Chinese Journal of Catalysis ›› 2013, Vol. 34 ›› Issue (2): 351-360.DOI: 10.3724/SP.J.1088.2013.20737

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Biotechnological production of 2,3-butanediol stereoisomers: synthetic mechanism and realized methods

SHEN Mengqiu1, JI Xiaojun1,a, NIE Zhikui1, XIA Zhifang1, YANG Han1, HUANG He1,2,b   

  1. 1College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 211816, Jiangsu, China; 2State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing University of Technology, Nanjing 210009, Jiangsu, China
  • Received:2012-08-10 Revised:2012-10-18 Online:2013-02-05 Published:2013-02-05

Abstract: 2,3-Butanediol, an important fine chemical, has been widely used in many areas. Containing two chiral centers, the molecule of 2,3-butanediol contains three stereoisomers, namely (S,S)-, (R,R)-, and meso-2,3-butanediol, which are especially crucial in providing chiral groups for the synthesis of fine chemicals and high-value pharmaceuticals. In this review, the synthetic mechanisms of different 2,3-butanediol stereoisomers are firstly revisited. Some strategies for efficient and economical pure 2,3-butanediol stereoisomers production, including constructing whole cell biocatalysts and constructing metabolic pathways using the emerging synthetic biology methods, are summarized. It is also pointed out that the focus of future research should be placed on improving the biosynthetic capability of different stereo- isomers using the synthetic biology methods, and establishing efficient downstream separation methods for economical 2,3-butanediol stereoisomers recovering process.

Key words: 2,3-butanediol, stereoisomer, synthetic mechanism, whole cell catalysis, synthetic biology