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Analysis and characterization of the IncFV plasmid pED208 transfer region
被引:36
作者:
Jun, L
Manchak, J
Klimke, W
Davidson, C
Firth, N
Skurray, RA
Frost, LS
机构:
[1] Univ Alberta, Dept Biol Sci, Edmonton, AB T6G 2E9, Canada
[2] Univ Sydney, Sch Biol Sci, Sydney, NSW 2006, Australia
来源:
基金:
澳大利亚研究理事会;
加拿大健康研究院;
关键词:
pED208;
F(0)lac transfer region;
DNA sequence;
conjugation;
regulation;
specificity;
coupling protein;
relaxase;
type IV secretion;
D O I:
10.1016/S0147-619X(02)00007-0
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
pED208 is a transfer-derepressed mutant of the IncFV plasmid, F(0)lac, which has an IS2 element inserted in its traY gene, resulting in constitutive overexpression of its transfer (tra) region. The pED208 transfer region, which encodes proteins responsible for pilus synthesis and conjugative plasmid transfer, was sequenced and found to be very similar to the F tra region in terms of its organization although most pED208 tra proteins share only about 45% amino acid identity. All the essential genes for F transfer had homologs within the pED208 transfer region with the exception of traQ, which encodes the chaperone for stable F-pilin expression. F(0)lac appears to have a fertility inhibition system different than the FinOP system of other F-like plasmids, and its transfer efficiency was increased in the presence of F or R 100, suggesting that it could be mobilized by these plasmids, The F-like transfer systems specified by F, R100, and F(0)lac were highly specific for their cognate origins of transfer (oriT) as measured by their abilities to mobilize chimeric oriT-containing plasmids. (C) 2002 Elsevier Science (USA). All rights reserved.
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页码:24 / 37
页数:14
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