CN100506995C - Method for production of 2-keto-L-gulonic acid - Google Patents
Method for production of 2-keto-L-gulonic acid Download PDFInfo
- Publication number
- CN100506995C CN100506995C CNB038212285A CN03821228A CN100506995C CN 100506995 C CN100506995 C CN 100506995C CN B038212285 A CNB038212285 A CN B038212285A CN 03821228 A CN03821228 A CN 03821228A CN 100506995 C CN100506995 C CN 100506995C
- Authority
- CN
- China
- Prior art keywords
- gluconobacter
- fermentation
- sorbitol powder
- kga
- microorganism
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/58—Aldonic, ketoaldonic or saccharic acids
- C12P7/60—2-Ketogulonic acid
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
The present invention relates to a process for the production of 2-KGA or a salt thereof from D-sorbitol by a multi-stage continuous or a single-stage semi-continuous fermentation mode using a mixed culture of microorganisms of the genus Gluconobacter or Acetobacter. One of the microorganisms is G. oxydans DSM 4025.
Description
Technical field
The present invention relates to from the D-Sorbitol Powder 2-keto-L-gulonic acid (2-keto-L-gulonicacid, 2-KGA) carry out the method for high yield fermentative production, described method is undertaken by utilizing the fermentation system of being made up of multistage continuous mode or single phase semicontinuous (repeated fed-batch) pattern.
Background technology
2-KGA is the important intermediate that is used to produce the L-xitix.This compound can be converted into the L-xitix according to known Reichstein method.The microorganism that belongs to by Acetobacter or Pseudomonas produces 2-KGA from the D-Sorbitol Powder method is disclosed in the Japanese patent application publication No. 40154/1976.Mentioned microorganism can produce 2-KGA, yet its output be very low, is less than 6g/L at oxidation D-Sorbitol Powder under the aerobic conditions.Because described low relatively output, aforesaid method far can not be used for plant-scale production, especially under the situation of D-Sorbitol Powder as starting raw material.
The known bacterial strain that some kinds of Acetobacter (being classified among the Gluconobacter now) arranged, for example A.xylinum and A.suboxydans can be from D-Sorbitol Powder High-efficient Production L-sorboses.The D-Sorbitol Powder is the raw material more more cheap than L-sorbose, but the L-sorbose can be converted into 2-KGA more efficiently.
Summary of the invention
The invention provides and be used for the method for producing 2-KGA with high yield from the D-Sorbitol Powder, described method is continuously fermented by the multistage or is fermented by single phase semicontinuous (repeated fed-batch) and carries out.
More specifically, the present invention relates to produce the method for 2-keto-L-gulonic acid (2-KGA) or its salt from the D-Sorbitol Powder, described method continuously ferment by the multistage or single phase semicontinuous fermentation carry out, wherein use and belong to Gluconobacter or the microorganism of Acetobacter genus and the mixed culture of G.oxydans DSM4025 (FERM BP-3812) or its mutant, described mutant has the identification mark of G.oxydans DSM 4025 (FERM BP-3812), and the described microorganism that belongs to Gluconobacter or Acetobacter genus can produce the L-sorbose from the D-Sorbitol Powder; Alternatively, described method also comprises reclaim 2-KGA from fermentation culture.
Embodiment
According to the regulation of " budapest treaty ", G.oxydans DSM 4025 was deposited on March 17th, 1987
The Deutsche Sammlung vonMikroorganismen und Zellkulturen (DSMZ) of (Germany) is numbered DSM No.4025.Depositor is that the eastern science instrument is imported and exported Group Co.,Ltd, and it is that Institute of Microorganism, Academia Sinica for No. 52, People's Republic of China (PRC) Sanlihe Road, Beijing delivers.Effectively depositor is described institute, and its full address is a The People's Republic of China Zhongguangcun, Haidian District, Beijing City Institute of Microorganism, Academia Sinica, 100080.
The subculture of this bacterial strain also has been deposited in NationalInstitute of Advanced Industrial Science and Technology (AIST) on March 30th, 1992, TsukubaCentral 6,1-1-1Higashi, Tsukuba, Ibaraki 305-8566, Japan, this also is the regulation according to " budapest treaty ", deposit number is FERM BP-3812.Depositor is NipponRoche K.K., 6-1, Shiba2-chrome, Minato-ku, Tokyo 105-8532 Japan.This subculture also be most preferably be used for of the present invention.
Multistage continuously ferments and comprises a more than fermenting container.An example of multistage continuous system is the system of continuously fermenting in two stages, and it is made of substratum storage tank, first fermentor tank, second fermentor tank and results container.By in whole process, using a more than fermenting container, make the output of this process reach best.
, discard biological substance after every batch and caused higher production cost in batches or in the fed-batch operation traditional, the reactor cleaning and (inoculation) the needed time of startup have caused the loss of reactor throughput.
Multistage cultured continuously pattern in the 2-KGA fermentation process can obtain higher to the throughput of 2-KGA and higher 2-KGA concentration, and does not have residual D-Sorbitol Powder and L-sorbose.This is the preferred method that is used for 2-KGA sodium preparation separating step.
In described initial link of continuously fermenting, can use in batches or fed-batch operation.
Among the present invention, need not fixing means at microorganism, chemical bond or be used for the physical method that cell keeps for example, for example matrix embedding also need not biological substance control or keeps, and for example the film system just may produce 2-KGA from the D-Sorbitol Powder.Therefore, after the multistage from the D-Sorbitol Powder to 2-KGA, the fermentative production system set up, to can from the D-Sorbitol Powder produce the microorganism of L-sorbose and G.oxydans DSM 4025 carry out mixed culture just can be easily and directly be used as 2-KGA fermentation process cheaply.
The D-Sorbitol Powder in initial production medium and the concentration that is used for the supplemented medium of continuous mode can be respectively: double continuous mode, and approximately 0g/L is to about 250g/L; For multistage continuous mode, 5g/L to 250g/L.In addition, the supplemented medium that is used for semicontinuous pattern can contain 20 the D-Sorbitol Powders to about 800g/L scope of having an appointment.The feed supplement volume that is used for fed-batch mode can change according to working volume and fermentation condition.In the concentration range of the supplemented medium D-Sorbitol Powder that is used for continuous mode, dilution rate can be set to about 0.01h
-1To about 0.05h
-1
The invention provides by continuously fermenting and produce the method for 2-KGA or its salt from the D-Sorbitol Powder, described method comprises:
(a) in one or more fermenting containers, in the nutritional medium that contains the D-Sorbitol Powder, cultivation belongs to microorganism and G.oxydansDSM 4025 (FERM BP-3812) or its mutant of Gluconobacter or Acetobacter genus, the described microorganism that belongs to Gluconobacter or Acetobacter genus can produce the L-sorbose from the D-Sorbitol Powder, and described mutant has the identification mark of G.oxydans DSM 4025 (FERM BP-3812);
(b) contain the nutritional medium that concentration is the D-Sorbitol Powder of the extremely about 250g/L of about 5g/L continuous the adding in fermenting container, and the dilution rate of fermentation is set to about 0.01h
-1To about 0.05h
-1
(c) from fermenting container, take out fermentation culture continuously; With
(d) from described fermentation culture, reclaim 2-KGA.
The invention still further relates to the single phase semicontinuous fermentation method of producing 2-KGA from the D-Sorbitol Powder.Described semicontinuous fermentation is to obtain from the method for D-Sorbitol Powder to the high productive capacity of 2-KGA, and wherein, the part nutrient solution is used as the seed of fermentation next time.After 48 hours the cultivation, all about 10% (v/v) in the nutrient solution can be used as the seed in second step, fills with fresh nutritional medium in fermentor tank, and cultivates.This round-robin is repeated can continue to carry out.Than traditional in batches or fed-batch operation, described semi continuous operation can utilize nutrient solution as the seed of cultivating next time.Therefore, described semi continuous operation can be applied to the fermentation of 2-KGA, and need not to carry out the step of several times from the inoculation of a small amount of seed, and the time that does not need to be used to prepare culture, for example cleaning and start time.In addition, reactor can both keep higher throughput in long fermenting process.
Therefore, an object of the present invention is to provide the method for producing 2-KGA or its salt from the D-Sorbitol Powder by semicontinuous fermentation, described method comprises:
(a) in fermenting container, in to contain starting point concentration be about 0g/L to the nutritional medium of the about D-Sorbitol Powder of 250g/L and to contain concentration be about 20g/L to the about supplemented medium that is used for fed-batch mode of the D-Sorbitol Powder of 800g/L, cultivation belongs to microorganism and G.oxydans DSM 4025 (FERM BP-3812) or its mutant of Gluconobacter or Acetobacter genus, the described microorganism that belongs to Gluconobacter or Acetobacter genus can produce the L-sorbose from the D-Sorbitol Powder, and described mutant has the identification mark of G.oxydans DSM 4025 (FERM BP-3812);
(b) with the part of fermentation culture as the inoculum of fed-batch fermentation next time;
(c) continue to repeat said process, and
(d) from fermentation culture, reclaim 2-KGA.
The volume ratio of seed and fermentation next time can be about 0.1% to the scope of about 90% (v/v), preferably about 5% to the scope of about 90% (v/v).
The cycle of a fed-batch fermentation can change according to be used for fermenting round-robin seed volume or fermentation condition next time, and described fermentation condition for example is the D-Sorbitol Powder in initial production medium with in the concentration of the supplemented medium that is used for fed-batch mode.
Therefore, in the present invention, a fed-batch fermentation round-robin cycle and the amount of the seed that is used for next time fermenting can be coordinated, to improve throughput to 2-KGA.
The concentration of D-Sorbitol Powder can be approximately between the extremely about 250g/L of 0g/L in the initial production medium.In addition, the supplemented medium that is used for fed-batch mode can contain the D-Sorbitol Powder of about 20g/L to the about 800g/L scope.
Described continuously and semicontinuous fermentation can be carried out in the fermentation culture dissolved oxygen concentration be about 0.1% to the situation of about 100% air saturation, be preferably about 5% to about 100% air saturation.
Therefore, one aspect of the present invention provides the method for producing 2-KGA or its salt from the D-Sorbitol Powder, described method continuously ferment by the multistage or single phase semicontinuous fermentation carry out, wherein use and belong to Gluconobacter or the microorganism of Acetobacter genus and the mixed culture of G.oxydans DSM 4025 (FERM BP-3812) or its mutant, described mutant has the identification mark of G.oxydansDSM 4025 (FERM BP-3812), and the described microorganism that belongs to Gluconobacter or Acetobacter genus can produce the L-sorbose from the D-Sorbitol Powder; In the described method, fermentation is carried out in the fermentation culture dissolved oxygen concentration under the situation between about 0.1% to about 100%.In a kind of preferred implementation, dissolved oxygen concentration is between about 5% to about 100%.
Except that being used as the D-Sorbitol Powder of starting raw material of the present invention, other carbon source material also can be added into, for example glycerine, D-glucose, D-N.F,USP MANNITOL, D-fructose, D-arabitol etc.
Some organic or inorganic materials also can be used as nitrogenous source, for example yeast extract, meat extract, peptone, casein, corn steep liquor, urea, amino acid, nitrate, ammonium salt etc.Can use sal epsom, potassiumphosphate, iron protochloride and inorganicss such as iron(ic) chloride, lime carbonate.
The amount of above-mentioned nutraceutical blending ratio and every kind of composition can change with the attribute of the microorganism of being adopted.The amount of starting raw material D-Sorbitol Powder, can details be as the case may be selected or determine by a kind of alternative relatively amount, inoculation times and other culture condition in the microorganism that inoculates.
Culture condition can also change according to the kind and the feature of microorganism used therefor.The composition of substratum certainly as the case may be details is carried out and selects or determine, with output program product most effectively, though culture temperature can remain between about 13 ℃ to about 36 ℃, preferably between about 18 ℃ to about 33 ℃, the pH value of substratum can remain between about 4.0 to about 9.0, preferably between about 6.0 to about 8.0.
Therefore, in one embodiment of the invention, above-mentioned be used for by the multistage continuously ferment or single phase the semicontinuous fermentation method of producing 2-KGA or its salt from the D-Sorbitol Powder, it is between about 4.0 to about 9.0 that described fermentation is carried out at pH.Preferred pH is between about 6.0 to about 8.0.
Another embodiment of the invention be above-mentioned be used for by the multistage continuously ferment or single phase the semicontinuous fermentation method of producing 2-KGA or its salt from the D-Sorbitol Powder, wherein, described fermentation be carried out at about 13 ℃ to about 36 ℃ temperature.A kind of preferred embodiment is that temperature is between about 18 ℃ to 33 ℃.
For keeping the pH value of substratum, any suitable acidity or the alkaline reagents that in described substratum, add appropriate amount proper time that can be in the training period.Perhaps, can reach same purpose by adding suitable damping fluid or culture being cushioned also.
Can be used by the bacterial strain of product 2-KGA from the L-sorbose that the production of D-Sorbitol Powder obtains by the bacterial strain that produces the L-sorbose, to make 2-KGA.Any microorganism that the D-Sorbitol Powder can be converted into the L-sorbose all can be used from the present invention with G.oxydans DSM 4,025 one.
What belong to that Gluconobacter or Acetobacter belong to can comprise G.suboxydans IFO 3130 from the example that the D-Sorbitol Powder is produced the microorganism of L-sorbose, G.suboxydans IFO 3255, G.suboxydans IFO 3256, G.suboxydans IFO 3257, G.suboxydans IFO3258, G.suboxydans IFO 3289, G.suboxydans IFO 3290, G.suboxydansIFO 3291, G.gluconicus IFO 3171, G.gluconicus IFO 3285, G.gluconicusIFO 3286, G.gluconicus IFO 3244, G.albidus IFO 3251, G.albidus IFO3253, G.industrius IFO 3261, G.cerinus IFO 3262, G.cerinus IFO 3263, G.cerinus IFO 3265, G.cerinus IFO 3266, G.cerinus IFO 3267, G.cerinusIFO 3270, G.diacetonicus IFO 3273, G.roseus IFO 3990, A.aceti spp.orleans IFO 3259, A.aceti spp.aceti IFO 3281, A.liquefaciens IFO 12257, A.liquefaciens IFO 12258, A.liquefaciens IFO 12388, A.aceti spp.xylinumIFO 3288, A.aceti spp.xylinum IFO 13693, A.aceti spp.xylinum IFO 13772 and A.aceti spp.xylinum IFO 13773.
Therefore, the present invention relates to by the multistage continuously ferment or single phase the semicontinuous fermentation method of producing 2-KGA or its salt from the D-Sorbitol Powder, wherein use and belong to Gluconobacter or the microorganism of Acetobacter genus and the mixed culture of G.oxydans DSM 4025 (FERM BP-3812) or its mutant, described mutant has the identification mark of G.oxydans DSM 4025 (FERM BP-3812), the described microorganism that belongs to Gluconobacter or Acetobacter genus can produce the L-sorbose from the D-Sorbitol Powder, and it is selected from the suboxydans by Gluconobacter, Gluconobacter rubiginosus, Gluconobacter albidus, Gluconobacterindustrius, Gluconobacter cerinus, Gluconobacter diacetonicus, Gluconobacter roseus, Gluconobacter gluconicus, Acetobacter aceti spp.orleans, the group that Acetobacter aceti spp.xylinum and Acetobacter liquefaciens are constituted.Preferred microorganism is selected from the group that is made of G.suboxydans IFO 3255, G.suboxydans IFO3256, G.suboxydans IFO 3258, G.suboxydans IFO 3290, G.suboxydansIFO 3291, G.gluconicus IFO 3285 and G.cerinus IFO 3267.More preferably, fermentation is undertaken by G.suboxydans IFO 3291 and G.oxydans DSM 4025 are carried out mixed culture.
Mentioned microorganism is stored in public depositary institution, is used to consign to any people who claims.One of this type of depositary institution is Institute of Fermentation, Osaka, Japan (IFO).
In the microorganism defined above, also comprise these type of species by defined synonym body (synonym) or the basinym body (basonym) of " international prokaryotic organism rules of nomenclature " (International Code of Nomenclature of Prokaryotes) with same physical-chemical attribute.
Described microorganism is incubated in the aqueous culture medium under aerobic conditions usually, contains D-Sorbitol Powder and suitable nutrition in the described substratum, for example nitrogenous source and trace element.Yet any traditional fermentation condition all can be used to implement method of the present invention.
Can isolate the 2-KGA that obtains according to present method from reaction mixture, for example, separate by forming salt, perhaps by utilizing product to separate with the difference of impurity attribute on every side, described attribute for example is the distribution coefficient between solubleness, absorbability and solvent.Absorption is for example carried out on ion exchange resin, is a kind of method that is used for separated product easily.Available traditional method is carried out further purifying to the product that obtains thus, for example, and by recrystallization or chromatogram.Perhaps, by esterification and subsequently enolization with lactonize, described reaction mixture can be directly used in the conversion to the L-xitix.
The following examples will be set forth the present invention.The calculating of transformation efficiency is based on the amount of the 2-KGA that the produces ratio with the amount of used D-Sorbitol Powder.
Embodiment 1 control DO says G.oxydans DSM 4025 and G.suboxydans IFO 3291
The row mixed culture is carried out two stage 2-KGA from 12% D-Sorbitol Powder and is continuously fermented
(1) inoculum of preparation G.oxydans DSM 4025 bacterial strains
Contain 8% L-sorbose (sterilization separately), 0.05% glycerine, 0.25% MgSO
47H
2O, 1.75% corn steep liquor, 5.0% bread yeast (pH is 7.0 before the sterilization), 0.5% CaCO
3, 0.5% urea (sterilization separately) and 0.03% defoamer (Actcol:Takeda) seed culture medium be loaded in the Erlenmeyer bottle of 500ml (every bottle of 100ml), and sterilized 20 minutes at 121 ℃.The cell inoculation of microorganism DSM4025 of one inoculation circular rector in this seed culture medium, was cultivated 24 hours at 30 ℃.
(2) inoculum of preparation G.suboxydans IFO 3291
Contain 2% D-Sorbitol Powder, 0.3% yeast extract (Oriental Yeast), 0.3% beef extract, 0.3% corn steep liquor, 1% polyprotein peptone, 0.1% urea, 0.1% KH
2PO
4, 0.02% MgSO
47H
2O, 0.1% CaCO
3The seed culture medium of (sterilization before pH be 7.0) and 0.03% defoamer is at 121 ℃ of autoclavings that carry out 20 minutes.The cell of G.suboxydans IFO 3291 of one inoculation circular rector is transferred in the 100ml seed culture medium in the 500ml Erlenmeyer bottle, cultivates 24 hours at 28 ℃.
(3) be inoculated in the Primary Fermentation
The each seed culture prepares 100ml (seed volume altogether is 200ml), is inoculated in the initial production medium of 2L, contains 4% D-Sorbitol Powder, 1% corn steep liquor, 0.01% MgSO in the described initial production medium
47H
2O, 0.025% KH
2PO
4, 0.4% yeast extract (BYF 100:Universal Foods) and 0.15% defoamer.When the concentration of 2-KGA is increased to 120g/L by fed-batch mode, (dissolvedoxygen DO) is on close level, and training mode is just changed into continuous mode afterwards for this stage and 90% dissolved oxygen.
(4) two stages continuously fermented
During continuously fermented system in described two stages, the vial fermentor tank had been equipped device same as described above.This fermentation system is made up of two fermentor tanks.The working volume of these two fermentor tanks all is 2L.For improving the dilution rate that throughput and the raising of 2-KGA are continuously fermented, used fed-batch operation in the initial link of continuously fermenting.The substratum that is used for fed-batch operation is by 60% D-Sorbitol Powder, 6.67% corn steep liquor, 0.0287% MgSO
47H
2O, 0.0717% KH
2PO
4Constitute with 0.2% defoamer.30 hours fed-batch operation stage, provide 600ml to be used for the supplemented medium of fed-batch mode to main fermentation tank with first peristaltic pump.After this, control continuous feeding speed with second peristaltic pump.The nutrient solution that will take out from first fermentor tank with the 3rd peristaltic pump is transferred in the subordinate phase fermentor tank further again.At last, with the 4th peristaltic pump nutrient solution is got in the results storage tank, and working volume is retained as 2L.Temperature is controlled in 28 ℃, and stirring velocity and Ventilation Rate are set to 800rpm and 1.0L/min respectively.With sodium hydroxide solution pH is controlled to be 7.0.
Known the process of producing 2-KGA from the D-Sorbitol Powder by above-mentioned mixed culture is carried out DO control, help to increase the cytoactive of G.suboxydans IFO 3291 and the output of 2-KGA.Therefore, between 9 to 52 hours after the fermentation beginning, the DO level of fs fermentor tank is controlled in 10%.The DO level is by providing the air that has mixed pure oxygen to control.In first fermentor tank and second fermentor tank, dilution rate (D) is set at 0.035h
-1To 0.045h
-1Scope in.Fermentation continues 250 hours.Table 1 has shown the fermentation activity of mixture in above-mentioned two stage continuous modes of G.oxydans DSM 4025 and G.suboxydans IFO 3291.In this continuous mode, average generation has gone out the 2-KGA of 74.5g/L.Under the steady state of this continuous mode, the throughput to 2-KGA in first fermentor tank is calculated as 2.57g/L/h.In addition, overall throughput is calculated as 1.33g/L/h, and total 2-KGA molar yield is 60.6%.
Table 1: the fermentation activity in the two stage continuous modes of use 3L fermentor tank
| State | Gross activity | Fs | Subordinate phase |
| Dilution rate (average: hour -1) | 0.0179 | 0.0443 | 0.0358 |
| 2-KGA concentration is (average: g/L) | 74.5 | 58.0 | 74.5 |
| Throughput (g/L/ hour) to 2-KGA | 1.33 | 2.57 | - |
| 2-KGA molar yield (%) | 60.6 | 52.9 | 60.6 |
Embodiment 2 is by the mixing to G.oxydans DSM 4025 and G.suboxydans IFO 3291
The D-Sorbitol Powder of cultivation from 13% carries out two stage 2-KGA and continuously ferments
Initial production medium and the supplemented medium that is used for fed-batch mode are by constituting with composition identical described in the embodiment 1.Described two stages continuously ferment according to the carrying out described in the embodiment 1.Use during described two stage 2-KGA continuously ferment and contain 13% D-Sorbitol Powder, 3% corn steep liquor, 0.25% MgSO
47H
2The continuous feeding substratum (10L) of O, 0.05% glycerine, yeast extract (BYF100) and 0.15% defoamer.
Fermentation has been carried out 160 hours.During fermentation kept metastable fermentation activity, in first and second fermentor tanks, average D is 0.0361h
-1The result is summarized in the table 2.Under the steady state of continuous mode, produced the 2-KGA of 88.2g/L.Under the steady state of this continuous mode, the throughput to 2-KGA in first fermentor tank is calculated as 2.28g/L/h.Total throughput is calculated as 1.59g/L/h, and the molar yield of D-Sorbitol Powder is 63.0%.Use this continuous feeding substratum, to the throughput of 2-KGA than described in the embodiment 1 high at least 19%.
Table 2: the fermentation activity in the two stage continuous modes of use 3L fermentor tank
| State | Gross activity | Fs | Subordinate phase |
| Dilution rate (average: hour -1) | 0.0181 | 0.0361 | 0.0361 |
| 2-KGA concentration is (average: g/L) | 88.2 | 63.4 | 88.2 |
| Throughput (g/L/ hour) to 2-KGA | 1.59 | 2.28 | - |
| 2-KGA molar yield (%) | 63.0 | 51.4 | 63.0 |
Embodiment 3 is by the mixing to G.oxydans DSM 4025 and G.suboxydans IFO 3291
The D-Sorbitol Powder of cultivation from 14% carries out two stage 2-KGA and continuously ferments
In continuously fermenting in this two stage, the concentration of D-Sorbitol Powder is 14% in the continuous feeding substratum.Identical in this continuous feeding substratum among other composition and the embodiment 2.Described two stages continuously ferment according to the carrying out described in the embodiment 1.Initial production medium is identical with the substratum described in the embodiment 1 with the supplemented medium that is used for fed-batch mode (600ml).
For first and second fermentor tanks, D is being respectively 0.015 to 0.060h appropriate opportunity
-1Scope in and 0.020 to 0.050h
-1Scope in change, the D-Sorbitol Powder is converted into 2-KGA fully and in final results jar, does not have the D-Sorbitol Powder and the D value of necessity that the L-sorbose is residual to work out.Fermentation was terminated at 700th hour.The fermentation activity of mixture in two stage continuous modes of having summarized G.oxydans DSM4025 and G.suboxydans IFO 3291 in the table 3.In this two stages continuous mode, apparent D is 0.0331h
-1Situation under, obtained to contain the nutrient solution of 75.1g/L 2-KGA, total dilution rate is calculated as 0.0166h
-1Total 2-KGA molar yield is 48.9%.Under the steady state of this continuous mode, in first fermentor tank throughput of 2-KGA and total throughput to 2-KGA are calculated as 2.07g/L/h and 1.24g/L/h respectively.This two stages continuation method has been used 10% DO control in first fermentor tank.In first fermentor tank, carry out DO control and can improve the activity that G.suboxydans IFO 3291 cells are converted into the D-Sorbitol Powder L-sorbose, and 2-ketone group-D-gulonic acid (2-keto-D-gluconicacid 2-KD) waits by product not accumulate in the nutrient solution of final fermentor tank.Can carry out more stable 2-KGA production by DO control.
Table 3: the fermentation activity in the two stage continuous modes of use 3L fermentor tank
| State | Gross activity | Fs | Subordinate phase |
| Dilution rate (average: hour -1) | 0.0166 | 0.0331 | 0.0331 |
| 2-KGA concentration is (average: g/L) | 75.1 | 62.6 | 75.1 |
| Throughput (g/L/ hour) to 2-KGA | 1.24 | 2.07 | - |
| 2-KGA molar yield (%) | 48.9 | 45.5 | 48.9 |
Embodiment 4 is by the mixing to G.oxydans DSM 4025 and G.suboxydans IFO 3291
Cultivation is carried out single phase 2-KGA semicontinuous fermentation from the D-Sorbitol Powder
As embodiment 1 described inoculum, get 100ml for every kind and be inoculated in the initial production medium of 1.5L, contain 2% D-Sorbitol Powder, 3% corn steep liquor, 0.25% MgSO in the described initial production medium
47H
2O, 0.05% glycerine, 0.4% BYF100 and 0.15% defoamer.The composition of supplemented medium (550ml) that is used for fed-batch mode is by 60% D-Sorbitol Powder, 10.67% corn steep liquor, 0.023% MgSO
47H
2O, 0.0573% KH
2PO
4Form with 0.2% defoamer.The semicontinuous production substratum of 2-KGA is made of the composition identical with initial production medium.The amount that is applied to the D-Sorbitol Powder in initial medium and each batch supplemented medium is respectively 30g and 330g.Be set to the pitch time of a fed-batch fermentation 30 hours.After initial D-Sorbitol Powder is by completely consumed, beginning fed-batch fermentation pattern.
Fed-batch fermentation was gathered in the crops the nutrient solution of 90% (v/v) after 30 hours for the first time.The nutrient solution of staying the residue 10% (v/v) in the fermentor tank is used as the seed of fermentation next time.In fermentor tank, fill with the semicontinuous production substratum that contains with the initial production medium identical component again.Afterwards, the G.suboxydans IFO 3291 with 5% (v/v) is inoculated in the main fermentation tank.By continuing to repeat this circulation, the fermentation in the main fermentation tank is able to constantly be repeated.With NaOH pH is controlled at 7.0 between yeast phase, semicontinuous fermentation is carried out 10% DO control.The 2-KGA semicontinuous fermentation that carries out from the D-Sorbitol Powder, temperature is controlled in 28 ℃.Stirring velocity and Ventilation Rate are set to 800rpm and 0.75L/ minute respectively.
Primary Fermentation repeats 5 times, and total fermentation time is 165 hours.For every batch operation, the total amount of D-Sorbitol Powder is 360g in initial medium and the supplemented medium.Table 4 has shown the 2-KGA fermentation activity in the semicontinuous pattern.The output of 2-KGA is in the scope of 119.5g/L to 130.7g/L, and average 2-KGA output is 124.6g/L.Every batch of throughput to 2-KGA is 4.14g/L/h to the average productive capacity of 2-KGA in the scope of 3.93g/L/h to 4.33g/L/h.The molar yield of D-Sorbitol Powder has surpassed 70.0%.This semi-continuous 2-KGA fermentation quite stable, this method can be produced the 2-KGA above 119g/L, and is easy to keep surpassing in producing for a long time the average productive capacity to 2-KGA of 4.00g/L/h.
Table 4: the fermentation activity of single phase in the semicontinuous pattern that uses the 3L fermentor tank
| Batch number | 1 | 2 | 3 | 4 | 5 |
| 2-KGA output (g/L) | 123.3 | 130.7 | 130.1 | 119.5 | 119.6 |
| Every batch of throughput (g/L/h) to 2-KGA | 4.11 | 4.33 | 4.30 | 3.99 | 3.96 |
| The D-Sorbitol Powder total amount (g) of every batch of use | 360.0 | 360.0 | 360.0 | 360.0 | 360.0 |
| 2-KGA productive rate (%) | 70.0 | 74.1 | 73.7 | 70.0 | 70.1 |
Embodiment 5 short batch pitch time to use new production substratum from the D-Sorbitol Powder to 2-
KGA says the influence of capable single phase semicontinuous fermentation
Be set to the pitch time of a fed-batch fermentation 24 hours.Use therein initial production medium and semicontinuous production substratum be identical substratum described in the embodiment 4.In the supplemented medium of this initial medium and each batch, the amount of D-Sorbitol Powder is respectively 30g and 330g.
Primary Fermentation has been repeated 5 times, and total fermentation time is 130 hours.In every batch operation, the total amount of the D-Sorbitol Powder in initial medium and supplemented medium is 360g.Table 5 has shown the 2-KGA fermentation activity in second continuous mode of situation of lacking every batch of pitch time.The output of 2-KGA is in the scope of 105.6g/L to 110.8g/L, and average 2-KGA output is 108.2g/L.In every batch to the throughput of 2-KGA in the scope of 4.40g/L/h to 4.62g/L/h, be 4.51g/L/h to the average productive capacity of 2-KGA.This throughput is described higher by 8.94% than embodiment 4.The molar yield of D-Sorbitol Powder has surpassed 61.0%.Be the average productive capacity that improved in 24 hours in the semi continuous operation 2-KGA pitch time.
Table 5: the fermentation activity of single phase in the semicontinuous pattern that uses the 3L fermentor tank
| Batch number | 1 | 2 | 3 | 4 | 5 |
| 2-KGA output (g/L) | 110.8 | 109.8 | 107.6 | 107.0 | 105.6 |
| Every batch of throughput (g/L/h) to 2-KGA | 4.62 | 4.58 | 4.48 | 4.46 | 4.40 |
| The D-Sorbitol Powder total amount (g) of every batch of use | 360.0 | 360.0 | 360.0 | 360.0 | 360.0 |
| 2-KGA productive rate (%) | 64.2 | 63.7 | 62.4 | 62.1 | 61.2 |
Claims (10)
1. one kind is used for from the method for D-Sorbitol Powder production 2-keto-L-gulonic acid (2-KGA) or its salt, described method by carry out in the nutritional medium that contains the D-Sorbitol Powder that the multistage continuously ferments or single phase semicontinuous fermentation carry out, wherein use to belong to microorganism of Gluconobacter (Gluconobacter) or acetobacter (Acetobacter) and the mixed culture of gluconobacter oxydans (G.oxydans) DSM 4025 (FERM BP-3812), the described microorganism that belongs to Gluconobacter or acetobacter can produce the L-sorbose from the D-Sorbitol Powder.
2. the method for claim 1 also comprises and reclaim 2-KGA from fermentation culture.
3. method as claimed in claim 1 or 2, the wherein said multistage continuously ferments and comprises the steps:
(a) in one or more fermenting containers, in the nutritional medium that contains the D-Sorbitol Powder, cultivation belongs to microorganism and the gluconobacter oxydans DSM4025 (FERM BP-3812) of Gluconobacter or acetobacter, and the described microorganism that belongs to Gluconobacter or acetobacter can produce the L-sorbose from the D-Sorbitol Powder;
(b) contain the nutritional medium that concentration is the D-Sorbitol Powder of 5g/L to 250g/L continuous the adding in fermenting container, and the dilution rate of fermentation is set to 0.01h
-1To 0.05h
-1
(c) from fermenting container, take out fermentation culture continuously; With
(d) from described fermentation culture, reclaim 2-KGA.
4. method as claimed in claim 1 or 2, wherein, described semicontinuous fermentation comprises the steps:
(a) in fermenting container, in contain starting point concentration be 0g/L to 250g/L the D-Sorbitol Powder nutritional medium and contain the supplemented medium that is used for fed-batch mode that concentration is the D-Sorbitol Powder of 20g/L to 800g/L, cultivation belongs to microorganism and the gluconobacter oxydans DSM4025 (FERM BP-3812) of Gluconobacter or acetobacter, and the described microorganism that belongs to Gluconobacter or acetobacter can produce the L-sorbose from the D-Sorbitol Powder;
(b) with the part of fermentation culture as the inoculum of fed-batch fermentation next time;
(c) continue to repeat said process, and
(d) from described fermentation culture, reclaim 2-KGA.
5. method as claimed in claim 4, wherein, the volume ratio of described inoculum and fed-batch fermentation next time is in 0.1% to 90%v/v scope.
6. method as claimed in claim 1 or 2, wherein said fermentation are carried out at the concentration of dissolved oxygen in the fermentation culture under the situation between 0.1% to 100%.
7. method as claimed in claim 1 or 2, wherein said fermentation are carried out in pH under the situation between 4.0 to 9.0.
8 methods as claimed in claim 1 or 2, wherein said fermentation are carried out in temperature between 13 ℃ to 36 ℃.
9. method as claimed in claim 1 or 2, the microorganism that wherein the D-Sorbitol Powder can be converted into the L-sorbose are to be selected from by weak glucose oxidation bacteria (Gluconobacter suboxydans), Gluconobacter rubiginosus, little white gluconobacter sp (Gluconobacter albidus), Gluconobacter industrius, wax shape gluconobacter sp (Gluconobacter cerinus), Gluconobacter diacetonicus, Gluconobacter roseus, Fu Shi gluconobacter sp (Gluconobacter gluconicus), acetify bacillus aceticus Sai Erlan subspecies (Acetobacteraceti spp.orleans), microorganism in the group that acetobacter xylinum (Acetobacter aceti spp.xylinum) and liquefaction bacillus aceticus (Acetobacter liquefaciens) are constituted.
10. method as claimed in claim 9, wherein said microorganism are selected from the group that is made of weak oxide gluconobacter suboxydans IFO 3255, weak glucose oxidation bacteria IFO 3256, weak oxide gluconobacter suboxydans IFO3258, weak oxide gluconobacter suboxydans IFO 3290, weak oxide gluconobacter suboxydans IFO 3291, G.gluconicus IFO 3285 and wax shape gluconobacter sp IFO 3267.
11. method as claimed in claim 1 or 2, wherein said fermentation is carried out by G.suboxydans IFO 3291 and oxidizing glucose acidfast bacilli DSM 4025 are carried out mixed culture.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02021598.4 | 2002-09-27 | ||
| EP02021598 | 2002-09-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1681933A CN1681933A (en) | 2005-10-12 |
| CN100506995C true CN100506995C (en) | 2009-07-01 |
Family
ID=32039095
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB038212285A Expired - Lifetime CN100506995C (en) | 2002-09-27 | 2003-09-22 | Method for production of 2-keto-L-gulonic acid |
Country Status (3)
| Country | Link |
|---|---|
| CN (1) | CN100506995C (en) |
| AU (1) | AU2003270233A1 (en) |
| WO (1) | WO2004029262A2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101348806B (en) * | 2008-09-04 | 2010-11-10 | 江西省德兴市百勤异Vc钠有限公司 | 2-keto-D-gluconic acid semicontinuous fermentation process |
| CN101845475B (en) * | 2010-04-30 | 2013-06-19 | 仪宏 | Nutrition-enhanced culture medium for preparing 2-KGA through fermentation and method thereof for preparing 2-KGA |
| CN102424830A (en) * | 2011-12-15 | 2012-04-25 | 江南大学 | Method for enhancing 2-keto-L-gulonic acid (2-KLG) production intensity of Ketogulonigenium vulgare by adding reduced glutathione (GSH) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1257127C (en) * | 2004-06-11 | 2006-05-24 | 张忠和 | Decorative boards |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2102481C1 (en) * | 1991-06-13 | 1998-01-20 | Ф.Хоффманн-Ля Рош, Аг | Method of 2-keto-l-gulonic acid or its salt preparing |
| EP0972843A1 (en) * | 1998-07-17 | 2000-01-19 | F. Hoffmann-La Roche Ag | Continuous fermentation process |
| DE19907115A1 (en) * | 1999-02-19 | 2000-08-24 | Basf Ag | New Gluconobacter oxydans strain with high tolerance to D-sorbitol, useful for converting D-sorbitol to L-sorbose in the production of ascorbic acid |
| US6204040B1 (en) * | 1999-04-22 | 2001-03-20 | Korea Research Institute Of Bioscience And Biotechnology | Gluconobacter suboxydans sorbitol dehydrogenase, genes and methods of use thereof |
-
2003
- 2003-09-22 AU AU2003270233A patent/AU2003270233A1/en not_active Abandoned
- 2003-09-22 CN CNB038212285A patent/CN100506995C/en not_active Expired - Lifetime
- 2003-09-22 WO PCT/EP2003/010490 patent/WO2004029262A2/en not_active Application Discontinuation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1257127C (en) * | 2004-06-11 | 2006-05-24 | 张忠和 | Decorative boards |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004029262A3 (en) | 2004-07-01 |
| WO2004029262A2 (en) | 2004-04-08 |
| AU2003270233A8 (en) | 2004-04-19 |
| CN1681933A (en) | 2005-10-12 |
| AU2003270233A1 (en) | 2004-04-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100357446C (en) | Microbial production of vitamin C | |
| CN1052512C (en) | Fermentation | |
| JP2719340B2 (en) | Fermentation method | |
| EP0366922B1 (en) | Fermentation process for producing 2-keto-L-gulonic acid | |
| CA1043283A (en) | Production of 2-keto-l-gulonic acid from glucose by mixed cultures | |
| CN1204260C (en) | Microbial micro-aerobe fermentation process of producing 1,3-propylene glycol | |
| CN100430471C (en) | Riboflavin-produced engineered strain and its method for producing riboflavin | |
| De Wulf et al. | Optimized synthesis of L‐sorbose by C5‐dehydrogenation of D‐sorbitol with Gluconobacter oxydans | |
| CN102250821B (en) | Method for producing 2-keto-L-gulonic acid vitamin C precursor by modifying Escherichia coli | |
| CN1351171A (en) | Microbial method for preparing L-ascorbic acid and D-isoascorbic acid | |
| CN100506995C (en) | Method for production of 2-keto-L-gulonic acid | |
| US4595659A (en) | Fermentation production of ascorbic acid from L-galactonic substrate | |
| CN110283789A (en) | Recombinant bacterial strain and its application | |
| CN100560728C (en) | The production method of 2-KGA | |
| EP0972843A1 (en) | Continuous fermentation process | |
| CN1080761C (en) | Improved production of 2-keto-L-gulonic acid | |
| KR20010102256A (en) | Method for Producing L-Sorbose | |
| US6238897B1 (en) | Continuous process for producing 2-keto-L-gulonic acid | |
| CN109593813B (en) | Culture medium for fermentation of 2-keto-L-gulonic acid and fermentation production method of 2-keto-L-gulonic acid | |
| CN115197982A (en) | Continuous method for producing sorbose | |
| Lakshmi | FERMENTATIVE PRODUCTION OF ANTIBIOTICS AND ORGANIC ACIDS | |
| JPS6296089A (en) | Production of polyol by fermentation using novel microorganism |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term |
Granted publication date: 20090701 |
|
| CX01 | Expiry of patent term |