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探索细菌拮抗剂和嗜盐球菌属ATCC 8456中的1-烯烃生物合成。

Exploring 1-alkene biosynthesis in bacterial antagonists and Jeotgalicoccus sp. ATCC 8456.

作者信息

Schweitzer Matthias, Friedrich Andrea Marianne, Dennig Alexander, Berg Gabriele, Müller Bogotá Christina Andrea

机构信息

Institute of Environmental Biotechnology, Graz University of Technology, Petersgasse 12/I, 8010 Graz, Austria.

Institute of Biotechnology and Biochemical Engineering, Graz University of Technology, Petersgasse 12/I, 8010 Graz, Austria.

出版信息

FEMS Microbiol Lett. 2025 Jan 10;372. doi: 10.1093/femsle/fnaf004.

DOI:10.1093/femsle/fnaf004
PMID:39805715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11776017/
Abstract

Terminal olefins are important platform chemicals, drop-in compatible hydrocarbons and also play an important role as biocontrol agents of plant pathogens. Currently, 1-alkenes are derived from petroleum, although microbial biosynthetic routes are known. Jeotgalicoccus sp. ATCC 8456 produces 1-alkenes via the fatty acid decarboxylase OleTJE. UndA and UndB are recently identified non-heme iron oxidases converting medium-chain fatty acids into terminal alkenes. Our knowledge about the diversity and natural function of OleTJE, UndA, and UndB homologs is scarce. We applied a combined screening strategy-solid-phase microextraction coupled with gas chromatography-mass spectrometry (SPME GC-MS) and polymerase chain reaction (PCR)-based amplification-to survey an environmental strain collection for microbial 1-alkene producers and their corresponding enzymes. Our results reinforce the high level of conservation of UndA and UndB genes across the genus Pseudomonas. In vivo production of defined 1-alkenes (C9-C13; C15; C19) was directed by targeted feeding of fatty acids. Lauric acid feeding enabled 1-undecene production to a concentration of 3.05 mg l-1 in Jeotgalicoccus sp. ATCC 8456 and enhanced its production by 105% in Pseudomonas putida 1T1 (1.10 mg l-1). Besides, whole genome sequencing of Jeotgalicoccus sp. ATCC 8456 enabled reconstruction of the 1-alkene biosynthetic pathway. These results advance our understanding of microbial 1-alkene synthesis and the underlying genetic basis.

摘要

末端烯烃是重要的平台化学品、可直接替代的碳氢化合物,并且在作为植物病原体的生物防治剂方面也发挥着重要作用。目前,1-烯烃来源于石油,尽管已知微生物生物合成途径。嗜盐放线菌属菌株ATCC 8456通过脂肪酸脱羧酶OleTJE产生1-烯烃。UndA和UndB是最近鉴定出的非血红素铁氧化酶,可将中链脂肪酸转化为末端烯烃。我们对OleTJE、UndA和UndB同源物的多样性和天然功能的了解很少。我们应用了一种联合筛选策略——固相微萃取结合气相色谱-质谱联用(SPME GC-MS)和基于聚合酶链反应(PCR)的扩增——来调查一组环境菌株,以寻找微生物1-烯烃生产者及其相应的酶。我们的结果强化了假单胞菌属中UndA和UndB基因的高度保守性。通过有针对性地投喂脂肪酸,可定向体内合成特定的1-烯烃(C9-C13;C15;C19)。投喂月桂酸可使嗜盐放线菌属菌株ATCC 8456中1-十一碳烯的产量达到3.05 mg l-1,并使恶臭假单胞菌1T1中的产量提高105%(达到1.10 mg l-1)。此外,嗜盐放线菌属菌株ATCC 8456的全基因组测序使得1-烯烃生物合成途径得以重建。这些结果推进了我们对微生物1-烯烃合成及其潜在遗传基础的理解。

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