Liu Yuanyuan, Tang Yuqi, Fu Zhiyang, Zhu Wangjie, Wang Hong, Zhang Huawei
School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, 310014, China.
School of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, 310014, China.
Metab Eng. 2025 Sep;91:1-29. doi: 10.1016/j.ymben.2025.03.018. Epub 2025 Mar 28.
Biosynthetic gene clusters (BGCs) in microbial genomes play a crucial role in the biosynthesis of diverse secondary metabolites (SMs) with pharmaceutical potential. However, most BGCs remain silent under conventional conditions, resulting in the frequently repeated discovery of known SMs. Fortunately, in the past two decades, the heterologous expression of BGCs in genetically tractable hosts has emerged as a powerful strategy to awaken microbial metabolic pathways for making novel microbial SMs. In this review, we comprehensively delineated the development and application of this strategy, highlighting various BGC cloning and assembly techniques and their technical characteristics. We also summarized 519 novel SMs from BGC hetero-expression-derived strains and described their occurrence, bioactivity, mode of action, and biosynthetic logic. Lastly, current challenges and future perspectives for developing more efficient BGC hetero-expression strategies were discussed in this review.
微生物基因组中的生物合成基因簇(BGCs)在具有药物潜力的多种次级代谢产物(SMs)的生物合成中起着关键作用。然而,大多数BGCs在传统条件下保持沉默,导致已知SMs的频繁重复发现。幸运的是,在过去二十年中,在遗传上易于处理的宿主中异源表达BGCs已成为一种强大的策略,用于唤醒微生物代谢途径以产生新型微生物SMs。在本综述中,我们全面描述了该策略的发展和应用,突出了各种BGC克隆和组装技术及其技术特点。我们还总结了来自BGC异源表达衍生菌株的519种新型SMs,并描述了它们的产生、生物活性、作用方式和生物合成逻辑。最后,本综述讨论了开发更高效的BGC异源表达策略当前面临的挑战和未来前景。