首页> 美国卫生研究院文献>Journal of Bacteriology >Bacterial Degradation of tert-Amyl Alcohol Proceeds via Hemiterpene 2-Methyl-3-Buten-2-ol by Employing the Tertiary Alcohol Desaturase Function of the Rieske Nonheme Mononuclear Iron Oxygenase MdpJ
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Bacterial Degradation of tert-Amyl Alcohol Proceeds via Hemiterpene 2-Methyl-3-Buten-2-ol by Employing the Tertiary Alcohol Desaturase Function of the Rieske Nonheme Mononuclear Iron Oxygenase MdpJ

机译:利用Rieske非血红素单核氧合酶MdpJ的叔醇去饱和酶功能,通过半萜烯2-甲基-3-丁烯-2-醇对半戊醇进行细菌降解

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摘要

Tertiary alcohols, such as tert-butyl alcohol (TBA) and tert-amyl alcohol (TAA) and higher homologues, are only slowly degraded microbially. The conversion of TBA seems to proceed via hydroxylation to 2-methylpropan-1,2-diol, which is further oxidized to 2-hydroxyisobutyric acid. By analogy, a branched pathway is expected for the degradation of TAA, as this molecule possesses several potential hydroxylation sites. In Aquincola tertiaricarbonis L108 and Methylibium petroleiphilum PM1, a likely candidate catalyst for hydroxylations is the putative tertiary alcohol monooxygenase MdpJ. However, by comparing metabolite accumulations in wild-type strains of L108 and PM1 and in two mdpJ knockout mutants of strain L108, we could clearly show that MdpJ is not hydroxylating TAA to diols but functions as a desaturase, resulting in the formation of the hemiterpene 2-methyl-3-buten-2-ol. The latter is further processed via the hemiterpenes prenol, prenal, and 3-methylcrotonic acid. Likewise, 3-methyl-3-pentanol is degraded via 3-methyl-1-penten-3-ol. Wild-type strain L108 and mdpJ knockout mutants formed isoamylene and isoprene from TAA and 2-methyl-3-buten-2-ol, respectively. It is likely that this dehydratase activity is catalyzed by a not-yet-characterized enzyme postulated for the isomerization of 2-methyl-3-buten-2-ol and prenol. The vitamin requirements of strain L108 growing on TAA and the occurrence of 3-methylcrotonic acid as a metabolite indicate that TAA and hemiterpene degradation are linked with the catabolic route of the amino acid leucine, including an involvement of the biotin-dependent 3-methylcrotonyl coenzyme A (3-methylcrotonyl-CoA) carboxylase LiuBD. Evolutionary aspects of favored desaturase versus hydroxylation pathways for TAA conversion and the possible role of MdpJ in the degradation of higher tertiary alcohols are discussed.
机译:叔醇,例如叔丁醇(TBA)和叔戊醇(TAA)和更高的同系物,只能通过微生物缓慢降解。 TBA的转化似乎是通过羟基化反应进行的,转化为2-甲基丙烷-1,2-二醇,然后被进一步氧化为2-羟基异丁酸。以此类推,由于该分子具有数个潜在的羟基化位点,因此预期会出现分支途径降解TAA。在Aquincola tertiaricarbonis L108和石油甲基乙霉菌PM1中,可能的羟基化候选催化剂是推定的叔醇单加氧酶MdpJ。但是,通过比较野生型L108和PM1菌株以及两个L108菌株的mdpJ敲除突变体中代谢产物的积累,我们可以清楚地表明MdpJ不会将TAA羟基化为二醇,而是起去饱和酶的作用,从而导致半萜烯的形成。 2-甲基-3-丁烯-2-醇。后者通过半萜烯醇,前体醇和3-甲基巴豆酸进一步加工。同样,3-甲基-3-戊醇通过3-甲基-1-戊烯-3-醇降解。野生型菌株L108和mdpJ敲除突变体分别由TAA和2-甲基-3-丁烯-2-醇形成异戊烯和异戊二烯。该脱水酶活性很可能被推测为2-甲基-3-丁烯-2-醇和泼尼醇的异构化的尚未表征的酶催化。在TAA上生长的L108菌株对维生素的需求以及3-甲基巴豆酸作为代谢产物的出现表明TAA和半萜烯的降解与氨基酸亮氨酸的分解代谢途径有关,包括涉及生物素依赖性的3-甲基巴豆酰基辅酶(3-甲基巴豆酰基-CoA)羧化酶LiuBD。讨论了有利于去饱和酶与羟基化途径进行TAA转化的进化方面,以及MdpJ在高级叔醇降解中的可能作用。

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