首页> 美国卫生研究院文献>Biochemical Journal >Microbial degradation of alkylbenzenesulphonates. Metabolism of homologues of short alkyl-chain length by an Alcaligenes sp
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Microbial degradation of alkylbenzenesulphonates. Metabolism of homologues of short alkyl-chain length by an Alcaligenes sp

机译:微生物降解烷基苯磺酸盐。 Alcaligenes sp代谢短链烷基链的同系物

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摘要

1. An organism isolated from sewage and identified as an Alcaligenes sp. utilized benzenesulphonate, toluene-p-sulphonate or phenylethane-p-sulphonate as sole source of carbon and energy for growth. Higher alkylbenzenesulphonate homologues and the hydrocarbons, benzene, toluene, phenylethane and 1-phenyldodecane were not utilized. 2. 2-Phenylpropanesulphonate was metabolized to 4-isopropylcatechol. 3. 1-Phenylpropanesulphonate was metabolized to an ortho-diol, which was tentatively identified, in the absence of an authentic specimen, as 4-n-propylcatechol. 4. In the presence of 4-isopropylcatechol, which inhibited catechol 2,3-dioxygenase, 4-ethylcatechol accumulated in cultures growing on phenylethane-p-sulphonate. 5. Authentic samples of catechol, 3-methylcatechol, 4-methylcatechol, 4-ethylcatechol and 3-isopropylcatechol were oxidized by heat-treated extracts to the corresponding 2-hydroxyalkylmuconic semialdehydes. Ring cleavage occurred between C-2 and C-3. 6. The catechol derived from 1-phenylpropanesulphonate was oxygenated by catechol 2,3-dioxygenase to a compound with all the properties of a 2-hydroxyalkylmuconic semialdehyde, but it was not rigorously identified. 7. The catechol 2,3-dioxygenase induced by growth on benzenesulphonate, toluene-p-sulphonate or phenylethane-p-sulphonate showed a constant ratio of specific activities with catechol, 3-methylcatechol, 4-methylcatechol and 4-ethylcatechol that was independent of the growth substrate. At 60°C, activity towards these substrates declined at an identical first-order rate. 8. Enzymes of the `ortho' pathway of catechol metabolism were present in small amounts in cells grown on benzenesulphonate, toluene-p-sulphonate or phenylethane-p-sulphonate. 9. The catechol 1,2-dioxygenase oxidized the alkylcatechols, but the rates and the total extents of oxidation were less than for catechol itself. The oxidation products of these alkylcatechols were not further metabolized.
机译:1.从污水中分离出来并被鉴定为产碱菌的一种生物。利用苯磺酸盐,甲苯对磺酸盐或苯乙烷对磺酸盐作为唯一的碳和能源增长来源。没有使用高级烷基苯磺酸盐的同系物,没有使用烃,苯,甲苯,苯乙烷和1-苯基十二烷。 2. 2-苯基丙磺酸酯代谢为4-异丙基邻苯二酚。 3. 1-苯基丙磺酸酯代谢为邻二醇,在没有真实标本的情况下,初步鉴定为4-正丙基邻苯二酚。 4.在抑制异丙基苯酚2,3-二加氧酶的4-异丙基邻苯二酚存在下,4-乙基邻苯二酚在苯乙烷-对磺酸酯上生长的培养物中积累。 5.通过热处理的提取物将邻苯二酚,3-甲基邻苯二酚,4-甲基邻苯二酚,4-乙基邻苯二酚和3-异丙基邻苯二酚的真实样品氧化为相应的2-羟基烷基粘康半醛。在C-2和C-3之间发生环断裂。 6.将衍生自1-苯基丙烷磺酸盐的邻苯二酚用邻苯二酚2,3-二加氧酶氧化成具有2-羟基烷基粘康半醛的所有性质的化合物,但未对其进行严格鉴定。 7.由苯磺酸盐,甲苯-对磺酸盐或苯乙烷-对磺酸盐的生长诱导的儿茶酚2,3-二加氧酶与儿茶酚,3-甲基邻苯二酚,4-甲基邻苯二酚和4-乙基邻苯二酚的比活性恒定比是独立的生长底物。在60°C下,对这些底物的活性以相同的一级速率下降。 8.苯磺酸盐,甲苯-对-磺酸盐或苯乙烷-对-磺酸盐上生长的细胞中少量存在儿茶酚代谢“邻位”途径的酶。 9.邻苯二酚1,2-二加氧酶氧化了烷基邻苯二酚,但氧化速率和总氧化程度低于邻苯二酚本身。这些烷基邻苯二酚的氧化产物不再被代谢。

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