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The Lipid A from the Lipopolysaccharide of the Phototrophic Bacterium Rhodomicrobium vannielii ATCC 17100 Revisited.


ABSTRACT: The structure of lipid A from lipopolysaccharide (LPS) of Rhodomicrobium vannielii ATCC 17100 (Rv) a phototrophic, budding bacterium was re-investigated using high-resolution mass spectrometry, NMR, and chemical degradation protocols. It was found that the (GlcpN)-disaccharide lipid A backbone was substituted by a GalpA residue that was connected to C-1 of proximal GlcpN. Some of this GalpA residue was ?-eliminated by alkaline de-acylation, which indicated the possibility of the presence of another so far unidentified substituent at C-4 in non-stoichiometric amounts. One Manp residue substituted C-4' of distal GlcpN. The lipid A backbone was acylated by 16:0(3-OH) at C-2 of proximal GlcpN, and by 16:0(3-OH), i17:0(3-OH), or 18:0(3-OH) at C-2' of distal GlcpN. Two acyloxy-acyl moieties that were mainly formed by 14:0(3-O-14:0) and 16:0(3-O-22:1) occupied the distal GlcpN of lipid A. Genes that were possibly involved in the modification of Rv lipid A were compared with bacterial genes of known function. The biological activity was tested at the model of human mononuclear cells (MNC), showing that Rv lipid A alone does not significantly stimulate MNC. At low concentrations of toxic Escherichia coli O111:B4 LPS, pre-incubation with Rv lipid A resulted in a substantial reduction of activity, but, when higher concentrations of E. coli LPS were used, the stimulatory effect was increased.

SUBMITTER: Komaniecka I 

PROVIDER: S-EPMC7795004 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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The Lipid A from the Lipopolysaccharide of the Phototrophic Bacterium <i>Rhodomicrobium vannielii</i> ATCC 17100 Revisited.

Komaniecka Iwona I   Susniak Katarzyna K   Choma Adam A   Heine Holger H   Holst Otto O  

International journal of molecular sciences 20201229 1


The structure of lipid A from lipopolysaccharide (LPS) of <i>Rhodomicrobium vannielii</i> ATCC 17100 (<i>Rv</i>) a phototrophic, budding bacterium was re-investigated using high-resolution mass spectrometry, NMR, and chemical degradation protocols. It was found that the (Glc<i>p</i>N)-disaccharide lipid A backbone was substituted by a Gal<i>p</i>A residue that was connected to C-1 of proximal Glc<i>p</i>N. Some of this Gal<i>p</i>A residue was β-eliminated by alkaline de-acylation, which indicat  ...[more]

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