Mo Xuhua, Gui Chun, Wang Qingji
Shandong Key Laboratory of Applied Mycology, School of Life Sciences, Qingdao Agricultural University, Qingdao 266109, China.
CAS Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, RNAM Center for Marine Microbiology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, 164 West Xingang Rd., Guangzhou 510301, China.
Bioorg Med Chem Lett. 2017 Sep 15;27(18):4431-4435. doi: 10.1016/j.bmcl.2017.08.010. Epub 2017 Aug 7.
Nocamycins belong to the tetramic acid family natural products and show potent antimicrobial activity. Recently, the biosynthetic gene cluster of nocamycin was identified from the rare actinomycete Saccharothrix syringae and an S-adenosylmethionine (SAM) dependent methyltransferase gene NcmP was found to be located within the gene cluster. In this report, the methyltransferase gene NcmP was disrupted and a new nocamycin intermediate nocamycin E was isolated from the mutant strain. Meanwhile, NcmP was heterologously expressed in Escherichia coli BL21 (DE3) and biochemically characterized as a carboxylate O-methyltransferase in nocamycin biosynthetic pathway. Compared to nocamycin I, nocamycin E showed inferior antibacterial activity, indicating the methyl group is essential to antibacterial activity.
诺卡霉素属于四嗪酸家族天然产物,具有强大的抗菌活性。最近,从稀有放线菌丁香糖丝菌中鉴定出了诺卡霉素的生物合成基因簇,并且发现一个依赖S-腺苷甲硫氨酸(SAM)的甲基转移酶基因NcmP位于该基因簇内。在本报告中,甲基转移酶基因NcmP被破坏,并且从突变菌株中分离出了一种新的诺卡霉素中间体诺卡霉素E。同时,NcmP在大肠杆菌BL21(DE3)中进行了异源表达,并被生化鉴定为诺卡霉素生物合成途径中的羧酸O-甲基转移酶。与诺卡霉素I相比,诺卡霉素E的抗菌活性较差,这表明甲基对抗菌活性至关重要。