Spirotetronate antibiotics with anti-Clostridium activity from Actinomadura sp 2EPS

被引:13
作者
Euanorasetr, Jirayut [1 ,2 ]
Intra, Bungonsiri [1 ,2 ]
Mongkol, Phayungsak [3 ]
Chankhamhaengdecha, Surang [3 ]
Tuchinda, Patoomratana [4 ]
Mori, Mihoko [5 ,6 ]
Shiomi, Kazuro [5 ,6 ]
Nihira, Takuya [2 ,7 ]
Panbangred, Watanalai [1 ,2 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Biotechnol, Bangkok 10400, Thailand
[2] Mahidol Univ, Mahidol Univ Osaka Univ Collaborat Res Ctr Biosci, Fac Sci, Bangkok 10400, Thailand
[3] Mahidol Univ, Dept Biol, Fac Sci, Bangkok 10400, Thailand
[4] Mahidol Univ, Dept Chem, Fac Sci, Bangkok 10400, Thailand
[5] Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
[6] Kitasato Univ, Grad Sch Infect Control Sci, Tokyo, Japan
[7] Osaka Univ, Int Ctr Biotechnol, Osaka, Japan
关键词
Actinomadura; Actinomycetes; Clostridium; Secondary metabolites; Spirotetronate antibiotics; SP MK73-NF4; SP-NOV; FERMENTATION; MICROMONOSPORA; DECATROMICINS; EVOLUTION; TAXONOMY; ORGANISM;
D O I
10.1007/s11274-014-1792-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 (H-1-NMR and C-13-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 A mu g/ml. Moreover, both 1 and 3 also exhibited strong activity, with similar MIC values, against Clostridium perfringens S107 at 0.63 A mu g/ml and C. difficile 630 at 0.08 A mu g/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.
引用
收藏
页码:391 / 398
页数:8
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