Chaudhry G R, Huang G H
Institute of Food and Agricultural Sciences, University of Florida, Gainesville 32611.
J Bacteriol. 1988 Sep;170(9):3897-902. doi: 10.1128/jb.170.9.3897-3902.1988.
A Flavobacterium sp. (strain 50001), capable of degrading 2,4-dichlorophenoxyacetate (2,4-D), 2-methyl-4-chlorophenoxyacetate, and 2-chlorobenzoate and imparting resistance to mercury, harbored a degradative plasmid, pRC10. Cured strains of the Flavobacterium sp. lost the plasmid as well as the ability to degrade these chlorinated compounds. Comparison of this plasmid with the well-characterized 2,4-D-degradative plasmid pJP4 from Alcaligenes eutrophus showed regions of homology between the two plasmids. Restriction fragments of plasmid pRC10 which shared homology with the regions conferring 2,4-D-degradative genes (tfd) of plasmid pJP4 were cloned into a broad-host-range plasmid and studied in Pseudomonas putida. From the results obtained, the cloned DNA fragment expressed the genes for 2,4-D monooxygenase (tfdA) and 2,4-dichlorophenol hydroxylase (tfdB). In spite of the similarity in function, the size (45 kilobases) and restriction pattern of plasmid pRC10 were considerably different from those of pJP4 (80 kilobases). This may be due to the difference in the microbial background during evolution of the two plasmids.
一种能够降解2,4-二氯苯氧乙酸(2,4-D)、2-甲基-4-氯苯氧乙酸和2-氯苯甲酸并赋予汞抗性的黄杆菌属菌株(菌株50001),携带一种降解性质粒pRC10。黄杆菌属的治愈菌株失去了该质粒以及降解这些氯化化合物的能力。将该质粒与来自嗜碱产碱杆菌的特征明确的2,4-D降解性质粒pJP4进行比较,发现这两种质粒之间存在同源区域。将与质粒pJP4中赋予2,4-D降解基因(tfd)的区域具有同源性的质粒pRC10的限制性片段克隆到一个广宿主范围质粒中,并在恶臭假单胞菌中进行研究。从获得的结果来看,克隆的DNA片段表达了2,4-D单加氧酶(tfdA)和2,4-二氯苯酚羟化酶(tfdB)的基因。尽管功能相似,但质粒pRC10的大小(45千碱基)和限制性图谱与pJP4(80千碱基)有很大不同。这可能是由于这两种质粒在进化过程中微生物背景的差异所致。