Reineke W, Knackmuss H J
J Bacteriol. 1980 May;142(2):467-73. doi: 10.1128/jb.142.2.467-473.1980.
Derivatives of Pseudomonas sp. B13 which had acquired the capability to utilize 4-chloro- and 3,5-dichlorobenzoate as a consequence of the introduction of genes of the TOL plasmid of Pseudomonas putida mt-2 were studied. The utilization of these substrates, a property not shared by the parent strains, was shown to depend upon the combined activities of enzymes from the donor and from the recipient. During growth on 3-chloro-, 4-chloro-, and 3,5-dichlorobenzoate, predominantly the toluate 1,2-deoxygenase and both dihydrodihydroxybenzoate dehydrogenases of the parent strains were induced. On the other hand, no catechol 2,3-dioxygenase from P. putida mt-2 was detectable, so that degradation of chlorocatechols by the nonproductive meta-cleavage pathway was avoided. Instead of that, chlorocatechols were subject to ortho cleavage and totally degraded by the preexisting enzymes of Pseudomonas sp. B13.
研究了恶臭假单胞菌mt-2的TOL质粒基因导入后获得利用4-氯苯甲酸和3,5-二氯苯甲酸能力的假单胞菌B13的衍生物。这些底物的利用(这是亲本菌株所没有的特性)被证明取决于供体和受体酶的联合活性。在以3-氯苯甲酸、4-氯苯甲酸和3,5-二氯苯甲酸为碳源生长期间,主要诱导了亲本菌株的甲苯酸1,2-双加氧酶和两种二氢二羟基苯甲酸脱氢酶。另一方面,未检测到来自恶臭假单胞菌mt-2的儿茶酚2,3-双加氧酶,因此避免了通过非生产性间位裂解途径降解氯代儿茶酚。取而代之的是,氯代儿茶酚通过假单胞菌B13预先存在的酶进行邻位裂解并完全降解。