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克鲁斯假丝酵母ZJB 09162产羰基还原酶的产酶条件 被引量:1

Optimization of Culture Conditions for Carbonyl Reductase by Candida krusei ZJB 09162
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摘要 研究了克鲁斯假丝酵母Candida krusei ZJB 09162产羰基还原酶的条件,确定了最适的培养基组成和培养条件:葡萄糖50.0 g/L,酵母膏50.0 g/L,(NH4)2HPO4 2.5 g/L,KH2PO4 2.5 g/L,NaCl 1.0 g/L,培养基初始pH6.0,装液量12%,接种量4%。将此条件下发酵培养60 h的菌体用于(R)-1,3-丁二醇的不对称合成,产物对映体过量值99%,产率85%。 (R)-1 ,3-butanediol is an important chiral building block and template in asymmetric synthesis. Car- bonyl reductase catalyzed asymmetric reduction of 4-hydroxy-2-butanone is an effective way for large scale production of (R)-1 ,3-butanediol. In this paper, culture conditions of Candida krusei ZJB 09162 producing carbonyl reductase were optimized as follows: glucose 50.0 g/L, yeast extract 50.0 g/L, ( NH4)2HPO4 2.5 g/L, KH2PO4 2.5 g/L, NaCI 1.0 g/L,initial pH 6.0, medium volume 12% , inoculum size 4%. Under these conditions, the yield of (R)- 1,3-butanediol reached 85% , with an optical purity of 99% e.e.
出处 《食品与发酵工业》 CAS CSCD 北大核心 2011年第7期17-21,共5页 Food and Fermentation Industries
基金 浙江省重大科技专项重点社会发展项目(2009C13033-3)
关键词 4-羟基-2-丁酮 (R)-1 3-丁二醇 不对称还原 克鲁斯假丝酵母 羰基还原酶 4-hydroxy-2-butanone, (R) -1,3-butanediol, asymmetric reduction, Candida krusei, carbonyl reductase
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  • 1Nakatsuka T, lwata H, Tanaka R, et al. A facile conversion of the phenyhhio group to acetoxy by copper reagents for a practical synthesis of 4-acetoxyazetidin-2-one derivatives from (R)-butane-1, 3-diol [J]. Journal of the Chemical Society, Chemical Communications, 1991, 9: 662 - 664.
  • 2Tanaka R, Iwata H, Ishiguro M. Synthesis of 5,6.-cis-penems [ J]. The Journal of Antibiotics, 1990, 43:1 068 - 1 610.
  • 3Ohloff G, Giersch W, Decorzant R, et al. Synthesis of the sesquirose oxides from rose oxide [ J ]. Helvetica Chimica Acta, 1980, 63:1 589- I 597.
  • 4Ferreira J T B, Ferreira B, Simonelli F. Synthesis of two stereoisomers of the propanoate ester of' 8-methyl-2-decanoi using remote asymmetric induction [ J ]. Tetrahedron, 1990, 46:6 311 -6 318.
  • 5Mori K, Miyake M. A new synthesis ot both the anantiomers of grandisol, the boll weevil phernomonLJ i . Tetrahedron, 1987, 43:2 229 -2 239.
  • 6Choi V M F, Elliott J D, Johnson W S A. Asymroetrie synthesis via chiral acetal templates. 7. Further studies of the eyanation reaction. The use of acetals derived from diols with one chiral center [ J ]. Tetrahedron Letters. 1984, 25:591 -594.
  • 7Marc Larcheveque, Lengo Mambu, Yves Petit. Preparation of enantiomericaliy pure 1 , 3-bu-tanediol from threonine [J]. Synthetic Communications, 1991, 21 (22) :2 295 - 2 300.
  • 8Sayo N, Satio T, Okeda Y, et al. Process for preparation optically active 3-hydroxybutanoic acid [ P ]. US, 4981992, 1991.
  • 9Tamotsu Eguchi, Kenichi Mochida. Lipase-catalyzed diacylation of 1,3-butanediol [ J ]. Biotechnology Letters, 1993, 15(9) :955 -960.
  • 10Hiroaki Yamamoto, Akinobu Matsuyama, Yoshinori Kobayashi. Synthesis of (R)-1,3-butandiol by enantiose lective oxidation using whole recombinant Eschertchia coli ceils expressing (S)-specif-ic secondary alcohol dehydro- genase [ J ]. Bioscience Biotechnology and Biochemistry, 2002, 66 (4) : 925 - 927.

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