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...
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Published in | Annals of microbiology Vol. 65; no. 2; pp. 929 - 935 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.06.2015
|
Subjects | |
Online Access | Get full text |
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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. |
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ISSN: | 1590-4261 1869-2044 |
DOI: | 10.1007/s13213-014-0936-6 |