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   <subfield code="a">Engineered Serratia marcescens for efficient (3 R )-acetoin and (2 R ,3 R )-2,3-butanediol production</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Fangmin Bai, Lu Dai, Jiying Fan, Ngoctu Truong, Ben Rao, Liaoyuan Zhang, Yaling Shen]</subfield>
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   <subfield code="a">(3R)-Acetoin and (2R,3R)-2,3-butanediol are important pharmaceutical intermediates. However, until now, the quantity of natural microorganisms with the ability to produce single configuration of optically pure (3R)-acetoin and (2R,3R)-2,3-butanediol is rare. In this study, a meso-2,3-butanediol dehydrogenase encoded by the slaC gene from Serratia marcescens MG1 was identified for meso-2,3-butanediol and (2S,3S)-2,3-butanediol biosynthesis. Inactivation of the slaC gene could significantly decrease meso-2,3-butanediol and (2S,3S)-2,3-butanediol and result in a large quantity of (3R)-acetoin accumulation. Furthermore, a (2R,3R)-2,3-butanediol dehydrogenase encoded by the bdhA gene from Bacillus subtilis 168 was introduced into the slaC mutant strain of Serratia marcescens MG1. Excess (2R,3R)-2,3-butanediol dehydrogenase could accelerate the reaction from (3R)-acetoin to (2R,3R)-2,3-butanediol and lead to (2R,3R)-2,3-butanediol accumulation. In fed-batch fermentation, the excess (2R,3R)-2,3-butanediol dehydrogenase expression strain could produce 89.81g/l (2R,3R)-2,3-butanediol with a productivity of 1.91g/l/h at 48h. These results provided potential applications for (3R)-acetoin and (2R,3R)-2,3-butanediol production.</subfield>
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   <subfield code="a">Society for Industrial Microbiology and Biotechnology, 2015</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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