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author:

Xiao, M.-T. (Xiao, M.-T..) [1] | Huang, Y.-Y. (Huang, Y.-Y..) [2] | Shi, X.-A. (Shi, X.-A..) [3] | Guo, Y.-H. (Guo, Y.-H..) [4]

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Scopus

Abstract:

Screening from 40 microorganisms belonging to different taxonomical groups (Saccharomyces cerevisiae, Lactoballius, Streptococcus faecalis and Candida albicans) was performed to select the strain with high production rate of R-(-)-mandelic acid (R-MA). A sp. strain S. cerevisiae FD11b with high yield and enantiomeric excess (e.e.) and little byproducts was obtained by means of UV-mutation breeding. In the optimal conditions of pH 6.5, 32°C, anaerobic and glucose supply rate (Fglu) 0.0833 mmol gdw-1 h -1, the strain FD11b showed a high specific MA production rate (qp = 0.35 mmol gdw-1 h-1) and enantioselectivity (e.e. = 97.1%). The phenylglyoxylic acid (PGA) concentration showed a remarkable effect on the apparent activity of MA dehydrogenase. The specific production rate (qp) reached the maximum at 30-40 mM of PGA concentrations. At higher concentrations of PGA more than 40 mM, the q p decreased obviously in a linear way. However, the e.e. of R-MA kept about 95-96.5%, when the PGA concentration was below 60 mM, even at the concentration of PGA 80 mM, the e.e. was still higher than 90%. A modified Monod type equation based on a hypothesis of substrate inhibition could fit the experimental data well. The estimated maximum specific production rate (q pm) and saturation constant (Ks) were 0.431 mmol gdw -1 h-1 and 5.88 mM, respectively. © 2005 Elsevier Inc. All rights reserved.

Keyword:

Asymmetric reduction; Chiral synthesis; Enantioselectivity; R-(-)-mandelic acid; Substrate inhibition

Community:

  • [ 1 ] [Xiao, M.-T.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou 350001, China
  • [ 2 ] [Xiao, M.-T.]Institute of Pharmaceutical Engineering, Huaqiao University, Quanzhou, 362021, China
  • [ 3 ] [Huang, Y.-Y.]Institute of Pharmaceutical Engineering, Huaqiao University, Quanzhou, 362021, China
  • [ 4 ] [Shi, X.-A.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou 350001, China
  • [ 5 ] [Guo, Y.-H.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou 350001, China

Reprint 's Address:

  • [Guo, Y.-H.]Institute of Pharmaceutical Biotechnology and Engineering, Fuzhou University, Fuzhou 350001, China

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Source :

Enzyme and Microbial Technology

ISSN: 0141-0229

Year: 2005

Issue: 6

Volume: 37

Page: 589-596

1 . 7 0 5

JCR@2005

3 . 4 0 0

JCR@2023

JCR Journal Grade:2

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 32

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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