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| Content Provider | Springer Nature Link |
|---|---|
| Author | Jiang, Feng Qi, Gaofu Ji, Zhixia Zhang, Shuling Liu, Jun Ma, Xin Chen, Shouwen |
| Copyright Year | 2011 |
| 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. |
| Starting Page | 1837 |
| Ending Page | 1840 |
| Page Count | 4 |
| File Format | |
| ISSN | 01415492 |
| Journal | Biotechnology Letters |
| Volume Number | 33 |
| Issue Number | 9 |
| e-ISSN | 15736776 |
| Language | English |
| Publisher | Springer Netherlands |
| Publisher Date | 2011-05-05 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Bacillus licheniformis Glutamate Glutamate racemase Poly-γ-glutamic acid Biotechnology Biochemistry Applied Microbiology Microbiology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine Bioengineering Applied Microbiology and Biotechnology Biotechnology |
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