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Structures and Biosynthetic Pathway of Pulvomycins B-D: 22-Membered Macrolides from an Estuarine Streptomyces sp.

Cited 16 time in Web of Science Cited 19 time in Scopus
Authors

Moon, Kyuho; Cui, Jinsheng; Kim, Eunji; Riandi, Evan Setiawan; Park, So Hyun; Byun, Woong Sub; Kal, Youngju; Park, Jun Young; Hwang, Sunghoon; Shin, Daniel; Sun, Jeongyoon; Oh, Ki-Bong; Cha, Sangwon; Shin, Jongheon; Lee, Sang Kook; Yoon, Yeo Joon; Oh, Dong-Chan

Issue Date
2020-07
Publisher
American Chemical Society
Citation
Organic Letters, Vol.22 No.14, pp.5358-5362
Abstract
Pulvomycins B-D (1-3) were discovered from an estuarine Streptomyces strain along with the known pulvomycin (4). The 22-membered macrocyclic lactone structures of 1-3 were determined based on the interpretation of NMR, UV, and MS data, the modified Mosher's method, and Kishi's bidentate chiral solvent NMR spectroscopy. Genomic analysis of the bacterial strain revealed the biosynthetic gene cluster of pulvomycin and enabled us to propose the trans-acyltransferase polyketide biosynthetic pathway. Pulvomycin D displayed potent cytotoxic activity against various cancer cell lines.
ISSN
1523-7060
URI
https://hdl.handle.net/10371/205955
DOI
https://doi.org/10.1021/acs.orglett.0c01249
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Chemical biology of natural products, Drug discovery from microbial natural products, Study of insect-microbial symbiosis, 미생물 유래 생리활성 천연물 발굴, 천연물 구조 분석

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