Chatfield L K, Williams P A
J Bacteriol. 1986 Nov;168(2):878-85. doi: 10.1128/jb.168.2.878-885.1986.
Structural genes for catechol 2,3-oxygenase (C23O) were cloned from the TOL plasmids pWW5, pWW14, pWW74, pWW84, and pWW88 isolated from Pseudomonas strains of diverse geographical origins. Each pKT230-based C23O+ recombinant plasmid carried a 2.05-kilobase XhoI insert which showed strong homology in Southern hybridizations with the xylE gene from the archetype TOL plasmid pWW0. Fragments were mapped for restriction endonuclease sites and were classified into two closely related groups on the basis of restriction maps. C23O structural genes were located on cloned fragments by a combination of subcloning and site-specific mutagenesis. All five TOL plasmids examined yielded clones whose maps differed from that of xylE of pWW0 by only a single XbaI site, but in addition plasmids pWW5, pWW74, and pWW88 carried a second, homologous C23O gene with seven further restriction site differences. The remaining plasmids, pWW14 and pWW84, carried a second nonhomologous C23O gene related to the second C23O gene (C23OII) of TOL plasmid pWW15 described previously (H. Keil, M. R. Lebens, and P. A. Williams, J. Bacteriol. 163:248-255, 1985). Thus, each naturally occurring TOL plasmid in this study appears to carry genes for two meta cleavage dioxygenases.
从源自不同地理区域的假单胞菌菌株中分离得到的TOL质粒pWW5、pWW14、pWW74、pWW84和pWW88中克隆了儿茶酚2,3-双加氧酶(C23O)的结构基因。每个基于pKT230的C23O+重组质粒都携带一个2.05千碱基的XhoI插入片段,该片段在Southern杂交中与原型TOL质粒pWW0的xylE基因显示出很强的同源性。对片段进行了限制性内切酶位点图谱分析,并根据限制性图谱将其分为两个密切相关的组。通过亚克隆和位点特异性诱变相结合的方法,将C23O结构基因定位在克隆片段上。所检测的所有五个TOL质粒产生的克隆,其图谱与pWW0的xylE图谱相比,仅在一个XbaI位点上有所不同,但此外,质粒pWW5、pWW74和pWW88还携带第二个同源的C23O基因,另有七个限制性位点差异。其余的质粒pWW14和pWW84携带第二个与先前描述的TOL质粒pWW15的第二个C23O基因(C23OII)相关的非同源C23O基因(H. Keil、M. R. Lebens和P. A. Williams,《细菌学杂志》163:248 - 255,1985年)。因此,本研究中每个天然存在的TOL质粒似乎都携带两种间位裂解双加氧酶的基因。