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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/33433
Title: Spirotetronate antibiotics with anti-Clostridium activity from Actinomadura sp. 2EPS
Authors: Jirayut Euanorasetr
Bungonsiri Intra
Phayungsak Mongkol
Surang Chankhamhaengdecha
Patoomratana Tuchinda
Mihoko Mori
Kazuro Shiomi
Takuya Nihira
Watanalai Panbangred
Mahidol University
Kitasato University
Osaka University
Keywords: Biochemistry, Genetics and Molecular Biology;Immunology and Microbiology
Issue Date: 1-Jan-2014
Citation: World Journal of Microbiology and Biotechnology. Vol.31, No.2 (2014), 391-398
Abstract: © 2014, Springer Science+Business Media Dordrecht. The rare actinomycetes strain 2EPS was isolated from soil and analysis of cultural, morphological characteristics, diaminopimelic acid content of its cell wall, and 16S rRNA gene sequence indicates that 2EPS belongs to genus Actinomadura. In addition, neighbor-joining phylogenetic tree also confirmed the relationships of this strain to other members of Actinomadura. A butanol extract with antibacterial activity was purified by reversed-phase chromatography to obtain three bioactive compounds, designated as compounds 1, 2 and 3. The structures of these compounds were determined using spectroscopic analysis (1H-NMR and13C-NMR) and mass spectrometric analysis (HR-TOF-MS). Compounds 1–3 were identified and found to be the same as those included in the Japanese patent number JP 09227587 for spirotetronate antibiotics and are BE-45722A (1), BE-45722B (2) and BE-45722C (3), respectively. All compounds were active against Gram-positive bacteria (Staphylococcus aureus ATCC 25923, Bacillus cereus ATCC 14579, and B. subtilis ATCC 6633) with low MIC values between 0.08 and 5.0 µg/ml. Moreover, both 1 and 3 also exhibited strong activity, with similar MIC values, against Clostridiumperfringens S107 at 0.63 µg/ml and C. difficile 630 at 0.08 µg/ml. These results suggest the identified spirotetronate compounds may have potential in the treatment of Clostridium infections. Overall, this analysis demonstrates that rare actinomycetes are a promising source for discovery of antimicrobial compounds.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84964300473&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/33433
ISSN: 15730972
09593993
Appears in Collections:Scopus 2011-2015

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