U.S. patent application number 10/500249 was filed with the patent office on 2005-03-31 for processes for producing coenzyme q10.
Invention is credited to Kanda, Akihisa, Kato, Takahisa, Kitamura, Shiro, Ueda, Yasuyoshi, Yajima, Kazuyoshi.
Application Number | 20050069996 10/500249 |
Document ID | / |
Family ID | 19189359 |
Filed Date | 2005-03-31 |
United States Patent
Application |
20050069996 |
Kind Code |
A1 |
Yajima, Kazuyoshi ; et
al. |
March 31, 2005 |
Processes for producing coenzyme q10
Abstract
The present invention relates to a process for producing reduced
coenzyme Q.sub.10 which comprises obtaining microbial cells
containing reduced coenzyme Q.sub.10 at a ratio of not less than 70
mole % among the entire coenzymes Q.sub.10, optionally disrupting
the cells and recovering thus-produced reduced coenzyme Q.sub.10.
The present invention also relates to a process for producing
oxidized coenzyme Q.sub.10 which comprises either recovering
oxidized coenzyme Q.sub.10 after oxidizing the above-mentioned
microbial cells or disrupted product thereof, or recovering reduced
coenzyme Q.sub.10 from the above-mentioned microbial cells or
disrupted product thereof to oxidize thus-obtained reduced coenzyme
Q.sub.10 thereafter. According to the processes of the present
invention, reduced coenzyme Q.sub.10 and oxidized coenzyme Q.sub.10
can be produced simply on the industrial scale.
Inventors: |
Yajima, Kazuyoshi; (Hyogo,
JP) ; Kato, Takahisa; (Hyogo, JP) ; Kanda,
Akihisa; (Osaka, JP) ; Kitamura, Shiro;
(Hyogo, JP) ; Ueda, Yasuyoshi; (Hyogo,
JP) |
Correspondence
Address: |
Brinks Hofer
Gilson & Lione
PO Box 10395
Chicago
IL
60610
US
|
Family ID: |
19189359 |
Appl. No.: |
10/500249 |
Filed: |
November 3, 2004 |
PCT Filed: |
December 27, 2002 |
PCT NO: |
PCT/JP02/13766 |
Current U.S.
Class: |
435/156 |
Current CPC
Class: |
C12P 7/66 20130101; C12P
7/22 20130101 |
Class at
Publication: |
435/156 |
International
Class: |
C12P 007/22 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 27, 2001 |
JP |
2001-398545 |
Claims
1. A process for producing the reduced coenzyme Q.sub.10
represented by the following formula (I): 5which comprises
culturing reduced coenzyme Q.sub.10-producing microorganisms in a
culture medium containing a carbon source, a nitrogen source, a
phosphorus source and a micronutrient to obtain microbial cells
containing reduced coenzyme Q.sub.10 at a ratio of not less than 70
mole % among the entire coenzymes Q.sub.10, optionally disrupting
the microbial cells and extracting thus-produced reduced coenzyme
Q.sub.10 by an organic solvent:
2. The process according to claim 1, wherein the reduced coenzyme
Q.sub.10 is contained at a ratio of not less than 70 mole % among
the entire coenzymes Q.sub.10.
3. (Canceled)
4. The process according to claim 1, wherein the culture is carried
out at 15 to 45.degree. C. and at a pH of 4 to 9.
5. The process according to claim 1, wherein the concentration of
the carbon source in the culture is controlled to a concentration
that no adverse effects are substantially caused on the
productivity of reduced coenzyme Q.sub.10.
6. (Canceled)
7. (Canceled)
8. (Canceled)
9. (Canceled)
10. (Canceled)
11. (Canceled)
12. (Canceled)
13. (Canceled)
14. (Canceled)
15. (Canceled)
16. The process according to claim 1, wherein the extraction of
reduced coenzymes Q.sub.10 is carried out from wet cells or dry
cells of the microbial cells or disrupted product thereof by using
a hydrophilic organic solvent.
17. (Canceled)
18. The process according to claim 1, wherein the extraction of the
reduced coenzymes Q.sub.10 is carried out from an aqueous
suspension of the microbial cells or disrupted product thereof by
using a hydrophobic organic solvent.
19. The process according to claim 18, wherein the hydrophobic
organic solvent is a hydrocarbon, a fatty acid ester or an
ether.
20. The process according to claim 18, wherein the hydrophilic
organic solvent is used as an auxiliary solvent in combination with
the hydrophobic organic solvent.
21. The process according to claim 20, wherein the hydrophobic
organic solvent is a hydrocarbon, and the hydrophilic organic
solvent is an alcohol.
22. (Canceled)
23. (Canceled)
24. The process according to claim 20, wherein the extraction is
carried out under the condition that the hydrophobic organic
solvent is contained in 25 to 65% by volume and the hydrophilic
organic solvent is contained in 5 to 50% by volume.
25. (Canceled)
26. (Canceled)
27. (Canceled)
28. (Canceled)
29. The process according to claim 1, wherein the reduced coenzyme
Q.sub.10 is contained at a ratio of not less than 70 mole % among
the entire coenzymes Q.sub.10 in the case that the reduced coenzyme
Q.sub.10-producing microorganisms are cultured with shaking
(amplitude: 2 cm, 310 reciprocation/min) at 25.degree. C. for 72
hours in 10 mL of a culture medium [(glucose: 20 g, peptone: 5 g,
yeast extract: 3 g, malt extract: 3 g)/L, pH: 6.0] using a test
tube (inner diameter: 21 mm, entire length: 200 mm), the obtained
broth is optionally concentrated, the obtained solution is
vigorously shaken for 3 minutes using 10 parts by volume of glass
beads (425 to 600 .mu.m) to disrupt the microorganisms under a
nitrogen atmosphere in the concomitant presence of 3 parts by
volume of isopropanol and 18.5 parts by volume of n-hexane relative
to 10 parts by volume of the broth, and the prepared hydrophobic
organic solvent phase (n-hexane phase) is analyzed by HPLC.
30. The process according to claim 29, wherein the reduced coenzyme
Q.sub.10-producing microorganisms have not less than 1 .mu.g/mL of
a productivity of reduced coenzyme Q.sub.10 per unit culture medium
when measured by HPLC under the condition according to claim
29.
31. The process according to claim 30, wherein the microorganisms
are microorganisms of the genus Agrobacterium, the genus
Aspergillus, the genus Acetobacter, the genus Aminobacter, the
genus Agromonas, the genus Acidiphilium, the genus Bulleromyces,
the genus Bullera, the genus Brevundimonas, the genus Cryptococcus,
the genus Chionosphaera, the genus Candida, the genus Cerinosterus,
the genus Exisophiala, the genus Exobasidium, the genus Fellomyces,
the genus Filobasidiella, the genus Filobasidium, the genus
Geotrichum, the genus Graphiola, the genus Gluconobacter, the genus
Kockovaella, the genus Kurtzmanomyces, the genus Lalaria, the genus
Leucosporidium, the genus Legionella, the genus Methylobacterium,
the genus Mycoplana, the genus Oosporidium, the genus Pseudomonas,
the genus Psedozyma, the genus Paracoccus, the genus petromyces,
the genus Rhodotorula, the genus Rhodosporidium, the genus
Rhizomonas, the genus Rhodobium, the genus Rhodoplanes, the genus
Rhodopseudomonas, the genus Rhodobacter, the genus Sporobolomyces,
the genus Sporidiobolus, the genus Saitoella, the genus
Schizosaccharomyces, the genus Sphingomonas, the genus
Sporotrichum, the genus Sympodiomycopsis, the genus
Sterigmatosporidium, the genus Tapharina, the genus Tremella, the
genus Trichosporon, the genus Tilletiaria, the genus Tilletia, the
genus Tolyposporium, the genus Tilletiopsis, the genus Ustilago,
the genus Udeniomyces, the genus Xanthophilomyces, the genus
Xanthobacter, the genus Paecilomyces, the genus Acremonium, the
genus Hyhomonus, or the genus Rhizobium.
32. (Canceled)
33. A process for producing the oxidized coenzyme Q.sub.10
represented by the following formula (II): 6which comprises
culturing reduced coenzyme Q.sub.10-producing microorganisms in a
culture medium containing a carbon source, a nitrogen source, a
phosphorus source and a micronutrient to obtain microbial cells
containing reduced coenzyme Q.sub.10 at a ratio of not less than 70
mole % among the entire coenzymes Q.sub.10, optionally disrupting
the microbial cells; and either oxidizing thus-produced reduced
coenzyme Q.sub.10 to oxidized coenzyme Q.sub.10 and then extracting
the resultant by an organic solvent, or extracting thus-produced
reduced coenzyme Q.sub.10 by an organic solvent, purifying
optionally and oxidizing the resultant to oxidized coenzyme
Q.sub.10.
34. (Canceled)
35. The process according to claim 33, wherein the culture is
carried out at 15 to 45.degree. C. and at a pH of 4 to 9.
36. The process according to claim 33, wherein the concentration of
the carbon source in the culture is controlled to a concentration
that no adverse effects are substantially caused on the
productivity of reduced coenzyme Q.sub.10.
37. (Canceled)
38. (Canceled)
39. (Canceled)
40. (Canceled)
41. (Canceled)
42. (Canceled)
43. (Canceled)
44. The process according to claim 33, wherein the extraction of
coenzymes Q.sub.10 is carried out from wet cells or dry cells of
the microbial cells or disrupted product thereof by using a
hydrophilic organic solvent.
45. (Canceled)
46. The process according to claim 33, wherein the extraction of
the coenzymes Q.sub.10 is carried out from an aqueous suspension of
the microbial cells or disrupted product thereof by using a
hydrophobic organic solvent.
47. (Canceled)
48. (Canceled)
49. (Canceled)
50. (Canceled)
51. (Canceled)
52. (Canceled)
53. (Canceled)
54. The process according to claim 33, wherein the reduced coenzyme
Q.sub.10 is contained at a ratio of not less than 70 mole % among
the entire coenzymes Q.sub.10 in the case that the reduced coenzyme
Q.sub.10-producing microorganisms are cultured with shaking
(amplitude: 2 cm, 310 reciprocation/min) at 25.degree. C. for 72
hours in 10 mL of a culture medium [(glucose: 20 g, peptone: 5 g,
yeast extract: 3 g, malt extract: 3 g)/L, pH: 6.0] using a test
tube (inner diameter: 21 mm, entire length: 200 mm), the obtained
broth is optionally concentrated, the obtained solution is
vigorously shaken for 3 minutes using 10 parts by volume of glass
beads (425 to 600 .mu.m) to disrupt the microorganisms under a
nitrogen atmosphere in the concomitant presence of 3 parts by
volume of isopropanol and 18.5 parts by volume of n-hexane relative
to 10 parts by volume of the broth, and the prepared hydrophobic
organic solvent phase (n-hexane phase) is analyzed by HPLC.
55. (Canceled)
56. The process according to claim 33, wherein the microorganisms
are microorganisms of the genus Agrobacterium, the genus
Aspergillus, the genus Acetobacter, the genus Aminobacter, the
genus Agromonas, the genus Acidiphilium, the genus Bulleromyces,
the genus Bullera, the genus Brevundimonas, the genus Cryptococcus,
the genus Chionosphaera, the genus Candida, the genus Cerinosterus,
the genus Exisophiala, the genus Exobasidium, the genus Fellomyces,
the genus Filobasidiella, the genus Filobasidium, the genus
Geotrichum, the genus Graphiola, the genus Gluconobacter, the genus
Kockovaella, the genus Kurtzmanomyces, the genus Lalaria, the genus
Leucosporidium, the genus Legionella, the genus Methylobacterium,
the genus Mycoplana, the genus Oosporidium, the genus Pseudomonas,
the genus Psedozyma, the genus Paracoccus, the genus petromyces,
the genus Rhodotorula, the genus Rhodosporidium, the genus
Rhizomonas, the genus Rhodobium, the genus Rhodoplanes, the genus
Rhodopseudomonas, the genus Rhodobacter, the genus Sporobolomyces,
the genus Sporidiobolus, the genus Saitoella, the genus
Schizosaccharomyces, the genus Sphingomonas, the genus
Sporotrichum, the genus Sympodiomycopsis, the genus
Sterigmatosporidium, the genus Tapharina, the genus Tremella, the
genus Trichosporon, the genus Tilletiaria, the genus Tilletia, the
genus Tolyposporium, the genus Tilletiopsis, the genus Ustilago,
the genus Udeniomyces, the genus Xanthophilomyces, the genus
Xanthobacter, the genus Paecilomyces, the genus Acremonium, the
genus Hyhomonus, or the genus Rhizobium.
57. (Canceled)
Description
TECHNICAL FIELD
[0001] The present invention relates to
[0002] a process for producing the reduced coenzyme Q.sub.10
represented by the following formula (I): 1
[0003] and a process for producing the oxidized coenzyme Q.sub.10
represented by the following formula (II): 2
[0004] More particularly,-the present invention relates to
[0005] a process for producing reduced coenzyme Q.sub.10
[0006] which comprises culturing reduced coenzyme
Q.sub.10-producing microorganisms to obtain microbial cells
containing reduced coenzyme Q.sub.10 at a ratio of not less than 70
mole % among the entire coenzymes Q.sub.10,
[0007] optionally disrupting the microbial cells and recovering
thus-produced reduced coenzyme Q.sub.10.
[0008] The present invention also relates to a process for
producing oxidized coenzyme Q.sub.10 which comprises either
recovering oxidized coenzyme Q.sub.10 after oxidizing the
above-mentioned microbial cells or disrupted product thereof, or
recovering reduced coenzyme Q.sub.10 from the above-mentioned
microbial cells or disrupted product thereof to oxidize
thus-obtained reduced coenzyme Q.sub.10 thereafter.
BACKGROUND ART
[0009] The reduced coenzyme Q.sub.10 (I) and the oxidized coenzyme
Q.sub.10 (II) are mitochondrial electron transport
system-constituting factors in cells of a living body of human and
deal with ATP production by working as electron carriers in
oxidative phosphorization reactions.
[0010] Conventionally, oxidized coenzyme Q.sub.10 has been widely
used for supplementary nutrient foods and cosmetic products in
addition to pharmaceutical products as a pharmaceutically and
physiologically effective substance for a variety of diseases.
[0011] On the other hand, reduced coenzyme Q.sub.10 has not so much
drawn attention so far; however, in these years, there has been
reported that reduced coenzyme Q.sub.10 is more effective in
various applications than oxidized coenzyme Q.sub.10.
[0012] For example, Japanese Kokai Publication Hei-10-330251
discloses an antihypercholesterolemia agent having excellent
cholesterol reducing function, an antihyperlipemia agent, and an
agent for curing and preventing arteriosclerosis which contain
reduced coenzyme Q.sub.10 as an active ingredient. In addition,
Japanese Kokai Publication Hei-10-109933 discloses a pharmaceutical
composition excellent in oral absorbability comprising coenzyme
Q.sub.10 including reduced coenzyme Q.sub.10 as an active
ingredient.
[0013] Furthermore, reduced coenzyme Q.sub.10 is effective as an
antioxidant and a radical scavenger. R. Stocker, et al. have
reported that reduced coenzyme Q.sub.10 prevented peroxidation of
human LDL more efficiently than .alpha.-tocopherol, lycopene and
.beta.-carotene (Proceedings of the National Academy of Science of
the United States of America, vol. 88, pp. 1646-1650, 1991).
[0014] It has been known that oxidized coenzyme Q.sub.10 and
reduced coenzyme Q.sub.10 are in a certain type of equilibrium in a
living body and that oxidized coenzyme Q.sub.10/reduced coenzyme
Q.sub.10 absorbed in the living body are mutually
reduced/oxidized.
[0015] Reduced coenzyme Q.sub.10 is supposedly produced by a
chemical synthesis method, similarly to the process for producing
oxidized coenzyme Q.sub.10. But the synthesis process is supposed
to be complicated, risky and costly. Moreover, in the case of
chemical synthesis methods, it will be necessary to minimize the
subgeneration and contamination of a (Z)-isomer, which is
suspiciously unsafe (Biomedical and Clinical Aspects of Coenzyme Q,
vol. 3, pp. 19-30, 1981). Europe Pharmacopoeia regulates that a
content of (Z)-isomer in oxidized coenzyme Q.sub.10 must be not
more than 0.1%.
[0016] As another process for producing reduced coenzyme Q.sub.10,
it can be supposed a method of utilizing microbial cells, that is,
a method for separating and recovering reduced coenzyme Q.sub.10
from reduced coenzyme Q.sub.10-producing microorganisms. However,
the reduced coenzyme Q.sub.10 produced by the microbial cells of
the above-mentioned microorganisms contains a large amount of
oxidized coenzyme Q.sub.10, and the separation and recovery of
reduced coenzyme Q.sub.10 by a conventional method results in high
cost.
[0017] The following are documents describing the presence of
reduced coenzyme Q.sub.10 in microbial cells and there have been
known the following examples of bacteria.
[0018] (1) An example describing that at lowest 5 to 10% by weight
and at highest. 30 to 60% by weight of reduced coenzyme Q.sub.10
are present among the entire coenzymes Q.sub.10 in culture cells of
photosynthesis bacteria (Japanese Kokai Publication
Sho-57-70834).
[0019] (2) An example describing that the genus Pseudomonas is
subjected to thermal extraction by an organic solvent in the
presence of sodium hydroxide and pyrogallol, and the resultant is
treated with 5% sodium hydrosulfite solution, and further
dehydrated and concentrated to collect an acetone-soluble portion,
and an oil containing reduced coenzyme Q.sub.10 is obtained
(Japanese Kokai Publication Sho-60-75294).
[0020] Both of the above (1) and (2) aim to convert a mixture of
the obtained reduced coenzyme Q.sub.10 and oxidized coenzyme
Q.sub.10 or the obtained reduced coenzyme Q.sub.10 into oxidized
coenzyme Q.sub.10 by further oxidation. Thus, reduced coenzyme
Q.sub.10 is only described as an intermediate substance in
producing oxidized coenzyme Q.sub.10.
[0021] In the above (1), photosynthesis bacteria are used, the
culture of which is complicated. Furthermore, in the microbial
cells of the above-mentioned microorganisms, when the production of
reduced coenzyme Q.sub.10 is aimed at, it cannot be said that the
ratio of reduced coenzyme Q.sub.10 among the entire coenzymes
Q.sub.10 is sufficient.
[0022] The above (2) comprises a process of converting oxidized
coenzyme Q.sub.10 contained in a hexane phase into reduced coenzyme
Q.sub.10 by sodium hydrosulfite, a reducing agent (see Example 3 in
Japanese Kokai Publication Sho-60-75294). Thus, the ratio of
reduced coenzyme Q.sub.10 among the entire coenzymes Q.sub.10 in
the microbial cells is not clear.
[0023] Furthermore, in both of the above (1) and (2), the
production amount of coenzymes Q in culture are not described.
[0024] As described above, microbial cells containing reduced
coenzyme Q.sub.10 at high ratio have not been reported yet. Still
less, it has not been known a fermentation production of reduced
coenzyme Q.sub.10 on the industrial scale, that is, a method
comprising culturing microorganisms to obtain microbial cells
containing reduced coenzyme Q.sub.10 at high ratio among the entire
coenzymes Q.sub.10, and recovering reduced coenzyme Q.sub.10 to
obtain high-purity reduced coenzyme Q.sub.10.
[0025] Under such circumstances, if a method for obtaining a large
quantity of coenzyme Q.sub.10 containing reduced coenzyme Q.sub.10
at high ratio by culturing microorganisms is found, it can be a
highly useful method for producing reduced coenzyme Q.sub.10.
SUMMARY OF THE INVENTION
[0026] It is an object of the present invention to provide a
process for producing reduced coenzyme Q.sub.10 safely and
efficiently on the industrial scale by culturing reduced coenzyme
Q.sub.10-producing microorganisms for obtaining microbial cells
containing reduced coenzyme Q.sub.10 at high ratio and suitably
recovering reduced coenzyme Q.sub.10 from the microbial cells.
[0027] It is another object of the present invention to provide a
process for producing oxidized coenzyme Q.sub.10 in simple
processes by culturing reduced coenzyme Q.sub.10-producing
microorganisms for obtaining microbial cells containing reduced
coenzyme Q.sub.10 at high ratio, and oxidizing the reduced coenzyme
Q.sub.10 obtained from the microbial cells as an intermediate
substance in producing oxidized coenzyme Q.sub.10.
[0028] That is, the present invention relates to
[0029] a process for producing the reduced coenzyme Q.sub.10
represented by the following formula (I): 3
[0030] which comprises culturing reduced coenzyme
Q.sub.10-producing microorganisms in a culture medium containing a
carbon source, a nitrogen source, a phosphorus source and a
micronutrient to obtain microbial cells containing reduced coenzyme
Q.sub.10 at a ratio of not less than 70 mole % among the entire
coenzymes Q.sub.10,
[0031] optionally disrupting the microbial cells and
[0032] extracting thus-produced reduced coenzyme Q.sub.10 by an
organic solvent.
[0033] Furthermore, the present invention also relates to
[0034] a process for producing the oxidized coenzyme Q.sub.10
represented by the following formula (II): 4
[0035] which comprises culturing reduced coenzyme
Q.sub.10-producing microorganisms in a culture medium containing a
carbon source, a nitrogen source, a phosphorus source and a
micronutrient to obtain microbial cells containing reduced coenzyme
Q.sub.10 at a ratio of not less than 70 mole % among the entire
coenzymes Q.sub.10,
[0036] optionally disrupting the microbial cells; and
[0037] either oxidizing thus-produced reduced coenzyme Q.sub.10 to
oxidized coenzyme Q.sub.10 and then extracting the resultant by an
organic solvent, or extracting thus-produced reduced coenzyme
Q.sub.10 by an organic solvent, purifying optionally and oxidizing
the resultant to oxidized coenzyme Q.sub.10.
[0038] According to the processes of the present invention, reduced
coenzyme Q.sub.10 can be produced cheaply on the industrial scale
by considerably simple steps comprising culturing microorganisms
and recovering reduced coenzyme Q.sub.10. In addition, oxidized
coenzyme Q.sub.10 can also be produced by simple processes.
Moreover, these coenzymes Q.sub.10 produced by microorganisms
basically do not contain (Z)-isomers thereof, and (all-E) isomers
thereof can be obtained, which are same as those contained in meat,
fish, etc.
DETAILED DESCRIPTION OF THE INVENTION
[0039] In the present invention, at first, reduced coenzyme
Q.sub.10-producing microorganisms are cultured to obtain microbial
cells containing reduced coenzyme Q.sub.10 at a ratio of not less
than 70 mole %, preferably not less than 75 mole %, among the
entire coenzymes Q.sub.10 (fermentation).
[0040] The microbial cells containing reduced coenzyme Q.sub.10 at
such high ratio among the entire coenzymes Q.sub.10 can be
basically obtained by culturing microorganisms capable of producing
reduced coenzyme Q.sub.10 at a ratio of not less than 70 mole %,
preferably not less than 75 mole %, among the entire coenzymes
Q.sub.10.
[0041] How much ratio the microorganisms can produce reduced
coenzyme Q.sub.10 among the entire coenzymes Q.sub.10 can be
evaluated, for example, by a method comprising culturing the
microorganisms with shaking (amplitude: 2 cm, 310
reciprocation/min) at 25.degree. C. for 72 hours in 10 mL of a
culture medium [(glucose: 20 g, peptone: 5 g, yeast extract: 3 g,
malt extract: 3 g)/L, pH: 6.0] using a test tube (inner diameter:
21 mm, entire length: 200 mm).
[0042] Although the preferable culture conditions for the
fermentation production on the industrial scale will be described
later, the above-mentioned culture condition is one method for
standardizing the ratio of reduced coenzyme Q.sub.10 produced,
which microorganisms have as its ability, so as to reflect the
ratio within the range without having significant inaccuracies.
[0043] Under the above-mentioned culture condition, it is
preferable to use microbial cells wherein a content of reduced
coenzyme Q.sub.10 is at a ratio of not less than 70 mole %,
preferably not less than 75 mole %, among the entire coenzymes
Q.sub.10, for the present invention. It is still more preferable to
use microorganisms having a productivity of reduced coenzyme
Q.sub.10 per unit culture medium of generally not less than 1
.mu.g/mL, preferably not less than 2 .mu.g/mL under the
above-mentioned culture condition.
[0044] The above-mentioned content of reduced coenzyme Q.sub.10 and
ratio of reduced coenzyme Q.sub.10 among the entire coenzymes
Q.sub.10 can be confirmed by physically disrupting the microbial
cells, extracting coenzyme Q.sub.10 from thus-obtained cells by an
organic solvent and performing HPLC analysis. Specifically, the
measurement can be carried out according to the following
procedures:
[0045] (1) The broth of microorganism is optionally concentrated,
10 parts by volume of the broth are displaced to a screw cap test
tube (inner diameter: 16.5 mm, entire length: 130 mm), and 10 parts
by volume of glass beads are added (425 to 600 .mu.m, manufactured
by SIGMA Co.);
[0046] (2) 3 parts by volume of isopropanol and 18.5 parts by
volume of n-hexane relative to 10 parts by volume of the broth are
added under a nitrogen atmosphere;
[0047] (3) microbial cell disruption and extraction are carried out
by vigorously shaking of the mixture for 3 minutes under a nitrogen
atmosphere; and
[0048] (4) the obtained hydrophobic organic solvent phase (n-hexane
phase) is evaporated (bath temperature: 40.degree. C.) under
reduced pressure to analyze the resultant by HPLC.
[0049] Column: YMC-Pack 4.6.times.250 mm (manufactured by YMC. Co.,
Ltd.)
[0050] Mobile phase: methanol/n-hexane=85/15
[0051] Flow rate: 1 mL/min,
[0052] Detection: UV 275 nm
[0053] Retention time: reduced coenzyme Q.sub.10 13.5 min oxidized
coenzyme Q.sub.10 22.0 min
[0054] The above-mentioned measurement method is provided for the
obtained result to reflect the reduced coenzyme Q.sub.10 content
and the ratio of reduced coenzyme Q.sub.10 among the entire
coenzymes Q.sub.10 as accurate as possible, and to standardize the
content and the ratio of reduced coenzyme Q.sub.10, which can be
guaranteed at the minimum. This method has been demonstrated, by
several experimentations performed by the present inventors, easy
and suitable to be carried out.
[0055] As the above-mentioned reduced coenzyme Q.sub.10-producing
microorganisms to be used in the present invention, bacteria, yeast
and fungi may be used without any specific limitation. As specific
examples of the above-mentioned microorganisms, there may be
mentioned, for example, microorganisms of the genus Agrobacterium,
the genus Aspergillus, the genus Acetobacter, the genus
Aminobacter, the genus Agromonas, the genus Acidiphilium, the genus
Bulleromyces, the genus Bullera, the genus Brevundimonas, the genus
Cryptococcus, the genus Chionosphaera, the genus Candida, the genus
Cerinosterus, the genus Exisophiala, the genus Exobasidium, the
genus Fellomyces, the genus Filobasidiella, the genus Filobasidium,
the genus Geotrichum, the genus Graphiola, the genus Gluconobacter,
the genus Kockovaella, the genus Kurtzmanomyces, the genus Lalaria,
the genus Leucosporidium, the genus Legionella, the genus
Methylobacterium, the genus Mycoplana, the genus Oosporidium, the
genus Pseudomonas, the genus Psedozyma, the genus Paracoccus, the
genus Petromyc, the genus Rhodotorula, the genus Rhodosporidium,
the genus Rhizomonas, the genus Rhodobium, the genus Rhodoplanes,
the genus Rhodopseudomonas, the genus Rhodobacter, the genus
Sporobolomyces, the genus Sporidiobolus, the genus Saitoella, the
genus Schizosaccharomyces, the genus Sphingomonas, the genus
Sporotrichum, the genus Sympodiomycopsis, the genus
Sterigmatosporidium, the genus Tapharina, the genus Tremella, the
genus Trichosporon, the genus Tilletiaria, the genus Tilletia, the
genus Tolyposporium, the genus Tilletiopsis, the genus Ustilago,
the genus Udeniomyce, the genus Xanthophllomyces, the genus
Xanthobacter, the genus Paecilomyces, the genus Acremonium, the
genus Hyhomonus, and the genus Rhizobium.
[0056] In terms of the culture easiness and productivity, bacteria
(preferably nonphotosynthetic bacteria) and yeast are preferred. As
the bacteria, there may be mentioned, for example, the genus
Agrobacterium, the genus Gluconobacter and the like. As the yeast,
there may be mentioned, for example, the genus Schizosaccharomyces,
the genus Saitoella and the like.
[0057] As preferable species, there may be mentioned, for example,
Agrobacterium tumefacience IFO13263, Agrobacterium radiobacter
ATCC4718, Aspergillus clavatus JCM1718, Acetobacter xylinum
IFO15237, Aminobacter aganouensis JCM7854, Agromonas oligotrophica
JCM1494, Acidiphilium multivorum JCM8867, Bulleromyces albus
IFO1192, Bullera armeniaca IFO10112, Brevundimonas diminuta
JCM2788, Cryptococcus laurentii IFO0609, Chionosphaera
apobasidialis CBS7430, Candida curvata ATCC10567, Cerinosterus
luteoalbus JCM2923, Exisophiala alcalophila JCM12519, Exobasidium
gracile IFO7788, Fellomyces fuzhouensis IFO10374, Filobasidiella
neoformans CBS132, Filobasidium capsuloigenum CBS1906, Geotrichum
capitatum JCM6258, Graphiola cylindrica IF06426, Gluconobacter
suboxydans IFO3257, Kockovaella imperatae JCM7826, Kurtzmanomyces
nectairei IFO10118, Lalaria cerasi CBS275.28, Leucosporidium
scottii IFO1212, Legionella anisa JCM7573, Methylobacterium
extorguens JCM2802, Mycoplana ramosa JCM7822, Oosporidium
margaritiferum CBS2531, Pseudomonas denitrificans IAM 12023,
Pseudomonas shuylkilliensis IAM 1092, Psedozyma aphidis CBS517.23,
Paracoccus denitrificans JCM6892, Petromyces alliaceus IFO7538,
Rhodotorula glutinis IF01125, Rhodotorula minuta IFO0387,
Rhodosporidium diobovatum ATCC1830, Rhizomonas suberifaciens
IFO15212, Rhodobium orients JCM9337, Rhodoplanes elegans JCM9224,
Rhodopseudomonas palustris JCM2524, Rhodobacter capsulatus SB1003,
Sporobolomyces holsaticus IFO1034, Sporobolomyces pararoseus
IFO0471, Sporidiobolus johnsonii IFO1840, Saitoella complicata
IFO10748, Schizosaccharomyces pombe IF00347, Sphingomonas
parapaucimobilis IFO15100, Sporotrichum cellulophilium ATCC20493,
Sympodiomycopsis paphiopedili JCM8318, Sterigmatosporidium
polymorphum IFO10121, Sphingomonas adhesiva JCM7370, Tapharina
caerulescens CBS351.35, Tremella mesenterica ATCC24438,
Trichosporon cutaneum IFO1198, Tilletiaria anomala CBS436.72,
Tilletia caries JCM1761, Tolyposporium bullatum JCM2006,
Tilletiopsis washintonesis CBS544, Ustilago esculenta IFO9887,
Udeniomyces megalosporus JCM5269, Xanthophllomyces dendrorhous
IFO10129, Xanthobacter flavus JCM1204, Paecilomyces lilacinus
ATCC10114, Acremonium chrysogenum ATCC11550, Hyphomonas hirschiana
ATCC33886, Rhizobium meliloti ATCC9930, and the like.
[0058] As the reduced coenzyme Q.sub.10-producing microorganisms,
not only the wild species of the above-mentioned microorganisms but
also microorganisms in which the transcription and translation
activities of the genes relevant to the biosynthesis of reduced
coenzyme Q.sub.10 in the above-mentioned microorganisms, or the
enzyme activity of the expressed protein are modified or improved
can be used preferably, for example.
[0059] As the means for modifying or improving the transcription
and translation activities of the genes or the enzyme activity of
the expressed protein, there may be mentioned gene recombination
(including gene improvement, amplification and destruction by
itself, external gene introduction, and gene improvement and
proliferation of thus-introduced external genes) and mutagenesis by
mutagens. In particular, the mutagenesis by mutagens is
preferred.
[0060] The more preferable microorganisms usable for the present
invention are microorganisms containing reduced coenzyme Q.sub.10
at a ratio of not less than 70 mole %, preferably not less than 75
mole %, more preferably not less than 80 mole %, still more
preferably not less than 85 mole %, and particularly preferably not
less than 90 mole %, among the entire coenzymes Q.sub.10 in the
case where the above-mentioned modified or improved microorganisms,
preferably microorganisms mutated by mutagens, are evaluated by the
above-mentioned proliferation method and the measurement method. In
the fermentation production on the industrial scale, it is
preferable to use microorganisms having a productivity of reduced
coenzyme Q.sub.10 per unit culture medium of not less than 1
.mu.g/mL, preferably not less than 2 .mu.g/mL, more preferably not
less than 3 .mu.g/mL, still more preferably not less than 5
.mu.g/mL, particularly preferably not less than 10 .mu.g/mL, much
more preferably not less than 15 .mu.g/mL, and most preferably not
less than 20 .mu.g/mL.
[0061] The mutagenesis may be carried out by a single mutagenesis;
however, mutagenesis is preferably carried out not less than 2
times. That is because it was found that the productivity of
reduced coenzyme Q.sub.10 can be improved in the respective
mutagenesis steps. It is needless to say that the candidates of the
microbial cells to be mutated are, generally, those having a
productivity of reduced coenzyme Q.sub.10 as high as possible in
the case where the evaluation is carried out by the above-mentioned
proliferation method and measurement method.
[0062] The mutagenesis can be carried out by using optional and
proper mutagens. The term "mutagen" encompasses, in a board
definition, not only chemical agents having mutagenesis effects,
for example, but also treatments such as UV radiation having
mutagenesis effects. As examples of proper mutangens, there may be
mentioned ethyl methanesulfonate, UV radiation,
N-methyl-N'-nitro-N-nitrosoguanidine, nucleotide base analogues
such as bromouracil, and acridines; however, they are not limited
to these examples.
[0063] According to a conventional mutagenesis technique,
successively to the mutagenesis, a proper selection of microbial
cells having high productivity of reduced coenzyme Q.sub.10 is
carried out. For that, the culture obtained from a single colony
should be evaluated, for example, by the above-mentioned
proliferation method and measurement method. Since a reduced
coenzyme Q.sub.10 crystal forms a white solid layer or a colorless
liquid phase, a productivity of reduced coenzyme Q.sub.10 can be
suitably evaluated by the above-mentioned measurement method at the
time of selection of the colony.
[0064] In the processes of the present invention, high productivity
of reduced coenzyme Q.sub.10 in the fermentation production on the
industrial scale can be achieved partially by using the microbial
cells containing reduced coenzyme Q.sub.10 at a ratio of not less
than 70 mole % among the entire coenzymes Q.sub.10 and, partially,
by using the suitable conditions of culture (fermentation) for
increasing a productivity of reduced coenzyme Q.sub.10 per unit
culture medium as described below. It is particularly preferable to
combinedly use suitable microbial cells described above and the
suitable conditions of culture (fermentation) as described
below.
[0065] The culture is carried out, in general, in a culture medium
containing major nutrients and micronutrients suited for
microorganism proliferation. As the above-mentioned nutrients,
there may be mentioned, for example, carbon sources (e.g.
hydrocarbons such as glucose, sucrose, maltose, starch, corn syrup
and molasses; alcohols such as methanol and ethanol), nitrogen
sources (e.g. corn steep liquor, ammonium sulfate, ammonium
phosphate, ammonium hydroxide, urea and peptone), phosphorus
sources (e.g. ammonium phosphate and phosphoric acid) and
micronutrients (e.g. minerals such as magnesium, potassium, zinc,
copper, iron, manganese, molybdenum, sulfuric acid and hydrochloric
acid; vitamins such as biotin, desthiobiotin and vitamin B1; amino
acids such as alanine and histidine; and natural raw materials
containing vitamins such as yeast extract and malt extract);
however, these are not limitative ones, and commonly used ones may
be used. Incidentally, in natural components of a culture medium,
such as yeast extract, phosphorus sources such as phosphates are
contained. The above-mentioned nutrients can be appropriately used
in combination.
[0066] The culture is generally carried out at a temperature range
of 15 to 45.degree. C., preferably 20 to 37.degree. C. If it is
below 15.degree. C., the proliferation speed of microorganisms
tends to be too slow to allow the industrial production and at high
temperatures exceeding 45.degree. C., the viability of
microorganisms tends to be easily hindered.
[0067] In general, the culture is carried out at a pH range of 4 to
9, preferably 5 to 8. If the pH is not more than 3 or not less than
10, proliferation of microorganisms tends to be easily
inhibited.
[0068] In the fermentation production on the industrial scale,
although it depends on the microorganism species, the concentration
of the carbon sources (including the produced alcohols) during the
culture is preferably controlled to a concentration that no adverse
effects are substantially caused on the productivity of reduced
coenzyme Q.sub.10. Accordingly, it is preferable to control the
culture so as to have the concentration of the carbon sources that
no adverse effects are substantially caused on the productivity of
reduced coenzyme Q.sub.10, that is, generally to not more than 20
g/L, preferably not more than 5 g/L, and more preferably not more
than 2 g/L in the broth.
[0069] To control the concentration of the carbon sources, a fed
batch culture method is preferably used. The carbon source
concentration in the broth can be controlled by adjusting the
supply of nutrient sources (especially carbon sources) based on the
culture control indexes such as pH, the dissolved oxygen
concentration (DO) or the remaining saccharide concentration.
Although it depends on the microorganism species, the supply of the
nutrient sources may be started from the initial stage of the
culture or during the culture. The supply of the nutrient sources
may be continuous or intermittent. Incidentally, in supplying the
nutrient sources, it is preferable to supply the above-mentioned
carbon sources to the culture medium separately from other
components.
[0070] The culture can be completed at the point when a desired
amount of reduced coenzyme Q.sub.10 is produced. The culture
duration is not particularly limited and it is generally 20 to 200
hours.
[0071] The above-mentioned culture is generally carried out
aerobically. The term "aerobically" means a condition that oxygen
is supplied so as not to cause oxygen limitation (oxygen
deficiency) during the culture, and preferably a condition that
oxygen is supplied sufficiently so as not to cause substantial
oxygen limitation during the culture. The culture is carried out
generally under an aeration condition, preferably under an aeration
and stirring condition.
[0072] By using the above-mentioned microorganisms and culture
conditions, it becomes possible to obtain microbial cells
containing reduced coenzyme Q.sub.10 at a ratio of not less than 70
mole %, preferably not less than 75 mole % among the entire
coenzymes Q.sub.10. Furthermore, the productivity of reduced
coenzyme Q.sub.10 of as high as not less than 1 .mu.g/mL,
preferably not less than 2 .mu.g/mL, and still more preferably not
less than 3 .mu.g/mL can be obtained.
[0073] Next, recovery of the reduced coenzyme Q.sub.10 produced by
the above-mentioned culture will be described.
[0074] In the present invention, an efficient production of reduced
coenzyme Q.sub.10 on the industrial scale is made to be possible
partially by the above-mentioned suitable culture and partially by
the suitable recovery process of reduced coenzyme Q.sub.10 as
described below.
[0075] Recovery of reduced coenzyme Q.sub.10 is carried out by
extraction from the microbial cells obtained by the above-mentioned
culture using an organic solvent.
[0076] In the extraction, cells can be disrupted optionally. The
cell disruption contributes to the efficient extraction of the
reduced coenzyme Q.sub.10 produced and accumulated in cells. It is
needless to say that the cell disruption and extraction can be
carried out at the same time.
[0077] Incidentally, "disruption" in the present invention may be
carried out to the extent that the surface structure such as a cell
wall is broken so as to make extraction of reduced coenzyme
Q.sub.10 possible; therefore, it is not necessary that microbial
cells are torn or fragmentated.
[0078] The above-mentioned cell disruption is not necessarily
required in the case of bacteria. However, in the case of yeast or
fungi, the cell disruption is generally required and, when cells
are not disrupted, it becomes difficult to efficiently recover the
reduced coenzyme Q.sub.10 produced and accumulated in the
cells.
[0079] The above-mentioned disruption of microbial cells can be
carried out by the following one or several disruption methods in
optional order. As the disruption method, there may be mentioned,
for example, a physical treatment, a chemical treatment, an enzymic
treatment as well as a heating treatment, an autolysis, an
osmolysis, a plasmoptysis and the like.
[0080] The above-mentioned physical treatment can be carried out,
for example, by using a high pressure homogenizer, an ultrasonic
homogenizer, a French press, a ball mill and the like or using them
in combination.
[0081] The above-mentioned chemical treatment can be carried out,
for example, by using an acid (preferably a strong acid) such as
hydrochloric acid and sulfuric acid, a base (preferably a strong
base) such as sodium hydroxide and potassium hydroxide and the like
or using them in combination.
[0082] The above-mentioned enzymic treatment can be carried out,
for example, by using lysozyme, zymolyase, glucanase, Novozyme,
protease, cellulase and the like or by using them appropriately in
combination.
[0083] The above-mentioned heating treatment can be carried out,
for example, by heating to the temperature range of 60 to
100.degree. C. for about 30 minutes to 3 hours.
[0084] The above-mentioned autolysis can be carried out, for
example, by treatment with a solvent such as ethyl acetate.
[0085] The osmolysis or the plasmoptysis for disrupting cells by
treating cells with a solution having a different salt
concentration from that in the cells are often combinedly used with
the above-mentioned physical treatment, chemical treatment, enzymic
treatment, heating treatment, autolysis and/or the like since the
above lytic method alone is insufficient in the disruption
effect.
[0086] As the cell disruption method as a pretreatment of
extraction and recovery of reduced coenzyme Q.sub.10, among the
above-mentioned disruption methods, the physical treatment, the
chemical treatment (particularly, an acid treatment and preferably
the one with a strong acid (e.g. an acid having a pKa value of not
more than 2.5 in the form of an aqueous solution) under the
condition that reduced coenzyme Q.sub.10 is protected from an
oxidation reaction as described below) and the heating treatment
are preferred. From the viewpoint of disruption efficiency, the
physical treatment is more preferred.
[0087] A conventional cell disruption method and coenzyme Q.sub.10
extraction method, specifically, a method comprising extracting
coenzyme Q.sub.10 by an organic solvent in the presence of sodium
hydroxide and pyrogallol has problems in terms of cost, waste
treatment, safety in effective utilization of waste microorganisms
(waste cells) such as recovery of protein, and the like. However,
the cell disruption method, particularly the physical treatment
method of the present invention, does not cause subgeneration of a
large quantity of salts by neutralization, and is a suitable method
from a viewpoint of the waste treatment and the effective
utilization of waste microorganisms (waste cells).
[0088] The form of the microbial cells to be used for the
above-mentioned cell disruption may be a broth, a concentrated
broth, microbial cells collected as wet cells from the broth, a
product obtained by washing them, a suspension of the wet cells in
a solvent (including, for example, water, physiological saline
solution, buffers and the like), dry cells obtained by drying the
above-mentioned wet cells, a suspension of the dry cells in a
solvent (including, for example, water, physiological saline
solution, buffers and the like), and the like. Preferred is an
aqueous suspension of microbial cells, and in terms of operability
and the like, more preferred are the broth, the concentrated broth,
and the product obtained by washing them.
[0089] The form of the above-mentioned microbial cells or disrupted
product thereof to be used for extraction and recovery of reduced
coenzyme Q.sub.10 is, similarly as described above, not
particularly limited and may be wet cells/dry cells of the
microbial cells/disrupted product thereof. Preferably, it is an
aqueous suspension of the microbial cells or disrupted product
thereof, and more preferably the broth, the concentrated and/or
washed broth, or solutions obtained by disrupting them (each of
them is an aqueous suspension).
[0090] The cell concentration in the above-mentioned suspension of
the microbial cells or disrupted product thereof is not
particularly limited and is generally 1 to 25% by weight on the
basis of dry weight. Preferably, it is 10 to 20% by weight in terms
of cost.
[0091] Reduced coenzyme Q.sub.10 can be recovered by extracting the
microbial cells and disrupted product thereof obtained in such a
manner by an organic solvent.
[0092] As the organic solvent to be used for the extraction, there
may be mentioned hydrocarbons, fatty acid esters, ethers, alcohols,
fatty acids, ketones, nitrogen compounds (including nitrites and
amides), sulfur compounds and the like.
[0093] Particularly, in extracting reduced coenzyme Q.sub.10, in
terms of protection from oxidation by a molecular oxygen, at least
one species of hydrocarbons, fatty acid esters, ethers, and
nitrites is preferably used. Among them, hydrocarbons and fatty
acid esters are particularly preferable, and hydrocarbons are most
preferable.
[0094] On the industrial production scale, complete oxygen
elimination is very difficult to be achieved and, furthermore,
fairly long periods of time are required for individual operations,
unlike laboratory scale production, so that residual oxygen exerts
a great adverse effect. The oxidation in question is directly
connected to a subgeneration of oxidized coenzyme Q.sub.10 from
reduced coenzyme Q.sub.10. Accordingly, use of the above-mentioned
organic solvent (such as hydrocarbons, fatty acid esters, ethers,
and nitriles) with high oxidation prevention effect in the
extraction of reduced coenzyme Q.sub.10 assists an efficient
extraction.
[0095] The hydrocarbons are not particularly restricted, but there
may be mentioned, for example, aliphatic hydrocarbons, aromatic
hydrocarbons, halogenated hydrocarbons, and the like. Preferred are
aliphatic hydrocarbons and aromatic hydrocarbons, and more
preferred are aliphatic hydrocarbons.
[0096] The aliphatic hydrocarbons are not particularly restricted,
and may be cyclic or acyclic, or saturated or unsaturated. However,
generally, saturated ones are preferably used. Usually, ones
containing 3 to 20 carbon atoms, preferably 5 to 12 carbon atoms,
and more preferably 5 to 8 carbon atoms are used. As specific
examples, there may be mentioned, for example, propane, butane,
isobutane, pentane, 2-methylbutane, hexane, 2-methylpentane,
2,2-dimethylbutane, 2,3-dimethylbutane, heptane, heptane isomers
(e.g. 2-methylhexane, 3-methylhexane, 2,3-dimethylpentane,
2,4-dimethylpentane), octane, 2,2,3-trimethylpentane, isooctane,
nonane, 2,2,5-trimethylhexane, decane, dodecane, 2-pentene,
1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene, cyclopentane,
methylcyclopentane, cyclohexane, methylcyclohexane,
ethylcyclohexane, p-menthane, cyclohexene, and the like. Preferred
are pentane, 2-methylbutane, hexane, 2-methylpentane,
2,2-dimethylbutane, 2,3-dimethylbutane, heptane, heptane isomers
(e.g. 2-methylhexane, 3-methylhexane, 2,3-dimethylpentane,
2,4-dimethylpentane), octane, 2,2,3-trimethylpentane, isooctane,
nonane, 2,2,5-trimethylhexane, decane, dodecane, cyclopentane,
methylcyclopentane, cyclohexane, methylcyclohexane,
ethylcyclohexane, p-menthane, and the like. More preferred are
pentane, 2-methylbutane, hexane, 2-methylpentane,
2,2-dimethylbutane, 2,3-dimethylbutane, heptane, heptane isomers
(e.g. 2-methylhexane, 3-methylhexane, 2,3-dimethylpentane,
2,4-dimethylpentane), octane, 2,2,3-trimethylpentane, isooctane,
cyclopentane, methylcyclopentane, cyclohexane, methylcyclohexane,
ethylcyclohexane, and the like.
[0097] Generally, heptanes, not only heptane but also heptane
isomers such as methylcyclohexane having 7 carbon atoms and a
mixture thereof are preferably used. More preferred are pentanes
(e.g. pentane and the like) having 5 carbon atoms, hexanes (e.g.
hexane, cyclohexane and the like) having 6 carbon atoms, and
heptanes (e.g. heptane, methylcyclohexane and the like) having 7
carbon atoms. Particularly preferred are heptanes (e.g. heptane,
methylcyclohexane and the like) in terms of especially high
protection effect from oxidation, and the most preferred is
heptane.
[0098] The aromatic hydrocarbons are not particularly restricted,
but generally ones containing 6 to 20 carbon atoms, preferably 6 to
12 carbon atoms, and more preferably 7 to 10 carbon atoms are used.
As specific examples, there may be mentioned, for example, benzene,
toluene, xylene, o-xylene, m-xylene, p-xylene, ethylbenzene,
cumene, mesitylene, tetralin, butylbenzene, p-cymene,
cyclohexylbenzene, diethylbenzene, pentylbenzene, dipentylbenzene,
dodecylbenzene, styrene, and the like. Preferred are toluene,
xylene, o-xylene, m-xylene, p-xylene, ethylbenzene, cumene,
mesitylene, tetralin, butylbenzene, p-cymene, cyclohexylbenzene,
diethylbenzene, pentylbenzene and the like. More preferred are
toluene, xylene, o-xylene, m-xylene, p-xylene, cumene, tetralin and
the like, and most preferred is cumene.
[0099] The halogenated hydrocarbons are not particularly
restricted, and may be cyclic or acyclic, or saturated or
unsaturated. However, acyclic ones are preferably used in general.
Usually, more preferred are chlorinated hydrocarbons and
fluorinated hydrocarbons, and chlorinated hydrocarbons are still
more preferred. Additionally, ones containing 1 to 6 carbon atoms,
preferably 1 to 4 carbon atoms, and more preferably 1 to 2 carbon
atoms are suitably used. As specific examples, for example, there
may be mentioned dichloromethane, chloroform, carbon tetrachloride,
1,1-dichloroethane, 1,2-dichloroethane, 1,1,1-trichloroethane,
1,1,2-trichloroethane, 1,1,1,2-tetrachloroethane,
1,1,2,2-tetrachloroetha- ne, pentachloroethane, hexachloroethane,
1,1-dichloroethylene, 1,2-dichloroethylene, trichloroethylene,
tetrachloroethylene, 1,2-dichloropropane, 1,2,3-trichloropropane,
chlorobenzene, 1,1,1,2-tetrafluoroethane, and the like. Preferred
are dichloromethane, chloroform, carbon tetrachloride,
1,1-dichloroethane, 1,2-dichloroethane, 1,1,1-trichloroethane,
1,1,2-trichloroethane, 1,1-dichloroethylene, 1,2-dichloroethylene,
trichloroethylene, chlorobenzene, 1,1,1,2-tetrafluoroethane, and
the like. More preferred are dichloromethane, chloroform,
1,2-dichloroethylene, trichloroethylene, chlorobenzene,
1,1,1,2-tetrafluoroethane and the like.
[0100] The fatty acid esters are not particularly restricted, but
there may be mentioned, for example, propionates, acetates,
formates, and the like. Preferred are acetates and formates, and
more preferred are acetates. Ester functional groups thereof are
not particularly restricted, but, in general, preferred are alkyl
esters having 1 to 8 carbon atoms and aralkyl esters having 7 to 12
carbon atoms, more preferred are alkyl esters having 1 to 6 carbon
atoms, and still more preferred are alkyl esters having 1 to 4
carbon atoms.
[0101] As specific examples of the propionates, there may be
mentioned, for example, methyl propionate, ethyl propionate, butyl
propionate, isopentyl propionate, and the like. Preferred are ethyl
propionate and the like.
[0102] As specific examples of the acetates, there may be
mentioned, for example, methyl acetate, ethyl acetate, propyl
acetate, isopropyl acetate, butyl acetate, isobutyl acetate,
sec-butyl acetate, pentyl acetate, isopentyl acetate, sec-hexyl
acetate, cyclohexyl acetate, benzyl acetate, and the like.
Preferred are methyl acetate, ethyl acetate, propyl acetate,
isopropyl acetate, butyl acetate, isobutyl acetate, sec-butyl
acetate, pentyl acetate, isopentyl acetate, sec-hexyl acetate,
cyclohexyl acetate, and the like. More preferred are methyl
acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl
acetate, isobutyl acetate, and the like. Most preferred is ethyl
acetate.
[0103] As specific examples of the formates, there may be
mentioned, for example, methyl formate, ethyl formate, propyl
formate, isopropyl formate, butyl formate, isobutyl formate,
sec-butyl formate, pentyl formate, and the like. Preferred are
methyl formate, ethyl formate, propyl formate, butyl formate,
isobutyl formate, pentyl formate, and the like. Most preferred is
ethyl formate.
[0104] The ethers are not particularly restricted, and may be
cyclic or acyclic, or saturated or unsaturated. But saturated ones
are preferably used in general. Generally, ones containing 3 to 20
carbon atoms, preferably 4 to 12 carbon atoms and more preferably 4
to 8 carbon atoms are used. As specific examples, there may be
mentioned, for example, diethyl ether, methyl tert-butyl ether,
dipropyl ether, diisopropyl ether, dibutyl ether, dihexyl ether,
ethyl vinyl ether, butyl vinyl ether, anisol, phenetole, butyl
phenyl ether, methoxytoluene, dioxane, furan, 2-methylfuran,
tetrahydrofuran, tetrahydropyran, ethylene glycol dimethyl ether,
ethylene glycol diethyl ether, ethylene glycol dibutyl ether,
ethylene glycol monomethyl ether, ethylene glycol monoethyl ether,
ethylene glycol monobutyl ether, and the like. Preferred are
diethyl ether, methyl tert-butyl ether, dipropyl ether, diisopropyl
ether, dibutyl ether, dihexyl ether, anisol, phenetole, butyl
phenyl ether, methoxytoluene, dioxane, 2-methylfuran,
tetrahydrofuran, tetrahydropyran, ethylene glycol dimethyl ether,
ethylene glycol diethyl ether, ethylene glycol dibutyl ether,
ethylene glycol monomethyl ether, ethylene glycol monoethyl ether,
and the like. More preferred are diethyl ether, methyl tert-butyl
ether, anisol, dioxane, tetrahydrofuran, ethylene glycol monomethyl
ether, ethylene glycol monoethyl ether, and the like. Still more
preferred are diethyl ether, methyl tert-butyl ether, anisol, and
the like, and most preferred is methyl tert-butyl ether.
[0105] The alcohols are not particularly restricted but may be
cyclic or acyclic, or saturated or unsaturated. Saturated ones are
generally preferred, however. Generally, ones containing 1 to 20
carbon atoms, more preferably 1 to 12 carbon atoms, and still more
preferably 1 to 6 carbon atoms are used. Among them, monohydric
alcohols containing 1 to 5 carbon atoms, dihydric alcohols
containing 2 to 5 carbon atoms, and trihydric alcohols containing 3
carbon atoms are preferred.
[0106] As specific examples of these alcohols, there may be
mentioned, for example, monohydric alcohols such as methanol,
ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutyl
alcohol, tert-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol,
2-methyl-1-butanol, isopentyl alcohol, tert-pentyl alcohol,
3-methyl-2-butanol, neopentyl alcohol, 1-hexanol,
2-methyl-1-pentanol, 4-methyl-2-pentanol, 2-ethyl-1-butanol,
1-heptanol, 2-heptanol, 3-heptanol, 1-octanol, 2-octanol,
2-ethyl-1-hexanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol,
allyl alcohol, propargyl alcohol, benzyl alcohol, cyclohexanol,
1-methylcyclohexanol, 2-methylcyclohexanol, 3-methylcyclohexanol,
4-methylcyclohexanol, and the like; dihydric alcohols such as
1,2-ethanediol, 1,2-propandiol, 1,3-propandiol, 1,2-butanediol,
1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 1,5-pentanediol,
and the like; and trihydric alcohols such as glycerol, and the
like.
[0107] As the monohydric alcohols, preferred are methanol, ethanol,
1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutyl alcohol,
tert-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol,
2-methyl-l-butanol, isopentyl alcohol, tert-pentyl alcohol,
3-methyl-2-butanol, neopentyl alcohol, 1-hexanol,
2-methyl-1-pentanol, 4-methyl-2-pentanol, 2-ethyl-1-butanol,
1-heptanol, 2-heptanol, 3-heptanol, 1-octanol, 2-octanol,
2-ethyl-1-hexanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol,
benzyl alcohol, cyclohexanol, 1-methylcyclohexanol,
2-methylcyclohexanol, 3-methylcyclohexanol, 4-methylcyclohexanol,
and the like. More preferred are methanol, ethanol, 1-propanol,
2-propanol, 1-butanol, 2-butanol, isobutyl alcohol, tert-butyl
alcohol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol,
isopentyl alcohol, tert-pentyl alcohol, 3-methyl-2-butanol,
neopentyl alcohol, 1-hexanol, 2-methyl-1-pentanol,
4-methyl-2-pentanol, 2-ethyl-1-butanol, cyclohexanol, and the like.
Still more preferred are methanol, ethanol, 1-propanol, 2-propanol,
1-butanol, 2-butanol, isobutyl alcohol, tert-butyl alcohol,
1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, isopentyl
alcohol, tert-pentyl alcohol, 3-methyl-2-butanol, neopentyl
alcohol, and the like. Particularly preferred are methanol,
ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutyl
alcohol, 2-methyl-1-butanol, isopentyl alcohol, and the like. Most
preferred is 2-propanol.
[0108] As the dihydric alcohols, preferred are 1,2-ethanediol,
1,2-propandiol, 1,3-propandiol, and the like. Most preferred is
1,2-ethanediol. As the trihydric alcohols, glycerol is
preferred.
[0109] As fatty acids, there may be mentioned, for example, formic
acid, acetic acid, propionic acid, and the like. Preferred are
formic acid and acetic acid, and most preferred is acetic acid.
[0110] The ketones are not particularly restricted, and ones having
3 to 6 carbon atoms are preferably used. As specific examples,
there may be mentioned, for example, acetone, methyl ethyl ketone,
methyl butyl ketone, methyl isobutyl ketone, and the like.
Preferred are acetone and methyl ethyl ketone, and most preferred
is acetone.
[0111] The nitriles are not particularly restricted, and may be
cyclic or acyclic, or saturated or unsaturated. However, saturated
ones are preferably used in general. Generally, ones containing 2
to 20 carbon atoms, preferably 2 to 12 carbon atoms, and more
preferably 2 to 8 carbon atoms are used.
[0112] As specific examples, there may be mentioned, for example,
acetonitrile, propiononitrile, malononitrile, butyronitrile,
isobutyronitrile, succinonitrile, valeronitrile, glutaronitrile,
hexanenitrile, heptylcyanide, octylcyanide, undecanenitrile,
dodecanenitrile, tridecanenitrile, pentadecanenitrile,
stearonitrile, chloroacetonitrile, bromoacetonitrile,
chloropropiononitrile, bromopropiononitrile, methoxyacetonitrile,
methyl cyanoacetate, ethyl cyanoacetate, tolunitrile, benzonitrile,
chlorobenzonitrile, bromobenzonitrile, cyanobenzoic acid,
nitrobenzonitrile, anisonitrile, phthalonitrile, bromotolunitrile,
methyl cyanobenzoate, methoxybenzonitrile, acetylbenzonitrile,
naphthonitrile, biphenylcarbonitrile, phenylpropiononitrile,
phenylbutyronitrile, methylphenylacetonitrile,
diphenylacetonitrile, naphthylacetonitrile,
nitrophenylacetonitrile, chlorobenzylcyanide,
cyclopropanecarbonitrile, cyclohexanecarbonitrile,
cycloheptanecarbonitrile, phenylcyclohexanecarbonitrile,
tolylcyclohexanecarbonitrile, and the like.
[0113] Preferred are acetonitrile, propiononitrile, succinonitrile,
butyronitrile, isobutyronitrile, valeronitrile, methyl
cyanoacetate, ethyl cyanoacetate, benzonitrile, tolunitrile and
chloropropiononitrile. More preferred are acetonitrile,
propiononitrile, butyronitrile and isobutyronitrile, and most
preferred is acetonitrile.
[0114] As the nitrogen compounds other than nitriles, there may be
mentioned, for example, amides such as formamide,
N-methylformamide, N, N-dimethylformamide, N,N-dimethylacetoamide,
N-methylpyrrolidone, and nitromethane, triethylamine, pyridine, and
the like.
[0115] As the sulfur compounds, there may be mentioned, for
example, dimethyl sulfoxide, sulfolane, and the like.
[0116] In selecting the organic solvent to be used from among the
organic solvents mentioned above, such properties as boiling point
and viscosity (e.g. the solvent should have a boiling point which
allows appropriate warming for increasing solubility and
facilitates a solvent removal from wet masses by drying and solvent
recovery from crystallization filtrates and the like (about 30 to
150.degree. C. at 1 atm), a melting point such that solidification
hardly occurs in handling at room temperature as well as upon
cooling to room temperature or below (not lower than about
0.degree. C., preferably not lower than about 10.degree. C., more
preferably not lower than about 20.degree. C.), and a low viscosity
(not higher than about 10 cp at 20.degree. C. and the like)) are
preferably taken into consideration.
[0117] The oxidation prevention effect on reduced coenzyme Q.sub.10
in a solvent tends to increase in a highly-concentrated solution of
reduced coenzyme Q.sub.10. Reduced coenzyme Q.sub.10 shows high
solubility in the above-mentioned organic solvents with high
oxidation prevention effect (e.g. hydrocarbons, fatty acid esters
and the like). The high solubility makes it possible to handle the
highly-concentrated solution and to promote the oxidation
prevention. A preferable concentration of reduced coenzyme Q.sub.10
for oxidation prevention at the time of extraction is not
particularly limited, but is generally not less than 0.001% by
weight, preferably not less than 0.01% by weight, and more
preferably not less than 0.1% by weight as the concentration of
reduced coenzyme Q.sub.10 in the above-mentioned organic solvent.
The upper limit is not particularly limited, however, in general,
it is not more than 10% by weight.
[0118] Among the above-mentioned organic solvents, to extract and
recover reduced coenzyme Q.sub.10 from wet cells and dry cells of
the microbial cells or disrupted product thereof, hydrophilic
organic solvents are preferably used. Specifically, there may be
mentioned acetone, acetonitrile, methanol, ethanol, 1-propanol,
2-propanol and the like.
[0119] Furthermore, among the above-mentioned organic solvents, to
extract and recover reduced coenzyme Q.sub.10 from the aqueous
suspension of the microbial cells or disrupted product thereof,
hydrophobic organic solvents are preferably used. Use of such
solvents assists the removal of water-soluble substances derived
from microorganisms. Many of hydrophobic organic solvents have high
oxidation prevention effect as described above, thus are very
advantageous.
[0120] As the hydrophobic organic solvents, hydrocarbons, fatty
acid esters and ethers are preferred.
[0121] In the case of the above-mentioned extraction operation,
when reduced coenzyme Q.sub.10 is extracted from the aqueous
suspension of the microbial cells or disrupted product thereof,
particularly from the aqueous suspension of the disrupted product,
further particularly the case in which the disrupted product is
physically treated, by an organic solvent, emulsions tend to be
partly formed because of the presence of cell components such as
proteins and phase separation tends to be difficult. Therefore, it
becomes important to suppress the formation of emulsions mentioned
above and to efficiently carry out extraction.
[0122] For that, as an extraction solvent, in addition to the
above-mentioned hydrophobic organic solvent, it is preferable to
use a hydrophilic organic solvent as an auxiliary solvent in
combination.
[0123] In this case, the hydrophobic organic solvent is not
particularly limited and those mentioned above may be used.
Preferred are hydrocarbons, and more preferred are aliphatic
hydrocarbons. Among the aliphatic hydrocarbons, those having 5 to 8
carbon atoms are preferably used.
[0124] As specific examples of the aliphatic hydrocarbons
containing 5 to 8 carbon atoms, there may be mentioned, for
example, pentane, 2-methylbutane, hexane, 2-methylpentane,
2,2-dimethylbutane, 2,3-dimethylbutane, heptane, heptane isomers
(e.g. 2-methylhexane, 3-methylhexane, 2,3-dimethylpentane,
2,4-dimethylpentane), octane, 2,2,3-trimethylpentane, isooctane,
cyclopentane, methylcyclopentane, cyclohexane, methylcyclohexane,
ethylcyclohexane, and the like. Particularly preferred are hexane,
heptane and methylcyclohexane, and most preferred are hexane and
heptane.
[0125] The hydrophilic organic solvent to be used in combination
with the above-mentioned hydrophobic organic solvent is not
particularly limited and those mentioned above may be used.
Preferred are alcohols. Among the alcohols, monohydric alcohols
having 1 to 5 carbon atoms are preferably used. As specific
examples thereof, there may be mentioned, for example, methanol,
ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutyl
alcohol, tert-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol,
2-methyl-1-butanol, isopentyl alcohol, tert-pentyl alcohol,
3-methyl-2-butanol, neopentyl alcohol, and the like. Particularly
preferred are methanol, ethanol, 1-propanol and 2-propanol, and
most preferred is 2-propanol.
[0126] The amounts of the above-mentioned hydrophilic organic
solvent and hydrophobic organic solvent to be used are not
particularly limited. But preferably, as the concentration at the
time of extraction, the hydrophilic organic solvent is used in a
range of 5 to 50% by volume and the hydrophobic organic solvent is
used in a range of 25 to 65% by volume relative to the total volume
of the entire solution.
[0127] In recovering reduced coenzyme Q.sub.10, the temperature at
the time of extraction is not particularly limited and is generally
in a range of 0 to 60.degree. C. and preferably 20 to 50.degree.
C.
[0128] As the extraction method, both batch extraction and
continuous extraction (preferably countercurrent multistage
extraction) may be used. However, the continuous extraction
(preferably countercurrent multistage extraction) is preferable in
terms of productivity. The stirring duration in the batch
extraction is not particularly limited but is generally not less
than 5 minutes. The average retention time in the continuous
extraction is not particularly limited but is generally not less
than 10 minutes.
[0129] In recovering reduced coenzyme Q.sub.10, it is preferable to
be careful so that reduced coenzyme Q.sub.10 is not decomposed
(e.g. so that reduced coenzyme Q.sub.10 is not oxidized to oxidized
coenzyme Q.sub.10). For that, the above-mentioned extraction
(including cell disruption) is preferably carried out under an
acidic to a weakly basic condition, and more preferably under an
acidic to a neutral condition. In the case where a pH is used as an
index, although it depends on the contact time, the pH is generally
not more than 10, preferably not more than 9, more preferably not
more than 8, and still more preferably not more than 7.
[0130] By the above-mentioned conditions, an oxidation reaction can
be substantially prevented and, optionally, more strictly, the
above-mentioned cell disruption and/or extraction are preferably
carried out under the condition that reduced coenzyme Q.sub.10 is
protected from an oxidation reaction. It is preferable to carry out
at least the extraction under this condition, and it is more
preferable to carry out the disruption and the extraction under
this condition.
[0131] As "the condition that reduced coenzyme Q.sub.10 is
protected from an oxidation reaction" means, for example, a
deoxygenized atmosphere (an atmosphere of an inert gas such as
nitrogen gas, carbon dioxide gas, helium gas, argon gas or hydrogen
gas, reduced pressure, a boiling condition); a high salt
concentration condition, for example, preferably a condition where
salts (e.g. inorganic salts such as sodium chloride and sodium
sulfate) are contained in not less than about 5% in an aqueous
phase; the condition in the presence of a strong acid (e.g. an acid
with a pKa value of not more than 2.5 in an aqueous solution), for
example, in the presence of not less than 0.1 mole % of the strong
acid relative to 1 mole of reduced coenzyme Q.sub.10; and the
condition in the presence of an antioxidant, for example, in the
concomitant presence of ascorbic acid, citric acid, salts and
esters thereof (e.g. not less than 0.1% by weight of them relative
to reduced coenzyme Q.sub.10). There may also be mentioned a
reduction condition (a condition in which oxidized coenzyme
Q.sub.10 can be converted into reduced coenzyme Q.sub.10), for
example, a condition involving a contact with a reducing agent such
as dithionous acid.
[0132] By the above-mentioned culture (fermentation) and
extraction, reduced coenzyme Q.sub.10 can be suitably produced and
recovered. Preferably, an extract containing not less than 70 mole
%, preferably not less than 75 mole % of reduced coenzyme Q.sub.10
among the entire coenzymes Q.sub.10 is obtained.
[0133] Thus-obtained extract containing reduced coenzyme Q.sub.10
is optionally purified by column chromatography, reduction
treatment, or the like and then subjected to crystallization to
obtain high-purity reduced coenzyme Q.sub.10 crystals.
Incidentally, also in this case, a series of treatment steps are
preferably carried out under "the condition that reduced coenzyme
Q.sub.10 is protected from an oxidation reaction" mentioned
above.
[0134] In the present invention, oxidized coenzyme Q.sub.10 can be
produced by oxidizing the above-mentioned microbial cells or
disrupted product thereof and then extracting oxidized coenzyme
Q.sub.10 by an organic solvent, or extracting reduced coenzyme
Q.sub.10 from the microbial cells or disrupted product thereof by
an organic solvent, purifying optionally and oxidizing the
resultant to oxidized coenzyme Q.sub.10.
[0135] The above-mentioned oxidation may be carried out by, for
example, mixing reduced coenzyme Q.sub.10 (preferably an aqueous
suspension of the microbial cells or disrupted product thereof
containing reduced coenzyme Q.sub.10, an extract containing reduced
coenzyme Q.sub.10 or the like) with an oxidizing agent (e.g.
manganese dioxide or the like) and then, for example, oxidizing the
mixture at room temperature (e.g. 30.degree. C.) for not less than
30 minutes. In the case where the microbial cells or disrupted
product thereof are oxidized, the extraction operation of oxidized
coenzyme Q.sub.10 can be carried out in the same manner as the
above-mentioned extraction operation of reduced coenzyme Q.sub.10.
Thereby, oxidized coenzyme Q.sub.10 can be efficiently recovered.
Incidentally, it is not necessary to carry out the recovery of
oxidized coenzyme Q.sub.10 under "the condition that reduced
coenzyme Q.sub.10 is protected from an oxidation reaction", which
is recommended for the recovery of reduced coenzyme Q.sub.10 and
the recovery may be carried out in consideration of general safe
operation and the like. The thus-obtained oxidized coenzyme
Q.sub.10 may be optionally purified by column chromatography or the
like, and, finally by conducting crystallization operation,
high-purity oxidized coenzyme Q.sub.10 crystals may be
obtained.
BRIEF DESCRIPTION OF THE DRAWINGS
[0136] FIG. 1 shows a schematic diagram of a countercurrent 3-step
continuous extraction apparatus used in Example 8.
BEST MODE FOR CARRYING OUT THE INVENTION
[0137] The following examples illustrate the present invention in
further detail. These examples are, however, by no means limitative
of the scope of the present invention.
EXAMPLE 1
[0138] Various coenzyme Q.sub.10-producing microorganisms shown in
the following Tables 1 to 3 were cultured with shaking (amplitude:
2 cm, 310 reciprocation/min) at 25.degree. C. for 72 hours in 10 mL
of culture media [(glucose: 20 g, peptone: 5 g, yeast extract: 3 g,
malt extract: 3 g)/L, pH: 6.0] using test tubes (inner diameter: 21
mm, entire length: 200 mm), and the obtained broth were optionally
concentrated. Under a nitrogen atmosphere, in the concomitant
presence of 3 parts by volume of isopropanol and 18.5 parts by
volume of n-hexane relative to 10 parts by volume of the broth, the
obtained solutions were vigorously shaken for 3 minutes using 10
parts by volume of glass beads (425 to 600 .mu.m) to carry out cell
disruption and extraction. The obtained hexane phases were
evaporated (at 40.degree. C.) under reduced pressure and analyzed
by high performance liquid chromatography (HPLC) to determine the
ratio and the production amount of reduced coenzyme Q.sub.10.
[0139] HPLC conditions
[0140] Column: YMC-Pack 4.6.times.250 mm (manufactured by YMC. Co.,
Ltd.)
[0141] Mobile phase: methanol/n-hexane=85/15
[0142] Flow rate: 1 mL/min
[0143] Detection: UV 275 nm.
[0144] The results are shown in Tables 1 to 3. The ratio of reduced
coenzyme Q.sub.10 means a mole percentage value of the ratio of
reduced coenzyme Q.sub.10 relative to the total of oxidized
coenzyme Q.sub.10 and reduced coenzyme Q.sub.10 on the basis of the
areas of the peaks of reduced coenzyme Q.sub.10 and oxidized
coenzyme Q.sub.10 and the ratio of the mole absorption coefficients
thereof (1:7.5).
1 TABLE 1 Upper stand: Ratio of reduced coenzyme Q10 (%) Lower
stand: Production amount of reduced coenzyme Strain name Q10
(.mu.g/ml) Agrobacterium tumefacience IFO 13263 82 7 Agrobacterium
radiobacter ATCC 4718 78 7 Aspergillus clavatus JCM 1718 83 2
Acetobacter xylinum IFO15237 77 2 Aminobacter aganouensis JCM 7854
70 3 Agromonas oligotrophica JCM 1494 75 2 Acidiphilium multivorum
JCM 8867 73 3 Bulleromyces albus IFO 1192 72 2 Bullera armeniaca
IFO 10112 85 7 Brevundimonas diminuta JCM 2788 82 5 Cryptococcus
laurentii IFO 0609 79 6 Chionosphaera apobasidialis CBS 7430 71 2
Candida curvata ATCC 10567 74 3 Cerinosterus luteoalbus JCM 2923 79
5 Exisophiala alcalophila JCM12519 77 3 Exobasidium gracile IFO7788
79 2 Fellomyces fuzhouensis IFO 10374 70 2 Filobasidiella
neoformans CBS 132 88 2 Filobasidium capsuloigenum CBS 1906 82 3
Geotrichum capitatum JCM 6258 77 3 Graphiola cylindrica IFO 6426 75
4 Gluconobacter suboxydans IFO 3257 86 6 Kockovaella imperatae JCM
7826 78 2
[0145]
2TABLE 2 Upper stand: Ratio of reduced coenzyme Q10 (%) Lower
stand: Production amount of reduced coenzyme Strain name Q10
(.mu.g/ml) Kurtzmanomyces nectairei IFO 10118 79 2 Lalaria cerasi
CBS 275.28 75 2 Leucosporidium scottii IFO 1212 88 6 Legionella
anisa JCM 7573 73 3 Methylobacterium extorguens JCM 2802 72 2
Mycoplana ramosa JCM 7822 80 2 Oosporidium margaritiferum CBS2531
76 2 Pseudomonas denitrificans IAM 12023 85 8 Pseudomonas
shuylkilliensis IAM 1092 84 6 Psedozyma aphidis CBS 517.23 79 5
Paracoccus denitrificans JCM 6892 83 5 Petromyces alliaceus IFO
7538 72 2 Rhodotorula glutinis IFO 1125 79 7 Rhodotorula minuta IFO
0387 74 8 Rhodosporidium diobovatum ATCC 1830 86 4 Rhizomonas
suberifaciens IFO 15212 82 2 Rhodobium orients JCM 9337 80 2
Rhodoplanes elegans JCM9224 74 2 Rhodopseudomonas palustris JCM2524
90 6 Rhodobacter capsulatus SB 1003 95 6 Sporobolomyces holsaticus
IFO 1034 72 9 Sporobolomyces pararoseus IFO 0471 93 8 Sporidiobolus
johnsonii IFO 1840 73 7 Saitoella complicata IFO 10748 97 9
[0146]
3TABLE 3 Upper stand: Ratio of reduced coenzyme Q10 (%) Lower
stand: Production amount of reduced coenzyme Strain name Q10
(.mu.g/ml) Schizosaccharomyces pombe IFO 0347 90 8 Sphingomonas
parapaucimobilis IFO 15100 78 7 Sporotrichum cellulophilium ATCC
20493 73 6 Sympodiomycopsis paphiopedili JCM 8318 80 6
Sterigmatosporidium polymorphum IFO 10121 72 2 Sphingomonas
adhesiva JCM 7370 80 3 Tapharina caerulescens CBS 351.35 81 2
Tremella mesenterica ATCC 24438 89 3 Trichosporon cutaneum IFO 1198
95 8 Tilletiaria anomala CBS 436.72 75 4 Tilletia caries JCM 1761
80 3 Tolyposporium bullatum JCM 2006 73 4 Tilletiopsis
washintonesis CBS 544 76 2 Ustilago esculenta IFO 9887 78 2
Udeniomyces megalosporus JCM 5269 87 2 Xanthophllomyces dendrorhous
IFO 10129 84 2 Xanthobacter flavus JCM1204 80 2 Paecilomyces
lilacinus ATCC10114 80 5 Acremonium chrysogenum ATCC11550 75 5
Hyphomonas hirschiana ATCC33886 72 3 Rhizobium meliloti ATCC9930 85
10
EXAMPLE 2
[0147] Rhodotorula glutinis IF01125 was aerobically cultured at
25.degree. C. for 48 hours in a culture medium (peptone: 5 g, yeast
extract: 3 g, malt extract: 3 g, glucose: 20 g/L, pH: 6.0). The
cells after the culture were collected by centrifugation and
suspended in a phosphoric acid buffer solution at pH 7 to which
N-methyl-N'-nitro-N-nitrosoguanidine have been added so as to have
its concentration of 200 .mu.g/mL. After maintaining the solution
at 25.degree. C. for 1 hour, the cells were washed for 5 times with
a 0.9% NaCl solution and further suspended in a 0.9% NaCl solution.
The obtained cell suspension was properly diluted and a colony was
to be formed on an agar plate of the above-mentioned culture
medium. The production amount and the ratio of reduced coenzyme
Q.sub.10 in the isolated mutant strain were determined in the same
manner as Example 1. The strains having higher production amount
and the ratio of reduced coenzyme Q.sub.10 as compared with those
of wild strains was further mutated repeatedly. As the result, by
repeating the mutagenesis for 10 times, mutant strains with
productivity of not less than 15 .mu.g/mL were obtained. In this
case, the ratio of reduced coenzyme Q.sub.10 was not less than 80
mole %.
EXAMPLE 3
[0148] Saitoella complicata IFO 10748 was aerobically cultured at
25.degree. C. for 72 hours in 10 L of a culture medium (peptone: 5
g, yeast extract: 3 g, malt extract: 3 g, glucose: 20 g/L, pH:
6.0). The obtained cells were disrupted for 2 times at 80 MPa of
disruption pressure by a pressure homogenizer (manufactured by
Lanni Co.) sealed with nitrogen gas to obtain a cell-disrupted
solution. The cell-disrupted solution was subjected to extraction
with 30 parts by volume of isopropanol and 40 parts by volume of
hexane for 3 times to obtain an extract. The extraction ratio was
99%. The ratio of reduced coenzyme Q.sub.10 was 97 mole %.
EXAMPLE 4
[0149] When mutant strains of Rhodotorula glutinis IF01125 were
aerobically cultured at 25.degree. C. in 10 L of a culture medium
(peptone: 10 g, yeast extract: 5 g, malt extract: 3 g, glucose: 20
g/L, pH: 6.0), glucose was fed at the rate of 4 g/h after the lapse
of 48 hours to 96 hours (fed glucose amount: 190 g). The production
amount of reduced coenzyme Q.sub.10 per culture medium was not less
than 20 .mu.g/mL and the ratio of reduced coenzyme Q.sub.10 was not
less than 80 mole %.
EXAMPLE 5
[0150] The extract obtained in Example 3 was subjected to solvent
substitution with a hexane solution, the resultant was adsorbed in
a column filled with silica gel and subjected to development and
elution by a solution of n-hexane/diethyl ether (9/1) to obtain a
fraction containing reduced coenzyme Q.sub.10. Furthermore, the
fraction was cooled to 2.degree. C. with stirring to obtain a white
slurry. All the above-mentioned operations were carried out in a
nitrogen atmosphere. The obtained slurry was filtered under reduced
pressure, the resulting wet crystals were washed with the
development solution same as used above (the temperature of the
solvent used for washing was 2.degree. C.), and the wet crystals
were dried under reduced pressure (20 to 40.degree. C., 1 to 30
mmHg) to obtain 81 mg of white dry crystals. The purity of the
obtained crystals was 99.9% and the ratio of reduced coenzyme
Q.sub.10 was 90 mole %.
EXAMPLE 6
[0151] The extract obtained in Example 3 was subjected to solvent
substitution with n-hexane, the resultant was added with 50 mg of
manganese dioxide, and the mixture was stirred at 30.degree. C. for
30 minutes. Thus-obtained reaction solution was fractionated and
purified in the same manner as Example 5 to obtain 74 mg of
high-purity oxidized coenzyme Q.sub.10.
EXAMPLE 7
[0152] Saitoella complicate IFO 10748 was aerobically cultured at
25.degree. C. for 72 hours in 500 mL of a culture medium (peptone:
5 g, yeast extract: 3 g, malt extract: 3 g, glucose: 20 g/L, pH:
6.0). The obtained cells were disrupted for 2 times at 80 MPa of
disruption pressure by a pressure homogenizer (manufactured by
Lanni Co.) sealed with nitrogen gas to obtain a cell-disrupted
solution. The ratio of reduced coenzyme Q.sub.10 in the
cell-disrupted solution was 97% relative to the entire coenzymes
Q.sub.10 including oxidized coenzyme Q.sub.10. 200 mL of the
cell-disrupted solution was mixed with isopropanol and n-hexane at
the ratios shown in the first extraction section in the following
Table 4 so as to adjust the total solvent amount to be 500 mL and
the mixtures were stirred at 40.degree. C. for 30 minutes to carry
out the first extraction. After completion of the extraction, the
resultants were kept standing for 10 minutes and the separated
upper layers were collected. The volume ratios of the lower layers
(residues) relative to the total solution amounts were defined as
indexes of separability and shown as the interface positions in
Table 4.
[0153] Furthermore, in order to carry out the second extraction,
the solvent concentrations of the residual layers were measured and
isopropanol and hexane were further added so as to keep the solvent
ratios in the entire solutions be the ratios shown in the second
extraction section in Table 4. The resulting solutions were stirred
at 40.degree. C. for 30 minutes. Then, the solutions were kept
standing for 10 minutes and the upper layers were collected in the
same manner as described above to determine the solvent
concentrations of the residual layers. Isopropanol and hexane were
added thereto so as to keep the solvent ratios in the entire
solutions be the ratios shown in the third extraction section in
Table 4, and the solutions were stirred at 25.degree. C. for 30
minutes to carry out the third extraction.
[0154] The ratios of the amounts of reduced coenzyme Q.sub.10
contained in the collected upper layers of each of the first,
second and third steps relative to the amount of reduced coenzyme
Q.sub.10 contained in the cell-disrupted solution or the extraction
residue before the extraction were defined as the extraction ratios
of reduced coenzyme Q.sub.10 in the respective steps. The
calculation results are shown in Table 4. The integrated extraction
ratios of reduced coenzyme Q.sub.10 in the second and third
extraction steps are also shown. In any steps, the static
separability was excellent and the integrated extraction ratio in
the case where extraction was repeated for 3 times was as high as
not less than 90% to show high recovery ratio. Particularly, in the
case where the isopropanol concentration was adjusted to be not
less than 30%, the recovery ratio was as high as not less than
99%.
4 TABLE 4 Solvent ratio Extraction ratio (%) (vol %) Respective
Integrated Isopro- Interface extraction extraction panol Hexane
position ratio ratio Case1 First 18.8 52.7 0.492 73.6 73.6 Second
19.0 52.4 0.624 47.6 86.2 Third 29.7 41.7 0.645 55.5 93.8 Case2
First 31.3 40.2 0.499 90.7 90.7 Second 37.7 33.7 0.549 83.7 98.5
Third 40.6 30.9 0.565 40.1 99.1 Case3 First 31.3 40.2 0.526 89.0
89.0 Second 34.1 37.3 0.553 85.8 98.3 Third 36.8 34.6 0.555 46.6
99.1 Case4 First 31.3 40.2 0.526 89.0 89.0 Second 34.1 37.3 0.553
85.8 98.3 Third 42.4 29.0 0.644 50.0 99.0 Case5 First 31.3 40.2
0.526 89.0 89.0 Second 40.1 31.4 0.595 88.1 98.6 Third 40.7 30.7
0.593 45.3 99.1 Case6 First 31.3 40.2 0.526 89.0 89.0 Second 40.1
31.4 0.595 88.1 98.6 Third 45.8 25.7 0.663 40.7 99.0
EXAMPLE 8
[0155] Saitoella complicata IFO 10748 was aerobically cultured at
25.degree. C. for 72 hours in 750 L of a culture medium (peptone: 5
g, yeast extract: 3 g, malt extract: 3 g, glucose: 20 g/L, pH:
6.0). The obtained cells were disrupted for 2 times at 140 MPa of
disruption pressure by a pressure homogenizer (manufactured by
Lanni Co.) sealed with nitrogen gas to obtain a cell-disrupted
solution. The cell-disrupted solution was subjected to continuous
extraction by a countercurrent 3-step continuous extraction
apparatus shown in FIG. 1. The capacity of the stirring tank was
630 L and the capacity of the static separation tank was 200 L. The
cell-disrupted solution was supplied to the first stirring tank and
isopropanol and n-hexane were supplied to respective steps. The
supply amount of the cell-disrupted solution was 2 L/min and the
supply amounts of isopropanol and n-hexane were adjusted to be 1.3
L/min for isopropanol and 3.7 L/min for n-hexane as the total of
the supply amounts in respective steps. In this case, the solvent
concentration in respective steps was properly adjusted so that the
isopropanol concentration of 5 to 50 v/v % and the n-hexane
concentration of 25 to 65 v/v % were kept. The extraction
temperature was 40.degree. C. and the treatment duration was 6
hours. At the point after the lapse of 6 hours, the recovery ratio
of reduced coenzyme Q.sub.10 extracted from the cell-disrupted
solution was calculated on the basis of reduced coenzyme Q.sub.10
remaining in the extraction residue in the static separation tank
in the third step to find the recovery ratio of 98.9%. The static
separation was well carried out during the entire operation period
and stable continuous extraction was possible.
Industrial Applicability
[0156] According to the processes of the present invention, reduced
coenzyme Q.sub.10 can be produced cheaply on the industrial scale
by considerably simple steps comprising culturing-microorganisms
and recovering reduced coenzyme Q.sub.10. In addition, oxidized
coenzyme Q.sub.10 can also be produced by simple processes.
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