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The Omp85 Protein of Neisseria Meningitidis is Required for Lipid Export to the Outer Membrane

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Journal EMBO J
Date 2003 Apr 19
PMID 12682011
Citations 39
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Abstract

In Gram-negative bacteria, lipopolysaccharide and phospholipid biosynthesis takes place at the inner membrane. How the completed lipid molecules are subsequently transported to the outer membrane remains unknown. Omp85 of Neisseria meningitidis is representative for a family of outer membrane proteins conserved among Gram-negative bacteria. We first demonstrated that the omp85 gene is co-transcribed with genes involved in lipid biosynthesis, suggesting an involvement in lipid assembly. A meningococcal strain was constructed in which Omp85 expression could be switched on or off through a tac promoter-controlled omp85 gene. We demonstrated that the presence of Omp85 is essential for viability. Depletion of Omp85 leads to accumulation of electron-dense amorphous material and vesicular structures in the periplasm. We demonstrated, by fractionation of inner and outer membranes, that lipopolysaccharide and phospholipids mostly disappeared from the outer membrane and instead accumulated in the inner membrane, upon depletion of Omp85. Omp85 depletion did not affect localization of integral outer membrane proteins PorA and Opa. These results provide compelling evidence for a role for Omp85 in lipid transport to the outer membrane.

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References
1.
Doerrler W, Reedy M, Raetz C . An Escherichia coli mutant defective in lipid export. J Biol Chem. 2001; 276(15):11461-4. DOI: 10.1074/jbc.C100091200. View

2.
Buchanan S, Smith B, Venkatramani L, Xia D, Esser L, Palnitkar M . Crystal structure of the outer membrane active transporter FepA from Escherichia coli. Nat Struct Biol. 1999; 6(1):56-63. DOI: 10.1038/4931. View

3.
Chang G, Roth C . Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette (ABC) transporters. Science. 2001; 293(5536):1793-800. DOI: 10.1126/science.293.5536.1793. View

4.
Dartigalongue C, Loferer H, Raina S . EcfE, a new essential inner membrane protease: its role in the regulation of heat shock response in Escherichia coli. EMBO J. 2001; 20(21):5908-18. PMC: 125713. DOI: 10.1093/emboj/20.21.5908. View

5.
Steeghs L, de Cock H, Evers E, Zomer B, Tommassen J, van der Ley P . Outer membrane composition of a lipopolysaccharide-deficient Neisseria meningitidis mutant. EMBO J. 2001; 20(24):6937-45. PMC: 125796. DOI: 10.1093/emboj/20.24.6937. View