Journal of Biological Chemistry · 1983 · 162 citations · 29 references
Life SciencesBiochemistryMolecular BiologyCarbohydrate BiochemistryLipid BiochemistryStructural BiologyFatty Acid BiosynthesisFatty Acid ChemistryLipid BiosynthesisLipid ChemistryLipid MetabolismLipid StructureAlpha Anomeric ConfigurationAnomeric Configuration EffectsBacterial Fatty Acid BiosynthesisBacterial Membrane Lipid CompositionEscherichia ColiFatty AcidsLipid Structural AnalysisLipopolysaccharide Biosynthesis
We have determined the complete structure of a glycolipid (designated lipid X) previously found to accumulate in certain Escherichia coli mutants defective in phosphatidylglycerol synthesis (Nishijima, M., and Raetz, C.R.H. (1979) J. Biol. Chem. 254, 7837-7844). Based on fast atom bombardment mass spectrometry and proton nuclear magnetic resonance studies, this substance is an acylated metabolite of glucosamine 1-phosphate. Lipid X of E. coli has a Mr = 711.87 as the free acid (C34H66NO12P) and contains two beta-hydroxymyristate moieties, one attached as an amide at the 2 position and the other as an ester at the 3 position of the sugar. It has free hydroxyl groups at the 4 and 6 positions, and the anomeric configuration is alpha. The structure of lipid X from E. coli closely resembles the reducing end subunit of lipid A, and it might represent a very early precursor in the biosynthesis of lipid A. To our knowledge, fatty acyl derivatives of glucosamine 1-phosphate have not been reported previously.
29
Phosphorus Assay in Column Chromatography
Grant R. Bartlett · Journal of Biological Chemistry · 1959 · 12.9K citations · Full text
A Text-Book of Practical Organic Chemistry
J. W. Cook · Nature · 1948 · 3.5K citations