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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-HyerkBan, Yeon HeeKim, Tae HoBae, Eun SeoShin, JongheonLee, Sang KookJang, JichanYoon, Yeo JoonOh, 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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