2,3-Dihydroxyisovalerate production byKlebsiella pneumoniae

2,3-Dihydroxyisovalerate is an intermediate of valine and leucine biosynthesis pathway; however, no natural microorganism has been found yet that can accumulate this compound.Klebsiella pneumoniaeis a useful bacterium that can be used as a workhorse for the production of a range of industrially desi...

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Veröffentlicht in:Applied microbiology and biotechnology 2020-08, Vol.104 (15), p.6601-6613
Hauptverfasser: Wang, Yike, Gu, Jinjie, Lu, Xiyang, Zhang, Zhongxi, Yang, Yang, Sun, Shaoqi, Kostas, Emily, Shi, Jiping, Gao, Mintian, Baganz, Frank, Lye, Gary J., Hao, Jian
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Sprache:eng
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Zusammenfassung:2,3-Dihydroxyisovalerate is an intermediate of valine and leucine biosynthesis pathway; however, no natural microorganism has been found yet that can accumulate this compound.Klebsiella pneumoniaeis a useful bacterium that can be used as a workhorse for the production of a range of industrially desirable chemicals. Dihydroxy acid dehydratase, encoded by theilvDgene, catalyzes the reaction of 2-ketoisovalerate formation from 2,3-dihydroxyisovalerate. In this study, anilvDdisrupted strain was constructed which resulted in the inability to synthesize 2-ketoisovalerate, yet accumulate 2,3-dihydroxyisovalerate in its culture broth. 2,3-Butanediol is the main metabolite ofK. pneumoniaeand its synthesis pathway and the branched-chain amino acid synthesis pathway share the same step of the alpha-acetolactate synthesis. By knocking out thebudAgene, carbon flow into the branched-chain amino acid synthesis pathway was upregulated, which resulted in a distinct increase in 2,3-dihydroxyisovalerate levels. Lactic acid was identified as a by-product of the process and by blocking the lactic acid synthesis pathway, a further increase in 2,3-dihydroxyisovalerate levels was obtained. The culture parameters of 2,3-dihydroxyisovalerate fermentation were optimized, which include acidic pH and medium level oxygen supplementation to favor 2,3-dihydroxyisovalerate synthesis. At optimal conditions (pH 6.5, 400 rpm), 36.5 g/L of 2,3-dihydroxyisovalerate was produced in fed-batch fermentation over 45 h, with a conversion ratio of 0.49 mol/mol glucose. Thus, a biological route of 2,3-dihydroxyisovalerate production with high conversion ratio and final titer was developed, providing a basis for an industrial process.
ISSN:0175-7598
1432-0614
DOI:10.1007/s00253-020-10711-y