaca gtggtcccaa 180agatggaccc ccacccacga ggagcatcgt ggaaaaagaa gacgttccaa ccacgtcttc 240aaagcaagtg gattgatgtg atggtccgat gtgagacttt tcaacaaagg gtaatatccg 300gaaacctcct cggattccat tgcccagcta tctgtcactt tattgtgaag atagtggaaa 360aggaaggtgg ctcctacaaa tgccatcatt gcgataaagg aaaggccatc gttgaagatg 420cctctgccga cagtggtccc aaagatggac ccccacccac gaggagcatc gtggaaaaag 480aagacgttcc aaccacgtct tcaaagcaag tggattgatg tgatatctcc actgacgtaa 540gggatgacgc acaatcccac tatccttcgc aagacccttc ctctatataa ggaagttcat 600ttcatttgga gaggacacgc tgacaagctg actctagcag atcctctaga accatcttcc 660acacactcaa gccacactat tggagaacac acagggacaa cacaccataa gatccaaggg 720aggcctccgc cgccgccggt aaccaccccg cccctctcct ctttctttct ccgttttttt 780ttccgtctcg gtctcgatct ttggccttgg tagtttgggt gggcgagagg cggcttcgtg 840cgcgcccaga tcggtgcgcg ggaggggcgg gatctcgcgg ctggggctct cgccggcgtg 900gatccggccc ggatctcgcg gggaatgggg ctctcggatg tagatctgcg atccgccgtt 960gttgggggag atgatggggg gtttaaaatt tccgccgtgc taaacaagat caggaagagg 1020ggaaaagggc actatggttt atatttttat atatttctgc tgcttcgtca ggcttagatg 1080tgctagatct ttctttcttc tttttgtggg tagaatttga atccctcagc attgttcatc 1140ggtagttttt cttttcatga tttgtgacaa atgcagcctc gtgcggagct tttttgtagg 1200tagaagtgat caacc atg gac aac aac cca aac atc aac gag tgc atc ccg 1251 Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro 1 5 10 tac aac tgc ctc agc aac cct gag gtc gag gtg ctc ggc ggt gag cgc 1299Tyr Asn Cys Leu Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg 15 20 25 atc gag acc ggt tac acc ccc atc gac atc tcc ctc tcc ctc acg cag 1347Ile Glu Thr Gly Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln 30 35 40 ttc ctg ctc agc gag ttc gtg cca ggc gct ggc ttc gtc ctg ggc ctc 1395Phe Leu Leu Ser Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu 45 50 55 60 gtg gac atc atc tgg ggc atc ttt ggc ccc tcc cag tgg gac gcc ttc 1443Val Asp Ile Ile Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe 65 70 75 ctg gtg caa atc gag cag ctc atc aac cag agg atc gag gag ttc gcc 1491Leu Val Gln Ile Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala 80 85 90 agg aac cag gcc atc agc cgc ctg gag ggc ctc agc aac ctc tac caa 1539Arg Asn Gln Ala Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln 95 100 105 atc tac gct gag agc ttc cgc gag tgg gag gcc gac ccc act aac cca 1587Ile Tyr Ala Glu Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro 110 115 120 gct ctc cgc gag gag atg cgc atc cag ttc aac gac atg aac agc gcc 1635Ala Leu Arg Glu Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala 125 130 135 140 ctg acc acc gcc atc cca ctc ttc gcc gtc cag aac tac caa gtc ccg 1683Leu Thr Thr Ala Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro 145 150 155 ctc ctg tcc gtg tac gtc cag gcc gcc aac ctg cac ctc agc gtg ctg 1731Leu Leu Ser Val Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu 160 165 170 agg gac gtc agc gtg ttt ggc cag agg tgg ggc ttc gac gcc gcc acc 1779Arg Asp Val Ser Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr 175 180 185 atc aac agc cgc tac aac gac ctc acc agg ctg atc ggc aac tac acc 1827Ile Asn Ser Arg Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr 190 195 200 gac cac gct gtc cgc tgg tac aac act ggc ctg gag cgc gtc tgg ggc 1875Asp His Ala Val Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly 205 210 215 220 cct gat tct aga gac tgg att cgc tac aac cag ttc agg cgc gag ctg 1923Pro Asp Ser Arg Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu 225 230 235 acc ctc acc gtc ctg gac att gtg tcc ctc ttc ccg aac tac gac tcc 1971Thr Leu Thr Val Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser 240 245 250 cgc acc tac ccg atc cgc acc gtg tcc caa ctg acc cgc gaa atc tac 2019Arg Thr Tyr Pro Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr 255 260 265 acc aac ccc gtc ctg gag aac ttc gac ggt agc ttc agg ggc agc gcc 2067Thr Asn Pro Val Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala 270 275 280 cag ggc atc gag ggc tcc atc agg agc cca cac ctg atg gac atc ctc 2115Gln Gly Ile Glu Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu 285 290 295 300 aac agc atc act atc tac acc gat gcc cac cgc ggc gag tac tac tgg 2163Asn Ser Ile Thr Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp 305 310 315 tcc ggc cac cag atc atg gcc tcc ccg gtc ggc ttc agc ggc ccc gag 2211Ser Gly His Gln Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu 320 325 330 ttt acc ttt cct ctc tac ggc acg atg ggc aac gcc gct cca caa caa 2259Phe Thr Phe Pro Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln 335 340 345 cgc atc gtc gct cag ctg ggc cag ggc gtc tac cgc acc ctg agc tcc 2307Arg Ile Val Ala Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser 350 355 360 acc ctg tac cgc agg ccc ttc aac atc ggt atc aac aac cag cag ctg 2355Thr Leu Tyr Arg Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu 365 370 375 380 tcc gtc ctg gat ggc act gag ttc gcc tac ggc acc tcc tcc aac ctg 2403Ser Val Leu Asp Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu 385 390 395 ccc tcc gct gtc tac cgc aag agc ggc acg gtg gat tcc ctg gac gag 2451Pro Ser Ala Val Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu 400 405 410 atc cca cca cag aac aac aat gtg ccc ccc agg cag ggt ttt tcc cac 2499Ile Pro Pro Gln Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His 415 420 425 agg ctc agc cac gtg tcc atg ttc cgc tcc ggc ttc agc aac tcg tcc 2547Arg Leu Ser His Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser 430 435 440 gtg agc atc atc aga gct cct atg ttc tct tgg ata cac cgt agt gct 2595Val Ser Ile Ile Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala 445 450 455 460 gag ttc aac aac atc att gca tcc gac agc att act caa ata ccc ttg 2643Glu Phe Asn Asn Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu 465 470 475 gtg aaa gca cat aca ctt cag tca ggt act act gtt gtc aga ggt cca 2691Val Lys Ala His Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro 480 485 490 ggg ttt aca gga gga gac att ctt cgt cgc aca agt gga gga ccc ttt 2739Gly Phe Thr Gly Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe 495 500 505 gct tac act att gtt aac atc aat ggc caa ttg ccc caa agg tat cgt 2787Ala Tyr Thr Ile Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg 510 515 520 gca aga atc cgc tat gcc tct act aca aat ctc agg atc tac gtg act 2835Ala Arg Ile Arg Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr 525 530 535 540 gtt gca ggt gaa agg atc ttt gct ggt cag ttc aac aag act atg gat 2883Val Ala Gly Glu Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp 545 550 555 acc ggt gac cct ttg aca ttc caa tct ttt agc tac gca act atc aac 2931Thr Gly Asp Pro Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn 560 565 570 aca gct ttt aca ttc cca atg agc cag agt agc ttc aca gta ggt gct 2979Thr Ala Phe Thr Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala 575 580 585 gac act ttc agc tca ggg aat gaa gtt tac atc gac agg ttt gaa ttg 3027Asp Thr Phe Ser Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu 590 595 600 att cca gtt act gca acc ctc gag gct gag tac aac ctt gag aga gcc 3075Ile Pro Val Thr Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala 605 610 615 620 cag aag gct gtg aac gcc ctc ttt acc tcc acc aat cag ctt ggc ttg 3123Gln Lys Ala Val Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu 625 630 635 aaa act aac gtt act gac tat cac att gac caa gtg tcc aac ttg gtc 3171Lys Thr Asn Val Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val 640 645 650 acc tac ctt agc gat gag ttc tgc ctc gac gag aag cgt gaa ctc tcc 3219Thr Tyr Leu Ser Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser 655 660 665 gag aaa gtt aaa cac gcc aag cgt ctc agc gac gag agg aat ctc ttg 3267Glu Lys Val Lys His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu 670 675 680 caa gac tcc aac ttc aaa gac atc aac agg cag cca gaa cgt ggt tgg 3315Gln Asp Ser Asn Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp 685 690 695 700 ggt gga agc acc ggg atc acc atc caa gga ggc gac gat gtg ttc aag 3363Gly Gly Ser Thr Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys

705 710 715 gag aac tac gtc acc ctc tcc gga act ttc gac gag tgc tac cct acc 3411Glu Asn Tyr Val Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr 720 725 730 tac ttg tac cag aag atc gat gag tcc aaa ctc aaa gcc ttc acc agg 3459Tyr Leu Tyr Gln Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg 735 740 745 tat caa ctt aga ggc tac atc gaa gac agc caa gac ctt gaa atc tac 3507Tyr Gln Leu Arg Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr 750 755 760 tcg atc agg tac aat gcc aag cac gag acc gtg aat gtc cca ggt act 3555Ser Ile Arg Tyr Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr 765 770 775 780 ggt tcc ctc tgg cca ctt tct gcc caa tct ccc att ggg aag tgt gga 3603Gly Ser Leu Trp Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly 785 790 795 gag cct aac aga tgc gct cca cac ctt gag tgg aat cct gac ttg gac 3651Glu Pro Asn Arg Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp 800 805 810 tgc tcc tgc agg gat ggc gag aag tgt gcc cac cat tct cat cac ttc 3699Cys Ser Cys Arg Asp Gly Glu Lys Cys Ala His His Ser His His Phe 815 820 825 tcc ttg gac atc gat gtg gga tgt act gac ctg aat gag gac ctc gga 3747Ser Leu Asp Ile Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly 830 835 840 gtc tgg gtc atc ttc aag atc aag acc caa gac gga cac gca aga ctt 3795Val Trp Val Ile Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu 845 850 855 860 ggc aac ctt gag ttt ctc gaa gag aaa cca ttg gtc ggt gaa gct ctc 3843Gly Asn Leu Glu Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu 865 870 875 gct cgt gtg aag aga gca gag aag aag tgg agg gac aaa cgt gag aaa 3891Ala Arg Val Lys Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys 880 885 890 ctc gaa tgg gaa act aac atc gtt tac aag gag gcc aaa gag tcc gtg 3939Leu Glu Trp Glu Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val 895 900 905 gat gct ttg ttc gtg aac tcc caa tat gat cag ttg caa gcc gac acc 3987Asp Ala Leu Phe Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr 910 915 920 aac atc gcc atg atc cac gcc gca gac aaa cgt gtg cac agc att cgt 4035Asn Ile Ala Met Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg 925 930 935 940 gag gct tac ttg cct gag ttg tcc gtg atc cct ggt gtg aac gct gcc 4083Glu Ala Tyr Leu Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala 945 950 955 atc ttc gag gaa ctt gag gga cgt atc ttt acc gca ttc tcc ttg tac 4131Ile Phe Glu Glu Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr 960 965 970 gat gcc aga aac gtc atc aag aac ggt gac ttc aac aat ggc ctc agc 4179Asp Ala Arg Asn Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser 975 980 985 tgc tgg aat gtg aaa ggt cat gtg gac gtg gag gaa cag aac aat cag 4227Cys Trp Asn Val Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln 990 995 1000 cgt tcc gtc ctg gtt gtg cct gag tgg gaa gct gaa gtg tcc caa 4272Arg Ser Val Leu Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln 1005 1010 1015 gag gtt aga gtc tgt cca ggt aga ggc tac att ctc cgt gtg acc 4317Glu Val Arg Val Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr 1020 1025 1030 gct tac aag gag gga tac ggt gag ggt tgc gtg acc atc cac gag 4362Ala Tyr Lys Glu Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu 1035 1040 1045 atc gag aac aac acc gac gag ctt aag ttc tcc aac tgc gtc gag 4407Ile Glu Asn Asn Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu 1050 1055 1060 gaa gaa atc tat ccc aac aac acc gtt act tgc aac gac tac act 4452Glu Glu Ile Tyr Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr 1065 1070 1075 gtg aat cag gaa gag tac gga ggt gcc tac act agc cgt aac aga 4497Val Asn Gln Glu Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg 1080 1085 1090 ggt tac aac gaa gct cct tcc gtt cct gct gac tat gcc tcc gtg 4542Gly Tyr Asn Glu Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val 1095 1100 1105 tac gag gag aaa tcc tac aca gat ggc aga cgt gag aac cct tgc 4587Tyr Glu Glu Lys Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys 1110 1115 1120 gag ttc aac aga ggt tac agg gac tac aca cca ctt cca gtt ggc 4632Glu Phe Asn Arg Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly 1125 1130 1135 tat gtt acc aag gag ctt gag tac ttt cct gag acc gac aaa gtg 4677Tyr Val Thr Lys Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val 1140 1145 1150 tgg atc gag atc ggt gaa acc gag gga acc ttc atc gtg gac agc 4722Trp Ile Glu Ile Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser 1155 1160 1165 gtg gag ctt ctc ttg atg gag gaa taa tga gatctatcga ttctagaagg 4772Val Glu Leu Leu Leu Met Glu Glu 1170 1175 cctgaattct gcatgcgttt ggacgtatgc tcattcaggt tggagccaat ttggttgatg 4832tgtgtgcgag ttcttgcgag tctgatgaga catctctgta ttgtgtttct ttccccagtg 4892ttttctgtac ttgtgtaatc ggctaatcgc caacagattc ggcgatgaat aaatgagaaa 4952taaattgttc tgattttgag tgcaaaaaaa aaggaatt 499081177PRTartificialSynthetic Construct 8Met Asp Asn Asn Pro Asn Ile Asn Glu Cys Ile Pro Tyr Asn Cys Leu 1 5 10 15 Ser Asn Pro Glu Val Glu Val Leu Gly Gly Glu Arg Ile Glu Thr Gly 20 25 30 Tyr Thr Pro Ile Asp Ile Ser Leu Ser Leu Thr Gln Phe Leu Leu Ser 35 40 45 Glu Phe Val Pro Gly Ala Gly Phe Val Leu Gly Leu Val Asp Ile Ile 50 55 60 Trp Gly Ile Phe Gly Pro Ser Gln Trp Asp Ala Phe Leu Val Gln Ile 65 70 75 80 Glu Gln Leu Ile Asn Gln Arg Ile Glu Glu Phe Ala Arg Asn Gln Ala 85 90 95 Ile Ser Arg Leu Glu Gly Leu Ser Asn Leu Tyr Gln Ile Tyr Ala Glu 100 105 110 Ser Phe Arg Glu Trp Glu Ala Asp Pro Thr Asn Pro Ala Leu Arg Glu 115 120 125 Glu Met Arg Ile Gln Phe Asn Asp Met Asn Ser Ala Leu Thr Thr Ala 130 135 140 Ile Pro Leu Phe Ala Val Gln Asn Tyr Gln Val Pro Leu Leu Ser Val 145 150 155 160 Tyr Val Gln Ala Ala Asn Leu His Leu Ser Val Leu Arg Asp Val Ser 165 170 175 Val Phe Gly Gln Arg Trp Gly Phe Asp Ala Ala Thr Ile Asn Ser Arg 180 185 190 Tyr Asn Asp Leu Thr Arg Leu Ile Gly Asn Tyr Thr Asp His Ala Val 195 200 205 Arg Trp Tyr Asn Thr Gly Leu Glu Arg Val Trp Gly Pro Asp Ser Arg 210 215 220 Asp Trp Ile Arg Tyr Asn Gln Phe Arg Arg Glu Leu Thr Leu Thr Val 225 230 235 240 Leu Asp Ile Val Ser Leu Phe Pro Asn Tyr Asp Ser Arg Thr Tyr Pro 245 250 255 Ile Arg Thr Val Ser Gln Leu Thr Arg Glu Ile Tyr Thr Asn Pro Val 260 265 270 Leu Glu Asn Phe Asp Gly Ser Phe Arg Gly Ser Ala Gln Gly Ile Glu 275 280 285 Gly Ser Ile Arg Ser Pro His Leu Met Asp Ile Leu Asn Ser Ile Thr 290 295 300 Ile Tyr Thr Asp Ala His Arg Gly Glu Tyr Tyr Trp Ser Gly His Gln 305 310 315 320 Ile Met Ala Ser Pro Val Gly Phe Ser Gly Pro Glu Phe Thr Phe Pro 325 330 335 Leu Tyr Gly Thr Met Gly Asn Ala Ala Pro Gln Gln Arg Ile Val Ala 340 345 350 Gln Leu Gly Gln Gly Val Tyr Arg Thr Leu Ser Ser Thr Leu Tyr Arg 355 360 365 Arg Pro Phe Asn Ile Gly Ile Asn Asn Gln Gln Leu Ser Val Leu Asp 370 375 380 Gly Thr Glu Phe Ala Tyr Gly Thr Ser Ser Asn Leu Pro Ser Ala Val 385 390 395 400 Tyr Arg Lys Ser Gly Thr Val Asp Ser Leu Asp Glu Ile Pro Pro Gln 405 410 415 Asn Asn Asn Val Pro Pro Arg Gln Gly Phe Ser His Arg Leu Ser His 420 425 430 Val Ser Met Phe Arg Ser Gly Phe Ser Asn Ser Ser Val Ser Ile Ile 435 440 445 Arg Ala Pro Met Phe Ser Trp Ile His Arg Ser Ala Glu Phe Asn Asn 450 455 460 Ile Ile Ala Ser Asp Ser Ile Thr Gln Ile Pro Leu Val Lys Ala His 465 470 475 480 Thr Leu Gln Ser Gly Thr Thr Val Val Arg Gly Pro Gly Phe Thr Gly 485 490 495 Gly Asp Ile Leu Arg Arg Thr Ser Gly Gly Pro Phe Ala Tyr Thr Ile 500 505 510 Val Asn Ile Asn Gly Gln Leu Pro Gln Arg Tyr Arg Ala Arg Ile Arg 515 520 525 Tyr Ala Ser Thr Thr Asn Leu Arg Ile Tyr Val Thr Val Ala Gly Glu 530 535 540 Arg Ile Phe Ala Gly Gln Phe Asn Lys Thr Met Asp Thr Gly Asp Pro 545 550 555 560 Leu Thr Phe Gln Ser Phe Ser Tyr Ala Thr Ile Asn Thr Ala Phe Thr 565 570 575 Phe Pro Met Ser Gln Ser Ser Phe Thr Val Gly Ala Asp Thr Phe Ser 580 585 590 Ser Gly Asn Glu Val Tyr Ile Asp Arg Phe Glu Leu Ile Pro Val Thr 595 600 605 Ala Thr Leu Glu Ala Glu Tyr Asn Leu Glu Arg Ala Gln Lys Ala Val 610 615 620 Asn Ala Leu Phe Thr Ser Thr Asn Gln Leu Gly Leu Lys Thr Asn Val 625 630 635 640 Thr Asp Tyr His Ile Asp Gln Val Ser Asn Leu Val Thr Tyr Leu Ser 645 650 655 Asp Glu Phe Cys Leu Asp Glu Lys Arg Glu Leu Ser Glu Lys Val Lys 660 665 670 His Ala Lys Arg Leu Ser Asp Glu Arg Asn Leu Leu Gln Asp Ser Asn 675 680 685 Phe Lys Asp Ile Asn Arg Gln Pro Glu Arg Gly Trp Gly Gly Ser Thr 690 695 700 Gly Ile Thr Ile Gln Gly Gly Asp Asp Val Phe Lys Glu Asn Tyr Val 705 710 715 720 Thr Leu Ser Gly Thr Phe Asp Glu Cys Tyr Pro Thr Tyr Leu Tyr Gln 725 730 735 Lys Ile Asp Glu Ser Lys Leu Lys Ala Phe Thr Arg Tyr Gln Leu Arg 740 745 750 Gly Tyr Ile Glu Asp Ser Gln Asp Leu Glu Ile Tyr Ser Ile Arg Tyr 755 760 765 Asn Ala Lys His Glu Thr Val Asn Val Pro Gly Thr Gly Ser Leu Trp 770 775 780 Pro Leu Ser Ala Gln Ser Pro Ile Gly Lys Cys Gly Glu Pro Asn Arg 785 790 795 800 Cys Ala Pro His Leu Glu Trp Asn Pro Asp Leu Asp Cys Ser Cys Arg 805 810 815 Asp Gly Glu Lys Cys Ala His His Ser His His Phe Ser Leu Asp Ile 820 825 830 Asp Val Gly Cys Thr Asp Leu Asn Glu Asp Leu Gly Val Trp Val Ile 835 840 845 Phe Lys Ile Lys Thr Gln Asp Gly His Ala Arg Leu Gly Asn Leu Glu 850 855 860 Phe Leu Glu Glu Lys Pro Leu Val Gly Glu Ala Leu Ala Arg Val Lys 865 870 875 880 Arg Ala Glu Lys Lys Trp Arg Asp Lys Arg Glu Lys Leu Glu Trp Glu 885 890 895 Thr Asn Ile Val Tyr Lys Glu Ala Lys Glu Ser Val Asp Ala Leu Phe 900 905 910 Val Asn Ser Gln Tyr Asp Gln Leu Gln Ala Asp Thr Asn Ile Ala Met 915 920 925 Ile His Ala Ala Asp Lys Arg Val His Ser Ile Arg Glu Ala Tyr Leu 930 935 940 Pro Glu Leu Ser Val Ile Pro Gly Val Asn Ala Ala Ile Phe Glu Glu 945 950 955 960 Leu Glu Gly Arg Ile Phe Thr Ala Phe Ser Leu Tyr Asp Ala Arg Asn 965 970 975 Val Ile Lys Asn Gly Asp Phe Asn Asn Gly Leu Ser Cys Trp Asn Val 980 985 990 Lys Gly His Val Asp Val Glu Glu Gln Asn Asn Gln Arg Ser Val Leu 995 1000 1005 Val Val Pro Glu Trp Glu Ala Glu Val Ser Gln Glu Val Arg Val 1010 1015 1020 Cys Pro Gly Arg Gly Tyr Ile Leu Arg Val Thr Ala Tyr Lys Glu 1025 1030 1035 Gly Tyr Gly Glu Gly Cys Val Thr Ile His Glu Ile Glu Asn Asn 1040 1045 1050 Thr Asp Glu Leu Lys Phe Ser Asn Cys Val Glu Glu Glu Ile Tyr 1055 1060 1065 Pro Asn Asn Thr Val Thr Cys Asn Asp Tyr Thr Val Asn Gln Glu 1070 1075 1080 Glu Tyr Gly Gly Ala Tyr Thr Ser Arg Asn Arg Gly Tyr Asn Glu 1085 1090 1095 Ala Pro Ser Val Pro Ala Asp Tyr Ala Ser Val Tyr Glu Glu Lys 1100 1105 1110 Ser Tyr Thr Asp Gly Arg Arg Glu Asn Pro Cys Glu Phe Asn Arg 1115 1120 1125 Gly Tyr Arg Asp Tyr Thr Pro Leu Pro Val Gly Tyr Val Thr Lys 1130 1135 1140 Glu Leu Glu Tyr Phe Pro Glu Thr Asp Lys Val Trp Ile Glu Ile 1145 1150 1155 Gly Glu Thr Glu Gly Thr Phe Ile Val Asp Ser Val Glu Leu Leu 1160 1165 1170 Leu Met Glu Glu 1175

Claims

1. An isolated nucleotide sequence encoding an insecticidal protein comprising an amino acid sequence as set forth in SEQ ID NO:2 from amino acid position 10 through amino acid position 600.

2. The isolated nucleotide sequence of claim 1 selected from the group consisting of SEQ ID NO:1 and SEQ ID NO:3.

3. The isolated nucleotide sequence of claim 2 for use in expressing said insecticidal protein in a crop plant.

4. The isolated nucleotide sequence of claim 3 wherein said crop plant is selected from the group consisting of a monocotyledonous crop plant and a dicotyledonous crop plant.

5. The isolated nucleotide sequence of claim 4 wherein said monocotyledonous plant is selected from the group of plants consisting of corn, wheat, oat, rice, sorghum, milo, buckwheat, rye, grass (fescue, timothy, brome, orchard, St. Augustine, Bermuda, bentgrass), and barley.

6. The isolated nucleotide sequence of claim 4 wherein said dicotyledonous plant is selected from the group of plants consisting of alfalfa, apple, apricot, asparagus, bean, berry, blackberry, blueberry, canola, carrot, cauliflower, celery, cherry, chickpea, citrus tree, cotton, cowpea, cranberry, cucumber, cucurbit, egg plant, fruit tree, grape, lemon, lettuce, linseed, melon, mustard, nut bearing tree, okra, orange, pea, peach, peanut, pear, plum, potato, soybeans, squash, strawberry, sugar beet, sunflower, sweet potato, tobacco, tomato, turnip, and vegetable.

7-20. (canceled)

21. A method of identifying in a biological sample a nucleotide sequence encoding a Cry1A.105 amino acid sequence, said method comprising contacting said sample with a polynucleotide that hybridizes to the nucleotide sequence under stringent hybridization conditions and detecting the binding of said polynucleotide to said nucleotide sequence, wherein said binding is diagnostic for said nucleotide sequence in said sample.

22. A method of identifying in a sample a Cry1A.105 protein, said method comprising contacting said sample with an antibody that binds specifically to said protein, and detecting the binding, wherein said binding is diagnostic for the presence of said protein in said sample.

23-36. (canceled)