拓展天然产物的视野:起始单位在非核糖体脂肽生物合成中的作用。

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2025-05-16 Epub Date: 2025-04-16 DOI:10.1021/acssynbio.4c00893
Lin Zhong, Seenivasan Boopathi, Xingyan Wang, Hanna Chen, Xianping Bai, Xingxing Shi, Qingsheng Yang, Xiaoying Bian, Youming Zhang
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引用次数: 0

摘要

非核糖体脂肽(nrlp)是结构复杂的天然产物,具有重要的生态和生物学作用。它们也是开发新药的宝贵资源和先导结构。这些化合物通常是用一种称为非核糖体肽合成酶(NRPSs)或杂交聚酮合成酶(NRPSs)的分子组装机制合成的。与传统NRPS不同,nrlp的特点是具有装载脂质链的启动模块和在起始阶段提供必要底物的底物合成途径。独特的脂质链是nrlp生物活性的关键决定因素。因此,通过组合生物合成来修饰这些脂质链对于释放它们的全部治疗潜力具有很大的希望。在本文中,我们使用术语“Starter Unit”来指代nrlp脂质链起始过程中涉及的初始模块和脂质起始途径。本文综述了启动单元组合生物合成的最新进展,并对未来的发展方向进行了展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expanding the Horizon of Natural Products: The Role of Starter Units in Nonribosomal Lipopeptide Biosynthesis.

Nonribosomal lipopeptides (NRLPs) are structurally complex natural products that play crucial ecological and biological roles. They are also valuable sources and lead structures for developing new pharmaceuticals. These compounds are typically synthesized using a molecular assembly machinery known as nonribosomal peptide synthetases (NRPSs) or hybrid polyketide synthases-NRPSs. Unlike conventional NRPS, NRLPs are characterized by a starter module that loads lipid chains and a substrate synthesis pathway that supplies the necessary substrates during the initiation stages. Unique lipid chains are critical determinants of the biological activity of NRLPs. Therefore, modifying these lipid chains through combinatorial biosynthesis holds great promise for unlocking their full therapeutic potential. Herein, we use the term "Starter Unit" to refer to the initial modules and lipoinitiation pathway involved in the lipid chain initiation process of NRLPs. This Review provides a comprehensive summary of recent advances in the combinatorial biosynthesis of starter units and offers insights into future directions for further development.

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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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