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Isolation and structural analysis of two lipid A precursors from a KDO deficient mutant of Salmonella typhimurium differing in their hexadecanoic acid content
Authors:Thomas Hansen-Hagge  Volker Lehmann  Ulrich Seydel  Buko Lindner  Ulrich Zähringer
Affiliation:(1) Max-Planck-Institut für Immunbiologie, Stübeweg 51, D-7800 Freiburg, Federal Republic of Germany;(2) Deutsches Krebsforschungszentrum, Institut für Immunologie und Genetik, Im Neuenheimer Feld 280, D-6900 Heidelberg, Federal Republic of Germany;(3) Forschungsinstitut Borstel, Institut für Experimentelle Biologie und Medizin, Parkallee 1-40, D-2061 Borstel, Federal Republic of Germany
Abstract:The extraction, purification and structural characterization of two lipid A precursors (Ia and Ib) differing only in one hexadecanoic acid are described. Both precursors were synthesized at elevated temperatures by a new mutant of Salmonella typhimurium (mutant Ts5) which is conditionally defective in synthesis of the 3-deoxy-d-manno-octulosonic acid region of lipopolysaccharides.Both precursors were purified by repeated phenol/chloroform/petroleum ether (PCP) extractions followed by thin layer chromatography. Teh precursor preparation was free of lipopolysaccharides and phospholipids and contained less than 0.1% protein. Structural analysis which included chemical degradation procedures as well as positive ion laser desorption (LDMS) mass spectroscopy of dephosphorylated lipid A precursors showed together that precursor Ia represents a diphosphorylated glucosamine disaccharide containing two ester, two amide-linked residues of 3-hydroxytetradecanoic acid and lacks the ester-linked dodecanoic, tetradecanoic and hexadecanoic acid as well as 3-deoxy-d-manno-octulosonic acid. Precursor Ib has the same basic structure as precursor Ia, but contains in addition one mol of hexadecanoic acid per mol disaccharide which is linked to the 3-hydroxy group of the amide-bound 3-hydroxy-tetradecanoic acid of the reducing, terminal glucosamine residue.The structure of precursor Ib supports the conclusion that hexadecanoic acid incorporation occurs at an early stage in lipid A biosynthesis prior to the attachment of 3-deoxy-d-manno-octulosonic acid and/or other polar substituents.Abbreviations LDMS laser desorption mass spectrometry - KDO 3-Deoxy-d-manno-octulosonic acid - Ts5 Salmonella typhimurium mutant Ts5 - PCP phenol/chloroform/petroleum ether - H2F2 hydrogen fluorideThis work is dedicated to Prof. Dr. Drews, Freiburg, on the occasion of his 60th birthday
Keywords:KDO mutant  Lipid A intermediates  Hexadecanoic acid substitution  Biosynthesis of lipid A
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