Chen Manyun, Dhakal Dipesh, Eckhardt Campbell W, Luesch Hendrik, Ding Yousong
Department of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development, University of Florida, Gainesville, FL 32610, USA.
Program in Cancer and Stem Cell Biology, Duke-NUS Medical School, Singapore, 169857, Singapore.
Nat Prod Rep. 2025 Apr 16. doi: 10.1039/d5np00009b.
Covering: 2014 to 2024Cyanobacteria are prolific producers of bioactive natural products, including promising drug leads for FDA-approved cancer therapeutics. Advances in genome sequencing and computational tools have revealed a wealth of cyanobacterial biosynthetic gene clusters (BGCs). However, progress in genome-driven discovery has been hindered by challenges in manipulating native hosts and the limited availability of efficient heterologous expression platforms. This highlight focuses on recent synthetic biology innovations on cyanobacterial systems that address these obstacles, facilitating the production of diverse cyanobacterial natural product families. We discuss key features of widely used cyanobacterial chassis, such as sp. PCC 6803, UTEX 2973, sp. PCC 7120, and emerging hosts. Advances in BGC cloning, combinatorial biosynthesis, transcriptional and translational regulation, and host engineering are also highlighted. Together, these synthetic biology developments provide a powerful framework for expanding cyanobacterial natural product discovery and production.
2014年至2024年
蓝细菌是生物活性天然产物的丰富生产者,包括有望用于美国食品药品监督管理局(FDA)批准的癌症治疗药物的先导化合物。基因组测序和计算工具的进步揭示了大量蓝细菌生物合成基因簇(BGCs)。然而,基因组驱动的发现进展受到操纵天然宿主方面的挑战以及高效异源表达平台可用性有限的阻碍。本综述重点关注蓝细菌系统的近期合成生物学创新,这些创新解决了这些障碍,促进了多种蓝细菌天然产物家族的生产。我们讨论了广泛使用的蓝细菌底盘的关键特征,如聚球藻属PCC 6803、UTEX 2973、集胞藻属PCC 7120以及新兴宿主。还强调了BGC克隆、组合生物合成、转录和翻译调控以及宿主工程方面的进展。总之,这些合成生物学进展为扩大蓝细菌天然产物的发现和生产提供了一个强大的框架。