Pertsova R N, Baskunov B P, Golovleva L A
Mikrobiologiia. 1982 Mar-Apr;51(2):275-80.
The purpose of this work was to study the process of oxidation of aromatic acids (benzoic, salicylic and phenylacetic acids) produced as the result of DDT degradation by Pseudomonas aeruginosa 640x. The cultural broth was analysed by thin-layer chromatography, chromato-mass spectrometry and the enzymes of aromatic acid oxidation were investigated. Benzoate was shown to be oxidized via p-hydroxybenzoic acid, protocatechuic acid and its ortho degradation. Phenylacetate, the principal of DDT degradation, was hydroxylated by the culture with simultaneous migration of the two-carbon fragment and decomposition of the resultant homogentisic acid. Salicylic acid was not oxidized by the culture; it was accumulated in the medium. Analysis of the enzymes involved in the oxidation of the aromatic cycle has shown that the culture lacks salicylate hydroxylase, metapyrocatechase and gentisate 1,2-dioxygenase. Instead, it manifested the activities of the enzymes catalysing ortho cleavage of the cycle, namely, pyrocatechase and protocatechoate 3 : 4 dioxygenase, as well as homogentisate oxygenase.
这项工作的目的是研究铜绿假单胞菌640x降解滴滴涕所产生的芳香酸(苯甲酸、水杨酸和苯乙酸)的氧化过程。通过薄层色谱法、色谱-质谱分析法对培养液进行了分析,并对芳香酸氧化酶进行了研究。结果表明,苯甲酸通过对羟基苯甲酸、原儿茶酸及其邻位降解途径被氧化。滴滴涕降解的主要产物苯乙酸被该培养物羟基化,同时两个碳原子片段发生迁移,生成的尿黑酸分解。水杨酸未被该培养物氧化,而是在培养基中积累。对参与芳香环氧化的酶的分析表明,该培养物缺乏水杨酸羟化酶、间原儿茶酸酶和尿黑酸1,2-双加氧酶。相反,它表现出催化该环邻位裂解的酶的活性,即原儿茶酸酶和原儿茶酸3:4双加氧酶,以及尿黑酸加氧酶。