Wei Qian, Bai Jian, Yan Daojiang, Bao Xiuqi, Li Wenting, Liu Bingyu, Zhang Dan, Qi Xiangbing, Yu Dequan, Hu Youcai
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.
National Institute of Biological Sciences, Beijing 102206, China.
Acta Pharm Sin B. 2021 Feb;11(2):572-587. doi: 10.1016/j.apsb.2020.07.020. Epub 2020 Aug 5.
Endophytic fungi are promising producers of bioactive small molecules. Bioinformatic analysis of the genome of an endophytic fungus revealed 43 biosynthetic gene clusters, exhibited its strong ability to produce numbers of secondary metabolites. However, this strain mainly produce rubratoxins alone with high yield in varied culture conditions, suggested most gene clusters are silent. Efforts for mining the cryptic gene clusters in , including epigenetic regulation and one-strain-many-compounds (OSMAC) approach were failed probably due to the high yield of rubratoxins. A metabolic shunting strategy by deleting the key gene for rubratoxins biosynthesis combining with optimization of culture condition successfully activated multiple silent genes encoding for other polyketide synthases (PKSs), and led to the trace compounds detectable. As a result, a total of 23 new compounds including azaphilone monomers, dimers, trimers with unprecedented polycyclic bridged heterocycle and spiral structures, as well as siderophores were identified. Some compounds showed significant cytotoxicities, anti-inflammatory or antioxidant activities. The attractive dual PKSs gene clusters for azaphilones biosynthesis were mined by bioinformatic analysis and overexpression of a pathway specific transcription factor. Our work therefor provides an efficient approach to mine the chemical diversity of endophytic fungi.
内生真菌是生物活性小分子的有前途的生产者。对一种内生真菌的基因组进行生物信息学分析,发现了43个生物合成基因簇,显示出其产生多种次生代谢产物的强大能力。然而,该菌株在不同培养条件下主要单独高产生产红曲毒素,这表明大多数基因簇是沉默的。挖掘其中隐秘基因簇的努力,包括表观遗传调控和“一菌多化合物”(OSMAC)方法,可能由于红曲毒素的高产而失败。通过删除红曲毒素生物合成的关键基因并结合培养条件优化的代谢分流策略成功激活了多个编码其他聚酮合酶(PKS)的沉默基因,并导致可检测到痕量化合物。结果,共鉴定出23种新化合物,包括氮杂蒽酮单体、二聚体、具有前所未有的多环桥连杂环和螺旋结构的三聚体以及铁载体。一些化合物表现出显著的细胞毒性、抗炎或抗氧化活性。通过生物信息学分析和途径特异性转录因子的过表达挖掘了用于氮杂蒽酮生物合成的有吸引力的双PKS基因簇。因此,我们的工作提供了一种挖掘内生真菌化学多样性的有效方法。