Lipid a modification systems in gram-negative bacteria

被引:993
作者
Raetz, Christian R. H. [1 ]
Reynolds, C. Michael
Trent, M. Stephen
Bishop, Russell E.
机构
[1] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
[2] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
[3] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
关键词
lipopolysaccharide; endotoxin; innate immunity; MsbA; LpxC;
D O I
10.1146/annurev.biochem.76.010307.145803
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
The lipid A moiety of lipopolysaccharide forms the outer monolayer of the outer membrane of most gram-negative bacteria. Escherichia coli lipid A is synthesized on the cytoplasmic surface of the inner membrane by a conserved pathway of nine constitutive enzymes. Following attachment of the core oligosaccharide, nascent core-lipid A is flipped to the outer surface of die inner membrane by the ABC transporter MsbA, where the O-antigen polymer is attached. Diverse covalent modifications of the lipid A moiety may occur during its transit from the outer surface of the inner membrane to the outer membrane. Lipid A modification enzymes are reporters for lipopolysaccharide trafficking within the bacterial envelope. Modification systems are variable and often regulated by environmental conditions. Although not required for growth, the modification enzymes modulate virulence of some gram-negative pathogens. Heterologous expression of lipid A modification enzymes may enable the development of new vaccines.
引用
收藏
页码:295 / 329
页数:35
相关论文
共 254 条
[31]   3-Deoxy-D-manno-oct-2-ulosonic acid (Kdo) transferase (WaaA) and Kdo kinase (KdkA) of Haemophilus influenzae are both required to complement a waaA knockout mutation of Escherichia coli [J].
Brabetz, W ;
Müller-Loennies, S ;
Brade, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (45) :34954-34962
[32]  
BRADE H, 1999, ENDOTOXIN HLTH DIS N
[33]   Imp/OstA is required for cell envelope biogenesis in Escherichia coli [J].
Braun, M ;
Silhavy, TJ .
MOLECULAR MICROBIOLOGY, 2002, 45 (05) :1289-1302
[34]   A formyltransferase required for polymyxin resistance in Escherichia coli and the modification of lipid a with 4-amino-4-deoxy-L-arabinose -: Identification and function of UDP-4-deoxy-4-formamido-L-arabinose [J].
Breazeale, SD ;
Ribeiro, AA ;
McClerren, AL ;
Raetz, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :14154-14167
[35]   Origin of lipid A species modified with 4-amino-4-deoxy-L-arabinose in polymyxin-resistant mutants of Escherichia coli -: An aminotransferase (ArnB) that generates UDP-4-amino-4-deoxy-L-arabinose [J].
Breazeale, SD ;
Ribeiro, AA ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (27) :24731-24739
[36]   Oxidative decarboxylation of UDP-glucuronic acid in extracts of polymyxin-resistant Escherichia coli -: Origin of lipid a species modified with 4-amino-4-deoxy-L-arabinose [J].
Breazeale, SD ;
Ribeiro, AA ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (04) :2886-2896
[37]   Lipopolysaccharide core glycosylation in Rhizobium leguminosarum - An unusual mannosyl transferase resembling the heptosyl transferase I of Escherichia coli [J].
Kadrmas, JL ;
Brozek, KA ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32119-32125
[38]   Lipopolysaccharide core glycosylation in Rhizobium leguminosarum - An unusual mannosyl transferase resembling the heptosyl transferase I of Escherichia coli [J].
Kadrmas, JL ;
Brozek, KA ;
Raetz, CRH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32119-32125
[39]  
BROZEK KA, 1989, J BIOL CHEM, V264, P6956
[40]  
BROZEK KA, 1987, J BIOL CHEM, V262, P5170