LC-MS Guided Discovery and Biosynthetic Pathway of Coprisamides E-H, Cinnamic Acid-Containing Metabolites from the Marine Algae-Derived Streptomyces thermolineatus NAK03196.

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2025-03-28 Epub Date: 2025-03-03 DOI:10.1021/acs.jnatprod.4c01439
Guo Dong Zhang, Zhi Wei Yang, Fang Zhou Yin, Zhang Yuan Yan, Zi Jun Xiong, Shuai Ma, Zhi Kai Guo, Rui Hua Jiao
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Abstract

Four cinnamoyl-containing nonribosomal peptides (CCNPs), coprisamides E-H (1-4), were isolated from the marine algae-associated actinomycete strain Streptomyces thermolineatus NAK03196. Their structures were elucidated to be unreported coprisamides by comprehensive analyses of HRESIMS, 1D and 2D NMR spectroscopic data, Marfey's method, and MS/MS analysis. Coprisamides E (1) and F (2) bear a characteristic nonproteinogenic amino acid, 2,3-diaminopropanoic acid. The biosynthetic pathways for these isolates were proposed through a comparison of their biosynthetic gene clusters with reported homologous gene clusters. Coprisamide E (1) exhibited weak antibacterial activity against the Gram-positive strain Staphylococcus aureus.

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热链霉菌NAK03196中含铜酰胺E-H、肉桂酸代谢物的LC-MS发现及其生物合成途径
从海洋藻类相关放线菌Streptomyces thermolineatus NAK03196中分离到4个含肉桂酰的非核糖体肽(CCNPs), coprisamides E-H(1-4)。通过hresms、1D和2D NMR数据、Marfey’s方法和MS/MS分析,证实其结构为未见报道的共维酰胺类化合物。corisamides E(1)和F(2)具有非蛋白性氨基酸,2,3-二氨基丙酸。通过将这些菌株的生物合成基因簇与已报道的同源基因簇进行比较,提出了这些菌株的生物合成途径。Coprisamide E(1)对革兰氏阳性金黄色葡萄球菌的抑菌活性较弱。
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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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