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A Third Transposable Element ISPpu12 from the Toluene-Xylene Catabolic Plasmid pWW0 of Pseudomonas putida mt-2

机译:来自恶臭假单胞菌mt-2的甲苯-二甲苯分解代谢质粒pWW0的第三个转座因子ISPpu12

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摘要

A 3,372-bp insertion sequence, ISPpu12, has been identified on the archetypal toluene-xylene TOL catabolic plasmid pWW0 from Pseudomonas putida mt-2. The insertion sequence element is located on the plasmid between bases 84397 and 87768 in a region which also contains the termini and transposase genes of the catabolic transposons Tn4651 and Tn4653 (A. Greated, L. Lambertson, P. A. Williams, and C. M. Thomas, Environ. Microbiol., in press). ISPpu12 has terminal inverted repeats of 24 bp with three mismatches and contains four open reading frames, a tnpA homologue and three open reading frames (lspA, orf1, and orf2) of undetermined function. After insertion in vitro of a Kmr cassette into ISPpu12 either in the intergenic region between orf1 and orf2 or directly into the orf1 gene and ligation into a suicide vector, the modified ISPpu12-Km transposes at high frequency, often in multiple copies, into the chromosome of a P. putida recipient. Inactivation of lspA, orf1, and orf2 by introducing a 7-bp deletion into the 5′ region of each gene had no major effect upon transposition, but a similar mutation of tnpA completely eliminated transposition. Analysis of the literature and of strains derived from the chlorobenzoate-degrading Pseudomonas sp. strain B13 suggests that the promiscuity of this element has played an important role in the history of plasmid pWW0. Database comparisons and the accompanying paper (A. J. Weightman, A. W. Topping, K. E. Hill, L. L. Lee, K. Sakai, J. H. Slater, and A. W. Thomas, J. Bacteriol. 184:6581-6591, 2002) show that ISPpu12 is a transposable element also found in other bacteria.
机译:在来自恶臭假单胞菌mt-2的原型甲苯-二甲苯TOL分解代谢质粒pWW0上已鉴定出3,372-bp的插入序列ISPpu12。插入序列元件位于质粒中84397和87768之间的区域中,该区域也包含分解代谢转座子Tn4651和Tn4653的末端和转座酶基因(A.Greated,L.Lambertson,PA Williams和CM Thomas,Environ。微生物,印刷中)。 ISPpu12具有24 bp的末端反向重复序列,具有三个错配,并包含四个开放阅读框,一个tnpA同源物和三个功能不确定的开放阅读框(lspA,orf1和orf2)。在体外将Km r 盒插入orf1和orf2之间的基因间区域中的ISPpu12中或直接插入orf1基因中并连接到自杀载体中后,修饰的ISPpu12-Km高频转座,通常多份复制到恶臭假单胞菌受体的染色体中。通过在每个基因的5'区域引入7 bp的缺失使lspA, orf1 orf2 失活,对转座没有重大影响,但是与< em> tnpA 完全消除了转座。降解氯苯甲酸假单胞菌 sp的文献和菌株分析。菌株B13表明该元件的混杂在质粒pWW0的历史中起了重要作用。数据库比较和随附的论文(AJ Weightman,AW Topping,KE Hill,LL Lee,K.Sakai,JH Slater和AW Thomas,J.Bacteriol。184:6581-6591,2002)表明IS Ppu12 < / em>是在其他细菌中也发现的转座因子。

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