Novel phosphotransferase genes revealed by bacterial genome sequencing: a gene cluster encoding a putative N-acetylgalactosamine metabolic pathway in Escherichia coli
Department of Biology, University of California at San Diego, La Jolla, CA 92093-0116, USA ABSTRACT Summary: We have analysed a gene cluster in the 67.4-76.0 min region of the Escherichia coli chromosome, revealed by recent systematic genome sequencing. The genes within this cluster include: (1) fiv...
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Veröffentlicht in: | Microbiology (Society for General Microbiology) 1996-02, Vol.142 (2), p.231-250 |
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Zusammenfassung: | Department of Biology, University of California at San Diego, La Jolla, CA 92093-0116, USA
ABSTRACT
Summary: We have analysed a gene cluster in the 67.4-76.0 min region of the Escherichia coli chromosome, revealed by recent systematic genome sequencing. The genes within this cluster include: (1) five genes encoding homologues of the E. coli mannose permease of the phosphotransferase system (IIB, IIB', IIC, IIC' and IID); (2) genes encoding a putative N -acetylgalactosamine 6-phosphate metabolic pathway including (a) a deacetylase, (b) an isomerizing deaminase, (c) a putative carbohydrate kinase, and (d) an aldolase; and (3) a transcriptional regulatory protein homologous to members of the DeoR family. Evidence is presented suggesting that the aldolase-encoding gene within this cluster is the previously designated kba gene that encodes tagatose-1,6-bisphosphate aldolase. These proteins and a novel IIA Man -like protein encoded in the 2.4-4.1 min region are characterized with respect to their sequence similarities and phylogenetic relationships with other homologous proteins. A pathway for the metabolism of N -acetylgalactosamine biochemically similar to that for the metabolism of N -acetylglucosamine is proposed.
Author for correspondence: Milton H. Saier, Jr. Tel: +1619 534 4084. Fax: +1619 534 7108. e-mail: msaier@ucsd.edu
Keywords: Escherichia coli genome, phosphotransferase system, sugar transport, N -acetylgalacrosamine, aldolases |
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ISSN: | 1350-0872 1465-2080 |
DOI: | 10.1099/13500872-142-2-231 |