Saint C P, McClure N C, Venables W A
School of Pure and Applied Biology, University of Wales College of Cardiff, UK.
J Gen Microbiol. 1990 Apr;136(4):615-25. doi: 10.1099/00221287-136-4-615.
A restriction endonuclease map was derived for the aromatic amine and m-toluate catabolic plasmid pTDN1 present in Pseudomonas putida UCC22, a derivative of P. putida mt-2. The plasmid is 79 +/- 1 kbp in size and can be divided into a restriction-site-deficient region of 51 +/- 1 kbp and a restriction-site-profuse region of 28 kbp which begins and ends with directly repeating sequences of at least 2 kbp in length. A mutant plasmid isolated after growth of the host on benzoate had lost the restriction-profuse region by a straightforward recombinational loss retaining one copy of the direct repeat. Analysis of clones, deletion and Tn5 insertion mutants strongly suggested that the meta-cleavage pathway of pTDN1 was situated in the region readily deleted. The catechol 2,3-dioxygenase (C23O) gene of pTDN1 showed no hybridization or restriction homology to previously described C23O genes of TOL plasmids pWW0 and pWW15. In addition, there was little homology between intact pTDN1, pWW0 and pWW15, suggesting the presence of a unique meta-cleavage pathway. We also demonstrated that pTDN1 did not originate from P. putida mt-2 chromosome.
推导了恶臭假单胞菌UCC22(恶臭假单胞菌mt-2的衍生物)中存在的芳香胺和间甲苯酸分解代谢质粒pTDN1的限制性内切酶图谱。该质粒大小为79±1kbp,可分为一个51±1kbp的限制性位点缺乏区和一个28kbp的限制性位点丰富区,该丰富区以至少2kbp长的直接重复序列开始和结束。宿主在苯甲酸上生长后分离出的一个突变质粒,通过直接重组缺失失去了限制性位点丰富区,保留了一份直接重复序列。对克隆、缺失和Tn5插入突变体的分析强烈表明,pTDN1的间位裂解途径位于容易缺失的区域。pTDN1的儿茶酚2,3-双加氧酶(C23O)基因与先前描述的TOL质粒pWW0和pWW15的C23O基因没有杂交或限制性同源性。此外,完整的pTDN1、pWW0和pWW15之间几乎没有同源性,表明存在独特的间位裂解途径。我们还证明pTDN1并非起源于恶臭假单胞菌mt-2染色体。