NOVEL PLASMID VECTORS FOR GENE CLONING IN PSEUDOMONAS

被引:10
作者
ITOH, N [1 ]
KOIDE, Y [1 ]
FUKUZAWA, H [1 ]
HIROSE, S [1 ]
INUKAI, T [1 ]
机构
[1] AMANO PHARMACEUT CO LTD, RES LAB, NISHIKASUGAI, AICHI 481, JAPAN
关键词
D O I
10.1093/oxfordjournals.jbchem.a123629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Novel host-vector systems have been developed for gene cloning in the metabolically versatile bacterial genus Pseudomonas. We found that a new Pseudomonas strain, Pseudomonas flavida IF-4, isolated from soil, carried two small cryptic plasmids, named pNI10 and pNI20. They were multi-copy, but not self-transmissible, and the genome size was 3.7 kb for pNI10 and 2.9 kb for pNI20. Several types of cloning vectors containing a kanamycin or streptomycin resistance (Km(r) or Sm(r)) gene were constructed from pNI10 and pNI20. These plasmid vectors were efficiently transformed into several strains of Pseudomonas at a frequency up to 4 x 10(5) transformants per 1-mu-g plasmid DNA by the usual competent cell method. The vectors derived from pNI10 replicated not only in Pseudomonas but also in some other Gram-negative enteric bacteria such as Escherichia coli, Enterobacter aerogenes, and Proteus mirabilis.
引用
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页码:614 / 621
页数:8
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