
Using conserved fingerprints in the glycosyltransferase (GTase) domain of high-molecular-weight penicillin-binding proteins (PBP), a gene (mgt) encoding a putative monofunctional glycosyltransferase has been identified in Haemophilus influenzae and in other bacteria] species. Here we report the cloning of the homologous Escherichia coli gene and show that the solubilised membrane fraction of E. coli cells overexpressing the mgt gene contain a significantly increased peptidoglycan synthesis activity. In contrast to the high-molecular-weight PBPs, this activity is not inhibited by Flavomycin.
Base Sequence, Sequence Homology, Amino Acid, Molecular Sequence Data, Glycosyltransferases, Membrane Proteins, Peptidoglycan, Recombinant Proteins, Species Specificity, Escherichia coli, Amino Acid Sequence, DNA Primers
Base Sequence, Sequence Homology, Amino Acid, Molecular Sequence Data, Glycosyltransferases, Membrane Proteins, Peptidoglycan, Recombinant Proteins, Species Specificity, Escherichia coli, Amino Acid Sequence, DNA Primers
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
