Scripps Institution of Oceanography and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California-San Diego, La Jolla, CA 92093, USA.
Nat Prod Rep. 2010 Jul;27(7):1048-65. doi: 10.1039/c000535e. Epub 2010 May 4.
Cyanobacteria are abundant producers of natural products well recognized for their bioactivity and utility in drug discovery and biotechnology applications. In the last decade, characterization of several modular gene clusters that code for the biosynthesis of these compounds has revealed a number of unusual enzymatic reactions. In this article, we review several mechanistic transformations identified in marine cyanobacterial biosynthetic pathways, with an emphasis on modular polyketide synthase(PKS)/non-ribosomal peptide synthetase (NRPS) gene clusters. In selected instances, we also make comparisons between cyanobacterial gene clusters derived from marine and freshwater strains. We then provide an overview of recent developments in cyanobacterial natural products biosynthesis made available through genome sequencing and new advances in bioinformatics and genetics.
蓝藻是天然产物的丰富生产者,其生物活性和在药物发现和生物技术应用中的实用性已得到广泛认可。在过去的十年中,对几种模块化基因簇的特征进行了描述,这些基因簇编码这些化合物的生物合成,揭示了许多不寻常的酶促反应。在本文中,我们综述了海洋蓝藻生物合成途径中鉴定的几种机制转化,重点介绍了模块化聚酮合酶(PKS)/非核糖体肽合酶(NRPS)基因簇。在某些情况下,我们还比较了来自海洋和淡水菌株的蓝藻基因簇。然后,我们概述了通过基因组测序以及生物信息学和遗传学的新进展,在蓝藻天然产物生物合成方面取得的最新进展。