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   <subfield code="a">Deletion of genes involved in glutamate metabolism to improve poly-gamma-glutamic acid production in B. amyloliquefaciens LL3</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Wei Zhang, Yulian He, Weixia Gao, Jun Feng, Mingfeng Cao, Chao Yang, Cunjiang Song, Shufang Wang]</subfield>
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   <subfield code="a">Here, we attempted to elevate poly-gamma-glutamic acid (γ-PGA) production by modifying genes involved in glutamate metabolism in Bacillus amyloliquefaciens LL3. Products of rocR, rocG and gudB facilitate the conversion from glutamate to 2-oxoglutarate in Bacillus subtillis. The gene odhA is responsible for the synthesis of a component of the 2-oxoglutarate dehydrogenase complex that catalyzes the oxidative decarboxylation of 2-oxoglutarate to succinyl coenzyme A. In-frame deletions of these four genes were performed. In shake flask experiments the gudB/rocG double mutant presented enhanced production of γ-PGA, a 38% increase compared with wild type. When fermented in a 5-L fermenter with pH control, the γ-PGA yield of the rocR mutant was increased to 5.83g/L from 4.55g/L for shake flask experiments. The gudB/rocG double mutant produced 5.68g/L γ-PGA compared with that of 4.03g/L for the wild type, a 40% increase. Those results indicated the possibility of improving γ-PGA production by modifying glutamate metabolism, and identified potential genetic targets to improve γ-PGA production.</subfield>
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