Molecular cloning of the Corynebacterium glutamicum ('Brevibacterium lactofermentum' AJ12036) odhA gene encoding a novel type of 2-oxoglutarate dehydrogenase
Central Research Laboratories, and Technology and Engineering Laboratories AJINOMOTO Co., Inc., 1-1 Suzuki-Cho, Kawasaki-ku, Kawasaki-shi 210, Japan ABSTRACT Summary: The Corynebacterium glutamicum (Brevibacterium lactofermentum AJ12036) odhA gene, encoding 2-oxoglutarate dehydrogenase (E1o subuni...
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Veröffentlicht in: | Microbiology (Society for General Microbiology) 1996-12, Vol.142 (12), p.3347-3354 |
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Zusammenfassung: | Central Research Laboratories, and Technology and Engineering Laboratories
AJINOMOTO Co., Inc., 1-1 Suzuki-Cho, Kawasaki-ku, Kawasaki-shi 210, Japan
ABSTRACT
Summary: The Corynebacterium glutamicum (Brevibacterium lactofermentum AJ12036) odhA gene, encoding 2-oxoglutarate dehydrogenase (E1o subunit of the 2-oxoglutarate dehydrogenase complex), has been isolated and identified as an homologous counterpart of the Escherichia coli sucA and Bacillus subtilis odhA genes. The nucleotide sequence of a 4394 bp chromosomal fragment containing the C. glutamicum odhA gene was determined. The odhA gene comprised 3771 bp (1257 codons, including the initiation codon) and a molecular mass of 138656 Da was predicted for the OdhA polypeptide. Northern blot analysis revealed a 3.9 kb transcript. The size of the transcript, together with the presence of a rho-independent terminator-like structure, suggests that C. glutamicum odhA is monocistronic. Cells harbouring plasmids carrying C. glutamicum odhA showed a threefold increase in specific 2-oxoglutarate dehydrogenase complex activity and expression of a protein with an apparent molecular mass of 136 kDa, in good agreement with the predicted size of the OdhA polypeptide. The C-terminal region of the C. glutamicum OdhA protein shows strong sequence similarity to E1os from other organisms. C. glutamicum OdhA has an N-terminal extension not found in previously reported E1os. The amino acid sequence of this extension shows similarity to that of the C-terminal region of dihydrolipoamide S -succinyltransferase (E2o) subunits of 2-oxoglutarate dehydrogenase complexes and dihydrolipoamide S -acetyltransferase (E2p) subunits of pyruvate dehydrogenase complexes. It suggests that the C. glutamicum odhA gene might encode a novel bifunctional protein with E1o and E2o activities.
Author for correspondence: Yoshihiro Usuda. Tel: +81 44 244 7138. Fax: +81 44 246 5093.
Keywords: Keywords: Corynebacterium glutamicum, , Brevibacterium lactofermentum, , 2-oxoglutarate dehydrogenase, odhA gene |
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ISSN: | 1350-0872 1465-2080 |
DOI: | 10.1099/13500872-142-12-3347 |