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Bahamaolide A from the marine-derived Streptomyces sp CNQ343 inhibits isocitrate lyase in Candida albicans

Cited 9 time in Web of Science Cited 11 time in Scopus
Authors

Lee, So-Hyoung; Moon, Kyuho; Kim, Heegyu; Shin, Jongheon; Oh, Dong-Chan; Oh, Ki-Bong

Issue Date
2014-09
Publisher
Pergamon Press Ltd.
Citation
Bioorganic and Medicinal Chemistry Letters, Vol.24 No.17, pp.4291-4293
Abstract
Bahamaolide A, a new macrocyclic lactone isolated from the culture of marine actinomycete Streptomyces sp. CNQ343, was evaluated for its inhibitory activity toward isocitrate lyase (ICL) from Candida albicans. These studies led to the identification of bahamaolide A as a potent ICL inhibitor with IC50 value of 11.82 mu M. The growth phenotype of ICL deletion mutants and quantitative RT-PCR analyses indicated that this compound inhibits the ICL mRNA expression in C albicans under C-2-carbon-utilizing conditions. The present data highlight the potential for bahamaolide A treatment of C. albicans infections via inhibition of ICL activity. (C) 2014 Elsevier Ltd. All rights reserved.
ISSN
0960-894X
URI
https://hdl.handle.net/10371/207381
DOI
https://doi.org/10.1016/j.bmcl.2014.07.021
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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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