Luo Mengna, Wang Mengyuan, Chang Shanshan, He Ning, Shan Guangzhi, Xie Yunying
CAMS Key Laboratory of Synthetic Biology for Drug Innovation, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Tiantan Xili No.1, Beijing 100050, China.
Antibiotics (Basel). 2022 Sep 25;11(10):1304. doi: 10.3390/antibiotics11101304.
Genome mining has become an important tool for discovering new natural products and identifying the cryptic biosynthesis gene clusters. Here, we utilized the flavin-dependent halogenase GedL as the probe in combination with characteristic halogen isotope patterns to mine new halogenated secondary metabolites from our in-house fungal database. As a result, two pairs of atropisomers, pestalachlorides A1a (1a)/A1b (1b) and A2a (2a)/A2b (2b), along with known compounds pestalachloride A (3) and SB87-H (4), were identified from Pestalotiopsis rhododendri LF-19-12. A plausible biosynthetic assembly line for pestalachlorides involving a putative free-standing phenol flavin-dependent halogenase was proposed based on bioinformatics analysis. Pestalachlorides exhibited antibacterial activity against sensitive and drug-resistant S. aureus and E. faecium with MIC values ranging from 4 μg/mL to 32 μg/mL. This study indicates that halogenase-targeted genome mining is an efficient strategy for discovering halogenated compounds and their corresponding halogenases.
基因组挖掘已成为发现新天然产物和鉴定隐秘生物合成基因簇的重要工具。在此,我们利用黄素依赖性卤化酶GedL作为探针,结合特征性卤素同位素模式,从我们的内部真菌数据库中挖掘新的卤化次级代谢产物。结果,从杜鹃拟盘多毛孢LF-19-12中鉴定出两对阻转异构体,即pestalachlorides A1a(1a)/A1b(1b)和A2a(2a)/A2b(2b),以及已知化合物pestalachloride A(3)和SB87-H(4)。基于生物信息学分析,提出了一条涉及假定独立的酚类黄素依赖性卤化酶的pestalachlorides可能的生物合成装配线。Pestalachlorides对敏感和耐药的金黄色葡萄球菌和屎肠球菌具有抗菌活性,MIC值范围为4μg/mL至32μg/mL。这项研究表明,以卤化酶为靶点的基因组挖掘是发现卤化化合物及其相应卤化酶的有效策略。