ASD-GFP vectors for in vivo expression technology in Pseudomonas aeruginosa and other gram-negative bacteria

被引:15
作者
Handfield, M
Schweizer, HP
Mahan, MJ
Sanschagrin, F
Hoang, T
Levesque, RC
机构
[1] Univ Laval, Fac Med, St Foy, PQ G1K 7P4, Canada
[2] Colorado State Univ, Ft Collins, CO 80523 USA
[3] Univ Calif Santa Barbara, Santa Barbara, CA 93106 USA
关键词
D O I
10.2144/98242st02
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe the construction of promoter probe vectors designed for identification of bacterial genes induced in vitro and/or in vivo and for measurement of gene expression levels for in vivo expression technology These plasmids use the Pseudomonas aeruginosa aspartate beta-semialdehyde dehydrogenase (asd) gene as a selectable marker and beta-galactosidase (pIVPRO, 10.88 kb) or mutant green fluorescent protein with enhanced fluorescence properties (mut3GFP, pIVET-GFP, 5.48 kb) as reporter gene systems. The proposed strategies can be adapted for use in most Gram-negative bacteria.
引用
收藏
页码:261 / 264
页数:4
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