Cloning, expression and characterization of glycerol dehydrogenase involved in 2,3-butanediol formation in Serratia marcescens H30
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- 作者：Liaoyuan Zhang (1)
Quanming Xu (1)
Xiaoqian Peng (1)
Boheng Xu (1)
Yuehao Wu (1)
Yulong Yang (1)
Shujing Sun (1)
Kaihui Hu (1)
Yaling Shen (2) - 关键词：Serratia marcescens ; 2 ; 3 ; Butanediol isomers ; Glycerol dehydrogenase ; Expression ; Enzymatic properties
- 刊名：Journal of Industrial Microbiology and Biotechnology
- 出版年：2014
- 出版时间：September 2014
- 年：2014
- 卷：41
- 期：9
- 页码：1319-1327
- 全文大小：1,339 KB
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Quanming Xu (1)
Xiaoqian Peng (1)
Boheng Xu (1)
Yuehao Wu (1)
Yulong Yang (1)
Shujing Sun (1)
Kaihui Hu (1)
Yaling Shen (2)
1. Key Laboratory of Biopesticide and Chemical Biology, Ministry of Education, College of Life Sciences, Gutian Edible Fungi Research Institute, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People’s Republic of China
2. State Key Laboratory of Bioreactor Engineering, New World Institute of Biotechnology, East China University of Science and Technology, Shanghai, 200237, People’s Republic of China - ISSN：1476-5535
文摘
The meso-2,3-butanediol dehydrogenase (meso-BDH) from S. marcescens H30 is responsible for converting acetoin into 2,3-butanediol during sugar fermentation. Inactivation of the meso-BDH encoded by budC gene does not completely abolish 2,3-butanediol production, which suggests that another similar enzyme involved in 2,3-butanediol formation exists in S. marcescens H30. In the present study, a glycerol dehydrogenase (GDH) encoded by gldA gene from S. marcescens H30 was expressed in Escherichia coli BL21(DE3), purified and characterized for its properties. In vitro conversion indicated that the purified GDH could catalyze the interconversion of (3S)-acetoin/meso-2,3-butanediol and (3R)-acetoin/(2R,3R)-2,3-butanediol. (2S,3S)-2,3-Butanediol was not a substrate for the GDH at all. Kinetic parameters of the GDH enzyme showed lower K m value and higher catalytic efficiency for (3S/3R)-acetoin in comparison to those for (2R,3R)-2,3-butanediol and meso-2,3-butanediol, implying its physiological role in favor of 2,3-butanediol formation. Maximum activity for reduction of (3S/3R)-acetoin and oxidations of meso-2,3-butanediol and glycerol was observed at pH 8.0, while it was pH 7.0 for diacetyl reduction. The enzyme exhibited relative high thermotolerance with optimum temperature of 60?°C in the oxidation–reduction reactions. Over 60?% of maximum activity was retained at 70?°C. Additionally, the GDH activity was significantly enhanced for meso-2,3-BD oxidation in the presence of Fe2+ and for (3S/3R)-acetoin reduction in the presence of Mn2+, while several cations inhibited its activity, particularly Fe2+ and Fe3+ for (3S/3R)-acetoin reduction. The properties provided potential application for single configuration production of acetoin and 2,3-butanediol .