Autor: |
Xiong G; Institut für Pharmakologie und Toxikologie, Justus-Liebig-Universität Giessen, Germany., Oepen P, Geiben R, el-Idrissi AH, Lutz F |
Jazyk: |
angličtina |
Zdroj: |
Virus research [Virus Res] 1996 Mar; Vol. 41 (1), pp. 77-87. |
DOI: |
10.1016/0168-1702(95)01279-6 |
Abstrakt: |
In bacteriophage phi CTX, the cohesive end sequences cos, the integrase gene int, the attachment site attP (the target site for int) and the gene ctx encoding a pore-forming cytotoxin CTX, are clustered. Phi CTX can infect some Pseudomonas aeruginosa strains with a subsequent induction of CTX expression. The 41 and 477 bp fragments containing cos ends of phi CTX DNA were cloned into the high copy number plasmid pHA10. After pretransformation with the cos ends containing plasmids, plaque formation of phi CTX and cytotoxin production in phi CTX-infected Pseudomonas aeruginosa cells decreased by 100- and 10-fold respectively. Twelve hours after phi CTX infection proteins binding with cooperativity to cos sequence containing cleavable ends and the 10 bp flanking sequences were detected by gel electrophoretic mobility retardation of [32P]cos DNA. The results suggest that the cos binding proteins of phi CTX are involved in phi CTX replication. |
Databáze: |
MEDLINE |
Externí odkaz: |
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