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author:

Li, Y.-N. (Li, Y.-N..) [1] | Shi, X.-A. (Shi, X.-A..) [2] | Zong, M.-H. (Zong, M.-H..) [3] | Meng, C. (Meng, C..) [4] | Dong, Y.-Q. (Dong, Y.-Q..) [5] | Guo, Y.-H. (Guo, Y.-H..) [6]

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Scopus

Abstract:

In the aqueous medium the asymmetric reduction of 2-octanone with Baker's yeast FD-12 was inhibited severely by the substrate and the product at higher concentrations, which resulted in a low yield and a low e.e. value of the object product (S)-2-octanol. Seven water/organic solvent biphasic systems were assayed in this work. FD-12 showed the best tolerance, catalytic activity and enantioselectivity in the water/n-dodecane system among the biphasic systems assayed. The metabolic activity retention (MAR) and viability of FD-12 in the n-dodecane containing system were 98% and 91.6%, respectively. The influence of the volume ratio Vaq/Vorg, temperature, pH value and the substrate concentration on the yield of 2-octanol and the e.e.(S) value was investigated. Under the optimum conditions (in the water/n-dodecane biphasic system, Vaq/Vorg 20/5, pH 8.0, 32 °C, 2-octanone concentration 500 mM), the final concentration of 2-octanol and the e.e.(S) value reached 105.60 mM and 89.38%, respectively, after 96 h reduction. The water/n-dodecane biphasic system with FD-12 was advantageous for the production of (S)-2-octanol of high final concentration and high e.e.(S) value. © 2006 Elsevier Inc. All rights reserved.

Keyword:

(S)-2-octanol; Asymmetric reduction; Baker's yeast; Water/organic solvent biphasic system

Community:

  • [ 1 ] [Li, Y.-N.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China
  • [ 2 ] [Shi, X.-A.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China
  • [ 3 ] [Shi, X.-A.]Laboratory of Applied Biocatalysis, South China University of Technology, Guangzhou, 510640, China
  • [ 4 ] [Zong, M.-H.]Laboratory of Applied Biocatalysis, South China University of Technology, Guangzhou, 510640, China
  • [ 5 ] [Meng, C.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China
  • [ 6 ] [Dong, Y.-Q.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China
  • [ 7 ] [Guo, Y.-H.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China

Reprint 's Address:

  • [Guo, Y.-H.]Institute of Pharmaceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, 350002, China

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Source :

Enzyme and Microbial Technology

ISSN: 0141-0229

Year: 2007

Issue: 5

Volume: 40

Page: 1305-1311

1 . 9 6 9

JCR@2007

3 . 4 0 0

JCR@2023

JCR Journal Grade:2

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: 1

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