Single amino acid substitutions in either YhjD or MsbA confer viability to 3-deoxy- d-manno-oct-2-ulosonic acid-depleted Escherichia coli

• Published in: Molecular microbiology 2008-02, Vol.67 (3), p.633-648
• Main Authors: Mamat, Uwe, Meredith, Timothy C, Aggarwal, Parag, Kühl, Annika, Kirchhoff, Paul, Lindner, Buko, Hanuszkiewicz, Anna, Sun, Jennifer, Holst, Otto, Woodard, Ronald W
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution; ATP-Binding Cassette Transporters - chemistry; ATP-Binding Cassette Transporters - genetics; ATP-Binding Cassette Transporters - physiology; Bacterial Proteins - chemistry; Bacterial Proteins - genetics; Bacterial Proteins - physiology; Bacteriology; Biochemistry; Biological and medical sciences; Carbohydrates; Cell Membrane - chemistry; E coli; Escherichia coli K12 - chemistry; Escherichia coli K12 - genetics; Escherichia coli K12 - physiology; Escherichia coli Proteins - genetics; Escherichia coli Proteins - physiology; Fundamental and applied biological sciences. Psychology; Genes, Essential; Glycolipids - analysis; Glycolipids - chemistry; Glycosylation; Lipid A - analogs & derivatives; Lipid A - analysis; Lipid A - chemistry; Mass Spectrometry; Membrane Proteins - genetics; Membrane Proteins - physiology; Membranes; Microbial Viability; Microbiology; Miscellaneous; Models, Molecular; Proteins; Sugar Acids - metabolism; Suppression, Genetic
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1111/j.1365-2958.2007.06074.x

The Escherichia coli K-12 strain KPM22, defective in synthesis of 3-deoxy- d-manno-oct-2-ulosonic acid (Kdo), is viable with an outer membrane (OM) composed predominantly of lipid IVA, a precursor of lipopolysaccharide (LPS) biosynthesis that lacks any glycosylation. To sustain viability, the presence of a second-site suppressor was proposed for transport of lipid IVA from the inner membrane (IM), thus relieving toxic side-effects of lipid IVA accumulation and providing sufficient amounts of LPS precursors to support OM biogenesis. We now report the identification of an arginine to cysteine substitution at position 134 of the conserved IM protein YhjD in KPM22 that acts as a compensatory suppressor mutation of the lethal ΔKdo phenotype. Further, the yhjD400 suppressor allele renders the LPS transporter MsbA dispensable for lipid IVA transmembrane trafficking. The independent derivation of a series of non-conditional KPM22-like mutants from the Kdo-dependent parent strain TCM15 revealed a second class of suppressor mutations localized to MsbA. Proline to serine substitutions at either residue 18 or 50 of MsbA relieved the Kdo growth dependence observed in the isogenic wild-type strain. The possible impact of these suppressor mutations on structure and function are discussed by means of a computationally derived threading model of MsbA.