Construction and application of a promoter-trapping vector with methyl parathion hydrolase gene mpd as the reporter

被引:19
作者
Cui, ZL [1 ]
Zhang, XZ [1 ]
Zhang, ZH [1 ]
Li, SP [1 ]
机构
[1] Nanjing Agr Univ, Dept Microbiol, MOA Key Lab Microbiol Engn Agr Environm, Nanjing 210095, Peoples R China
关键词
Bacillus subtilis; gene expression; genomic promoter library; methyl parathion hydrolase; promoter-trapping vector;
D O I
10.1023/B:BILE.0000035481.03854.41
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A facilitative and efficient promoter-trapping vector, pUC-mpd, was constructed with the promoterless methyl parathion hydrolase gene as the reporter. This reporter gene is easily used to clone promoters with different promoting strength on selective plates. Promoter regions of the ytkA and ywoF genes with strong promoting and signal peptide functions were cloned from the Bacillus subtilis 168 genomic promoter library with this vector.
引用
收藏
页码:1115 / 1118
页数:4
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