Structures and Biosynthetic Pathway of Coprisamides C and D, 2-Alkenylcinnamic Acid-Containing Peptides from the Gut Bacterium of the Carrion Beetle Silpha perforata
- Authors
- Shin, Yern-Hyerk; Ban, Yeon Hee; Kim, Tae Ho; Bae, Eun Seo; Shin, Jongheon; Lee, Sang Kook; Jang, Jichan; Yoon, Yeo Joon; Oh, Dong-Chan
- Issue Date
- 26-Feb-2021
- Publisher
- American Chemical Society
- Citation
- Journal of Natural Products, v.84, no.2, pp 239 - 246
- Pages
- 8
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Natural Products
- Volume
- 84
- Number
- 2
- Start Page
- 239
- End Page
- 246
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/4069
- DOI
- 10.1021/acs.jnatprod.0c00864
- ISSN
- 0163-3864
1520-6025
- Abstract
- Coprisamides C and D (1 and 2) were isolated from a gut bacterium, Micromonospora sp. UTJ3, of the carrion beetle Silpha perforata. Based on the combined analysis of UV, MS, and NMR spectral data, the planar structures of 1 and 2 were elucidated to be unreported derivatives of coprisamides A and B, cyclic depsipeptides bearing a 2-alkenylcinnamic acid unit and the unusual amino acids beta-methylaspartic acid and 2,3-diaminopropanoic acid. The absolute configuration of 1 was determined using the advanced Marfey's method, phenylglycine methyl ester derivatization, and J-based configuration analysis. The biosynthetic gene clusters for the coprisamides were investigated based on genomic data from coprisamide-producing strains Micromonospora sp. UTJ3 and Streptomyces sp. SNU533. Coprisamide C (1) was active against the Mycobacterium tuberculosis mc(2) 6230 strain.
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