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首页> 外文期刊>Applied and Environmental Microbiology >Biological synthesis of the analgesic hydromorphone, an intermediate in the metabolism of morphine, by Pseudomonas putida M10.
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Biological synthesis of the analgesic hydromorphone, an intermediate in the metabolism of morphine, by Pseudomonas putida M10.

机译:恶臭假单胞菌M10生物合成镇痛性氢吗啡酮,是吗啡代谢的中间体。

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摘要

The morphine alkaloid hydromorphone (dihydromorphinone) was identified as an intermediary metabolite in the degradation of morphine by Pseudomonas putida M10. A constitutive NADH-dependent morphinone reductase capable of catalyzing the reduction of the 7,8-unsaturated bond of morphinone and codeinone, yielding hydromorphone and hydrocodone, respectively, was shown to be present in cell extracts. The structures have been identified by 1H nuclear magnetic resonance and mass spectrometry. Morphinone reductase has been partially purified by anion-exchange and gel filtration chromatography. This enzyme has potential applications as a biocatalyst for the synthesis of the highly potent analgesic hydromorphone and the antitussive hydrocodone.
机译:吗啡生物碱氢吗啡酮(dihydromorphinone)被鉴定为恶臭假单胞菌M10降解吗啡的中间代谢物。结果表明,细胞提取物中存在一种能催化吗啡酮和可待因酮的7,8-不饱和键还原的组成型NADH依赖性吗啡酮还原酶,分别可产生氢吗啡酮和氢可酮。结构已通过1H核磁共振和质谱鉴定。吗啡酮还原酶已通过阴离子交换和凝胶过滤色谱法部分纯化。该酶作为生物催化剂用于合成高效止痛氢吗啡酮和镇咳氢可酮具有潜在的应用。

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