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辅酶 F430 生物合成酶和中间产物的制备。

Preparation of coenzyme F430 biosynthetic enzymes and intermediates.

机构信息

Department of Chemistry and Biochemistry, Auburn University, Auburn, AL, United States.

Department of Chemistry and Biochemistry, Auburn University, Auburn, AL, United States.

出版信息

Methods Enzymol. 2024;702:147-170. doi: 10.1016/bs.mie.2024.06.008. Epub 2024 Jul 20.

Abstract

Methyl-coenzyme M reductase (MCR) is the key enzyme in pathways for the formation and anaerobic oxidation of methane. As methane is a potent greenhouse gas and biofuel, investigations of MCR catalysis and maturation are of interest for the development of both methanogenesis inhibitors and natural gas conversion strategies. The activity of MCR is dependent on a unique, nickel-containing coenzyme F430, the most highly reduced tetrapyrrole found in nature. Coenzyme F430 is biosynthesized from sirohydrochlorin in four steps catalyzed by the CfbABCDE enzymes. Here, methods for the expression and purification of the coenzyme F430 biosynthesis enzymes are described along with conditions for the synthesis and purification of biosynthetic intermediates on the milligram scale from commercially available porphobilinogen.

摘要

甲基辅酶 M 还原酶(MCR)是甲烷形成和厌氧氧化途径中的关键酶。由于甲烷是一种强效温室气体和生物燃料,因此对 MCR 催化和成熟的研究对于开发甲烷生成抑制剂和天然气转化策略都具有重要意义。MCR 的活性依赖于一种独特的含镍辅酶 F430,它是自然界中发现的还原程度最高的四吡咯。辅酶 F430 由 CfbABCDE 酶催化,经过四个步骤从硅烷氯化氢中生物合成。本文描述了辅酶 F430 生物合成酶的表达和纯化方法,以及在商业可得的卟胆原的毫克级规模上合成和纯化生物合成中间体的条件。

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