GltS, the sodium-coupled L-glutamate uptake system of Corynebacterium glutamicum: identification of the corresponding gene and impact on L-glutamate production
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作者:
C. Trötschel
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机构:Institut für Biochemie der Universität zu Köln,
C. Trötschel
S. Kandirali
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机构:Institut für Biochemie der Universität zu Köln,
S. Kandirali
P. Diaz-Achirica
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机构:Institut für Biochemie der Universität zu Köln,
P. Diaz-Achirica
A. Meinhardt
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机构:Institut für Biochemie der Universität zu Köln,
A. Meinhardt
S. Morbach
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机构:Institut für Biochemie der Universität zu Köln,
S. Morbach
R. Krämer
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机构:Institut für Biochemie der Universität zu Köln,
R. Krämer
A. Burkovski
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机构:Institut für Biochemie der Universität zu Köln,
A. Burkovski
机构:
[1] Institut für Biochemie der Universität zu Köln,
[2] Zülpicher-Strasse 47,undefined
[3] 50674 Cologne,undefined
[4] Germany,undefined
来源:
Applied Microbiology and Biotechnology
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2003年
/
60卷
A screening procedure was established to identify Corynebacterium glutamicum transposon mutants with an altered L-glutamate excretion behaviour. By this microtiter plate-based approach seven non- or less excreting C. glutamicum strains and two hyper-excreters were found. The subsequently carried out molecular analysis of a hyper-producing clone led to the identification of the gltS gene, which codes for the sodium-coupled secondary L-glutamate uptake system in C. glutamicum. Characterization of a gltS deletion strain revealed that this transporter has a weak but significant impact on L-glutamate production induced by biotin limitation in the wild type. Obviously, GltS leads to the re-uptake of excreted L-glutamate causing a futile cycle. In accord with this hypothesis, the overexpression of gltS decreased L-glutamate production.