A Dynamic Network of Proteins Facilitate Cell Envelope Biogenesis in Gram-Negative Bacteria

被引:16
作者
Graham, Chris L. B. [1 ]
Newman, Hector [1 ]
Gillett, Francesca N. [1 ,2 ]
Smart, Katie [1 ]
Briggs, Nicholas [1 ]
Banzhaf, Manuel [2 ]
Roper, David I. [1 ]
机构
[1] Univ Warwick, Sch Life Sci, Coventry CV4 7AL, W Midlands, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
peptidoglycan; interactions; Escherichia coli; outer membrane; envelope; network; protein-protein; seds; complexes; dynamic; gram-negative; cell division; cytoskeleton; PEPTIDOGLYCAN CROSS-LINKING; ESCHERICHIA-COLI; LYTIC TRANSGLYCOSYLASES; ACTIN CYTOSKELETON; GLYCAN STRANDS; SYNTHASE PBP1B; SHAPE MUTANTS; WALL; DIVISION; MREB;
D O I
10.3390/ijms222312831
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
Bacteria must maintain the ability to modify and repair the peptidoglycan layer without jeopardising its essential functions in cell shape, cellular integrity and intermolecular interactions. A range of new experimental techniques is bringing an advanced understanding of how bacteria regulate and achieve peptidoglycan synthesis, particularly in respect of the central role played by complexes of Sporulation, Elongation or Division (SEDs) and class B penicillin-binding proteins required for cell division, growth and shape. In this review we highlight relationships implicated by a bioinformatic approach between the outer membrane, cytoskeletal components, periplasmic control proteins, and cell elongation/division proteins to provide further perspective on the interactions of these cell division, growth and shape complexes. We detail the network of protein interactions that assist in the formation of peptidoglycan and highlight the increasingly dynamic and connected set of protein machinery and macrostructures that assist in creating the cell envelope layers in Gram-negative bacteria.
引用
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页数:23
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