Abstract

The glr gene, which encodes glutamate racemase involved in the conversion of L-glutamic acid to its D-isomer, was cloned and expressed in Bacillus licheniformis WX-02. Overexpression of the glr gene not only increased the production of poly-γ-glutamic acid (γ-PGA) by 22.5% but also increased the proportion of D-glutamate in γ-PGA from 77 to 85%. The activity of glutamate racemase was higher than in the original strain throughout cultivation. This is the first report that overexpression of the glr gene could enhance the L- and D-glutamate conversion in B. licheniformis WX-02 and increase the proportion of D-glutamate in γ-PGA and the yield of γ-PGA.

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