The VirB4 family of proposed traffic nucleoside triphosphatases: Common motifs in plasmid RP4 TrbE are essential for conjugation and phage adsorption

被引:57
作者
Rabel, C
Grahn, AM
Lurz, R
Lanka, E
机构
[1] Max Planck Inst Mol Genet, Abt Lehrach, D-14195 Berlin, Germany
[2] Univ Helsinki, Viikki Bioctr, Dept Biosci, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Viikki Bioctr, Inst Biotechnol, FIN-00014 Helsinki, Finland
关键词
D O I
10.1128/JB.185.3.1045-1058.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Proteins of the VirB4 family are encoded by conjugative plasmids and by type IV secretion systems, which specify macromolecule export machineries related to conjugation systems. The central feature of VirB4 proteins is a nucleotide binding site. In this study,we asked whether members of the VirB4 protein family have similarities in their primary structures and whether these proteins hydrolyze nucleotides. A multiple-sequence alignment of 19 members of the VirB4 protein family revealed striking overall similarities. We defined four common motifs and one conserved domain. One member of this protein family, TrbE of plasmid RP4, was genetically characterized by site-directed mutagenesis. Most mutations in trbE resulted in complete loss of its activities, which eliminated pilus production, propagation of plasmid-specific phages, and DNA transfer ability in Escherichia coli. Biochemical studies of a soluble derivative of RP4 TrbE and of the full-length homologous protein R388 TrwK revealed that the purified forms of these members of the VirB4 protein family do not hydrolyze ATP or GTP and behave as monomers in solution.
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页码:1045 / 1058
页数:14
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