Robertson J B, Spain J C, Haddock J D, Gibson D T
Air Force Civil Engineering Support Agency, Tyndall Air Force Base, Florida 32403.
Appl Environ Microbiol. 1992 Aug;58(8):2643-8. doi: 10.1128/aem.58.8.2643-2648.1992.
Pseudomonas putida F1 and Pseudomonas sp. strain JS150 initiate toluene degradation by incorporating molecular oxygen into the aromatic nucleus to form cis-1,2-dihydroxy-3-methylcyclohexa-3,5-diene. When toluene-grown cells were incubated with 2- and 3-nitrotoluene, the major products identified were 2- and 3-nitrobenzyl alcohol, respectively. The same cells oxidized 4-nitrotoluene to 2-methyl-5-nitrophenol and 3-methyl-6-nitrocatechol. Escherichia coli JM109(pDTG601), which contains the toluene dioxygenase genes from P. putida F1 under the control of the tac promoter, oxidized the isomeric nitrotoluenes to the same metabolites as those formed by P. putida F1 and Pseudomonas sp. strain JS150. These results extend the range of substrates known to be oxidized by this versatile enzyme and demonstrate for the first time that toluene dioxygenase can oxidize an aromatic methyl substituent.
恶臭假单胞菌F1和假单胞菌属菌株JS150通过将分子氧掺入芳香核中以形成顺式-1,2-二羟基-3-甲基环己-3,5-二烯来启动甲苯降解。当用2-和3-硝基甲苯培养以甲苯为生长底物的细胞时,鉴定出的主要产物分别是2-和3-硝基苄醇。相同的细胞将4-硝基甲苯氧化为2-甲基-5-硝基苯酚和3-甲基-6-硝基儿茶酚。大肠杆菌JM109(pDTG601)含有受tac启动子控制的来自恶臭假单胞菌F1的甲苯双加氧酶基因,它将异构体硝基甲苯氧化为与恶臭假单胞菌F1和假单胞菌属菌株JS150形成的相同代谢物。这些结果扩展了已知可被这种多功能酶氧化的底物范围,并首次证明甲苯双加氧酶可以氧化芳香甲基取代基。