Outer membrane composition of a lipopolysaccharide-deficient Neisseria meningitidis mutant

被引:110
作者
Steeghs, L
de Cock, H
Evers, E
Zomer, B
Tommassen, J
van der Ley, P
机构
[1] Natl Inst Publ Hlth & Environm, RIVM, Lab Vaccine Res, NL-3720 BA Bilthoven, Netherlands
[2] Natl Inst Publ Hlth & Environm, RIVM, Lab Organ Analyt Chem, NL-3720 BA Bilthoven, Netherlands
[3] Univ Utrecht, Biomembrane Inst, NL-3584 CH Utrecht, Netherlands
关键词
capsular polysaccharide; lipopolysaccharide; Neisseria meningitidis; outer membrane proteins; phospholipids;
D O I
10.1093/emboj/20.24.6937
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the pathogen Neisseria meningitidis, a completely lipopolysaccharide (LPS)-deficient but viable mutant can be obtained by insertional inactivation of the lpxA gene, encoding UDP-GlcNAc acyltransferase required for the first step of lipid A biosynthesis. To study how outer membrane structure and biogenesis are affected by the absence of this normally major component, inner and outer membranes were separated and their composition analysed. The expression and assembly of integral outer membrane proteins appeared largely unaffected. However, the expression of iron limitation-inducible, cell surface-exposed lipoproteins was greatly reduced. Major changes were seen in the phospholipid composition, with a shift towards phosphatidylethanolamine and phosphatidylglycerol species containing mostly shorter chain, saturated fatty acids, one of which was unique to the LPS-deficient outer membrane. The presence of the capsular polysaccharide turned out to be essential for viability without LPS, as demonstrated by using a strain in which LPS biosynthesis could be switched on or off through a tac promoter-controlled lpxA gene. Taken together, these results can help to explain why meningococci have the unique ability to survive without LPS.
引用
收藏
页码:6937 / 6945
页数:9
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