cellulose has been researched along with alpha-hydroxymyristic-acid* in 1 studies
1 other study(ies) available for cellulose and alpha-hydroxymyristic-acid
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Accumulation of a polyisoprene-linked amino sugar in polymyxin-resistant Salmonella typhimurium and Escherichia coli: structural characterization and transfer to lipid A in the periplasm.
Polymyxin-resistant mutants of Escherichia coli and Salmonella typhimurium accumulate a novel minor lipid that can donate 4-amino-4-deoxy-l-arabinose units (l-Ara4N) to lipid A. We now report the purification of this lipid from a pss(-) pmrA(C) mutant of E. coli and assign its structure as undecaprenyl phosphate-alpha-l-Ara4N. Approximately 0.2 mg of homogeneous material was isolated from an 8-liter culture by solvent extraction, followed by chromatography on DEAE-cellulose, C18 reverse phase resin, and silicic acid. Matrix-assisted laser desorption ionization/time of flight mass spectrometry in the negative mode yielded a single species [M - H](-) at m/z 977.5, consistent with undecaprenyl phosphate-alpha-l-Ara4N (M(r) = 978.41). (31)P NMR spectroscopy showed a single phosphorus atom at -0.44 ppm characteristic of a phosphodiester linkage. Selective inverse decoupling difference spectroscopy demonstrated that the undecaprenyl phosphate group is attached to the anomeric carbon of the l-Ara4N unit. One- and two-dimensional (1)H NMR studies confirmed the presence of a polyisoprene chain and a sugar moiety with chemical shifts and coupling constants expected for an equatorially substituted arabinopyranoside. Heteronuclear multiple-quantum coherence spectroscopy analysis demonstrated that a nitrogen atom is attached to C-4 of the sugar residue. The purified donor supports in vitro conversion of lipid IV(A) to lipid II(A), which is substituted with a single l-Ara4N moiety. The identification of undecaprenyl phosphate-alpha-l-Ara4N implies that l-Ara4N transfer to lipid A occurs in the periplasm of polymyxin-resistant strains, and establishes a new enzymatic pathway by which Gram-negative bacteria acquire antibiotic resistance. Topics: Amino Sugars; Anti-Bacterial Agents; Bacterial Proteins; Carbohydrate Sequence; Carbohydrates; Cell Nucleus; Cell-Free System; Chromatography; DEAE-Cellulose; Escherichia coli; Ethanolamines; Hydrolysis; Lipid A; Lipids; Magnetic Resonance Spectroscopy; Models, Chemical; Molecular Sequence Data; Mutation; Myristic Acids; Palmitic Acid; Periplasm; Phosphorus; Polymyxins; Protein Binding; Protein Conformation; Protein Prenylation; Salmonella typhimurium; Silicic Acid; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 2001 |