Harayama S, Rekik M, Wasserfallen A, Bairoch A
Department of Medical Biochemistry, University Medical Center, University of Geneva, Switzerland.
Mol Gen Genet. 1987 Dec;210(2):241-7. doi: 10.1007/BF00325689.
TOL plasmid pWW0 and plasmid NAH7 encode catabolic enzymes required for oxidative degradation of toluene and naphthalene, respectively. The gene order of the catabolic operon of NAH7 for salicylate oxidation was determined to be: promoter--nahG (the structural gene for salicylate hydroxylase)--nahH (catechol 2.3-dioxygenase)--nahI (hydroxymuconic semialdehyde dehydrogenase)--nahN (hydroxymuconic semialdehyde hydrolase)--nahL (2-oxopent-4-enoate hydratase). This order is identical to that of the isofunctional genes of TOL plasmid pWW0. The complete nucleotide sequence of nahH was determined and compared with that of xylE, the isofunctional gene of TOL plasmid pWW0. There were 20% and 16% differences in their nucleotide and amino acid sequences, respectively. The homology between the NAH7 and TOL pWW0 plasmids ends upstream of the Shine-Dalgarno sequences of nahH and xylE, but the homology continues downstream of these genes. This observation suggested that genes for the catechol oxidative enzymes of NAH7 and TOL pWW0 were derived from a common ancestral sequence which was transferred as a discrete segment of DNA between plasmids.
TOL质粒pWW0和质粒NAH7分别编码甲苯和萘氧化降解所需的分解代谢酶。已确定NAH7水杨酸氧化分解代谢操纵子的基因顺序为:启动子--nahG(水杨酸羟化酶的结构基因)--nahH(儿茶酚2,3-双加氧酶)--nahI(羟粘康酸半醛脱氢酶)--nahN(羟粘康酸半醛水解酶)--nahL(2-氧代戊-4-烯酸水合酶)。这个顺序与TOL质粒pWW0的同功能基因的顺序相同。测定了nahH的完整核苷酸序列,并与TOL质粒pWW0的同功能基因xylE的核苷酸序列进行了比较。它们的核苷酸序列和氨基酸序列分别有20%和16%的差异。NAH7和TOL pWW0质粒之间的同源性在nahH和xylE的Shine-Dalgarno序列上游终止,但在这些基因的下游同源性仍在继续。这一观察结果表明NAH7和TOL pWW0的儿茶酚氧化酶基因源自一个共同的祖先序列,该序列作为一段离散的DNA片段在质粒之间转移。