Method for producing .epsilon.-poly-L-lysine

BACKGROUND OF THE INVENTION
This invention relates to a mutant which mass-produces .epsilon.-poly-L-lysine (abbreviated as .epsilon.PL in the following), a method for using the mutant and a method for producing .epsilon.PL. .epsilon.PL is a high-molecular weight compound as described in the following equation in which amino groups of .epsilon.-positions of L-lysine are linked to adjacent carboxyl groups of L-lysine by amide bond formation. ##STR1##
As this material is a polymer of L-lysine which is an essential amino-acid, it has high safety and particular physical properties because of its high cation content. Accordingly, it is useful in toiletry supplies, beauty aids, feed additives, pharmaceuticals, agricultural medicines, food additives, electronic materials, etc. is bacause of these properties.
Hitherto, this material was obtained by cultivating the strain of Streptomyces albulus subsp. lysinopolymerus No. 346-D (deposit No. 3834 of microorganisms of FRI) which is an .epsilon.PL producing bacterium belonging to Streptomyces in a culture medium, separating it from the obtained culture materials and refining it (Japanese Patent Publication 59-20359).
However, .epsilon.PL was produced at most 0.5g per liter of culture solution from the said strain. Accordingly, the production cost of this material was high and its wide utilization was prevented.
The inventors of the present invention have obtained a strain which mass-produce .epsilon.PL, investigated repeatedly in order to produce .epsilon.PL in large quantities by using the said strain, and attained the following invention.
SUMMARY OF THE INVENTION
The present invention provides a mutant mass-producing .epsilon.PL which is obtained by mutant treatment of a strain producing .epsilon.PL. Further, the present invention provides a method for using the mutant strain, characterized in that the mutant is cultured in a cultivated medium, .epsilon.PL is mass-produced and stored in the culture solution, and the stored .epsilon.PL is collected from the solution. The present invention also provides a method for producing .epsilon.PL, characterized in that a strain which produces .epsilon.PL is mutation-treated, the obtained mutant is cultivated in a culture medium to which L-lysine or L-lysine and one or more sugars are added, .epsilon.PL is mass-produced and stored in the culture solution, and the stored .epsilon.PL is collected from the solution. The mutant is a strain which produces .epsilon.PL in large quantities, preferably it is a mutant which has tolerance to an analogue of L-lysine of Streptomyces albulus subsp. lysinopolymerus No.346-D strain or a chloramphenicol-treated mutant amplified of the same bacterium.
The analogue material of L-lysine is preferably either a mixture of S-aminoethyl-L-cysteine or S-aminoethyl-L-cysteine and one or more materials selected from the group of L-threonine, glycine, L-homoserine and L-methionine.
Further, the chloramphenicol-treated mutant of Streptomyces albulus subsp. lysinopolymerus No.346-D strain is a strain which is obtained by chloramphenicol treatment and a chloramphenicol-treated mutant 50833 strain (deposit No.1110 of microorganisms of FRI) obtained by chloramphenicol treatment can be exemplified.
The following description serves to illustrate the invention more specifically.
Firstly, a method for obtaining the mutant of the present invention is described. The mutants which have tolerance to an L-lysine analogue such as S-aminoethyl-L-cysteine are prepared, e.g., from the following method.
Spores of Streptomyces albulus subsp. lysinopolymerus No.346-D strain are suspended in tris-maleic acid buffer solution (pH 9.0) and N-methyl-N-nitro-N'-nitrosoguanidine is added to the solution.
After shaking the solution, the spores are collected by centrifugation, washed with sterilized water and inoculated in a culture medium. By shaking the medium, bacteria are cultivated. The culture medium containing the bacteria (hereinafter the medium is referred to as culture solution) is diluted. Then, S-aminoethyl-L-cysteine or S-aminoethyl-L-cysteine and one or more materials selected from the group of glycine, L-threonine, L-homoserine and L-methionine is added to an agar culture medium having the same composition as the above medium.
In this case, S-aminoethyl-L-cysteine in concentration from 0.5 to 10 mg per ml of the agar culture medium, preferably 2 mg, or S-aminoethyl-L-cysteine in the same concentration and one or more amino acids selected from the above group in concentration from 0.2 to 5 mg per ml of the agar culture medium, preferably 1 mg, is usable. The above diluted culture solution is applied to this agar culture medium. After incubating the applied agar culture medium, S-aminoethyl-L-cysteine mutants are obtained as colonies. The mutant cultivated in the agar culture medium containing S-aminoethyl-L-cysteine alone is a tolerance mutant 81512. strain. The mutant cultivated in the agar culture medium containing S-aminoethyl-L-cysteine and glycine is a tolerant mutant 11011A-1 strain (deposit No.1109 of microorganisms of FRI). Further, the strain cultivated in the agar culture medium containing S-aminoethyl-L-cysteine and L-threonine is a tolerant mutant strain 81502. Fermentation Research Institute, an Agency of Industrial Science and Technology, Ministry of International Trade and Industry, is located at 1-3, Yatabemachi Higashi 1-chome, Tsukubagun, Ibarakiken, Japan 305;
Next, the chloramphenicol-treated mutant strains are obtained by chloramphenicol treatment, e.g., by the following method. Streptomyces albulus subsp. lysinopolymerus No.346-D strain or S-aminoethyl-L-cysteine tolerance mutant strain is inoculated in a culture medium. After shaking the medium, chloramphenicol is added to the medium, and cultivation is continued. Cultivated bacteria are collected by centrifugation, washed, and applied to an agar culture meduim. After static cultivation, a conventional agar culture medium containing Staphylococcus aureus is overlapped on the said medium. After further cultivation, the strains which formed a large zone of inhibition of growth of Staphylococcus aureus are the desired chloramphenical-treated mutant 50833 strain (deposit No. 1110 of microorganims of FRI). Among these mutant strains, the mycological properties of the 11011A-1 strain and the 50833 strain are as follows:
1. Morphological properties:
Aerical Mycel and Substrate Mycelium of the 11011A-1 strain and the 50833 strain which were grown on a sucrose-nitrate agar culture medium at 30.degree. C. for ten days were observed by a microscope. The result is as follows.
1) Ramification and morphology of the sporogenesis mycelia: simple ramification, and closed spiral.
2) Spore number: several tens.
3) Surface structure and spore size: spiny, about 1.2-1.5.mu., and round or oval shape.
4) Existence of flagellum spores, bacterium nucleuses and sporangia: none.
5) Insertion position of Sporophore: on Aerical Mycel.
2. Growth conditions on various culture mediums
Properties of the strains on the following various culture mediums are shown as observation results after cultivating at 30.degree. C. for 10-14 days.
a) The 11011A-1 strain (deposit No. 1109 of microorganisms of FRI)
______________________________________Culture Substrate Aerical SolubleMedium Mycelium Mycel pigment______________________________________Sucrose-nitrate pale gray noneagar yellow brownGlucose-aspara- pale white, palegine agar yellow powdery yellowGlycerol-aspara- pale yellow, bad growth palegine agar then, of Aerical yellow yellow brown MycelTyrosine agar pale white, brown brown rich, powderyNutrient agar pale white, none yellow richYeast-maltose pale yellow white, noneagar wrinkled powdery, gray brown spotsOatmeal agar pale white, none gray then, gray brown______________________________________ b) The 50833 strain (deposit No. 1110 of micro-organisms of FRI)
______________________________________Culture Substrate Aerical SolubleMedium Mycelium Mycel pigment______________________________________Sucrose-nitrate pale gray noneagar yellow brownGlucose-aspara- pale white, palegine agar brown powdery yellowGlycerol-aspara- pale yellow, bad growth palegine agar then, of Aerical yellow yellow brown MycelTyrosine agar brown white, brown powdery, richNutrient agar pale white, none yellow richYeast-maltose pale yellow white, noneagar wrinkled powdery, gray brown spotsOatmeal agar pale white, none gray then, gray brown______________________________________
3. Physiological properties
The physiological properties of the 11011A-1 strain and the 50833 strain are as follows.
1) Range of growth temperatures: about 15.degree.-40.degree. C. The optimum growth temperature: about 30.degree. C.
2) Liquefaction of gelatine, hydrolysis of starch and peptonization of skim milk: all positive.
3) Coagulation of skim milk: negative.
4) Formation of melanon-like pigments: a brown pigment is produced on the tyrosine agar culture medium.
5) Composition of cell walls: the analytical result obtained by the method of Becker et al. (Applied Microbiology, 13, 236 (1965)) shows that the type of diaminopimelic acid in the composition of cell walls was L, L type.
4. Assimilability of various carbon sources on the Pridham Gottliep agar culture medium:
______________________________________ L-arabinose - D-xylose - D-glucose + D-fructose + L-rhamnose - D-galactose + sucrose - raffinose - D-mannitol + i-inositol + salicin -______________________________________ notes: +: assimilate, -: dissimilate
As described above, the properties of the mutants of the present invention are similar to the properties of Streptomyces albulus subsp. lysinopolymerus No. 346-D strain which is an original strain. Then .epsilon.PL is prepared by the present invention using the mutants obtained by the above described methods. Further, % in this specification indicates weight(g)/volume(ml) % unless otherwise noted.
Firstly, the obtained mutants are inoculated in a culture medium, e.g., adding L-lysine or L-lysine and one or more sugars, and cultivated. The .epsilon.PL obtained from the culture medium containing the culture materials (abbreviated as culture solution hereinafter) is separated and purified. Any culture mediums containing carbon sources, nitrogen sources, inorganic salts and vitamin can be used. Although not limiting, a medium containing 5% of glucose or 5% of glycerin as the carbon source, and ammonium sulfate, L-lysine or peptone as the nitrogen source is preferred. In the course of the cultivation, the carbon source and the nitrogen source can be added successively or continuously to the culture medium.
When L-lysine and sugars are added to the culture solution, L-lysine and sugars can be added anytime from the beginning to the ending of the cultivation, preferably in the middle of the cultivation when pH is balling. As L-lysine to be added, L-lysine monohydrochloride can be used in the range of 0.05-2% based on the total volume of the culture solution, preferably 0.5%. For the sugars, one or more sugars selected from the group of glucose, sucrose, maltose, starch, galactose, etc., and glycerine can be used in the range of 0.5-5% based on the total volume of the culture solution, preferably 2.5% of glucose can be used.
In successive addition, L-lysine and sugars are added when the sugar concentration in the culture solution is balls below a fixed %. For example, 2.5% of glucose and 0.5% of L-lysine are preferably added when the sugar concentration is lowered below 0.1%.
In continuous addition, a glucose solution and an L-lysine solution can be passed through a culture tank and the culture solution can be eliminated so as to maintain, for example, the glucose concentration, e.g., at 1% and, for example, L-lysine concentration, e.g., at 0.2% in the culture solution. Further, a defoaming agent-can be added to the culture solution.
The pH value can be left to drop up to 4.0 at the beginning of the cultivation, and then maintained at 4.0 by adding an alkali solution such as an aqueous sodium hydroxide solution. After removing the cultivated bacteria with a centrifuge or a filter from the culture solution, the filtrate is purified, decolorized and concentrated. .epsilon.PL is crystallized out of the concentrated solution by using an organic solvent such as acetone, ethanol, etc..
The effects of the present invention are as follows.
The mutants strains of the present invention have the ability to mass-produce .epsilon.PL. By cultivating the said mutants strains, the mutants produce more .epsilon.PL than the known strains. Further, according to the present invention, when the mutant strains of the strains producing .epsilon.PL are cultivating, the mutants can produce .epsilon.PL in large quantities by adding L-lysine or L-lysine and one or more sugars to the culture solution.
Accordingly, the production cost of .epsilon.PL can be greatly lowered in comparison with the conventional methods.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
The following non-limiting examples illustrate the present invention more specifically.
EXAMPLE 1
Obtention of mutants strains tolerant to S-aminoethyl-L-cysteine:
Spores of Streptomyces albulus subsp. lysinopolymerus No. 346-D strain in quantities of a platinum earpick were suspended in tris-maleic acid buffer solution (pH 9.0) and N-methyl-N-nitro-N'-nitrosoguanidine was added to the solution. After shaking the solution at 30.degree. C. for 30 minutes, the spores were collected with a centrifuge, washed with sterilized water and inoculated in 5 ml of the culture medium of pH 6.8 that contains 5% of glucose, 1% of ammonium sulfate, 0.5% of yeast extract, 0.136% of potassium dihydrogen phosphate heptahydrate, 0.158% of disodium hydrogen phosphate dodecahydrate, 0.05% of magnesium sulfate heptahydrate, 0.004% of zinc sulfate heptahydrate, 0.003% of ferrous sulfate heptahydrate (the medium is abbreviated as the first culture medium hereinafter). By shaking cultivation at 30.degree. C. for a whole day and night, bacteria were grown.
The culture solution was diluted 5000-fold by adding the MS solution which contains of 0.05% of magnesium sulfate heptahydrate, 0.5% of sodium chloride and 0.05% of Tween 80 (Trade mark). Then, the diluted culture solution was applied to the agar culture medium having the same component as that of the first culture medium in addition to S-aminoethyl-L-cysteine or S-aminoethyl-L-cysteine in concentration of 2 mg per ml of the agar culture medium and glycine or L-threonine in concentration of 1 mg per ml of the agar culture medium. The applied agar culture medium was incubated at 30.degree. C. for 48 hours to grow strains as colonies, and mutants strains tolerant to S-aminoethyl-L-cysteine were obtained.
In this case, the mutant obtained from the agar culture medium to which only S-aminoethyl-L-cysteine was added, was the 81512 strain. The mutant obtained from the agar culture medium to which S-aminoethyl-L-cysteine and glycine were added, was the 11011A-1 strain (deposit No. 1109 of microorganisms of FRI). The mutant obtained from the agar culture medium to which S-aminoethyl-L-cysteine and L-threonine were added, was the 81502 strain.
Production of .epsilon.PL:
S-Aminoethyl-L-cysteine tolerant 81512 strain in quantities of a platinum earpick was inoculated in 5 ml of the culture medium having the same composition as that of the above first culture medium, cultivated with shaking at 30.degree. C. for eight days. At the conclusion of the cultivation, the concentration of .epsilon.PL in the culture solution was determined by the method of Itzhaki.
The yield of .epsilon.PL per liter of the culture solution was 0.67 gr.
EXAMPLES 2 and 3
Using the same method as used in Example 1 except that the mutants strain 81512 strain tolerant to S-aminoethyl-L-cysteine was changed to the mutant strain 11011A-1 tolerant to S-aminoethyl-L-cysteine and glycine (deposit No. 1109 of microorganisms of FRI) (Example 2) and the mutant 81502 strain tolerant to S-aminoethyl-L-cysteine and L-threonine (Example 3), .epsilon.PL was produced and its concentration was determined by the same method as in Example 1.
The yields of .epsilon.PL per liter of the culture solution were 0.88 gr.(Example 2) and 0.72 gr.(Example 3), respectively.
EXAMPLE 4
Obtention of the chloramphenicol-treated mutant strains:
The mutant strain tolerant to S-aminoethyl-L-cysteine that was obtained in Example 1 was inoculated in 5 ml of the culture medium having the same composition as that of the first culture medium as described in Example 1.
After shaking the culture medium at 30.degree. C. for two days, chloramphenicol in quantities from 50 to 500 mg per liter of the culture solution, preferably 100 mg, was added to the solution, and the cultivation was continued for further 5-10 hours, preferably eight hours. The cultivated bacteria were collected by centrifugation, washed with sterilized water or a physiological saline solution and applied to an agar culture medium having the same composition as that of the first culture medium in addition to 1.7% of agar.
After static cultivation at 30.degree. C. for 8 days, a conventional agar culture medium containing Staphylococcus aureus was overlapped on the said medium. After cultivating further one night, the strains which formed a large zone of inhibition of growth of Staphylococcus aureus were the desired chloramphenicol-treated mutant 50833 stain deposit No. 1110 of microorganisms of FRI).
Production of .epsilon.PL:
Using the same method as described in Example 1 except that the 81512 strain was changed to the obtained plasmid amplified 50833 strain, .epsilon.PL was produced and its concentration was determined by the same method as in Example 1.
The yield of .epsilon.PL per liter of the culture solution was 1.80 gr.
COMPARATIVE EXAMPLE 1
Using the same method as described in Example 1 except that strain of the mutant 81512 strain tolerant to S-aminoethyl-L-cysteine was changed to Streptomyces albulus subsp. lysinopolymerus No. 346-D strain, .epsilon.PL was produced and its concentration was determined by the same method as in Example 1.
The yield of .epsilon.PL per liter of the culture solution was 0.20 gr. cl EXAMPLE 5
Using the same method as described in Example 4 except that the production of .epsilon.PL was conducted as follows.
The chloramphenicol-treated mutant 50833 in quantities of a platinum earpick were inoculated in 5 ml of the culture medium having the same composition as that of the above culture medium with the addition to 0.5% of L-lysine monohydrochloride, cultivated with shaking at 30.degree. C. for eight days. At the conclusion of the cultivation, the concentration of .epsilon.PL in the culture solution was determined by the method of Itzhaki. The yield of .epsilon.PL per liter of the culture solution was 1.85 gr.
COMPARISON EXAMPLE 2
Using the same method as described in Example 5 except that the chloramphenicol-treated mutant 50833 strain was changed to Streptomyces albulus subsp. lysinopolymerus No. 346-D strain, .epsilon.PL was produced and its concentration was determined by the same method as in Example 5.
The yield of .epsilon.PL per liter of the culture solution was 0.16 gr.
EXAMPLE 6
To 1.5 liter of the culture medium containing the same component as that of the first culture medium described in Example 1, 0.05 volume % of a defoaming agent of a polyoxyalkylene glycol derivative was added. The culture solution 50 ml in which the mutant 11011A-1 strain tolerant to S-aminoethyl-L-cysteine was precultivated was inoculated in the said medium, and the mutant was cultivated with shaking of 600 rpm at 30.degree. C. in an air flow rate of 2 1/min..
After 24 hours, 5% of glucose and 1% of ammonium sulfate were sterilely added to the medium. After lowering of the pH, 6N of sodium hydroxide was added while the pH was automatically and continuously controlled with a pH controller so as not to ball below 4.0. After the cultivation, the bacteria were removed with a centrifuge and .epsilon.PL in the culture solution was purified with an anion exchange resin of IRA-402, a cation exchange resin of IRC-50 and active carbon of Carboraffin 50 w, and the purity of the obtained .epsilon.PL was 99.9 weight % and the yield of .epsilon.PL per liter of the culture solution was 4.77 gr.
COMPARATIVE EXAMPLE 3
Using the same method as described in Example 6 except that the mutant 11011A-1 strain tolerant to S-aminoethyl-L-cysteine was changed to Streptomyces albulus subsp. lysinopolymerus No. 346-D strain, .epsilon.PL was produced. The purity of the obtained .epsilon.PL was 97.8 weight % and the yield of .epsilon.PL per liter of the culture solution was 0.56 gr.
EXAMPLE 7
To 1.5 liter of the culture medium containing the same component as that of the first culture medium described in Example 1, 0.05 volume % of a defoaming agent of a polyoxyalkylene glycol derivative was added. 50 ml of the culture solution in which the chloramphenical-amplified treated mutant 50833 strain was precultivated was inoculated in the said medium, and the mutant was cultivated with aeration and stirring at 30.degree. C. for eight days. When the pH of the culture solution began to drop, 2.5% of glucose and 0.5% of L-lysine monohydrochloride were sterilely added to the medium. Thereafter, so as not to lower the glucose concentration of the culture solution below 2%, 2.5% of glucose was sterilily added successively. After lowering the pH, 6N of sodium hydroxide was added while the pH was automatically and continuously controlled with a pH controller so as not to decrease below 4.0.
After the cultivation, the bacteria were removed with a centrifuge and the concentration of .epsilon.PL in the culture solution was determined by the method Itzhaki. The yield of .epsilon.PL per liter of the culture solution was 20.3 gr.
COMPARISON EXAMPLE 4
Using the same method as described in Example 7 except that the chloramphenical-treated mutant 50833 strain was changed to Streptomyces albulus subsp. lysinopolymerus No. 346-D strain, the concentration of .epsilon.PL was determined by the same method as in Example 7.
The yield of .epsilon.PL per liter of the culture solution was 0.20 gr.
EXAMPLE 8
To 1.5 liter of the culture medium containing the same component as that of the first culture medium described in Example 1, 0.05 volume % of a defoaming agent of a polyoxyalkylene glycol derivative was added. 50 ml of the culture solution in which the chloramphenical treated 50833 strain was precultivated was inoculated in the said medium, and the mutant was cultivated with shaking of 600 rpm at 30.degree. C. in an air flow rate of 2 1/min..
After 24 hours, as the pH of the culture solution began to decrease, a glucose solution and a L-lysine solution were passed through the culture tank so as to maintain the concentrations of 1% of gulucose and 0.2% of L-lysine, and exhausted the culture solution. After the pH was lowered, 6N of sodium hydroxide was added while the pH was automatically and continuously controlled with a pH controller so as not to decrease below 4.0.
After the cultivation, the bacteria were removed with a centrifuge, and .epsilon.PL in the culture solution was purified with an anion exchange resin of IRA-402, a cation exchange resin of IRC-50 and active carbon of Carboraffin 50w. Then .epsilon.PL was crystallized with alcohol. The purity of the obtained .epsilon.PL was 99.9 weight % and the yield was 5.02 gr.

Number	Date	Country	Kind
61-192157	Aug 1986	JPX
61-192158	Aug 1986	JPX

Number	Date	Country
072896	Jun 1978	JPX
59-20359	Jul 1984	JPX

	Number	Date	Country
Parent	864182	Apr 1992
Parent	391267	Aug 1989

Method for producing .epsilon.-poly-L-lysine

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (2)

Parent Case Info

US Referenced Citations (1)

Foreign Referenced Citations (2)

Non-Patent Literature Citations (1)

Divisions (1)

Continuations (2)

Continuation in Parts (1)