Putative lmbI and lmbH genes form a single lmbIH ORF in Streptomyces lincolnensis type strain ATCC 25466
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Genes, Bacterial MeSH
- Bacterial Proteins chemistry genetics metabolism MeSH
- Lincomycin biosynthesis MeSH
- Molecular Sequence Data MeSH
- Multigene Family MeSH
- Open Reading Frames genetics MeSH
- Escherichia coli Proteins * MeSH
- Protein Biosynthesis * MeSH
- Gene Expression Regulation, Bacterial MeSH
- Amino Acid Sequence MeSH
- Sequence Analysis, DNA MeSH
- Streptomyces genetics metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- Lincomycin MeSH
- LmbIH protein, Streptomyces lincolnensis MeSH Browser
- Escherichia coli Proteins * MeSH
- TldD protein, E coli MeSH Browser
The lincomycin-production gene cluster of the industrial overproduction strain Streptomyces lincolnensis 78-11 has been sequenced (Peschke et al. 1995) and twenty-seven putative open reading frames with biosynthetic or regulatory functions (lmb genes) identified. Two distinct hypothetical genes, lmbI and lmbH, were found downstream of the lmbJ gene, coding for LmbJ protein, which is believed to participate in the last lincomycin biosynthetic step, i.e. conversion of N-demethyllincomycin (NDL) to lincomycin. In the present study, we demonstrate the presence of a single larger open reading frame, called lmbIH, in the lincomycin low-production type strain Streptomyces lincolnensis ATCC 25466, instead of two smaller lmbI and lmbH genes. The product, LmbIH, is a protein of an unknown function and is homologous with the T1dD protein family. Escherichia coli T1dD protein was previously shown to be involved in the control of DNA gyrase by LetD protein. Moreover, our experiments indicate co-regulation of lmbJ and lmbIH expression. This translation coupling probably reflects an eight nucleotide overlap between the lmbJ and lmbIH genes, as well as the lack of a Shine-Dalgarno sequence upstream of the lmbIH gene.
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