Bridging cell wall biosynthesis and bacterial morphogenesis

被引:64
作者
Mattei, Pierre-Jean [1 ]
Neves, David [1 ]
Dessen, Andrea [1 ]
机构
[1] Inst Biol Struct, Bacterial Pathogenesis Grp, UMR CNRS CEA UJF 5075, F-38027 Grenoble, France
关键词
BETA-LACTAM RESISTANCE; PENICILLIN-BINDING PROTEINS; CRYSTAL-STRUCTURE; ESCHERICHIA-COLI; PEPTIDOGLYCAN SYNTHESIS; BACILLUS-SUBTILIS; ACTIVE-SITE; MREB; SHAPE; COMPLEX;
D O I
10.1016/j.sbi.2010.09.014
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 bacterial cell wall is a complex three-dimensional structure that protects the cell from environmental stress and ensures its shape. The biosynthesis of its main component, the peptidoglycan, involves the coordination of activities of proteins present in the cytoplasm, the membrane, and the periplasm, some of which also interact with the bacterial cytoskeleton. The sheer complexity of the cell wall elongation process, which is the main focus of this review, has created a significant challenge for the study of the macromolecular interactions that regulate peptidoglycan biosynthesis. The availability of new structural and biochemical data on a number of components of peptidoglycan assembly machineries, including a complex between MreB and RodZ as well as structures of penicillin-binding proteins (PBPs) from a number of pathogenic species, now provide novel insight into the underpinnings of an intricate molecular machinery.
引用
收藏
页码:749 / 755
页数:7
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