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Updated: Sep 16, 2025

Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products
Published on: March 12, 2020
Discovery and Biosynthesis of Nyuzenamides D and E by Genome Mining in Streptomyces hygroscopicus
Kah Yean Lum1, Rohitesh Kumar1, Zhijie Yang1
1Department of Biotechnology and Biomedicine, Technical University of Denmark, So̷ltofts Plads 221, Lyngby DK 2800, Denmark.
Abstract:
Nyuzenamides belong to a class of bioactive cinnamoyl moieties containing nonribosomal peptides. Genome mining revealed a putative nyu BGC in Streptomyces hygroscopicus DSM 40578. Two new analogues, nyuzenamides D (1) and E (2), were subsequently isolated, and their structures were elucidated by detailed nuclear magnetic resonance spectroscopic and mass spectrometric data analyses. The absolute configuration of 1 was determined by a single-crystal X-ray diffraction study. Through retrobiosynthesis and CRISPR genome editing, the nonribosomal peptide synthetase biosynthetic gene cluster for nyuzenamides was confirmed. Nyuzenamides D and E are likely derived from nyuzenamide C through nonenzymatic hydrolysis. Our discovery enriches the diversity of cinnamoyl-containing nonribosomal peptides and validates the biosynthetic gene clusters for future genome mining research.
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