An Joon Soo, Lim Hyung-Ju, Lee Ji Yun, Jang Yong-Joon, Nam Sang-Jip, Lee Sang Kook, Oh Dong-Chan
Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
Natura Center of Life and Environment, Seoul 08826, Republic of Korea.
J Nat Prod. 2022 Apr 22;85(4):936-942. doi: 10.1021/acs.jnatprod.1c01075. Epub 2022 Apr 1.
A new bicyclic macrolide, hamuramicin C (), was isolated from sp. MBP16, a gut bacterial strain of the wasp . Its 22-membered macrocyclic lactone structure was determined by NMR and mass spectrometry. The relative configurations of hamuramicin C () were assigned by -based configuration analysis utilizing H rotating frame Overhauser effect spectroscopy and heteronuclear long-range coupling NMR spectroscopy. Genomic and bioinformatic analyses of the bacterial strain enabled identification of the type-I polyketide synthase pathway, which employs a -acyltransferase system. The absolute configurations of were proposed based on the analysis of the sequences of ketoreductases in the modular gene cluster. Moreover, hamuramicin C () demonstrated significant inhibitory activity against diverse human cancer cell lines (HCT116, A549, SNU-638, SK-HEP-1, and MDA-MB-231).
一种新的双环大环内酯类化合物,哈穆拉霉素C(),是从黄蜂肠道细菌菌株sp. MBP16中分离得到的。其22元大环内酯结构通过核磁共振(NMR)和质谱测定。哈穆拉霉素C()的相对构型通过基于H旋转框架奥弗豪泽效应光谱和异核远程耦合核磁共振光谱的构型分析来确定。对该细菌菌株的基因组和生物信息学分析使得能够鉴定出采用α-酰基转移酶系统的I型聚酮合酶途径。基于对模块化基因簇中酮还原酶序列的分析,提出了的绝对构型。此外,哈穆拉霉素C()对多种人类癌细胞系(HCT116、A549、SNU-638、SK-HEP-1和MDA-MB-231)表现出显著的抑制活性。