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许建和, You-Yan Liu b, Jian-He Xua, *, Hui-Yuan Wu a, Duan Shen a
Journal of Biotechnology 110(2004)209~217,-0001,():
-1年11月30日
The two processes for the partial purification and for the immobilization of a crude lipase preparation (Candida rugosa Lipase OF) have been successfully integrated into one by simple adsorption of the enzyme onto a cation ion exchanger resin (SP-Sephadex C-50) at pH 3.5. Due to selective removal of the unfavorable lipase isoenzyme (L1), the enzyme components (mainly L2 and L3) that are tightly fixed on the resin displayed a significantly improved enantioselectivity (E value: 50 versus 13 with addition of Tween-80) in the biocatalytic hydrolysis of 2-chloroethyl ester of rac-ketoprofen. The activity yields of the immobilized lipase were 48 and 70%, respectively when emulsified and non-emulsified substrates were employed for enzyme assay. Moreover, the concentration of Tween-80 was found to be a factor affecting the lipase enantioselectivity. By using such an immobilized enzyme as biocatalyst, the process for preparing enantiopure (S)-ketoprofen becomes simpler and more practical as compared with the previously reported procedures and the product was obtained with >94% ee at 22.3% conversion in the presence of an optimal concentration (0.5mg/ml) of Tween-80 at pH 3.5. Furthermore, the operational stability of the immobilized biocatalyst was examined in different types of reactors. In an air-bubbled column reactor, the productivity was much higher than that in a packed-bed column reactor, in spite of a slightly lower stability. Under optimal conditions, the air-bubbled column reactor could be operated smoothly for at least 350 h, remaining nearly 50% activity.
Enzymatic resolution, Ketoprofen, Candida rugosa lipase, Purification, Immobilization, Process integration, Air-bubbled column reactor
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许建和, Jiang Pan, Jian-He Xu*
Enzyme and Microbial Technology 33(2003)527~533,-0001,():
-1年11月30日
The fermentation of an epoxide hydrolase by a newly isolated Trichosporon loubierii strain ECU1040 was optimized. The epoxide hydrolase production was enhanced by 6.9-fold from an initial activity of 45 U/l with the incorporation of substrate induction, optimization of medium composition and other culture conditions, and the implementation of a fed-batch process. It was found that phenyl glycidyl ether (PGE) could efficiently induce biosynthesis of the epoxide hydrolase, though it strongly inhibited the cell growth. To reduce the toxicity of PGE, dibutyl o-phthalate was used in flask cultivation to dissolve PGE, keeping a low concentration of PGE in the broth. Glucose was added to promote cell growth in the presence of PGE, though glycerol was identified as the best single carbon source for the highest specific activity. Trace elements have significant effect on the epoxide hydrolase synthesis.With addition of trace elements and glucose and adjustment of phosphate concentration, the total activity was enhanced by 150%. To further increase the epoxide hydrolase production, a fed-batch culture with PGE in the feed solution was performed in a 5-l jar fermenter. The maximum production of the epoxide hydrolase was 312 U/l, with a specific activity of 23.7 U/g DCW (dry cell weight).
Epoxide hydrolase, Trichosporon loubierii, Medium optimization, Enzyme induction, Fed-batch fermentation, Phenyl glycidyl ether
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许建和, Peng-Fei Gong, Jian-He Xu*
Enzyme and Microbial Technology 36(2005)252~257,-0001,():
-1年11月30日
Optically active epoxides can be prepared by kinetic resolution of racemic mixtures using stereospecific epoxide hydrolases. To increase the bio-resolution efficiency of a sparingly water-soluble epoxide (glycidyl phenyl ether, GPE), we investigated the use of organic/aqueous two-phase system.Various conditions were systematically examined and optimized in shake flasks. Isooctanewas found to be the most suitable solvent as the organic phase. The phase volume ratio (φo/w) and biocatalyst concentration were shown to be sensitive parameters affecting both the reaction rate and the enzyme enantiospecificity in the biphase system. An isooctane/aqueous system was developed to overcome the low solubility and instability of GPE in the aqueous phase, resulting in a significant improvement of enatiomeric ratio (E-value) from 39.5 to 94.0 and an average productivity of 18.8mg GPE/(h g) biocatalyst to 48.9mg GPE/(h g) biocatalyst, respectively. Resolution of a 90.1g/l solution of racemic glycidyl phenyl ether in isooctane phase was successfully carried out in a mechanically stirred reactor (120ml), affording (S)-glycidyl phenyl ether in high (100%) enantiomeric excess with a yield of 44.5%.
Kinetic resolution, Glycidyl phenyl ether, Epoxide hydrolase, Bacillus megaterium, Enantiospecific hydrolysis, Organic-aqueous two-liquid system, Stirred reactor
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许建和, Yi Xu, Jian-He Xu*, Jiang Pan, Liang Zhao, Si-Liang Zhang
Journal of Molecular Catalysis B: Enzymatic 27(2004)155~159,-0001,():
-1年11月30日
Biocatalytic resolution of 3-(2'-nitrophenoxy)propylene oxide (1a), 3-(3'-nitrophenoxy)propylene oxide (1b) and 3-(4'-nitrophenoxy)propylene oxide (1c) were exploited by using lyophilized cells of yeast Trichosporon loubierii ECU1040 with epoxide hydrolase (EH) activity, which preferentially hydrolyzes (S)-enantiomers of the epoxides (1a-c), yielding (S)-diols and (R)-epoxides. The activity increased as the nitro group in the phenyl ring was shifted from 4'-position (1c) to 2'-position (1a). When the substrate concentration of 1a was increased from 10 to 80mM, the E-value increased at first, until reaching a peak at 40mM, and then decreased at higher concentrations (>40mM). The optically active epoxide (R)-1a was prepared at gram-scale (97% ee, 41% yield). Furthermore, a simple method was developed to predict the enantiomeric excess of substrate (ees) at any time of the whole reaction course based on the ees value determined at a certain reaction time at a relatively lower substrate concentration. This will be helpful for terminating the reaction at a proper time to get both higher optical purity and higher yield of the remaining epoxides.
Nitro-substituted phenoxypropylene oxide, Trichosporon loubierii, Epoxide hydrolase, Kinetic resolution, Theoretical prediction, Enantioselective hydrolysis
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许建和, Ai-Min Tong a, Jian-He Xu a, *, Wen-Ya Lu b, Guo-Qiang Lin b
Journal of Molecular Catalysis B: Enzymatic 32(2005)83~88,-0001,():
-1年11月30日
A monophasic organic-water system for efficient enzymatic synthesis ofβ-d-glucopyranoside by reverse hydrolysis was constructed and optimized. p-Nitrobenzyl alcohol (pNBA), selected as a model substrate alcohol, was readily glucosylated with d-glucose through reverse hydrolysis using almond β-d-glucosidase in a monophasic aqueous-organic medium, producing a new glucoside, p-nitrobenzylβ-d-glucopyranoside (pNBG). The effects of different buffers, organic solvents and water contents were investigated. Buffer type and Ph affected the initial reaction rate but had little effect on the final yields. The ratio of organic solvent to water plays a crucial role in shifting the reaction equilibrium toward synthesis, but a minimum amount of water is necessary to maintain the enzyme activity. Dioxane, which was previously known as an unsuitable solvent forβ-d-glucosidase-catalyzed reactions, was found to be the most appropriate solvent for this synthetic procedure. The reaction equilibrium and enzyme stability in the reaction medium were also investigated. Under the optimal reaction conditions, i.e. 90% dioxane (v/v) + 10% buffer (Na2HPO4–KH2PO4, 70mM, pH 6.0) with alcohol-to-glucose molar ratio of 9:1, p-nitrobenzylβ-d-glucopyranoside was produced with a maximum yield (13.3%).
Reversed hydrolysis, β-d-Glucopyranoside, Almond β-d-glucosidase, Organic medium, Dioxane-water system
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