利用重组可溶性甲烷单加氧酶和重组甲基辅酶 M 还原酶捕获甲烷。

IF 5.7 2区 生物学 Microbial Biotechnology Pub Date : 2024-08-19 DOI:10.1111/1751-7915.70000
Viviana Sanchez-Torres, Thomas K. Wood
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引用次数: 0

摘要

通过氧化捕获甲烷被认为是催化领域的 "圣杯 "之一(Tucci 和 Rosenzweig,2024 年)。甲烷也是一种主要温室气体,必须在 10 年内减少 12 亿吨,才能使全球升温降低 0.23°C (He 和 Lidstrom,2024 年);因此,需要采用新技术来降低大气中的甲烷含量。在自然界中,甲烷可被甲烷营养菌有氧捕获,也可被厌氧甲烷营养古细菌厌氧捕获;但厌氧过程占主导地位。在这里,我们描述了利用已克隆的具有捕获甲烷活性的两种非凡酶的历史和潜力:通过可溶性甲烷单加氧酶进行需氧捕获和通过甲基辅酶 M 还原酶进行厌氧捕获。我们认为,这两种酶可在解决目前的全球变暖危机方面发挥突出的、可持续的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Capturing methane with recombinant soluble methane monooxygenase and recombinant methyl-coenzyme M reductase

Methane capture via oxidation is considered one of the ‘Holy Grails’ of catalysis (Tucci and Rosenzweig, 2024). Methane is also a primary greenhouse gas that has to be reduced by 1.2 billion metric tonnes in 10 years to decrease global warming by only 0.23°C (He and Lidstrom, 2024); hence, new technologies are needed to reduce atmospheric methane levels. In Nature, methane is captured aerobically by methanotrophs and anaerobically by anaerobic methanotrophic archaea; however, the anaerobic process dominates. Here, we describe the history and potential of using the two remarkable enzymes that have been cloned with activity for capturing methane: aerobic capture via soluble methane monooxygenase and anaerobic capture via methyl-coenzyme M reductase. We suggest these two enzymes may play a prominent, sustainable role in addressing our current global warming crisis.

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来源期刊
Microbial Biotechnology
Microbial Biotechnology Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
11.20
自引率
3.50%
发文量
162
审稿时长
1 months
期刊介绍: Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes
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