Wu Yunqiang, Wang Min, Liu Liwei
Health Science Center, Ningbo University, Ningbo, Zhejiang, 315211, China; Department of Marine Pharmacy, College of Food and Pharmaceutical Sciences, Ningbo University, Ningbo, Zhejiang, 315832, China.
School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, 529020, China.
Eur J Med Chem. 2023 Dec 15;262:115890. doi: 10.1016/j.ejmech.2023.115890. Epub 2023 Oct 20.
Trans-AT polyketides represent a class of natural compounds utilizing independent acyltransferase during their biosynthesis. They are well known for their diverse chemical structures and potent bioactivities. Trans-AT polyketides are synthesized through biosynthetic gene clusters predominantly composed of polyketide synthases (PKS), but often found in hybrid with non-ribosomal peptide synthetases (NRPS). This genetic hybridization results in the incorporation of amino acid residues into polyketide structures, significantly enhancing their structural diversity. Numerous amino acid-containing trans-AT polyketides have been identified, drawing significant attention to the mechanisms underlying amino acid incorporation and their impact on the biological activity of polyketides. Here, we discussed their origins, structures, biological activities, and the specific roles of amino acids in modulating both the bioactivity and biosynthesis of 38 trans-AT polyketides containing amino acids for the first time. This comprehensive analysis will serve as a crucial reference for the exploration of novel compounds and the improvement of structures and activities.
反式聚酮化合物是一类在生物合成过程中利用独立酰基转移酶的天然化合物。它们以其多样的化学结构和强大的生物活性而闻名。反式聚酮化合物通过主要由聚酮合酶(PKS)组成的生物合成基因簇合成,但经常与非核糖体肽合成酶(NRPS)杂交发现。这种基因杂交导致氨基酸残基掺入聚酮化合物结构中,显著增强了它们的结构多样性。已经鉴定出许多含氨基酸的反式聚酮化合物,这引起了人们对氨基酸掺入机制及其对聚酮化合物生物活性影响的极大关注。在这里,我们首次讨论了它们的起源、结构、生物活性以及氨基酸在调节38种含氨基酸的反式聚酮化合物的生物活性和生物合成中的具体作用。这种全面的分析将为新型化合物的探索以及结构和活性的改进提供关键参考。