Characterization, modification, and overexpression of 3-phosphoglycerate dehydrogenase in Corynebacterium glutamicum for enhancing l-serine production

The direct fermentative production of l -serine from renewable biomass using Corynebacterium glutamicum is attracting increasing attention. In this study, wild-type C. glutamicum SYPS-062 produced up to 6.65 ± 0.23 g/L l -serine; to further improve l -serine production, the serA gene was cloned, and...

Full description

Saved in:
Bibliographic Details
Published inAnnals of microbiology Vol. 65; no. 2; pp. 929 - 935
Main Authors Xu, Guoqiang, Jin, Xuexia, Guo, Wen, Dou, Wenfang, Zhang, Xiaomei, Xu, Zhenghong
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.06.2015
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The direct fermentative production of l -serine from renewable biomass using Corynebacterium glutamicum is attracting increasing attention. In this study, wild-type C. glutamicum SYPS-062 produced up to 6.65 ± 0.23 g/L l -serine; to further improve l -serine production, the serA gene was cloned, and the C-terminal domain of 3-phosphoglycerate dehydrogenase (PGDH) from this strain was truncated. When expressed in Escherichia coli , the resultant mutein SerAΔ197 showed a specific PGDH activity of 1.092 ± 0.05 U/mg protein, representing a decrease of 25.87 % from that encoded by serA , and was no longer sensitive to high concentrations of l -serine. When serA Δ591 was overexpressed in C. glutamicum SYPS-062, the activity of PGDH in C. glutamicum pJC1- tac - serA Δ591 increased by 47.72 %, and the resultant strain C. glutamicum pJC1- tac - serA Δ591 could accumulate 7.69 ± 0.22 g/L l -serine. Furthermore, when serA Δ591 was overexpressed in C. glutamicum SYPS-062 ΔsdaA , the resultant strain could accumulate 8.84 ± 0.23 g/L l -serine at 102 h, and the yield of l -serine on cells (Y p/x) improved by 60 % when compared with that noted in the control. These results demonstrate that l -serine production in C. glutamicum SYPS-062 could be improved by overexpressing a C-terminal truncation of PGDH in combination with other genetic modifications.
ISSN:1590-4261
1869-2044
DOI:10.1007/s13213-014-0936-6