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Main Authors: Zhang, Guo Dong, Yang, Zhi Wei, Yin, Fang Zhou, Yan, Zhang Yuan, Xiong, Zi Jun, Ma, Shuai, Guo, Zhi Kai, Jiao, Rui Hua
Format: Artículo científico
Language:en
Published: Journal of natural products 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/40030089/
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author Zhang, Guo Dong
Yang, Zhi Wei
Yin, Fang Zhou
Yan, Zhang Yuan
Xiong, Zi Jun
Ma, Shuai
Guo, Zhi Kai
Jiao, Rui Hua
author_facet Zhang, Guo Dong
Yang, Zhi Wei
Yin, Fang Zhou
Yan, Zhang Yuan
Xiong, Zi Jun
Ma, Shuai
Guo, Zhi Kai
Jiao, Rui Hua
Zhang, Guo Dong
Yang, Zhi Wei
Yin, Fang Zhou
Yan, Zhang Yuan
Xiong, Zi Jun
Ma, Shuai
Guo, Zhi Kai
Jiao, Rui Hua
collection PubMed - marine biology
contents LC-MS Guided Discovery and Biosynthetic Pathway of Coprisamides E-H, Cinnamic Acid-Containing Metabolites from the Marine Algae-Derived NAK03196. Zhang, Guo Dong Yang, Zhi Wei Yin, Fang Zhou Yan, Zhang Yuan Xiong, Zi Jun Ma, Shuai Guo, Zhi Kai Jiao, Rui Hua Streptomyces Staphylococcus aureus Molecular Structure Anti-Bacterial Agents Marine Biology Cinnamates Microbial Sensitivity Tests Chromatography, Liquid Nuclear Magnetic Resonance, Biomolecular Biosynthetic Pathways Multigene Family Liquid Chromatography-Mass Spectrometry Four cinnamoyl-containing nonribosomal peptides (CCNPs), coprisamides EH (-), were isolated from the marine algae-associated actinomycete strain 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 () and F () 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 () exhibited weak antibacterial activity against the Gram-positive strain .
format Artículo científico
id pubmed_40030089
institution PubMed
language en
publishDate 2025
publisher Journal of natural products
record_format pubmed
spellingShingle LC-MS Guided Discovery and Biosynthetic Pathway of Coprisamides E-H, Cinnamic Acid-Containing Metabolites from the Marine Algae-Derived NAK03196.
Zhang, Guo Dong
Yang, Zhi Wei
Yin, Fang Zhou
Yan, Zhang Yuan
Xiong, Zi Jun
Ma, Shuai
Guo, Zhi Kai
Jiao, Rui Hua
Streptomyces
Staphylococcus aureus
Molecular Structure
Anti-Bacterial Agents
Marine Biology
Cinnamates
Microbial Sensitivity Tests
Chromatography, Liquid
Nuclear Magnetic Resonance, Biomolecular
Biosynthetic Pathways
Multigene Family
Liquid Chromatography-Mass Spectrometry
LC-MS Guided Discovery and Biosynthetic Pathway of Coprisamides E-H, Cinnamic Acid-Containing Metabolites from the Marine Algae-Derived NAK03196. Zhang, Guo Dong Yang, Zhi Wei Yin, Fang Zhou Yan, Zhang Yuan Xiong, Zi Jun Ma, Shuai Guo, Zhi Kai Jiao, Rui Hua Streptomyces Staphylococcus aureus Molecular Structure Anti-Bacterial Agents Marine Biology Cinnamates Microbial Sensitivity Tests Chromatography, Liquid Nuclear Magnetic Resonance, Biomolecular Biosynthetic Pathways Multigene Family Liquid Chromatography-Mass Spectrometry Four cinnamoyl-containing nonribosomal peptides (CCNPs), coprisamides EH (-), were isolated from the marine algae-associated actinomycete strain 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 () and F () 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 () exhibited weak antibacterial activity against the Gram-positive strain .
title LC-MS Guided Discovery and Biosynthetic Pathway of Coprisamides E-H, Cinnamic Acid-Containing Metabolites from the Marine Algae-Derived NAK03196.
topic Streptomyces
Staphylococcus aureus
Molecular Structure
Anti-Bacterial Agents
Marine Biology
Cinnamates
Microbial Sensitivity Tests
Chromatography, Liquid
Nuclear Magnetic Resonance, Biomolecular
Biosynthetic Pathways
Multigene Family
Liquid Chromatography-Mass Spectrometry
url https://pubmed.ncbi.nlm.nih.gov/40030089/