The role of galacturonic acid in outer membrane stability in Klebsiella pneumoniae

被引:28
作者
Frirdich, E
Bouwman, C
Vinogradov, E
Whitfield, C [1 ]
机构
[1] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
[2] Natl Res Council Canada, Ottawa, ON K1A 0R6, Canada
关键词
D O I
10.1074/jbc.M504987200
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 most members of the Enterobacteriaceae, including Escherichia coli and Salmonella, the lipopolysaccharide core oligosaccharide backbone is modified by phosphoryl groups. The negative charges provided by these residues are important in maintaining the barrier function of the outer membrane. Mutants lacking the core heptose region and the phosphate residues display pleiotrophic defects collectively known as the deep-rough phenotype, characterized by changes in outer membrane structure and function. Klebsiella pneumoniae lacks phosphoryl residues in its core, but instead contains galacturonic acid. The goal of this study was to determine the contribution of galacturonic acid as a critical source of negative charge. A mutant was created lacking all galacturonic acid by targeting UDP-galacturonic acid precursor synthesis through a mutation in gla(KP). Gla(KP) is a K. pneumoniae UDP-galacturonic acid C4 epimerase providing UDP-galacturonic acid for core synthesis. The glaKP gene was inactivated and the structure of the mutant lipopolysaccharide was determined by mass spectrometry. The mutant displayed characteristics of a deep-rough phenotype, exhibiting a hypersensitivity to hydrophobic compounds and polymyxin B, an altered outer membrane profile, and the release of the periplasmic enzyme beta-lactamase. These results indicate that the negative charge provided by the carboxyl groups of galacturonic acid do play an equivalent role to the core oligosaccharide phosphate residues in establishing outer membrane integrity in E. coli and Salmonella.
引用
收藏
页码:27604 / 27612
页数:9
相关论文
共 87 条
[1]  
ALBERTI S, 1995, INFECT IMMUN, V63, P903
[2]   ELECTROTRANSFORMATION IN SALMONELLA-TYPHIMURIUM LT2 [J].
BINOTTO, J ;
MACLACHLAN, PR ;
SANDERSON, KE .
CANADIAN JOURNAL OF MICROBIOLOGY, 1991, 37 (06) :474-477
[3]   Biogenesis of the gram-negative bacterial outer membrane [J].
Bos, MP ;
Tommassen, J .
CURRENT OPINION IN MICROBIOLOGY, 2004, 7 (06) :610-616
[4]   Folding and insertion of the outer membrane protein OmpA is assisted by the chaperone Skp and by lipopolysaccharide [J].
Bulieris, PV ;
Behrens, S ;
Holst, O ;
Kleinschmidt, JH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (11) :9092-9099
[5]   LEAKAGE OF PERIPLASMIC ENZYMES FROM LIPOPOLYSACCHARIDE-DEFECTIVE MUTANTS OF SALMONELLA-TYPHIMURIUM [J].
CHATTERJEE, AK ;
ROSS, H ;
SANDERSON, KE .
CANADIAN JOURNAL OF MICROBIOLOGY, 1976, 22 (10) :1549-1560
[6]   Molecular characterization of a 17-kDa outer-membrane protein from Klebsiella pneumonia [J].
Climent, N ;
Ferrer, S ;
Rubires, X ;
Merino, S ;
Tomas, JM ;
Regue, M .
RESEARCH IN MICROBIOLOGY, 1997, 148 (02) :133-143
[7]  
Collins Carleen M., 1996, P299
[8]   The RcsCB His-Asp phosphorelay system is essential to overcome chlorpromazine-induced stress in Escherichia coli [J].
Conter, A ;
Sturny, R ;
Gutierrez, C ;
Cam, K .
JOURNAL OF BACTERIOLOGY, 2002, 184 (10) :2850-2853
[9]   Aeromonas salmonicida possesses two genes encoding homologs of the major outer membrane protein, OmpA [J].
Costello, GM ;
Vipond, R ;
MacIntyre, S .
JOURNAL OF BACTERIOLOGY, 1996, 178 (06) :1623-1630
[10]   Expression of SHV-2 β-lactamase and of reduced amounts of OmpK36 porin in Klebsiella pneumoniae results in increased resistance to cephalosporins and carbapenems [J].
Crowley, B ;
Benedí, VJ ;
Doménech-Sánchez, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3679-3682