Abstract
The Corynebacterium glutamicum glutamine synthetase I (GSI) structural gene glnA was cloned by a PCR approach using oligonucleotide primers derived from conserved amino acid sequences of the GSI proteins from various bacteria. Disruption or deletion of this gene in C. glutamicum led to a glutamine auxotrophic phenotype and complete loss of glutamine synthetase activity, indicating the key role of this enzyme in nitrogen metabolism. Additionally, indications for a second glutamine synthetase, GSII, were found.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acids / metabolism
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Blotting, Southern
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Cloning, Molecular
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Corynebacterium / enzymology*
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Corynebacterium / genetics*
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DNA, Bacterial / analysis
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Gene Deletion
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Glutamate-Ammonia Ligase / genetics*
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Molecular Sequence Data
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Mutagenesis
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Nitrogen / metabolism
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Sequence Analysis, DNA
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Sequence Homology, Amino Acid
Substances
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Amino Acids
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DNA, Bacterial
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glutamine synthetase 2
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glutamine synthetase I
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Glutamate-Ammonia Ligase
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Nitrogen
Associated data
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GENBANK/Q10377
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GENBANK/Q10378
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GENBANK/Y13221