Redefining the Requisite Lipopolysaccharide Structure in Escherichia coli

• Published in: ACS chemical biology 2006-02, Vol.1 (1), p.33-42
• Main Authors: Meredith, Timothy C, Aggarwal, Parag, Mamat, Uwe, Lindner, Buko, Woodard, Ronald W
• Format: Article
• Language: English
• Subjects: Carbohydrate Sequence; Cell Membrane - enzymology; Endotoxins - chemistry; Escherichia coli - chemistry; Gram-Negative Bacteria - chemistry; Lipid A - chemistry; Lipid Bilayers; Lipopolysaccharides - chemistry; Lipopolysaccharides - isolation & purification; Molecular Sequence Data; Phospholipases - metabolism; Sugar Acids - chemistry; Thermodynamics
• ISSN: 1554-8929; 1554-8937
• DOI: 10.1021/cb0500015

Gram-negative bacteria possess an asymmetric lipid bilayer surrounding the cell wall, the outer membrane (OM). The OM inner leaflet is primarily composed of various glycerophospholipids, whereas the outer leaflet predominantly contains the unique amphiphilic macromolecule, lipopolysaccharide (LPS or endotoxin). The majority of all Gram-negative bacteria elaborate LPS containing at least one 2-keto 3-deoxy-d-manno-octulosonate (Kdo) molecule. The minimal LPS structure required for growth of Escherichia coli has long been recognized as two Kdo residues attached to lipid A, inextricably linking viability to toxicity. Here we report the construction and characterization of the nonconditional E. coli K-12 suppressor strain KPM22 that lacks Kdo and is viable despite predominantly elaborating the endotoxically inactive LPS precursor lipid IVA. Our results challenge the established E. coli Kdo2-lipid A dogma, indicating that the previously observed and well-documented dependence of cell viability on the synthesis of Kdo stems from a lethal pleiotropy precipitated after the depletion of the carbohydrate, rather than an inherent need for the Kdo molecule itself as an indispensable structural component of the OM LPS layer. Inclusion of the inner membrane LPS transporter MsbA on a multicopy plasmid partially suppresses the lethal ΔKdo phenotype directly in the auxotrophic parent strain, suggesting increased rates of nonglycosylated lipid A transport can, in part, compensate for Kdo depletion. The unprecedented nature of a lipid IVA OM redefines the requisite LPS structure for viability in E. coli.