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1. (CSDB ID: 2189) | report error |
| a-L-Rhap-(1-5)-+ | EtN-(1--P--7)--a-Kdop-(2-4)-+ | | a-Kdop-(2-4)-+ | | EtN-(1---P---P---4)-+ | | | a-D-Galp-(1-6)-+ | P-4)-+ | | | | | Hepp-(1-6)-a-D-Glcp-(1-2)-a-D-Glcp-(1-3)-a-D-Glcp-(1-3)-L-gro-a-D-manHepp-(1-3)-L-gro-a-D-manHepp-(1-5)-a-Kdop-(2--/lipid A/ | L-gro-a-D-manHepp-(1-7)-+ | Show graphically |
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Escherichia coli K12
(NCBI TaxID 83333,
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uoguelph.caThe waa gene cluster is responsible for the biosynthesis of the lipopolysaccharide (LPS) core region in Escherichia coli and Salmonella: Homologs of the waaZ gene product are encoded by the waa gene clusters of Salmonella enterica and E. coli strains with the K-12 and R2 core types. Overexpression of WaaZ in E. coli and S. enterica led to a modified LPS structure showing core truncations and (where relevant) to a reduction in the amount of O-polysaccharide side chains. Mass spectrometry and nuclear magnetic resonance spectroscopy were used to determine the predominant LPS structures in an E. coli isolate with an R1 core (waaZ is lacking from the type R1 waa gene cluster) with a copy of the waaZ gene added on a plasmid. Novel truncated LPS structures, lacking up to 3 hexoses from the outer core, resulted from WaaZ overexpression. The truncated molecules also contained a KdoIII residue not normally found in the R1 core
Lipopolysaccharide, biosynthesis, LPS, structure, core, gene, isolate, microbiology, strain, polysaccharide, cell, chain, molecule, Research, side chain, Escherichia, Escherichia coli, type, predominant, cluster, gene cluster, O-polysaccharide, O polysaccharide, spectrometry, Salmonella, core region, region, mass spectrometry, reduction, biochemistry, biophysics, hexose, Hexoses, homolog, inner core, lead, Magnetic Resonance Spectroscopy, medicine, modification, modified, nuclear, nuclear magnetic resonance, nuclear magnetic resonance spectroscopy, plasmid, resonance, Salmonella enterica, spectroscopy, surface
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