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author:

Shi, X.-A. (Shi, X.-A..) [1] (Scholars:石贤爱) | Li, C.-Y. (Li, C.-Y..) [2] | Fu, J. (Fu, J..) [3] | Meng, C. (Meng, C..) [4] (Scholars:孟春) | Guo, Y.-H. (Guo, Y.-H..) [5] (Scholars:郭养浩) | Lou, W.-Y. (Lou, W.-Y..) [6] | Wu, H. (Wu, H..) [7] | Zong, M.-H. (Zong, M.-H..) [8]

Indexed by:

Scopus PKU CSCD

Abstract:

In aqueous buffer system containing surfactants of SDS, CTAB and Emulsifier OP-6, the asymmetric reduction of 2-octanone to (S)-2-octanol with Saccharomyces cerevisiae cells was studied. The results indicated that the yield and product e.e. were disappointingly low due to the serious reverse reaction and side reaction in the surfactant-free system. Particularly, at the substrate concentration of 10 mmol/L, they were 77.4% and 78.8% for 96 h reaction. With addition of surfactants to the system, the rates of reverse and side reactions were decreased by Emulsifier OP-6 and CTAB, with the effective increase of the average positive reaction rate. In the systems containing 0.4 mmol/L Emulsifier OP-6 or 0.04 mmol/L CTAB, the yield and e.e. value were 88.4%, 91.1% and 97.0%, 94.5%), respectively, obviously higher than those in the reaction system without surfactant. The further work showed that the enhancement of efficiency and enantioselectivity of the asymmetric reduction resulted from the effect of the surfactants on the cell characteristics such as growth, membrane penetrability, etc. Among the surfactants investigated, Emulsifier OP-6 performed best.

Keyword:

2-octanone; Asymmetric bioreduction; Enantioselectivity; Saccharomyces cerevisiae; Surfactant

Community:

  • [ 1 ] [Shi, X.-A.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China
  • [ 2 ] [Shi, X.-A.]Lab. Appl. Biocatai, South China University of Technology, Guangzhou, Guangdong 510640, China
  • [ 3 ] [Li, C.-Y.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China
  • [ 4 ] [Fu, J.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China
  • [ 5 ] [Meng, C.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China
  • [ 6 ] [Guo, Y.-H.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China
  • [ 7 ] [Lou, W.-Y.]Lab. Appl. Biocatai, South China University of Technology, Guangzhou, Guangdong 510640, China
  • [ 8 ] [Wu, H.]Lab. Appl. Biocatai, South China University of Technology, Guangzhou, Guangdong 510640, China
  • [ 9 ] [Zong, M.-H.]Lab. Appl. Biocatai, South China University of Technology, Guangzhou, Guangdong 510640, China

Reprint 's Address:

  • 石贤爱

    [Shi, X.-A.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou, Fujian 350002, China

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Source :

The Chinese Journal of Process Engineering

ISSN: 1009-606X

CN: 11-4541/TQ

Year: 2010

Issue: 2

Volume: 10

Page: 339-343

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 3

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