Yang Jie, Zhu Xiaoyu, Cao Mingming, Wang Changbao, Zhang Chong, Lu Zhaoxin, Lu Fengxia
College of Food Science and Technology, Nanjing Agricultural University , 1 Weigang, Nanjing 210095, China.
J Agric Food Chem. 2016 Nov 23;64(46):8811-8820. doi: 10.1021/acs.jafc.6b04455. Epub 2016 Nov 15.
Fmb60 is a wild-type Bacillus subtilis isolated from compost with significant broad-spectrum antimicrobial activities. Two novel PKS clusters were recognized in the genome sequence of fmb60, and then three polyene antibiotics, aurantinins B, C, and D, 1-3, were obtained by bioactivity-guided isolation from the fermentation of fmb60. The structures of aurantinins B-D were elucidated by LC-HRMS and NMR data analysis. Aurantinins C and D were identified as new antimicrobial compounds. The three aurantinins showed significant activity against multidrug-resistant Staphylococcus aureus and Clostridium sporogenes. However, aurantinins B-D did not exhibit any cytotoxicity (IC50 > 100 μg/mL) against LO2 and Caco2 cell lines by MTT assay. Furthermore, using S. aureus as a model bacterium to explore the antibacterial mechanism of aurantinins B-D, it was revealed that the bactericidal activity of aurantinins B-D was related to their ability to disrupt the cell membrane.
Fmb60是从堆肥中分离出的野生型枯草芽孢杆菌,具有显著的广谱抗菌活性。在fmb60的基因组序列中识别出两个新的聚酮合酶(PKS)基因簇,然后通过生物活性导向分离从fmb60的发酵产物中获得了三种多烯抗生素,即金霉素B、C和D(1-3)。通过液相色谱-高分辨质谱(LC-HRMS)和核磁共振(NMR)数据分析阐明了金霉素B-D的结构。金霉素C和D被鉴定为新型抗菌化合物。这三种金霉素对耐多药金黄色葡萄球菌和产芽孢梭菌显示出显著活性。然而,通过MTT法检测,金霉素B-D对LO2和Caco2细胞系未表现出任何细胞毒性(半数抑制浓度IC50>100μg/mL)。此外,以金黄色葡萄球菌为模型细菌探索金霉素B-D的抗菌机制,结果表明金霉素B-D的杀菌活性与其破坏细胞膜的能力有关。