Re-Engineering Fungal Nonribosomal Peptide Synthetases by Module Dissection and Duplicated Thiolation Domains

文献类型： 外文期刊

第一作者： Yin, Miaomiao

作者： Yin, Miaomiao;Xie, Linan;Chen, Kang;Zhang, Liwen;Yue, Qun;Wang, Chen;Zeng, Juntian;Hao, Xiaoyang;Gu, Xiaofeng;Xu, Yuquan;Xie, Linan;Zhang, Liwen;Yue, Qun;Wang, Chen;Xu, Yuquan;Molnar, Istvan

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关键词： nonribosomal peptide synthetase; heterologous expression; natural products; combinatorial biosynthesis; synthetic biology

期刊名称：ANGEWANDTE CHEMIE-INTERNATIONAL EDITION （ 影响因子：16.1； 五年影响因子：16.2 ）

ISSN： 1433-7851

年卷期： 2024 年 63 卷 33 期

页码：

收录情况： SCI

摘要： Unnatural product (uNP) nonribosomal peptides promise to be a valuable source of pharmacophores for drug discovery. However, the extremely large size and complexity of the nonribosomal peptide synthetase (NRPS) enzymes pose formidable challenges to the production of such uNPs by combinatorial biosynthesis and synthetic biology. Here we report a new NRPS dissection strategy that facilitates the engineering and heterologous production of these NRPSs. This strategy divides NRPSs into "splitting units", each forming an enzyme subunit that contains catalytically independent modules. Functional collaboration between the subunits is then facilitated by artificially duplicating, at the N-terminus of the downstream subunit, the linker - thiolation domain - linker fragment that is resident at the C-terminus of the upstream subunit. Using the suggested split site that follows a conserved motif in the linker connecting the adenylation and the thiolation domains allows cognate or chimeric splitting unit pairs to achieve productivities that match, and in many cases surpass those of hybrid chimeric enzymes, and even those of intact NRPSs, upon production in a heterologous chassis. Our strategy provides facile options for the rational engineering of fungal NRPSs and for the combinatorial reprogramming of nonribosomal peptide production. A new strategy is presented to dissect fungal nonribosomal peptide synthetases into "splitting unit" pairs (SUPs). Collaboration in SUPs is facilitated by artificial duplication of the thiolation domain and its linkers, and an optimized split site. The productivities of SUPs match or exceed those of the corresponding single-subunit chimeras or even those of native fungal enzymes, boding well for generating novel peptide natural product analogues. image

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