NTF2-Like Enzymes as Versatile Biocatalysts in Fungal Natural Product Biosynthesis

IF 3.9 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2024-10-22 DOI:10.1002/cctc.202401495
Dr. Yanqin Li, Prof. Junfeng Wang, Prof. Yan Yan
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Abstract

Fungal natural products (NPs), known for their potent bioactivities, can be utilized as human therapeutics and agrochemicals. These bioactive and structurally complex compounds are biosynthesized through condensation of monomeric building blocks to construct core scaffolds, followed by various modification steps. Recent studies have revealed that a unique class of enzymes from the NTF2-like protein family plays important roles in the biosynthesis of complex fungal NPs. These NTF2-like enzymes belong to a large group of related proteins that share a common fold with nuclear transport factor 2, and are capable of catalyzing various reactions. In this study, we summarize the recent progress in discovering and characterizing the catalytic functions of fungal-derived NTF2-like enzymes, including dehydratases, epimerases, isomerases, semipinacolases, pericyclases, and aldolases. These findings not only provide valuable insights into new catalytic reactions and mechanisms, but also offer opportunities to discover novel NPs and biocatalysts through genome mining.

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ntf2样酶作为真菌天然产物生物合成的多功能生物催化剂
真菌天然产物(NPs)以其强大的生物活性而闻名,可用于人类治疗和农用化学品。这些具有生物活性和结构复杂的化合物是通过单体构建块的缩合来构建核心支架,然后经过各种修饰步骤进行生物合成的。最近的研究表明,一类来自ntf2样蛋白家族的独特酶在复杂真菌NPs的生物合成中起着重要作用。这些ntf2样酶属于与核转运因子2有共同折叠的一大相关蛋白群,能够催化各种反应。在本研究中,我们总结了近年来发现和表征真菌衍生的ntf2样酶的催化功能的进展,包括脱水酶、外膜酶、异构酶、半脂酶、周环酶和醛缩酶。这些发现不仅为新的催化反应和机制提供了有价值的见解,而且为通过基因组挖掘发现新的NPs和生物催化剂提供了机会。
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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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