U.S. patent application number 13/688570 was filed with the patent office on 2013-05-30 for cyclopropene amine compounds.
This patent application is currently assigned to NORTH CAROLINA STATE UNIVERSITY. The applicant listed for this patent is North Carolina State University. Invention is credited to Edward C. Sisler.
Application Number | 20130137575 13/688570 |
Document ID | / |
Family ID | 39761007 |
Filed Date | 2013-05-30 |
United States Patent
Application |
20130137575 |
Kind Code |
A1 |
Sisler; Edward C. |
May 30, 2013 |
CYCLOPROPENE AMINE COMPOUNDS
Abstract
Methods of applying cyclopropene amine derivatives and
compositions thereof to inhibit ethylene receptors in plants and
plant material are disclosed. Methods include applying to the plant
an effective ethylene response-inhibiting amount of at least one
cyclopropene amine compound or composition thereof. Cyclopropene
amine compounds, enantiomers, stereoisomers or salts thereof are
also provided.
Inventors: |
Sisler; Edward C.; (Raleigh,
NC) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
North Carolina State University; |
Raleigh |
NC |
US |
|
|
Assignee: |
NORTH CAROLINA STATE
UNIVERSITY
Raleigh
NC
|
Family ID: |
39761007 |
Appl. No.: |
13/688570 |
Filed: |
November 29, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13248917 |
Sep 29, 2011 |
8329954 |
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13688570 |
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12138548 |
Jun 13, 2008 |
8093430 |
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13248917 |
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60945777 |
Jun 22, 2007 |
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60961183 |
Jul 19, 2007 |
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Current U.S.
Class: |
504/115 ;
426/321; 504/326; 564/455 |
Current CPC
Class: |
A01N 33/04 20130101;
A23B 7/144 20130101; A23B 7/154 20130101; C07C 211/25 20130101;
C07C 211/45 20130101; C07C 211/48 20130101; C07C 2601/02
20170501 |
Class at
Publication: |
504/115 ;
564/455; 504/326; 426/321 |
International
Class: |
A01N 33/04 20060101
A01N033/04; C07C 211/25 20060101 C07C211/25 |
Goverment Interests
STATEMENT OF GOVERNMENT SUPPORT
[0002] Aspects of this research are supported by the Binational
Agricultural Research and Development Fund (BARD) under grant
number US-IS-3493-03CR. The U.S. Government has certain rights to
this invention.
Claims
1. A compound having the following structure: ##STR00017## or an
enantiomer, stereoisomer or a salt thereof.
2. The compound of claim 1, wherein the compound is
N-(cycloprop-1-en ylmethyl)-N-ethylethanamine.
3. A composition comprising: (a) A compound having the following
structure: ##STR00018## or an enantiomer, stereoisomer or a salt
thereof; and (b) an adjuvant.
4. The composition of claim 3, wherein the adjuvant is an
agriculturally acceptable carrier.
5. The compound of claim 1, wherein the salt of the compound is
selected from the group consisting of phosphate, acetate, formate,
carbonate, hydrobromide, hydrochloride, sulfate, bisulfate,
nitrate, trifluoroacetate, oxalate, valerate, oleate, palmitate,
stearate, laurate, borate, benzoate, lactate, tosylate, citrate,
maleate, fumarate, succinate, tartrate, naphthylate, mesylate,
glucoheptonate, lactiobionate and laurylsulfonate salts.
6. The compound of claim 1, wherein the salt of the compound is
selected from the group consisting of phosphate, acetate, formate
and carbonate salts.
7. The compound of claim 1, wherein the salt of the compound is a
carbonate salt.
8. A method of inhibiting an ethylene response in a plant,
comprising applying to the plant an effective ethylene
response-inhibiting amount of a compound having the following
structure: ##STR00019## or an enantiomer, stereoisomer or a salt
thereof.
9. The method of claim 8, wherein said salt of the compound is
selected from the group consisting of phosphate, acetate, formate,
carbonate, hydrobromide, hydrochloride, sulfate, bisulfate,
nitrate, trifluoroacetate, oxalate, valerate, oleate, palmitate,
stearate, laurate, borate, benzoate, lactate, tosylate, citrate,
maleate, fumarate, succinate, tartrate, naphthylate, mesylate,
glucoheptonate, lactiobionate and laurylsulfonate salts.
10. The method of claim 8, wherein said salt of the compound is
selected from the group consisting of phosphate, acetate, formate
and carbonate salts.
11. The method of claim 8, wherein said salt of the compound is a
carbonate salt.
12. The method of claim 8, wherein application is carried out by
contacting said plant to a gas of said compound.
13. The method of claim 8, wherein application is carried out by
contacting said plant to a solid comprising said compound.
14. The method of claim 8, wherein application is carried out by
contacting said plant to a gas, salt or mixture thereof.
15. The method of claim 8, wherein application is carried out by
applying a spray comprising said compound.
16. The method of claim 8, wherein application is carried out by
dipping said plant in a composition comprising said compound.
17. The method of claim 8, wherein application is carried out by
addition of said compound to a container containing said plant.
18. The method of claim 8, wherein said plant is a cut flower.
19. The method of claim 8, wherein said ethylene response is one or
more of ripening or senescence of flowers, fruits, and vegetables;
abscission of foliage, flowers, and fruit; the shortening of life
of ornamental plants, cut flowers, shrubbery, seeds, or dormant
seedlings; inhibition of growth; stimulation of growth; auxin
activity; inhibition of terminal growth; control of apical
dominance; increase in branching; increase in tillering; changing
the morphology of plants; modifying the susceptibility to plant
pathogens such as fungi; changing bio-chemical compositions;
inducing pest resistance; abortion or inhibition of flowering or
seed development; lodging effects; stimulation of seed germination;
breaking of dormancy; hormone effects; and epinasty effects.
20. The method of claim 8, wherein said compound can be applied in
a closed system.
21. The method of claim 8, wherein said compound can be applied in
an open system.
22. The method of claim 8, wherein said plant is a whole plant and
or any portions thereof, a field crop, landscape plant, potted
plant, cut flower, or harvested fruit or vegetable.
23. A method of inhibiting an ethylene response in a plant grown in
a field crop, comprising applying to the field crop an effective
ethylene response-inhibiting amount of a spray formulation
comprising the following compound: ##STR00020## or an enantiomer,
stereoisomer or a salt thereof.
24. The method of claim 23, wherein said compound is a salt.
25. A method of prolonging the life of a landscape plant comprising
applying to the landscape plant an effective ethylene
response-inhibiting amount of a formulation comprising the
following compound: ##STR00021## or an enantiomer, stereoisomer or
a salt thereof.
Description
RELATED APPLICATION DATA
[0001] This application is a continuation of U.S. application Ser.
No. 13/248,917, now allowed, filed on Sep. 29, 2011, which claims
the benefit of U.S. application Ser. No. 12/138,548, filed on Jun.
13, 2008, issued as U.S. Pat. No. 8,093,430 on Jan. 10, 2012, which
claims the benefit of U.S. Provisional Application Ser. No.
60/945,777, filed on Jun. 22, 2007, and U.S. Provisional
Application Ser. No. 60/961,183, filed on Jul. 19, 2007. The
disclosure of each application is incorporated by reference herein
in its entirety.
FIELD OF THE INVENTION
[0003] The present invention generally relates to methods of
inhibiting ethylene responses in plants and plant materials by
applying cyclopropene amine compounds and compositions thereof to
plants. The invention further relates to cyclopropene amine
compounds, enantiomers, stereoisomers and salts thereof.
BACKGROUND OF THE INVENTION
[0004] Ethylene is known to mediate a variety of growth phenomena
in plants. See generally Fritz et al. U.S. Pat. No. 3,879,188. This
activity is understood to be achieved through a specific ethylene
receptor in plants. Many compounds other than ethylene interact
with this receptor: some mimic the action of ethylene; while others
prevent ethylene from binding and thereby counteract its
action.
[0005] Many compounds that block the action of ethylene do so by
binding to the ethylene binding site. Unfortunately, they often
diffuse from the binding site over a period of several hours. See
E. Sisler and C. Wood, Plant Growth Reg. 7, 181-191 (1988). These
blocking compounds may be used to counteract ethylene action.
However, a problem with such compounds is that exposure must be
continuous if the effect is to last for more than a few hours.
[0006] Photoaffinity labeling has been used in biological studies
to label binding sites in a permanent manner--usually by generating
a carbene or nitrene intermediate. Such intermediates are generally
reactive and react rapidly and indiscriminately with many
compositions. A compound already bound, however, would react mostly
with the binding site. In a preliminary study, it was shown that
cyclopentadiene was an effective blocking agent for ethylene
binding. See E. Sisler et al., Plant Growth Reg. 9, 157-164 (1990).
Methods of combating the ethylene response in plants with
diazocyclopentadiene and derivatives thereof are described in U.S.
Pat. No. 5,100,462 to Sisler et al. U.S. Pat. No. 5,518,988 to
Sisler et al. describes the use of cyclopropenes having a C.sub.1
to C.sub.4 alkyl group to block the action of ethylene.
[0007] Notwithstanding these efforts, however, there remains a need
in the art for additional methods providing improved plant
maturation and degradation regulation as well as those for
counteracting ethylene-induced processes in agricultural produce
and/or horticultural products.
SUMMARY OF THE INVENTION
[0008] The present invention includes cyclopropene compounds of
Formula I:
##STR00001##
[0009] wherein:
[0010] n is an integer from 1 to 4;
[0011] R is
##STR00002##
[0012] wherein;
[0013] m is an integer from 1 to 3,
[0014] R.sub.1 and R.sub.2 are independently hydrogen,
C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5 alkenyl, C.sub.2-C.sub.5
alkynyl, C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.8 cycloalkenyl,
C.sub.3-C.sub.8 cycloalkynyl, heterocyclyl or aryl, wherein said
cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl or aryl is
optionally attached to the nitrogen via a C.sub.1-C.sub.5 alkyl,
C.sub.2-C.sub.5 alkenyl or C.sub.2-C.sub.5 alkynyl group, or
[0015] an enantiomer, stereoisomer or a salt thereof.
[0016] In some embodiments, the salt of the compound as described
above is selected from the group consisting of phosphate, acetate,
formate and carbonate salts.
[0017] In particular embodiments, the compound has the following
structure:
##STR00003##
or
[0018] an enantiomer, stereoisomer or a salt thereof.
[0019] Embodiments of the present invention further provide
compositions including: (a) at least one compound of Formula I; and
(b) an adjuvant such as an agriculturally acceptable carrier.
[0020] The present invention further includes methods of inhibiting
ethylene responses in plants and plant materials. Methods include
inhibiting an ethylene response in a plant, comprising applying to
the plant an effective ethylene response-inhibiting amount of a
compound of Formula I or a composition including at least one
compound of Formula I; and an adjuvant.
[0021] Application of the compounds to a plant may be carried out
by contacting the plant to a gaseous form or salt form of the
compound or a mixture thereof, contacting the plant with a solid
including the compound, applying a spray including the compound,
dipping the plant in a composition including the compound, and
addition of the compound to a container containing the plant.
Additionally, compounds of the present invention can be applied in
an open or closed system. In particular embodiments, compounds of
the present invention can be used outside, for example, on field
crops or landscaping plants.
[0022] Embodiments of the present invention further provide methods
of prolonging the life of a cut flower or fresh produce, including
applying to the cut flower or fresh produce an effective
life-prolonging amount of the cyclopropene amine compounds
described herein.
[0023] Aspects of the present invention may result in the
prolongation of storability and shelf life of produce, such as
fruits and vegetables, extension of the storage and vase life of
cut flowers, extension of the harvest timing for field crops and/or
prolongation of life of landscape plants.
[0024] According to further aspects of the present invention, the
compounds described herein are useful to provide protection against
ethylene regulated processes in vascular plants.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] FIG. 1. Protection of banana peel by
N,N-dipropyl(1-cyclopropenylmethyl)amine as acetic acid salt.
[0026] FIG. 2. Protection of banana peel by
N,N-dipropyl(1-cyclopropenylmethyl)amine as a gas or as the
carbonate salt. The amount of chlorophyll was measured 7 days after
the treatment with the compound and 6 days after the treatment with
ethylene.
[0027] FIG. 3. Effect of N,N Dimethyl(1-cyclopropenylmethyl)amine
and N,N Dibutyl(1-cyclopropenylmethyl)amine acetate salts on
protecting chlorophyll degradation in banana peel. The treatment
levels of 4 samples each were adjusted so that each had equal
activities for the compound as a gas. The lowest sample in each
case would be equal in activity to a minimum protection level as a
gas. Exposure was for 24 hours then ethylene was applied.
[0028] FIG. 4. Gaseous phase. These bananas show results of the gas
compound exposure to the dipropyl compound after seven days. Marked
with an E, the banana is treated with only ethylene--This shows the
fastest ripening since no compound has been applied. Higher
concentrations of the compound show more extensive ethylene
blockage by comparing the level of green intensity. The check mark
represents the control that has remained completely untreated. 10
and 15 .mu.L of the dipropyl compound had already begun showing an
ethylene response.
[0029] FIG. 5. Aqueous phase. The four bananas on the left show
results of the dimethyl compound. The three bananas on the right
are results of the dibutyl compound. Compounds were swabbed onto
the top half and pictures were taken four days after exposure to
ethylene gas. Brown spots on the dibutyl bananas indicate a more
extensive ripening, and therefore, less protection after the same
number of days. Numbers indicate the .mu.L amount pipetted onto the
banana.
[0030] FIG. 6. Results of various compounds. The graph shown in
FIG. 6A shows the percent of chlorophyll in banana peels. All but
the last two bananas have been treated using acetic acid. A control
is considered to be at a 100% chlorophyll level since it has not
been treated with compounds or ethylene (ethylene induces
ripening). The first black bar is the dimethyl compound control;
the following four bars show ascending concentrations to have
increasingly higher chlorophyll levels. Higher levels of
chlorophyll indicate a higher level of protection because a
ripening yellow banana has less chlorophyll than a fresher green
banana. The next four show a control for the dibutyl compound along
with bananas of ascending concentrations to have increasing levels
of chlorophyll. The last set is using the dipropyl compound. The
last two bars correspond with the dipropyl compound but were made
with carbonic acid.
[0031] There is a concentration curve among cyclopropene compounds.
The last two compounds shown on the graph at FIG. 6B indicate
compounds that may be less weak and/or less active. The graph at
FIG. 6C shows a numeric version of the aqueous phase picture shown
in FIG. 5. The numbers on the y-axis represent the amount of
chlorophyll in each banana relative to a control that was left
untreated.
[0032] FIG. 7. Protection of flowers (Krigia dandelion) by
N,N-dipropyl(1-cyclopropenylmethyl)amine (100 nl) as a gas or as
the carbonate salt. Treatment included check (control), ethylene,
gas form, salt form of N,N-dipropyl(1-cyclopropenylmethyl)amine,
from left to right. The flowers were immersed for 48 hours in water
or a salt solution. All except check were subjected to ethylene for
24 hours.
[0033] FIG. 8. Protection of flowers (Petunia hybridia) by
N,N-dipropyl(1-cyclopropenylmethyl)amine (100 nl) as a gas or as
the carbonate salt. Treatment included check (control), ethylene,
gas form, salt form of N,N-dipropyl(1-cyclopropenylmethyl)amine,
from left to right. All except check were subjected to ethylene for
24 hours.
DETAILED DESCRIPTION
[0034] The compounds disclosed herein may exhibit significant
anti-ethylene activity. In some embodiments, the compound described
herein can block the ethylene receptor and may be applied as either
a gas or as a salt or as a mixture thereof. Application may be
carried out by a spraying or dipping technique. In some
embodiments, the compounds can be applied as a salt with a response
rate that parallels that of a gaseous form.
[0035] Unless otherwise defined, all technical and scientific terms
used herein have the same meaning as commonly understood by one of
ordinary skill in the art to which this invention belongs. Further,
all publications, U.S. patent applications, U.S. patents and other
references cited herein are incorporated by reference in their
entireties.
[0036] The present invention can be practiced based upon the
disclosure described herein, in light of the knowledge of persons
skilled in the art, and in light of the information set forth in
U.S. Pat. No. 6,365,549; U.S. Pat. No. 6,194,350; and U.S. Pat. No.
5,518,988.
[0037] Cyclopropene amine compounds that may be used to carry out
the present invention may be prepared by using various methods
known to those skilled in the art. For example, as described by
Baird et al. in Preparation and Lithiation of 1-Halogenocyclop
ropenes, J. CHEM. SOC. PERKIN TRANS. I 1845-53 (1986).
Additionally, cyclopropene amine compounds can be prepared using
methods described by N. I. Yakushkina and I. G. Bolesov in
Dehydrohalogenation of onohalogenocyclopropanes as a Method for the
Synthesis of Sterically Screened Cyclopropenes, RUSSIAN J. OF
ORGANIC CHEM. 15:853-59 (1979).
[0038] The cyclopropene amine compounds of the present invention
include those of Formula I:
##STR00004##
[0039] wherein n is an integer from 1 to 4.
[0040] R is
##STR00005##
wherein:
[0041] m is an integer from 1 to 1 R.sub.1 and R.sub.2 are
independently hydrogen, C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5
alkenyl, C.sub.2-C.sub.5 alkynyl, C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.5 cycloalkenyl, C.sub.3-C.sub.8 cycloalkynyl,
heterocyclyl or aryl, wherein said cycloalkyl, cycloalkenyl,
cycloalkynyl, heterocyclyl or aryl is optionally attached to the
nitrogen via a C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5 alkenyl or
C.sub.2-C.sub.5 alkynyl group.
[0042] In some embodiments, at least one of R.sub.1 or R.sub.2 is
C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5 alkenyl, C.sub.2-C.sub.5
alkynyl, C.sub.3-C.sub.8 cycloalkyl, C.sub.3-C.sub.8 cycloalkenyl,
C.sub.3-C.sub.5 cycloalkynyl, heterocyclyl or aryl. In further
embodiments, m is 1 and in some embodiments, n is 1. In further
embodiments, R.sub.1 and R.sub.2 are independently C.sub.1-C.sub.5
alkyl. In some embodiments, R.sub.1 and R.sub.2 are both the same
C.sub.1-C.sub.5 alkyl group. In some embodiments, at least one of
R.sub.1 or R.sub.2 is aryl. In other embodiments, at least one of
R.sub.1 or R.sub.2 is C.sub.3-C.sub.8 cycloalkenyl and said
cycloalkenyl is attached to the nitrogen via a C.sub.1-C.sub.5
alkyl group.
[0043] Embodiments of the present invention further include
enantiomers, stereoisomers and salts of the cyclopropene amine
compounds described herein.
[0044] In some embodiments, the salt of Formula I is selected from
the group consisting of phosphate, acetate, formate, carbonate,
hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate,
trifluoroacetate, oxalate, valerate, oleate, palmitate, stearate,
laurate, borate, benzoate, lactate, tosylate, citrate, maleate,
fumarate, succinate, tartrate, naphthylate, mesylate,
glucoheptonate, lactiobionate and laurylsulfonate salts. In some
embodiments, the salt of the Formula I is selected from the group
consisting of phosphate, acetate, formate and carbonate salts. In
particular embodiments, the salt of Formula I is a carbonate
salt.
[0045] According to embodiments of the present invention, the
compounds are N,N-dicyclopropenylmethylamine,
N,N-dimethyl(1-cyclopropenylmethyl)amine,
N,N-diethyl(1-cyclopropenylmethyl)amine,
N,N-dipropyl(1-cyclopropenylmethyl)amine,
N,N-dibutyl(1-cyclopropenylmethyl)amine or
N-(1-methylcyclopropene)-aniline. In particular embodiments, the
compounds have the following structure:
##STR00006##
[0046] The terms "alkyl", "alkenyl", and "alkynyl", as used herein,
refer to linear or branched alkyl, alkenyl or alkynyl substituents,
which may be unsubstituted or substituted. Moreover, a range, such
as C.sub.1-C.sub.5, means that the carbon chain can be C.sub.1,
C.sub.2, C.sub.3, C.sub.4 or C.sub.5 or any range inclusive of any
of the values included in the range, for example, C.sub.2-C.sub.4.
As used herein, the term "heterocyclyl", heterocycle" or
"heterocyclic" refer to saturated or partially unsaturated
monocyclic, bicyclic or tricyclic groups having from 3 to 15 atoms,
in some instances 3 to 7, with at least one heteroatom in at least
one of the rings. As used herein, "aryl" refers to an aromatic
group in a single or fused carbocyclic ring system having from 6 to
15 ring atoms, in some instances 6 to 10, and includes substituted
aromatic groups. Examples of aryl groups include, but are not
limited to, phenyl, 1-naphthyl, 2-naphthyl and benzyl.
[0047] Embodiments of the present invention further include a
composition comprising, consisting essentially of or consisting of
(a) at least one of a compound of Formula I:
##STR00007##
[0048] wherein n is an integer from 1 to 4; R is
##STR00008##
wherein m is an integer from 1 to 3, R.sub.1 and R.sub.2 are
independently hydrogen, C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5
alkenyl, C.sub.2-C.sub.5 alkynyl, C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.8 cycloalkenyl, C.sub.3-C.sub.8 cycloalkynyl,
heterocyclyl or aryl, wherein said cycloalkyl, cycloalkenyl,
cycloalkynyl, heterocyclyl or aryl is optionally attached to the
nitrogen via a C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5 alkenyl or
C.sub.2-C.sub.5 alkynyl group, or an enantiomer, stereoisomer or a
salt thereof; and (b) an adjuvant such as an agriculturally
acceptable carrier.
[0049] Agricultural compositions including the cyclopropene amine
compounds described herein are also encompassed by the invention.
In some embodiments, the compositions include 0.005% to 99%, by
weight; in other embodiments 1% to 95%, by weight; in further
embodiments 2% to 90%, by weight; in still further embodiments 3%
to 80%, by weight; and in some embodiments, 4% to 70%, by weight,
of the active compounds of the present invention. As used herein,
all percentages are percent by weight and all parts are parts by
weight, unless otherwise specified, and are inclusive and
combinable. All ratios are by weight and all ratio ranges are
inclusive and combinable. All molar ranges are inclusive and
combinable.
[0050] These compositions may include one or more adjuvants, such
as, for example, carriers, extenders, binders, lubricants,
surfactants and/or dispersants, wetting agents, spreading agents,
dispersing agents, stickers, adhesives, defoamers, thickeners, and
emulsifying agents. Such adjuvants commonly used in the art can be
found in the John W. McCutcheon, Inc. publication Detergents and
Emulsifiers, Annual, Allured Publishing Company, Ridgewood, N.J.,
U.S.A. The term "agriculturally acceptable carrier" refers to
adjuvants that are ordinarily used in agricultural formulation
technology.
[0051] Numerous organic solvents may be used as carriers for the
active compounds of the present invention, e.g., hydrocarbons such
as hexane, benzene, toluene, xylene, kerosene, diesel oil, fuel oil
and petroleum naphtha, ketones such as acetone, methyl ethyl ketone
and cyclohexanone, chlorinated hydrocarbons such as carbon
tetrachloride, esters such as ethyl acetate, amyl acetate and butyl
acetate, ethers, e.g., ethylene glycol monomethyl ether and
diethylene glycol monomethyl ether, alcohols, e.g., ethanol,
methanol, isopropanol, amyl alcohol, ethylene glycol, propylene
glycol, butyl carbitol acetate and glycerine.
[0052] Mixtures of water and organic solvents, either as solutions
or emulsions, can also be employed as inert carriers for the active
compounds.
[0053] The active compounds of the present invention may also
include adjuvants or carriers such as talc, pyrophyllite, synthetic
fine silica, attapulgus clay (attaclay), kieselguhr, chalk,
diatomaceous earth, lime, calcium carbonate, bentonite, fuller's
earth, cottonseed hulls, wheat flour, soybean flour pumice,
tripoli, wood flour, walnut shell flour, redwood flour and
lignin.
[0054] It may be desirable to incorporate a wetting agent in the
compositions of the present invention. Such wetting agents may be
employed in both the solid and liquid compositions. The wetting
agent can be anionic, cationic or nonionic in character.
[0055] Typical classes of wetting agents include alkyl sulfonate
salts, alkylaryl sulfonate salts, alkyl sulfate salts, alkylamide
sulfonate salts, alkylaryl polyether alcohols, fatty acid esters of
polyhydric alcohols and the alkylene oxide addition products of
such esters, and addition products of long chain mercaptans and
alkylene oxides. Typical examples of such wetting agents include
the sodium alkylbenzene sulfonates having 10 to 18 carbon atoms in
the alkyl group, alkylphenol ethylene oxide condensation products,
e.g., p-isooctylphenol condensed with 10 ethylene oxide units,
soaps, e.g., sodium stearate and potassium oleate, sodium salt of
propylnaphthalene sulfonic acid (di-2-ethylhexyl), ester of sodium
sulfosuccinic acid, sodium lauryl sulfate, sodium stearate and
potassium oleate, sodium salt of the sulfonated monoglyceride of
coconut fatty acids, sorbitan, sesquioleate, lauryl trimethyl
ammonium chloride, octadecyl trimethyl ammonium chloride,
polyethylene glycol lauryl ether, polyethylene esters of fatty
acids and rosin acids (e.g., Ethofat.RTM. 7 and 13, commercially
available from Akzo Nobel Chemicals, Inc. of Chicago, Ill.), sodium
N-methyl-N-oleyltaurate, Turkey Red oil, sodium dibutylnaphthalene
sulfonate, sodium lignin sulfonate (Marasperse.RTM. N, commercially
available from LignoTech USA of Rothschild, Wis.), polyethylene
glycol stearate, sodium dodecylbenzene sulfonate, tertiary dodecyl
polyethylene glycol thioether, long chain ethylene oxide-propylene
oxide condensation products (e.g., Pluronic.RTM. 61 (molecular
weight 1,000) commercially available from BASF of Mount Olive,
N.J.), sorbitan sesquioleate, polyethylene glycol ester of tall oil
acids, sodium octyl phenoxyethoxyethyl sulfate, polyoxyethylene
(20) sorbitan monolaurate (Tween.RTM. 20, commercially available
from ICI Americas Inc. of Wilmington, Deleware) tris
(polyoxyethylene) sorbitan monostearate (Tween 60, commercially
available from ICI Americas Inc. of Wilmington, Deleware), and
sodium dihexyl sulfosuccinate.
[0056] Solid, liquid, and gaseous formulations can be prepared by
various conventional procedures. Thus, the active ingredient, in
finely divided form if a solid, may be tumbled together with finely
divided solid carrier. Alternatively, the active ingredient in
liquid form, including mixtures, solutions, dispersions, emulsions
and suspensions thereof, may be admixed with a solid carrier in
finely divided form. Furthermore, the active ingredient in solid
form may be admixed with a liquid carrier to form a mixture,
solution, dispersion, emulsion, suspension or the like.
[0057] Embodiments of the present invention further include methods
of inhibiting an ethylene response in a plant, comprising,
consisting essentially of or consisting of applying to the plant an
effective ethylene response-inhibiting amount of at least one
compound of Formula I:
##STR00009##
wherein n is an integer from 1 to 4; R is
##STR00010##
wherein m is an integer from 1 to 3, R.sub.1 and R.sub.2 are
independently hydrogen, C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5
alkenyl, or C.sub.2-C.sub.5 alkynyl, C.sub.3-C.sub.8 cycloalkyl,
C.sub.3-C.sub.8 cycloalkenyl, C.sub.3-C.sub.8 cycloalkynyl,
heterocyclyl or aryl, wherein said cycloalkyl, cycloalkenyl,
cycloalkynyl, heterocyclyl or aryl is optionally attached to the
nitrogen via a C.sub.1-C.sub.5 alkyl, C.sub.2-C.sub.5 alkenyl or
C.sub.2-C.sub.5 alkynyl group, or an enantiomer, stereoisomer, salt
or a composition thereof.
[0058] In some embodiments, m is 1 and in other embodiments, n is
1. In some embodiments, R.sub.1 and R.sub.2 are independently
C.sub.1-C.sub.5 alkyl. In further embodiments, R.sub.1 and R.sub.2
are both the same C.sub.1-C.sub.5 alkyl group. In some embodiments,
at least one of R.sub.1 or R.sub.2 is aryl. In some embodiments, at
least one of R.sub.1 or R.sub.2 is C.sub.3-C.sub.8 cycloalkenyl and
said cycloalkenyl is attached to the nitrogen via a C.sub.1-C.sub.5
alkyl group.
[0059] In some embodiments, the salt of Formula I is selected from
the group consisting of phosphate, acetate, formate, carbonate,
hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate,
trifluoroacetate, oxalate, valerate, oleate, palmitate, stearate,
laurate, borate, benzoate, lactate, tosylate, citrate, maleate,
fumarate, succinate, tartrate, naphthylate, mesylate,
glucoheptonate, lactiobionate and laurylsulfonate salts. In some
embodiments, the salt of Formula I is selected from the group
consisting of phosphate, acetate, formate and carbonate salts. In
particular embodiments, the salt of Formula I is a carbonate
salt.
[0060] In some embodiments, when the compounds are applied as a
salt, in a non-volatile form, the response rate may parallel that
of the gas form. Accordingly, the salt application, in at least
some instances, can be used more effectively commercially and the
contact between the compound and receptor may be increased.
[0061] Additionally, ethylene receptors are thought to form
higher-order clusters composed of receptor dimer subunits. The
receptor dimers can influence the signaling states of neighboring
dimers through direct contact. Accordingly, transmitters from many
receptors may be altered by a single ligand-binding event. Some
compounds of the present invention can be involved in cross-linking
in ethylene receptor clusters.
[0062] The active compounds of the present invention can be applied
to plants by various suitable means. For example, an active
compound may be applied alone in gaseous, liquid, or solid form or
a mixture of any combination thereof by contacting the compound
with the plant to be treated. Additionally, the active compound may
be converted to the salt form, and then applied to the plants.
Alternatively, compositions containing one or more active compounds
of the present invention may be formed. The compositions may be
applied in gaseous, liquid or solid form or a mixture of any
combination thereof by contacting the composition with the plant to
be treated. Such compositions may include an inert carrier.
Suitable solid carriers include dusts. Similarly, when in gaseous
form, the compound may be dispersed in an inert gaseous carrier to
provide a gaseous solution. The active compound may also be
suspended in a liquid solution such as an organic solvent or an
aqueous solution that may serve as the inert carrier. Solutions
containing the active compound may be heterogeneous or homogeneous
and may be of various forms including mixtures, dispersions,
emulsions, suspensions and the like.
[0063] The active compounds and compositions thereof can also be
applied as aerosols, e.g., by dispersing them in air using a
compressed gas such as, for example, nitrogen, carbon dioxide,
dichlorodifluoromethane, trichlorofluoromethane, or other
halocarbons.
[0064] Accordingly, in some embodiments, methods of the present
invention can be carried out by contacting a plant to a gaseous
form of at least one cyclopropene amine compound described herein,
contacting said plant to a solid including at least one
cyclopropene amine compound described herein, applying a spray
including at least one cyclopropene amine compound described
herein, dipping the plant in a composition including at least one
cyclopropene amine compound described herein, and/or addition of at
least one cyclopropene amine compound described herein to a
container containing said plant. In some embodiments, the plant is
a cut flower.
[0065] The present invention can be employed to modify a variety of
different ethylene responses. Ethylene responses may be initiated
by either exogenous or endogenous sources of ethylene. Ethylene
responses include, for example, the ripening and/or senescence of
flowers, fruits and vegetables, abscission of foliage, flowers and
fruit, the shortening of the life of ornamentals such as potted
plants, cut flowers, shrubbery, and dormant seedlings, in some
plants (e.g., pea) the inhibition of growth, and in other plants
(e.g., rice) the stimulation of growth. Additional ethylene
responses or ethylene-type responses that may be inhibited by
active compounds of the present invention include, but are not
limited to, auxin activity, inhibition of terminal growth, control
of apical dominance, increase in branching, increase in tillering,
changing bio-chemical compositions of plants (such as increasing
leaf area relative to stem area), abortion or inhibition of
flowering and seed development, lodging effects, stimulation of
seed germination and breaking of dormancy, and hormone or epinasty
effects. Thus, in some embodiments, the cyclopropene amine
compounds described herein inhibit one or more of ripening or
senescence of flowers, fruits, and vegetables; abscission of
foliage, flowers, and fruit; the shortening of life of ornamental
plants, cut flowers, shrubbery, seeds, or dormant seedlings;
inhibition of growth; stimulation of growth; auxin activity;
inhibition of terminal growth; control of apical dominance;
increase in branching; increase in tillering; changing the
morphology of plants; modifying the susceptibility to plant
pathogens such as fungi; changing bio-chemical compositions;
inducing pest resistance; abortion or inhibition of flowering or
seed development; lodging effects; stimulation of seed germination;
breaking of dormancy; hormone effects; and epinasty effects. In
some embodiments, the plant is a whole plant and or any portions
thereof, a field crop, potted plant, cut flower, or harvested fruit
or vegetable. In some embodiments, the ethylene response is fruit
ripening, vegetable ripening, and/or flower senescence.
[0066] In some embodiments, the compounds can be applied in a
closed or open system. In some embodiments, the compounds can be
used as a gas in a closed system, for example, indoors or applied
to a plant in a container or in a greenhouse. In other embodiments,
the compounds can be used a salt, which can be used, for example,
in a spray, in an open system, such as outdoors, for example, on
field crops or landscape plants.
[0067] The term "plant" is used in a generic sense herein, and
includes woody-stemmed plants such as trees and shrubs and further
includes vascular plants. See also LH Bailey Manual of Cultivated
Plants. MacMillan Publishing Company; revised edition (June 1949)
for a list of other suitable plants.
[0068] Plants to be treated by the methods described herein include
whole plants and any portions thereof, field crops, landscape
plants, potted plants, cut flowers (stems and flowers), and
harvested fruits and vegetables. Accordingly, plants include
agricultural produce, such as fresh produce and landscape plants
such as trees, shrubs, potted plants and ornamental plants
including flowers.
[0069] Plants treated with the compounds and by the methods of the
present invention are treated with a non-phytotoxic amount of the
active compound.
[0070] Vegetables which may be treated by the method of the present
invention to inhibit ripening and/or senescence include leafy green
vegetables such as lettuce (e.g., Lactuea sativa), spinach (Spinaca
oleracea), and cabbage (Brassica oleracea), various roots, such as
potatoes (Solanum tuberosum) and carrots (Daucus), bulbs, such as
onions (Allium sp.), herbs, such as basil (Ocimum basilicum),
oregano (Origanum vulgare), dill (Anethum graveolens), as well as
soybean (Glycine max), lima beans (Phaseolus limensis), peas
(Lathyrus spp.), corn (Zea mays), broccoli (Brassica oleracea
italica), cauliflower (Brassica oleracea botrytis), and asparagus
(Asparagus officinalis).
[0071] Fruits which may be treated by the method of the present
invention to inhibit an ethylene response, such as ripening,
include tomatoes (Lycopersicon esculentum), apples (Malus
domestica), bananas (Musa sapientum), pears (Pyrus communis),
papaya (Carica papaya), mangoes (Mangifera indica), peaches (Prunus
persica), apricots (Prunus armeniaca), nectarines (Prunus persica
nectarina), oranges (Citrus sp.), lemons (Citrus limonia), limes
(Citrus aurantifolia), grapefruit (Citrus paradisi), tangerines
(Citrus nobilis deliciosa), kiwi (Actinidia chinenus), melons such
as cantaloupe (C. cantalupensis) and musk melon (C. melo),
pineapple (Aranas comosus), persimmon (Diospyros sp.), various
small fruits including berries such as strawberries (Fragaria),
blueberries (Vaccinium sp.) and raspberries (e.g., Rubus ursinus),
green beans (Phaseolus vulgaris), members of the genus Cucumis such
as cucumber (C. sativus), and avocados (Persea americana).
[0072] Ornamental plants that may be treated by the method of the
present invention to inhibit an ethylene response, such as
senescence and/or shortening of flower life and, thus prolong
flower life and appearance (e.g., delay wilting), include potted
ornamentals, and cut flowers. Potted ornamentals and cut flowers
which may be treated with the present invention include azalea
(Rhododendron spp.), hydrangea (Macrophylla hydrangea), hybiscus
(Hibiscus rosasanensis), snapdragons (Antirrhinum sp.), poinsettia
(Euphorbia pulcherima), cactus (e.g. Cactaceae schlumbergera
truncata), begonias (Begonia sp.), roses (Rosa spp.), tulips
(Tulipa sp.), daffodils (Narcissus spp.), dandelions (Taraxacum
offinale), petunias (Petunia hybrida), carnation (Dianthus
caryophyllus), lily (e.g., Lilium sp.), gladiolus (Gladiolus sp.),
alstroemeria (Alstoemeria brasiliensis), anemone (e.g., Anemone
blanda), columbine (Aquilegia sp.), aralia (e.g., Aralia
chinensis), aster (e.g., Aster carolinianus), bougainvillea
(Bougainvillea sp.), camellia (Camellia sp.), bellflower (Campanula
sp.), cockscomb (celosia sp.), falsecypress (Chamaecyparis sp.),
chrysanthemum (Chrysanthemum sp.), clematis (Clematis sp.),
cyclamen (Cyclamen sp.), freesia (e.g., Freesia refracta), and
orchids of the family Orchidaceae.
[0073] Plants which may be treated by the methods of the present
invention to inhibit an ethylene response, such as abscission of
foliage, flowers and fruit, include cotton (Gossypium spp.),
apples, pears, cherries (Prunus avium), pecans (Carva illinoensis),
grapes (Vitis vinifera), olives (e.g. Vitis vinifera and Olea
europaea), coffee (Coffea arabica), snapbeans (Phaseolus vulgaris),
and weeping fig (ficus benjamina), as well as dormant seedlings
such as various fruit trees including apple, ornamental plants,
shrubbery, and tree seedlings. In addition, shrubbery which may be
treated according to the present invention to inhibit an ethylene
response, such as abscission of foliage, include privet (Ligustrum
sp.), photinea (Photinia sp.), holly (Ilex sp.), ferns of the
family Polypodiaceae, schefflera (Schefflera sp.), aglaonema
(Aglaonema sp.), cotoneaster (Cotoneaster sp.), barberry (Berberis
sp.), waxmyrtle (Myrica sp.), abelia (Abelia sp.), acacia (Acacia
sp.) and bromeliades of the family Bromeliaceae.
[0074] Field crops which may be treated by the methods of the
present invention include a plurality of, or at least more than
one, tree, bush, shrub, plant, etc. including the vegetables,
fruits, ornamental plants and plants discussed herein.
[0075] Active compounds of the present invention have proven to be
unexpectedly potent inhibitors of ethylene action on plants, fruits
and vegetables, even when applied at low concentrations and varying
temperatures. Among other things, compounds of the present
invention may result in a longer period of insensitivity to
ethylene than compounds found in the prior art. This longer period
of insensitivity may occur even when compounds of the present
invention are applied at a lower concentration than previous
compounds, at varying temperatures and/or when applied as a gas or
spray. In some situations, a higher concentration can be used or a
longer time interval can be used.
[0076] The present invention is explained in greater detail in the
following non-limiting examples. In these examples, .mu.l means
microliters; ml means milliliters; nl means nanoliters; l means
liters; cm means centimeters; and temperatures are given in degrees
Celsius.
EXAMPLES
Materials and Methods
1. Preparation of Compounds
A. The preparation of cyclopropene,
N,N-dimethyl-(1-cyclopropenylmethyl) amine
[0077] The cyclopropene, N,N-dimethyl-(1-cyclopropenylmethyl) amine
was prepared from 2-bromo-3-(N,N-dimethyamino) propene.
2-bromo-3-(N,N-dimethyamino) propene was synthesized from
2,3-dibromopropene and dimethylamine by a modified procedure of
Corey, et al. (1971) (See E. J. Corey, et. al., The synthesis of
racemic .alpha.-trans- and .beta.-trans-bergamotene, J. Am. Chem.
Soc., 93, 7016-7021 (1971).) 2-bromo-3-(N,N-dimethyamino) propene
reacted with bromoform in the presence of 50% NaOH and subsequently
reacted with methyllithium to provide the cyclopropene
N,N-dimethyl-(1-cyclopropenylmethyl)amine by using the procedure of
Al Dulayymi et al. (1996 and 1997) and (Al Dulayymi et al. 1997)
(See Al Dulayymi JR., et al., Structure based interference with
insect behaviour-Cyclopropenes analogs of pheromones containing
Z-Alkenes, Tetrahedron, 52, 12509-12520 (1996); Al Dulayymi A. R.,
et al., Simple four and five carbon cyclopropane and cyclopropene
synthetic intermediates, Russian. J. Org. Chem., 33, 798-816
(1997); Al Dulayymi J. R., et al., Synthesis of Putative .about.6-,
12 and .about.15-Desaturase Inhibitors., Tetrahedron, 53, 1099-1110
(1997)).
B. The preparation of N,N-diethyl-(1-cyclopropenylmethyl)amine,
N,N-dipropyl-(1-cyclopropenylmethyl)amine and
N,N-dibutyl-(1-cyclopropenylmethyl)amine
[0078] By applying a similar procedure,
N,N-diethyl-(1-cyclopropenylmethyl)amine,
N,N-dipropyl-(1-cyclopropenylmethyl)amine and
N,N-dibutyl-(1-cyclopropenylmethyl)amine can also be prepared by
using the appropriate diamines and 2,3-dibromopropene.
C. The preparation of N,N-dicyclopropenylmethylamine
[0079] N,N-dicyclopropenylmethylamine was prepared by a modified
procedure of Bottini et al. (1973) and Bottini and Olsen (1973)
followed by reaction with bromoform and 50% NaOH and subsequently
reacted with methyl lithium by using the procedure of Al Dulayymi
et al. (1996) to provide the cyclopropene. (See Bottini A. T. Dey,
et al., 2-Bromoallylamine In Organic Synthesis Collective Vol. 5,
John Wiley and Sons New York., 121-124, (1973); Bottini, A T, et
al., N-(2-bromoallyl)ethylamine In Organic Synthesis Collective
Volume 5 John Wiley and Sons New York. 124-126, (1973); Al Dulayymi
J. R., et al., Structure based interference with insect
behaviour-Cyclopropenes analogs of pheromones containing Z-Alkenes,
Tetrahedron, 52, 12509-12520 (1996)).
D. The preparation of N-(1-cyclopropenylmethyl)aniline
[0080] N-(1-cyclopropenylmethyl)aniline was prepared by a modified
procedure of Bottini and Olsen (1973) followed by treatment with
50% NaOH and subsequently with methyl lithium by the procedure of
Al Dulayymi et al. (1996) to provide the cyclopropene. (See
Bottini, A T, et al., N-(2-bromoallyl)ethylamine In Organic
Synthesis Collective Volume 5 John Wiley and Sons New York.
124-126, (1973); Al Dulayymi J. R., et al., Structure based
interference with insect behaviour-Cyclopropenes analogs of
pheromones containing Z-Alkenes, Tetrahedron, 52, 12509-12520
(1996)).
[0081] The structures of exemplary cyclopropene amine compounds are
further illustrated in Table 1 below.
TABLE-US-00001 TABLE 1 Minimum Protection Concentration Time
Structure and Name (nl/l) (Days) ##STR00011## 5.7 33 ##STR00012##
73 34 ##STR00013## 59 32 ##STR00014## 30 33 ##STR00015## 184 33
##STR00016## 248 32 Minimum concentration is the amount of compound
as a gas in nl/l that would protect bananas by a 24 hour exposure.
All bananas remained green for 26-28 days and remained hard for
32-34 days.
2. Plant Material
[0082] Untreated mature green bananas (Musa paradisiaca L) from
Costa Rica which were ready for market were obtained from the local
Farmers Market and were kept at 14.5.degree. C. until use. Bananas
were used within 24 hours of arrival. Experiments were conducted at
approximately 22-23.degree. C. No damaged fruit were used in the
experiments.
[0083] In experiments to study effects of the compounds described
herein on the ethylene response in flowering plants, the petunia
(Petunia hybridia), a well known ethylene sensitive flower, and the
dandelion (Krigia dandelion) were used in the experiments.
3. Treatment
[0084] To obtain gas phase values, compounds in the gaseous phase
were applied to the bananas by pipetting an ether solution of the
compound onto filter paper in order to increase the surface area in
a 3 liter jar and then allowed to stand for 24 hours to allow the
compounds to evaporate and diffuse to the binding site. The jars
were then vented and ethylene was injected and allowed to stand for
a minimum of 15 hours and then allowed to stand at 23.degree. C.
until ethylene responses developed.
[0085] When the effect of the respective salts of the cyclopropenes
were assayed, the salt was mixed with the desired amount of water
containing Tween 20 as a wetting agent and the acid. Usually 200: l
of water, 20: l of Tween 20 and 100: l of 0.1 M acid and the
compound dissolved in ether were used. These salts were applied to
the banana. The peels were swabbed to spread the mixture and
increase the exposed surface area. The bananas were placed in an
unsealed 3-liter jar and allowed to stand 24 hours. In the case of
the carbonate salt, the compound was exposed to carbon dioxide in
water long enough for the salt to form. In this case, the carbonate
salt was formed by mixing the compound dissolved in water with
CO.sub.2. The concentration of CO.sub.2 in water at 1 atmosphere
and 25.degree. C. is reported to be 0.0338 M (Daniels and Alberty
1955) (See Daniels, F, et al., Physical Chemistry, John Wiley and
Sons New York, 200 (1955). Only about 1% of the CO.sub.2 is present
as carbonic acid but equilibrium is fairly rapid and as the
carbonic acid is consumed more is produced. Carbonic acid is a much
stronger acid than the usually published pK.sub.a of 6.38 would
indicate. When corrected for the equilibrium a pK.sub.a value of
3.58 is obtained for carbonic acid (Cotton et al. 1999), which
indicates that carbonic acid is generally stronger than formic
acid. (See Cotton, et al., Advanced Inorganic Chemistry John Wiley
and Sons. New York, 152 (1999). At the end of 24 hours, ethylene
was injected and the jars were sealed. After 15 hours exposure, the
bananas were removed and observed for several days for the effect
of ethylene. An untreated check banana and a similar untreated
banana treated with ethylene only were included in each experiment
for comparison.
[0086] In some studies, only part of the peel was treated. When the
peel was exposed to ethylene, the pulp which was not protected
began to ripen and produce large amounts of ethylene. The untreated
part of the peel ripened quickly but the treated part remained
green for many days. In some instances there was a substantial
portion of the treated peel green after 18 days.
[0087] For gaseous phase treatment, the compound is applied to
bananas by pipetting solution onto filter paper. Filter paper is
used to increase surface area in a 3 L jar. The jar is sealed for
24 hours to give enough time to diffuse through plant tissue to the
ethylene binding sites. 333 ul/L of ethylene gas is added to the
jars. The jars are then resealed for 15 hours. This allows for
maximal exposure to ethylene to measure effectiveness of the
compounds. Firmness was recorded over a number of days.
Disappearance of chlorophyll was determined by extracting
chlorophyll from banana peels. Absorbance was measured in a
spectrometer.
[0088] For aqueous phase (salts) treatment, compounds were
alternatively tested by mixing the solutions in acid and a
detergent. The detergent, Tween 20, was used as a wetting agent.
Solutions were then applied at various concentrations to the banana
with a cotton swab. Bananas were then sealed in a jar and treated
in the same manner as with the gas compound procedures described
above.
4. Minimum Amount Required for Protection
[0089] The minimum amount of cyclopropene necessary to protect
bananas from ethylene was determined after the bananas had been
exposed to the compound for 24 hours. Following this time, the
fruits were vented for 10 minutes and then exposed to 333l.sup.-l
of ethylene gas treatment. This has been the procedure for most
other studies involving cyclopropene compounds and bananas. This
time was used so that a reasonable comparison could be made with
previous work (Sister. et al. 1996 a; 1996b; 1999; 2001; 2003).
(See Sister E. C., et al., Effect of 1-methylcyclopropene, and
methylenecyclopropene on ethylene binding and ethylene action in
cut carnations, Plant Growth Reg., 18, 79-86, (1996a); Sister E. C.
et al., Comparison of cyclopropene, 1-MCP and
3,3-dimethylcyclopropene as ethylene antagonist in plants, Plant
Growth Reg., 18, 169-174, (1996b); Sister E. C., et al., Inhibition
of ethylene responses by 1-methylcyclopropene and
3-methylcyclopropene, Plant Growth Reg., 27, 105-111 (1999);
Sister, E. C., et al., The effect of chemical structure on the
antagonism by cyclopropenes of ethylene responses in banana, Plant
Growth Reg., 33, 107-110 (2001); Sister, E. C., et al.,
1-Substituted cyclopropenes: Effective blocking agents for ethylene
action in plants, Plant Growth Reg, 40, 221-228 (2003)).
5. Time of Protection
[0090] Bananas were treated to an amount of compound believed to
saturate the receptor sites (10 times the minimum amount for
protection). The bananas were exposed for 24 hours then vented.
They were kept on a laboratory bench and each day a sample was
exposed to ethylene. The day the bananas were treated with ethylene
and the day the bananas turned yellow and became soft were
recorded. Generally, this observation occurred about 3 days after
the ethylene treatment day. The treatment day the bananas first
ripened was considered to be the time of protection.
6. Chlorophyll Determination
[0091] Chlorophyll was determined by the method of Amon (Amon, D I
(1949) Copper content in isolated chloroplasts. Polyphenoloxidase
in Beta vulgaris. Plant Physiology 24:1-15) or by using a
reflective chlorophyll meter (Field Scout CM 1000 Spectronic
Technologies Inc.). To extract chlorophyll, a measured area of peel
was cut from representative areas of the peel and placed in boiling
water for 3 minutes. The samples were then removed and blended with
acetone. After standing overnight in the dark, they were filtered
then concentrated in a hood and chlorophyll determined by the
method of Arnon (1949) according to the procedures outlined by
Holden (1965).
7. Gas Chromatography and Spectrophotometry
[0092] Gas chromatographic measurements were made on a GP Carbopack
C 80/100 0.2% Carbowax 1500 Supelco Supelco Park Bellefonte Park
Pa. 16823-0048 Separation was performed according to the procedure
of Sisler et al. 2003. (See Sisler, E. C., et al., 1-Substituted
cyclopropenes: Effective blocking agents for ethylene action in
plants. Plant Growth Reg. 40, 221-228 (2003)).
[0093] Banana peel samples were cut and mixed with acetone to
extract chlorophyll. Samples were made in an ether solution and
absorbance measured at 663 nm.
8. Experimental Results
[0094] The effectiveness of the compounds was measured by the
amount of chlorophyllpresent in bananas after some number of
days.
A. Effect of Concentration of Cyclopropene Compounds Applied as a
Gas
[0095] The results of cyclopropenes applied as a gas are reported
in Table 1 below. The minimum concentration of the compound
N,N-dicyclopropenylmethylamine required for protection of bananas
by a 24 hour exposure was 5.3 nl l.sup.-l of the compound as a gas.
The protection time was 33 days. The minimum concentration of
N,N-dimethyl-(1-cyclopropenylmethyl) amine required for protection
by a 24 hour exposure was 73 nl.l.sup.-l of the compound as a gas.
The protection time was 34 days. The minimum concentration of
N,N-diethyl (1-cyclopropenyl methyl)amine required for protection
by a 24 hour exposure was 59 of the compound as a gas. The
protection time was 32 days. The minimum concentration of
N,N-dipropyl-(1-cyclopropenylmethyl)amine required for protection
by a 24 hour exposure was 30 nl.l.sup.-l of the compound as a gas.
The protection time was 33 days. The minimum concentration of
N,N-dibutyl (1cyclopropenylmethyl) amine required for protection by
a 24 hour exposure was 184 nl.l.sup.-l of the compound as a gas.
The protection time was 33 days. The minimum concentration of
N-(1-methylcyclopropene-1-aniline required for protection by a 24
hour exposure was 248 nl l.sup.-l of the compound as a gas. The
protection time was 32 days.
B. Effect of Concentration of Cyclopropene on Chlorophyll Content
of Banana Peel when Applied as a Salt
[0096] Experiments were conducted to treat the bananas with the
cyclopropene compounds as a salt. Fruit color changes offer some
advantages and provide useful information regarding the interaction
of the compounds with the ethylene receptor and further provide a
good assay system for the compounds to measure diffusion in the
tissue.
C. Effect of Different Acids on the Stability of the Cyclopropene
Compounds
[0097] When N,N-dibutyl-(1-cyclopropenylmethyl)amine was incubated
with different acids or salts at different pH values down to pH 1.5
for a period of 1 hour, followed by compound re-isolation and use
in the usual treatments, little or no inactivation occurred (See
Table 2). However, these compounds are thought to be unstable under
very acidic conditions. Liao et al. in some synthetic procedures
lower the pH to 1-3.
TABLE-US-00002 TABLE 2 Effect of pH on stability of N,N-
dibutyl-(1-cyclopropenylmethyl)amine. Chlorophyll Treatment (% of
control) Gas control 100 H.sub.2O 98 Sodium acetate (0.1M, pH 4.75)
100 Sodium formate (0.1M, pH 3.0) 100 Phosphoric acid (.1M, pH 1.5)
98 Incubated 1 hour at the indicated pH values -and then
neutralized with NaOH and extracted with ether. Bananas were
exposed to this extract in the usual manner as a gas for 24 hours
and then ethylene for 15 hours. Readings at 7 days.
D. Effect of Salts on the Application and Protection of the
Peel
[0098] When a water solution of different salts (phosphate, acetate
and formate) of the cyclopropene compound was applied, the peel was
protected in all cases. See Table 3 below.
TABLE-US-00003 TABLE 3 Effect of pH on
N,N-dipropyl-(1-cyclopropenylmethyl)amine salt activity on
protection of chlorophyll in bananas. Chlorophyll Treatment (% of
control) Control 100 DP Gas 100 0.1M Acetic acid 31 0.1M Acetic
acid buffer (pH 4.75) 33 0.1M Formic acid 30 Phosphoric acid (pH
1.5) 30 The sample was applied with a swab to 1/2 banana with 20
.mu.l of Tween 20 and water to 200 .mu.l for 24 hours and then
exposed to ethylene for 15 hours. Readings made at 5 days.
[0099] These did not differ much in effect. At high levels where
the acid was in excess, injury occurred with some salt-acid
mixtures. Up to 0.2 M acid concentrations did not seem to cause
injury.
[0100] Some experiments were conducted using the carbonate salt
(see Table 4 below). It appeared to be as effective as the other
acids, and it has the advantage of not leaving a residue if an
excess of acid is applied. Any excess is likely to be lost rapidly
as carbon dioxide. Other acids can be used. Generally, those with a
pH above 1.0 are suitable. When one-half of the banana was treated
and the other half was not treated with the compound, the treated
half was protected and the untreated half was not. The untreated
peel ripened when exposed to ethylene. The peel covering the half
of the banana treated with the compound did not ripen when the
amount of the compound was sufficiently high for protection. (FIG.
2). If an amount of surface equivalent to one-half of the banana
was treated in the middle of the banana, both ends ripened upon
exposure to ethylene but the treated portion did not. These results
show that the salts penetrate the peel surface and may inactivate
the receptor. There did not appear to be diffusion from the applied
area into areas that had no cyclopropene compound applied. The pulp
of the banana ripened in the treated fruits. Ethylene treatment
(300 .mu.l l.sup.-1) started after 24 hours and lasted 15 hours.
This protocol should have stopped the action of the unbound
cycloprenes rapidly and essentially stopped any further
inactivation of the receptors.
TABLE-US-00004 TABLE 4 Comparison of
N,N-dipropyl-(1-cyclopropenylmethyl)amine acetate and carbonate
salts on chlorophyll content of banana peel. Chlorophyll Treatment
(% of Control) Untreated control 100 Carbonic acid + 200 .mu.l
dipropyl compound 48 Carbonic + 50 .mu.l dipropyl compound 47
Acetic acid + 200 .mu.l dipropyl compound 46 Acetic acid + 50 .mu.l
dipropyl compound 43 Ethylene 0 Exposure was to the dipropyl
compound for 24 hours and after venting 15 hours to ethylene (300
.mu.l/l) Chlorophyll values were taken 5 days after the ethylene
was added.
[0101] In FIG. 3, the lines represent a comparison between
N,N-dimethyl-(1-cyclopropenyl methyl) amine and
N,N-dibutyl-(1-cyclopropenylmethyl) amine in their uptake and
protection of bananas against ethylene. The compounds were applied
on an equal activity basis in a series of concentrations starting
at 219 nl for the dimethyl compound and 552 nl for the dibutyl
cyclopropene. Each of these were increased by 0, 5.times. for the
second point and also 0.5.times. for third point and by 1.times.
for the fourth point. The series in both cases would be 1, 1.5. 2,
and 2.5. The initial point in both cases was 3 times the minimum
for the compound as a gas (see Table 1). Since the activity of the
volume of the gas of the jar in determining the minimum value is 3
L, the amount used in the first point would be close to the minimum
value for amount of the gas to protect the banana. The lowest of
the applied compounds started at 3 times the minimum protection
value of 73 nl l.sup.-1 and 184 nl l.sup.-1 given in FIG. 3. Each
point in the two series should have the same activity as the
counterpart point in the other series. The lines resemble each
other except in one respect. The difference between the highest and
lowest value for the dimethyl cyclopropene was 30.9% of the control
and the dibutyl cyclopropene was 48% of the control. The dibutyl
compound appears to inactivate the receptor at all concentrations
during a 24 hour exposure according to the amount present. It is
1.55.times. more rapid than the dimethyl compound.
E. Effect of Compounds of Flowering Plants
[0102] FIGS. 7 and 8 present the results of using 100 nI
N,N-dipropyl(1-cyclopropenylmethyl)amine on dandelions and
petunias, respectively. The Krigia dandeloin is commonly known as a
weed that can be found along roads during particular times of the
year such as spring and summer. It is of interest because ethylene
can cause the plant to become dormant and, as a defense mechanism,
the plant can become dormant when there is drought. As shown in
FIG. 7, at 5 days, the dandelion treated with the compound, using
either a gas or carbonate salt form, shows that these compounds can
be used to regulate physiological processes in dandelions. The
petunia is a well-known ethylene sensitive flower. As noted in FIG.
8, at 5 days, the petunia treated with the compound, using either a
gas or carbonate salt form, appears to withstand the ethylene
response.
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[0127] The foregoing embodiments and examples are illustrative of
the present invention and are not to be construed as limiting
thereof. The invention is defined by the following claims, with
equivalents of the claims to be included therein.
* * * * *