A SIMPLE AND EFFICIENT SYSTEM FOR THE CONSTRUCTION OF PHOA GENE FUSIONS IN GRAM-NEGATIVE BACTERIA

被引:4
作者
DUCHENE, AM [1 ]
PATTE, J [1 ]
GUTIERREZ, C [1 ]
CHANDLER, M [1 ]
机构
[1] CNRS,MOLEC GENET & MICROBIOL UNIT,118 ROUTE NARBONNE,F-31062 TOULOUSE,FRANCE
关键词
ENVELOPE PROTEINS; ALKALINE PHOSPHATASE; BETA-LACTAMASE; TRANSPOSON; PLASMID;
D O I
10.1016/0378-1119(92)90714-Z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have developed a two-plasmid system for generating gene fusions between phoA and cloned genes encoding envelope proteins. The vector plasmid carries a temperature-sensitive replication system and can be rescued at high temperature by insertion of an IS1-based transposon carrying the ori region of pBR322 and a phoA gene lacking transcription and translation initiation signals. The vector plasmid also carries the transfer origin of the conjugative plasmid, F, permitting transfer into a suitable recipient strain. We have used this system in the analysis of the bla gene cloned from pBR322.
引用
收藏
页码:103 / 107
页数:5
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