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author:

Shi, X. (Shi, X..) [1] | Lin, H. (Lin, H..) [2] | Wang, X. (Wang, X..) [3] | Fang, S. (Fang, S..) [4]

Indexed by:

Scopus PKU CSCD

Abstract:

In the water/n-dodecane biphasic reaction system, the influence of organic solvent treatment on the gene expression level of isozymes of alcohol dehydrogenase (ADH) 1~3 was investigated to probe their correlation in asymmetric reduction of the substrate 2-octanone by Saccharomyces cerevisiae type II. The results showed that after treatment with organic media, the relative expression level of isozymes of alcohol dehydrogenase (ADH) varied, along with the different properties shown in asymmetric reduction of 2-octanone treatmented by Saccharomyces cerevisiae, the gene expression level of ADH 1 was severely inhibited by toluene and 2-octanol, but it was not obviously influenced by n-dodecane, n-octane and n-hexane, while substantially enhanced by 2-octanone. However, the gene expression level of ADH 2 was highly increased by toluene and 2-octanol, but inhibited by n-dodecane, n-octane, n-hexane, and 2-octanone. Furthermore, the inhibition of ADH 1 gene expression would reduce the catalytic activity, and inhibition of ADH 2 gene expression would improve the enantiomeric selectivity, while the gene expression level of ADH 3 would not influence both the activity and selectivity. The isozyme ADH 1 which has good enantio selectivity is the key oxidoreductase for catalyzing asymmetric reduction of 2-ocatnone by Saccharomyces cerevisiae type II, and the isozyme ADH 2 is of poor enantio selectivity while it conducts the same reaction. © 2017, Science Press. All right reserved.

Keyword:

Alcohol dehydrogenase; Asymmetric reduction; Gene expression level; Isozyme; Saccharomyces cerevisiae

Community:

  • [ 1 ] [Shi, X.]College of Biological Science and Technology, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 2 ] [Shi, X.]Institute of Pharmarceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 3 ] [Shi, X.]Fujian Key Lab of Medical Instrument and Pharmarceutical Technology, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 4 ] [Lin, H.]College of Biological Science and Technology, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 5 ] [Wang, X.]College of Biological Science and Technology, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 6 ] [Fang, S.]College of Biological Science and Technology, Fuzhou University, Fuzhou, Fujian 350108, China
  • [ 7 ] [Fang, S.]Institute of Pharmarceutical Biotechnology and Bioengineering, Fuzhou University, Fuzhou, Fujian 350108, China

Reprint 's Address:

  • [Shi, X.]College of Biological Science and Technology, Fuzhou UniversityChina

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Source :

The Chinese Journal of Process Engineering

ISSN: 1009-606X

Year: 2017

Issue: 4

Volume: 17

Page: 827-833

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 1

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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