β-二羰基促进工程微生物的溴甲烷合成。

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2024-03-25 DOI:10.1021/acssynbio.4c00005
Thomas D. Loan, Claudia E. Vickers, Michael Ayliffe* and Ming Luo*, 
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引用次数: 0

摘要

反刍家畜产生的甲烷排放量约占全球人为甲烷排放量的 24%。动物瘤胃中的甲烷生成在很大程度上受到溴甲烷的抑制,而溴甲烷在天门冬属海藻中含量丰富。这促使人们开发基于拟南芥的家畜饲料添加剂,以减少甲烷排放,尽管仅靠这种方法不太可能满足全球需求。在这里,我们设计了一种非本地生物合成途径,以酵母作为替代生物源在体内生产溴甲烷,从而实现可持续、可扩展的发酵溴甲烷生产。研究发现,具有低 pKa 值的β-二羰基化合物是生产溴仿的必要底物,并能在表达依赖于钒酸盐的卤过氧化物酶基因的工程酵母中合成溴仿。除了为溴甲烷的大规模可持续生物生产提供了一条潜在途径外,这项工作还推动了新型卤化微生物生物合成途径的发展。
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β-Dicarbonyls Facilitate Engineered Microbial Bromoform Biosynthesis

Ruminant livestock produce around 24% of global anthropogenic methane emissions. Methanogenesis in the animal rumen is significantly inhibited by bromoform, which is abundant in seaweeds of the genus Asparagopsis. This has prompted the development of livestock feed additives based on Asparagopsis to mitigate methane emissions, although this approach alone is unlikely to satisfy global demand. Here we engineer a non-native biosynthesis pathway to produce bromoform in vivo with yeast as an alternative biological source that may enable sustainable, scalable production of bromoform by fermentation. β-dicarbonyl compounds with low pKa values were identified as essential substrates for bromoform production and enabled bromoform synthesis in engineered Saccharomyces cerevisiae expressing a vanadate-dependent haloperoxidase gene. In addition to providing a potential route to the sustainable biological production of bromoform at scale, this work advances the development of novel microbial biosynthetic pathways for halogenation.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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