CLONING, SEQUENCING, AND OVEREXPRESSION OF GENE-16 OF SALMONELLA BACTERIOPHAGE-P22

被引:10
作者
UMLAUF, B [1 ]
DREISEIKELMANN, B [1 ]
机构
[1] UNIV BIELEFELD,FAK BIOL,LEHRSTUHL GENTECHNOL MIKROBIOL,POSTFACH 8640,W-4800 BIELEFELD,GERMANY
关键词
D O I
10.1016/0042-6822(92)90503-H
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It has been suggested that gene product 16 of bacteriophage P22 forms a pore for DNA transfer and/or that it functions as a pilot protein guiding the DNA across the membrane. We have cloned gene 16 and determined the nucleotide sequence. Within the sequenced region there is an open reading frame that could encode a protein of 609 amino acids having a molecular weight of 64,366. The hydropathic plot of this protein does not reveal putative membrane-spanning regions as expected for a protein forming a membrane pore. Overproduction of gene product 16 in Escherichia coli was successful only in a mutant in which the La protease was inactivated. Gene 16 mutants of phage P22 were not able to infect recBCD mutants of Salmonella typhimurium nor was protein 16, synthesized in E. coli from a plasmid, able to substitute for the pilot protein of phage T4. It seems that gene product 16 is not a pilot protein in the meaning of binding to the ends of linear DNA, thus protecting it from degradation by nucleases. © 1992.
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页码:495 / 501
页数:7
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