UIDA-ANTIBIOTIC-RESISTANCE CASSETTES FOR INSERTION MUTAGENESIS, GENE FUSIONS AND GENETIC CONSTRUCTIONS

被引:45
作者
BARDONNET, N
BLANCO, C
机构
[1] UNIV RENNES 1, GENET & PHYSIOL MICROBIENNES,CNRS,URA 256, CAMPUS BEAULIEU, F-35042 RENNES, FRANCE
[2] INST NATL SCI APPL, MICROBIOL LAB, F-69621 VILLEURBANNE, FRANCE
关键词
BETA-GLUCURONIDASE; REGULATION STUDIES; RECOMBINANT DNA; CASSETTE;
D O I
10.1111/j.1574-6968.1992.tb05105.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have constructed a series of promoter-probe cassettes that provides powerful tools for insertion mutagenesis, transcription fusions and genetic constructions. These cassettes contain the Tn9 chloramphenicol (Cm(R)) and the Tn903 kanamycin (Km(R)) resistance genes which are expressed in a large variety of microorganisms; these antibiotic-resistance markers were associated with the uidA promoterless gene. This beta-glucuronidase-encoding gene of Escherichia coli K-12 has been successfully used as reporter gene for various organisms including prokaryotes and eukaryotes. The resulting 'uidA-KM(R) and 'uidA-CM(R) cassettes (truncated at the ') can be excized with most of the commonly used restriction enzymes. Furthermore, they are borne by Ap(R) or CM(R) plasmids which facilitate their utilization. These promoter-probe cassettes allow transcriptional signal localization and regulation studies.
引用
收藏
页码:243 / 248
页数:6
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