Function of the usher N-terminus in catalysing pilus assembly

被引:22
|
作者
Henderson, Nadine S. [1 ]
Ng, Tony W. [1 ]
Talukder, Iehab [1 ]
Thanassi, David G. [1 ]
机构
[1] SUNY Stony Brook, Ctr Infect Dis, Dept Mol Genet & Microbiol, Stony Brook, NY 11794 USA
基金
美国国家卫生研究院;
关键词
UROPATHOGENIC ESCHERICHIA-COLI; BACTERIAL OUTER-MEMBRANE; DONOR-STRAND EXCHANGE; CHAPERONE-SUBUNIT COMPLEXES; DRIVES FIBER FORMATION; TYPE-1; PILI; STRUCTURAL BASIS; FIMH ADHESIN; PAPC USHER; BIOGENESIS;
D O I
10.1111/j.1365-2958.2010.07505.x
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 chaperone/usher (CU) pathway is a conserved bacterial secretion system that assembles adhesive fibres termed pili or fimbriae. Pilus biogenesis by the CU pathway requires a periplasmic chaperone and an outer membrane (OM) assembly platform termed the usher. The usher catalyses formation of subunit-subunit interactions to promote polymerization of the pilus fibre and provides the channel for fibre secretion. The mechanism by which the usher catalyses pilus assembly is not known. Using the P and type 1 pilus systems of uropathogenic Escherichia coli, we show that a conserved N-terminal disulphide region of the PapC and FimD ushers, as well as residue F4 of FimD, are required for the catalytic activity of the ushers. PapC disulphide loop mutants were able to bind PapDG chaperone-subunit complexes, but did not assemble PapG into pilus fibres. FimD disulphide loop and F4 mutants were able to bind chaperone-subunit complexes and initiate assembly of pilus fibres, but were defective for extending the pilus fibres, as measured using in vivo co-purification and in vitro pilus polymerization assays. These results suggest that the catalytic activity of PapC is required to initiate pilus biogenesis, whereas the catalytic activity of FimD is required for extension of the pilus fibre.
引用
收藏
页码:954 / 967
页数:14
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