CN100362108C - Microbial process of producing validamycin anamine and validamycin amine - Google Patents
Microbial process of producing validamycin anamine and validamycin amine Download PDFInfo
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- CN100362108C CN100362108C CNB2005100613641A CN200510061364A CN100362108C CN 100362108 C CN100362108 C CN 100362108C CN B2005100613641 A CNB2005100613641 A CN B2005100613641A CN 200510061364 A CN200510061364 A CN 200510061364A CN 100362108 C CN100362108 C CN 100362108C
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Abstract
The present invention discloses a microbe capable of cracking validamycin into validamycin enamine and validamycin amine, which belongs to the alcaligenes faecalis of the alcaligenes of which the CCTCC number is M205095. The present invention also discloses a method capable of using the microbe to crack validamycin to prepare validamycin enamine and validamycin amine.
Description
Technical field
The Alcaligenes faecalis (Alcaligenes faecalis) of the new microorganism Alcaligenes (Alcaligenes) that the present invention relates to screen from soil also relates to the method that this new bacterial strain cracking validamycin (claiming jingganmycin again) of utilization is produced effective mildew enamine and validamine.
Background technology
Effective mildew enamine that the present invention relates to (valienamine) and validamine (validamine) structural formula following (Chem.Rev.2003,103:1955～1977):
Effective mildew enamine claims valienamine again, and molecular formula is C
7H
13NO
4, important group has: a primary amino (NH
2), a carbon-carbon double bond (C=C), a methylol (CH
2OH), three hydroxyls (OH).Its hydrochloride (C
7H
13NO
4HCl) [a]
D 23Be+68.6 ° (1N-HCl), pentacetate (C
17H
23NO
9) fusing point be 95 ℃, [a]
D 23Be+30.2 ° of (CHCl
3), meet the triketohydrindene hydrate color reaction.
Validamine claims the well ridge mould amine again, and molecular formula is C
7H
15NO
4, important group has: a primary amino (NH
2), a methylol (CH
2OH), three hydroxyl (OH), its hydrochloride (C
7H
13NO
4HCl) [a]
D 23Be+57.4 ° (1N-HCl) that fusing point is 229 ℃-232 ℃, [a]
D 21Be+60.6 ° of (H
2O), meet the triketohydrindene hydrate color reaction.
Effective mildew enamine and validamine are two kinds of stronger glycosidase inhibitors, also are simultaneously the core textures of a lot of other glycosidase inhibitors, can be used for synthetic effective Valiolamine (valiolamine) and voglibose (voglibose).
About the research of the production method of effective mildew enamine and validamine has had the history in more than 30 year, people such as Japanese tortoise field once adopted thalline degraded Validacin (Takeda) or the effective mould ylidene amines A of denitration pseudomonas, separate obtaining effective mildew enamine and validamine again, can not on the substratum that only is sole carbon source, grow with validamycin class material; And very weak to the capacity of decomposition of validamycin, be not suitable for the mass production of effective mildew enamine and validamine.
Japanese tortoise field etc. is separated to the bacterial strain that a strain can be decomposed into validamycin effective mildew enamine and validamine and has a liking for sugared Flavobacterium (Flavobacterium saccharophilum) IFO13948 (open special permission: JP57-54593) in soil.
Japanese tortoise fields etc. adopt Cytophaga microbes producing cellulase (Cytophaga heparina) IFO12017 (ATCC13125) and IFO14087 strain degraded validamycin or effective mould ylidene amines to produce effective mildew enamine and validamine [special permission communique (B2): flat 2-26957].
The microorganism of soil Pseudomonas (Agrobacterium) or Aeromonas (Aeromonas) has been found in Japanese tortoise field etc. and their variant can decompose validamycin or effective mould ylidene amines is produced effective mildew enamine and validamine.Such as soil Pseudomonas (Agrobacterium) microorganism, Agrobacterum Radiobacter IFO 12664 (ATCC 4718) strain is arranged, IFO 13258 (ATCC13332) strain, IFO 13259 (ATCC 13333) strain, IFO 13532 (ATCC 19358) strain, IFO13533 (ATCC 25235) strain, and Agrobacterium tumefaciens IFO 3058 strains etc.; Aeromonas (Aeromonas) microorganism, Aeromonas hydrophila subsp.Anaerogenes IFO 13282 is arranged, with subspecies subsp.hydrophila IFO 13286, subsp.proteolytica IFO 13287, Aeromonas punctata subsp.cavice IFO 13288, and Aeromonas salmonicida subsp.salmonicida IFO 12659 etc. [special permission communique (B2): flat 6-69380].
Consult the result according to document and patent, the patent bacterial classification of the validamycin of having reported of degrading comprises Rhodopseudomonas (Pseudomonas, 1 kind, Pseudomonas denitrificans, denitrifying pseudomonas), Flavobacterium (Flavobacterium, 3 kinds), have a liking for Cellulomonas (Cytophaga1 kind, 3 bacterial strains), soil Pseudomonas (Agrobacterium, 2 kinds, wherein Agrobacterium radiobacter has 5 bacterial strains, Agrobacterium tumefaciens, a kind), Aeromonas (Aeromonas, 5 kinds).Concrete outcome sees attached list 1.
Table 1 degraded validamycin patent [special permission communique (B2)] bacterial classification gathers
| Bacterial classification | Patent |
| ?Pseudomonas?denitrificans | Flat 2-26957 (1982), flat 2-2598 |
| ?Flavobacterium?saccharophilum?IFO?13984 | Flat 2-26957, flat 2-2598 |
| ?Flavobacterium?heparinum | Flat 2-26957 |
| ?Flavobacterium?keratolyticus | Flat 2-26957 |
| ?Cytophaga?heparina?IFO?12017 | Flat 2-26957 |
| ?Cytophaga?heparina?ATCC?13125 | Flat 2-26957 |
| ?Cytophaga?heparina?IFO?14087 | Flat 2-26957 |
| ?Flavobacterium?saccharophilum?n.sp. | Flat 2-2598 |
| ?Flavobacterium?saccharophilum?FERM-P | Flat 2-2598 |
| ?Flavobacterium?saccharophilum?NO.5707 | Flat 2-2598 |
| ?Agrobacterium?Radiobacter?IFO?12664(ATCC?4718) | Flat 6-69380 |
| ?Agrobacterium?Radiobacter?IFO?13258(ATCC?13332) | Flat 6-69380 |
| ?Agrobacterium?Radiobacter?IFO?13259(ATCC?13333) | Flat 6-69380 |
| ?Agrobacterium?Radiobacter?IFO?13532(ATCC?19358) | Flat 6-69380 |
| ?Agrobacterium?Radiobacter?IFO?13533(ATCC?25235) | Flat 6-69380 |
| ?Agrobacterium?tumefaciens?IFO?3058 | Flat 6-69380 |
| ?Aeromonas?hydrophila?subsp.anaerogenes?IFO?13282 | Flat 6-69380 |
| ?Aeromonas?hydrophila?subsp.hydrophila?IFO?13286 | Flat 6-69380 |
| ?Aeromonas?hydrophila?subsp.proteolytica?IFO?13287 | Flat 6-69380 |
| ?Aeromonas?punctata?subsp.cavice?IFO?13288 | Flat 6-69380 |
| ?Aeromonas?salmonicida?subsp.salmonicida?IFO?12659 | Flat 6-69380 |
In addition, in April, 2004, people such as the Zhejiang Polytechnical University abundant state of Zheng have screened germ oligotrophy unit cell (Stenotrophomonas maltrophilia) (CN 1563397), and this bacterium can be used for the production of effective mildew enamine and validamine.2004, Japan also reported the production technology (JP 3586684 B1) of utilizing Paenibacillus to prepare validamine and effective mildew enamine.
Summary of the invention
The invention provides a kind of new microorganism strains that validamycin can be cracked into effective mildew enamine and validamine that from soil, screens; Next provides a kind of method of utilizing this new microbial lytic validamycin to produce effective mildew enamine and validamine.
New microorganism strains provided by the invention belongs to the Alcaligenes faecalis (Alcaligenes faecalis) of Alcaligenes (Alcaligenes), oneself is preserved in Chinese typical culture collection center this bacterial strain on September 2nd, 2005, be called for short CCTCC, deposit number is CCTCC No.M 205095.
The new strain characteristic that the present invention screens from soil is as follows:
Cellular form: tyrothricin
Colonial morphology: aerobic, cultivated 2 days for 30 ℃, rounded at the bacterium colony that beef extract-peptone is dull and stereotyped to be cultivated, diameter 1 millimeter, projecting shape are lens-shaped, neat in edge is smooth, the moistening easy picking of quality, color and luster is creamy white, and is translucent.
Physiological and biochemical property: Gram-negative, the indiffusion of beef extract-peptone inclined-plane was cultivated muddiness 2 days for 30 ℃ in the test tube beef-protein medium, there is flocks to form, oxidase positive, the catalase positive is not moved, edwardsiella hoshinae, the lecithinase positive, hydrolyzed starch not, ornithine decarboxylase feminine gender, the arginine decarboxylase feminine gender, the lysine decarboxylase feminine gender, phenylalanine deaminase feminine gender, esterase (Tween 80) feminine gender, the VP reaction negative, casein hydrolysis feminine gender, the tyrosine hydrolysis positive does not produce 3-ketone group lactose.Glucose sugar oxidized form, nonfermented ethanol, the clark and Lubsreaction feminine gender, the V-P reaction negative, starch hydrolysis feminine gender, the nitrate reduction feminine gender, the nitrite reduction is negative, the denitrification positive, the urase positive, liquefy gelatin not, produce hydrogen sulfide, can utilize malonate, acetate, the DL-lactic acid salt, propionic salt, valerate, Citrate trianion, 3-hydroxyl-butyrates, the L-proline(Pro) can not utilize rhamnosyl, the N-acetylglucosamine, ribose, inositol, sucrose, maltose, methylene-succinic acid, suberate, the L-L-Ala, 5-ketone group-gluconate, glycogen, 3-hydroxy-benzoic acid salt, N.F,USP MANNITOL, D-glucose, salicin, the D-melibiose, the L-Fucose, the D-sorbyl alcohol, L-arabinose, caprate, Histidine, 2-ketone group-gluconate, 4-hydroxy-benzoic acid salt, the L-Serine.
According to above bacterial characteristics, this new bacterial strain is belonged to the Alcaligenes faecalis (Alcaligenes faecalis) of Alcaligenes (Alcaligenes) by evaluation, and this microorganism has the ability that the cracking validamycin is produced effective mildew enamine and validamine.
The new bacterial strain Alcaligenes faecalis (Alcaligenes faecalis) that the present invention screens does not belong to any of above-mentioned own publication bacterial classification.
The used raw material of the present invention is a kind of agricultural antibiotic of widespread use a---validamycin, it is jingganmycin, it is a kind of efficient, safe agricultural antibiotic, free from environmental pollution, to the person poultry harmless, become at present that China's usable floor area is wide, mu is minimum with cost, safety, public nuisance-free agricultural chemicals, be an important kind of pesticide industry.Validamycin is the aminoglycoside agricultural antibiotic, and main ingredient has A, B, C, D, E, F etc., can find from the structure of validamycin, and validamycin is made up of effective mildew enamine, validamine and β-structures such as D-glucose.
New microorganism of the present invention belongs to the Alcaligenes faecalis (Alcaligenes faecalis) of Alcaligenes (Alcaligenes), CCTCC No.M 205095.This new bacterial strain all can be grown under 20 ℃～40 ℃ culture temperature, and the suitableeest growth temperature is 25 ℃～37 ℃, culture condition: pH value 6.0～8.0, the suitableeest growth pH value are neutral or approaching neutral.The bacterial classification that this is new or its thalline aerobic fermentation on the substratum that contains the microbiotic validamycin has the ability that the cracking validamycin prepares effective mildew enamine and validamine.
The substratum that is used for bacterial classification CCTCC No.M 205095 of the present invention is that some contain and can be utilized nutritive substance by above-mentioned bacterial strains, as carbon source, nitrogenous source, inorganic salt etc., as carbon source except validamycin, can also have: glucose, lactose, maltose, dextrin, starch, glycerine, N.F,USP MANNITOL, sorbyl alcohol, lipid (soya-bean oil, lard etc.); As having of nitrogenous source: gravy, yeast extract paste, dry yeast, soyflour, corn steep liquor, peptone, urea, ammonia salt (ammonium sulfate, ammonium chloride, ammonium nitrate, Ammoniom-Acetate etc.), peptide class (dipeptides, tripeptides etc.); Inorganic salts has: metallic salt and organic acid salts such as phosphoric acid salt, acetate such as Na, K, Ca, Mg, Fe, Mn, Zn, Co, Ni; In addition, the material that also can add on a small quantity has: amino acids (as L-glutamic acid, aspartic acid, Methionin, glycine, methionine(Met) etc.), little element (V that gives birth to
B1, V
B2, V
B12, V
C, V
E, nicotinic acid etc.), nucleic acid class (as purine, pyrimidine and derivative thereof etc.).PH value with mineral acid or organic acid, bases are regulated substratum also can add appropriate amount of defoamer, opposes as bubble etc.Liquid culture, solid culture all can, but during a large amount of suitability for industrialized production, liquid nutrient medium is comparatively suitable.Can adopt training method to have: to leave standstill cultivation, wave and culture or ventilation stir culture etc., the appropriate to the occasion employing deep ventilation of mass production effective mildew enamine and validamine stir culture.
The Alcaligenes faecalis (Alcaligenesfaecalis) of new microorganism Alcaligenes (Alcaligenes) of the present invention, CCTCC No.M 205095, this bacterial strain Alcaligenes faecalis (Alcaligenes faecalis), CCTCC No.M 205095, after cultivating, seed culture medium inserts the decomposition substrate that ferments in the fermention medium that contains the substrate validamycin, or seed culture medium cultivation back separation obtains thalline, the thalline that obtains is added in the solution of validamycin and carry out the reaction decomposes substrate, then decomposed solution is separated, purify, obtain effective mildew enamine and validamine.
Seed culture medium bulking value of the present invention such as down (g/L): glucose 10～40, peptone 5～20, yeast extract paste 1～10, MgSO
40.1～1, the tap water preparation.
Main component is a validamycin in the fermention medium, other component is the carbon source that can be utilized by new microorganism of the present invention, nitrogenous source, inorganic salt etc., fermention medium of the present invention form each bulking value such as down (g/L): validamycin 5～50, glucose 1～20, peptone 1～10, yeast powder 1～10, MgSO
40.1～1, prepare with tap water.
With new bacterial strain Alcaligenes faecalis of the present invention (Alcaligenes faecalis), CCTCC No.M205095 decomposes the substrate validamycin and produces effective mildew enamine and validamine, and its method has:
(1) utilize this new microbial fermentation to decompose the substrate validamycin and prepare effective mildew enamine and validamine: bacterial classification CCTCC No.M 205095 is through overactivation, the seed culture medium that inserts above-mentioned sterilization is cultivated and to be made seed liquor, seed liquor is linked into cultivation and fermentation in the fermention medium of above-mentioned preparation sterilization.
The control condition of seed culture is as follows: 25 ℃～37 ℃ of culture temperature, and pH6.0～8.0, incubation time 24h～48h, the pH value, is carried out to good under ventilate stirring or oscillating condition for well near neutral;
The control condition of fermentation culture: 25 ℃～37 ℃ of temperature, pH is 6.0～8.0, and fermentation time is 72h～192h, and the pH value, is carried out to good under ventilate stirring or oscillating condition for well near neutral.Validamycin during substratum is formed in this method is the carbon source that microorganism utilizes, again by the substrate of microbial lytic; The substrate validamycin is cracked into effective mould ylidene amines, and effective mould ylidene amines has two kinds of A, B, and effective mould ylidene amines passes through cracking again, generates effective mildew enamine (valienamine) and validamine (validamine)
(2) utilize this new microorganism cells, utilize cell catalysis cracking substrate validamycin to prepare effective mildew enamine and validamine: bacterial classification CCTCC No.M 205095 is through overactivation, insert in the seed culture medium of sterilizing and cultivate, 25 ℃～37 ℃ of culture temperature, pH6.0～8.0, it is centrifugal to the logarithmic growth after date to cultivate thalline, collects thalline; The thalline that obtains is added in the substrate validamycin solution, utilize cellular lysate substrate validamycin to produce effective mildew enamine and validamine;
Validamycin concentration, with the ratio of bulking value represent (kg/L, %): 1.0%～10.0%; 25 ℃～37 ℃ of temperature of reaction, reaction times 4h～96h carries out to good under the condition that stirs or vibrate of ventilating.
The pH value is regulated control with mineral acid or organic acid, bases in cracking validamycin process.
Effective mildew enamine and validamine are alkaline matter soluble in water, thereby can adopt separation, the process for purification of water-soluble alkaline material, for example ion exchange resin, gac, porous polymer, dextrane gel, ion-exchanger etc. adsorb back desorb, chromatography etc.
Sepn process is as follows: it is centrifugal or remove by filter thalline to contain the fermented liquid of effective mildew enamine and validamine or cell catalysis reaction solution, again supernatant liquor or filtrate are carried out ion-exchange with macroporous ion exchange resin, use the ammonia soln wash-out, collect elutriant, concentrating under reduced pressure, concentrated solution carries out chromatography with the strong basicity chromatographic resin, and water is collected the part that only contains effective mildew enamine or validamine as eluent.Lyophilize obtains finished product.Method with thin-layer chromatography and gas phase analysis is analyzed effective mildew enamine and the validamine produced, operating process and experiment condition are pressed document J.Antibiot, 1984, the method for 37:1301～1305 and patent documentation EP0063456 is carried out, and resulting result and they are in full accord.This shows, utilize microorganism of the present invention to produce effective mildew enamine and validamine by the cracking validamycin.
Specific embodiments
The following examples can make those skilled in the art more fully understand the present invention, but do not limit the present invention in any way.
Embodiment 1
Seed culture medium (g/L): glucose 20, peptone 10, yeast extract paste 5, MgSO
40.2, the tap water preparation, it is standby to sterilize.
Fermention medium (g/L): validamycin 15, glucose 5, peptone 10, yeast powder 10, MgSO
40.2 with the tap water preparation, it is standby to sterilize.
The preparation of seed liquor: get the 500mL seed culture medium, average mark is contained in 10 250mL triangular flasks, sterilization.Insert inclined-plane CCTCC No.M 205095 and cultivate, shaking speed 200r/min cultivates 36h as seed liquor at 30 ℃ of shaking tables.
Fermentation: the 10L fermention medium of in the 15L fermentor tank, packing into, sterilization.Then, insert seed liquor and ferment inoculum size 5% (V/V promptly inserts the 0.5L seed liquor), 30 ℃ of leavening temperatures, pH7.0, ventilation 3.5vvm, fermentation time 96h.
The separation of product: collect above-mentioned fermented liquid 10L, thalline is removed in centrifugation, supernatant liquor upper prop (D113 resin, NH
4 +), carry out ion-exchange, behind distilled water wash, use the ammoniacal liquor wash-out of 0.5mol/L again, concentrating under reduced pressure, (Dowex 1 * 2, OH with column chromatography on the concentrated solution again
-), use the distilled water wash-out, analyze (silica-gel plate G: Haiyang Chemical Plant, Qingdao with the thin-layer chromatography method; The chromatography agent, n-propyl alcohol/acetic acid/water=4: 1: 1; The colour developing of 0.5% triketohydrindene hydrate, effective mildew enamine R
f=0.45, the R of validamine
f=0.39), the Fractional Collections elutriant is collected the part that only contains effective mildew enamine or validamine, carries out vacuum lyophilization then.Obtain 8.1 gram effective mildew enamines and 2.4 gram validamines.
Embodiment 2
Seed culture medium (g/L): glucose 10, peptone 20, yeast extract paste 1, MgSO
40.1, the tap water preparation, it is standby to sterilize.
Fermention medium (g/L): validamycin 20, glucose 5, peptone 10, yeast powder 10, MgSO
40.2 with the tap water preparation, it is standby to sterilize.
The preparation of seed liquor: get the 150mL seed culture medium, average mark is contained in 3 250mL triangular flasks, sterilization.Insert inclined-plane CCTCC No.M 205095 and cultivate, shaking speed 200r/min cultivates 48h as seed liquor at 25 ℃ of shaking tables.
Fermentation: in the triangular flask of 20 500mL, every bottled 100mL fermention medium of going into, sterilization inserts seed liquor then and ferments, inoculum size 5% (promptly inserting the 5mL seed liquor), 28 ℃ of leavening temperatures, pH7.0, shaking speed 200r/min, fermentation time 144h.
Collect above-mentioned fermented liquid 1.8L, separate, purifying, step is with embodiment 1.Obtain 1.9 gram effective mildew enamines and 0.4 gram validamine.
Embodiment 3
Seed culture medium (g/L): glucose 40, peptone 5, yeast extract paste 10, MgSO
41, the tap water preparation, it is standby to sterilize.
Fermention medium (g/L): validamycin 30, glucose 5, peptone 10, yeast powder 10, MgSO
40.2 with the tap water preparation, it is standby to sterilize.
The preparation of seed liquor: get the 150mL seed culture medium, average mark is contained in 3 250mL triangular flasks, sterilization.Insert inclined-plane CCTCC No.M 205095 and cultivate, shaking speed 200r/min cultivates 24h as seed liquor at 37 ℃ of shaking tables.
Fermentation: in the triangular flask of 20 500mL, every bottled 100mL fermention medium of going into, sterilization inserts seed liquor then and ferments, 35 ℃ of leavening temperatures, pH7.2, shaking speed 200r/min, fermentation time 144h.
Collect above-mentioned fermented liquid 1.8L, separate, purifying, step obtains 2.1 gram effective mildew enamines and 0.8 gram validamine with embodiment 1.
Embodiment 4
Seed culture medium (g/L): glucose 25, peptone 15, yeast extract paste 5, MgSO
40.4, the tap water preparation, it is standby to sterilize.
The preparation of seed liquor is with embodiment 1.
Fermention medium (g/L): validamycin 50, glucose 1, peptone 10, yeast powder 1, MgSO
41, with the tap water preparation, it is standby to sterilize.
Fermentation: in the triangular flask of 20 500mL, every bottled 100mL fermention medium of going into, sterilization inserts seed liquor then and ferments, 25 ℃ of leavening temperatures, pH6.0, shaking speed 200r/min, fermentation time 192h.
Collect above-mentioned fermented liquid 1.8L, separate, purifying, step obtains 2.2 gram effective mildew enamines and 0.9 gram validamine with embodiment 1.
Embodiment 5
Seed culture medium (g/L): glucose 30, peptone 8, yeast extract paste 6, MgSO
40.5, the tap water preparation, it is standby to sterilize.
The preparation of seed liquor is with embodiment 1.
Fermention medium (g/L): validamycin 5, glucose 20, peptone 1, yeast powder 10, MgSO
40.1 with the tap water preparation, it is standby to sterilize.
Fermentation: in the triangular flask of 20 500mL, every bottled 100mL fermention medium of going into, sterilization inserts seed liquor then and ferments, 37 ℃ of leavening temperatures, pH8.0, shaking speed 200r/min, fermentation time 72h.
Collect above-mentioned fermented liquid 1.8L, separate, purifying, step obtains 0.7 gram effective mildew enamine and 0.2 gram validamine with embodiment 1.
Embodiment 6
Seed culture medium (g/L): glucose 20, peptone 10, yeast extract paste 5, MgSO
40.2, the tap water preparation, it is standby to sterilize.
The preparation of thalline: get the 500mL seed culture medium, average mark is contained in 10 250mL triangular flasks, sterilization.Insert inclined-plane CCTCC No.M 205095 and cultivate, shaking speed 200r/min cultivates thalline to logarithmic phase at 30 ℃ of shaking tables, and is centrifugal, collects thalline.
Cell catalysis reaction: the thalline that collection is obtained joins 100mL and contains in 5.0% the validamycin aqueous solution 30 ℃ of temperature of reaction, reaction times 48h.
Collect above-mentioned fermented liquid 100mL, separate, purifying, step obtains 0.4 gram effective mildew enamine and 0.1 gram validamine with embodiment 1.
Embodiment 7
Seed culture medium (g/L): glucose 10, peptone 20, yeast extract paste 10, MgSO
40.1, the tap water preparation, it is standby to sterilize.
The preparation of thalline is with embodiment 6.
The cell catalysis reaction: the thalline that collection is obtained joins in the validamycin aqueous solution of 100mL 1.0% 37 ℃ of temperature of reaction, reaction times 4h.
Collect above-mentioned fermented liquid 100mL, separate, purifying, step obtains 0.09 gram effective mildew enamine and 0.04 gram validamine with embodiment 1.
Embodiment 8
Seed culture medium (g/L): glucose 40, peptone 5, yeast extract paste 1, MgSO
41, the tap water preparation, it is standby to sterilize.
The preparation of thalline is with embodiment 6.
The cell catalysis reaction: the thalline that collection is obtained joins in the validamycin aqueous solution of 100mL 10.0% 25 ℃ of temperature of reaction, reaction times 96h.
Collect above-mentioned fermented liquid 100mL, separate, purifying, step obtains 0.5 gram effective mildew enamine and 0.2 gram validamine with embodiment 1.
Claims (6)
1. method of utilizing microorganism Alcaligenes faecalis cracking validamycin to prepare effective mildew enamine and validamine, it is characterized in that described microorganism belongs to the Alcaligenes faecalis of Alcaligenes (Alcaligenes) (Alcaligenes faecalis), CCTCC No.M 205095; Described Alcaligenes faecalis (Alcaligenesfaecalis), CCTCC No.M 205095, after cultivating, seed culture medium inserts the decomposition substrate that ferments in the fermention medium that contains the substrate validamycin, or seed culture medium cultivation back separation obtains thalline, the thalline that obtains is added in the solution of validamycin and carry out the reaction decomposes substrate, then decomposed solution is separated, purified, obtain effective mildew enamine and validamine.
2. method according to claim 1 is characterized in that described seed culture medium, the ratio of the bulking value that each is formed, and promptly g/L is: glucose 10～40, peptone 5～20, yeast extract paste 1～10, MgSO
40.1～1, the tap water preparation.
3. method according to claim 1 is characterized in that described fermention medium, the ratio of the bulking value that each is formed, and promptly g/L is: validamycin 5～50, glucose 1～20, peptone 1～10, yeast powder 1～10, MgSO
40.1～1, prepare with tap water.
4. according to claim 1 or 2 or 3 described methods, it is characterized in that in seed culture medium, inserting microorganism CCTCC No.M 205095 and cultivate, 25 ℃～37 ℃ of culture temperature, pH6.0～8.0, incubation time 24h～48h obtains seed liquor; Seed liquor inserts in the fermention medium that contains the substrate validamycin ferments, and its fermentation condition is: 25 ℃～37 ℃ of leavening temperatures, and pH6.0～8.0, fermentation time is 72h～192h.
5. method according to claim 1 and 2 is characterized in that inserting microorganism CCTCC No.M 205095 and cultivates 25 ℃～37 ℃ of culture temperature in seed culture medium, pH6.0～8.0, cultivate thalline to logarithmic phase, centrifugation then obtains thalline; With the thalline that separation obtains, add in the solution that contains the substrate validamycin and react, utilize thalline to decompose substrate, 25 ℃～37 ℃ of temperature of reaction, reaction times 4h～96h.
6. method according to claim 5, the concentration that it is characterized in that the substrate validamycin is 1.0%～10.0%.
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|---|---|---|---|---|
| JPS5754593A (en) * | 1980-09-16 | 1982-04-01 | Takeda Chem Ind Ltd | Preparation of valienamine |
| JPS586684B2 (en) * | 1978-05-23 | 1983-02-05 | 日立造船株式会社 | Energy saver for contact type sulfuric acid production equipment |
| JPS58152496A (en) * | 1982-03-04 | 1983-09-10 | Takeda Chem Ind Ltd | Production of valienamine and validamine |
| JPS62181793A (en) * | 1985-10-08 | 1987-08-10 | Takeda Chem Ind Ltd | Production of valineamine and validamine |
| JP3586684B1 (en) * | 2003-10-28 | 2004-11-10 | 合同酒精株式会社 | Novel microorganisms that convert validamycin to valienamin and validamin |
| CN1563397A (en) * | 2004-04-05 | 2005-01-12 | 浙江工业大学 | Microbe method for preparing enamine and amine from valinemia |
-
2005
- 2005-11-01 CN CNB2005100613641A patent/CN100362108C/en not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS586684B2 (en) * | 1978-05-23 | 1983-02-05 | 日立造船株式会社 | Energy saver for contact type sulfuric acid production equipment |
| JPS5754593A (en) * | 1980-09-16 | 1982-04-01 | Takeda Chem Ind Ltd | Preparation of valienamine |
| JPS58152496A (en) * | 1982-03-04 | 1983-09-10 | Takeda Chem Ind Ltd | Production of valienamine and validamine |
| JPS62181793A (en) * | 1985-10-08 | 1987-08-10 | Takeda Chem Ind Ltd | Production of valineamine and validamine |
| JP3586684B1 (en) * | 2003-10-28 | 2004-11-10 | 合同酒精株式会社 | Novel microorganisms that convert validamycin to valienamin and validamin |
| CN1563397A (en) * | 2004-04-05 | 2005-01-12 | 浙江工业大学 | Microbe method for preparing enamine and amine from valinemia |
Non-Patent Citations (1)
| Title |
|---|
| 微生物转化法裂解井冈霉素生产井冈霉亚基胺A. 张宪锋，郑裕国，沈寅初.中国抗生素杂志，第29卷第4期. 2004 * |
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|---|---|
| CN1772914A (en) | 2006-05-17 |
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Assignee: Zhejiang Tonglu Huifeng Biochemistry Co., Ltd. Assignor: Zhejiang University of Technology Contract record no.: 2011330000825 Denomination of invention: Microbial process of producing validamycin anamine and validamycin amine Granted publication date: 20080116 License type: Exclusive License Open date: 20060517 Record date: 20110627 |
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