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灰色链霉菌:一种具有 N-加氧酶活性的新型生物催化剂。

Streptomyces griseus: A new biocatalyst with N-oxygenase activity.

机构信息

Universidad Nacional de Quilmes, CONICET, Departamento de Ciencia y Tecnología, LBB, Roque Sáenz Peña 352, Quilmes, 1876, Argentina.

Universidad Nacional de Quilmes, CONICET, Departamento de Ciencia y Tecnología, LBB, Roque Sáenz Peña 352, Quilmes, 1876, Argentina.

出版信息

J Biotechnol. 2021 Feb 10;327:36-42. doi: 10.1016/j.jbiotec.2020.12.008. Epub 2020 Dec 26.

DOI:10.1016/j.jbiotec.2020.12.008
PMID:33373628
Abstract

Aromatic nitro compounds are key building blocks for many industrial syntheses and are also components of explosives, drugs and pesticides. Due to the environmentally unfriendly experimental conditions involved in their chemical syntheses, industrial processes would benefit from the use of biocatalysts. Among potentially useful enzymes, N-oxygenases, whose role is to oxygenate primary amines, are becoming relevant. These enzymes are involved in different secondary metabolic pathways in Streptomyces and in few other bacteria, forming part of the enzyme pools implicated in antibiotic synthesis. In this work, a group of Streptomyces strains, whose biomass was obtained from simple and novel culture media, were identified as new sources of N-oxygenase activity. Furthermore, the use of unspecific metabolic stimulation strategies allowed substantial improvements in the activity of whole cells as biocatalysts. It is remarkable the 6 to 50-fold increase in nitro compound yields compared to the biotransformation under standard conditions when Streptomyces griseus was the biocatalyst. In addition, biocatalyst substrate acceptance was studied in order to determine the biocatalytic potential of this enzyme.

摘要

芳香族硝基化合物是许多工业合成的关键构建块,也是爆炸物、药物和农药的组成部分。由于其化学合成涉及到对环境不友好的实验条件,因此工业过程将受益于生物催化剂的使用。在潜在有用的酶中,N-加氧酶的作用是氧化伯胺,它变得越来越重要。这些酶参与链霉菌和少数其他细菌中的不同次级代谢途径,构成了参与抗生素合成的酶库的一部分。在这项工作中,一组从简单新颖的培养基中获得生物质的链霉菌菌株被鉴定为 N-加氧酶活性的新来源。此外,使用非特异性代谢刺激策略可以显著提高作为生物催化剂的全细胞的活性。与标准条件下使用灰色链霉菌作为生物催化剂相比,硝基化合物产率提高了 6 到 50 倍,这是值得注意的。此外,还研究了生物催化剂的底物接受能力,以确定该酶的生物催化潜力。

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