Cong Zhanren, Mukoma Njeru Joe, Yin Qiang, Zhu Bin, She Lingwei, Hsiang Tom, Zhang Lixin, Jiang Lan, Liu Xueting
State Key Laboratory of Bioreactor Engineering, East China University of Science of Technology, Shanghai 200237, China.
Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education, and Laboratory of Pharmaceutical Crystal Engineering & Technology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China.
J Agric Food Chem. 2024 Dec 11;72(49):27225-27234. doi: 10.1021/acs.jafc.4c07653. Epub 2024 Dec 2.
Terpenoids derived from phytopathogenic fungi are major participants in interactions among microorganisms, plants, and animals. The modifications catalyzed by cytochrome P450s significantly influence the structural and bioactivity diversity of the terpenoids. To conduct genome mining of P450s in pathogenic fungi, in this study, we developed a new software called atural roducts iloring Enzymes enome ining (NPtagM). By optimizing the workflow and gene prediction software, NPtagM demonstrated a 3-fold increase in the number of predicted P450s and an 8-fold reduction in runtime compared to antiSMASH. We then used it to extract 1189 dereplicated terpenoid P450s from our in-house fungal genomes. Using a sequence similarity network analysis, we identified a family that potentially produced eremophilane-type sesquiterpenoids. The heterologous expression in resulted in the production of two new and four known eremophilanes. Our results highlight the potential of NPtagM in genome mining for tailoring enzymes from phytopathogenic fungi.
源自植物病原真菌的萜类化合物是微生物、植物和动物之间相互作用的主要参与者。细胞色素P450催化的修饰显著影响萜类化合物的结构和生物活性多样性。为了对病原真菌中的P450进行基因组挖掘,在本研究中,我们开发了一种名为天然产物着色酶基因组挖掘(NPtagM)的新软件。通过优化工作流程和基因预测软件,与antiSMASH相比,NPtagM预测的P450数量增加了3倍,运行时间减少了8倍。然后,我们用它从我们内部的真菌基因组中提取了1189个去重复的萜类P450。通过序列相似性网络分析,我们鉴定出一个可能产生雅槛蓝烷型倍半萜的家族。在[具体表达系统]中的异源表达导致产生了两种新的和四种已知的雅槛蓝烷。我们的结果突出了NPtagM在从植物病原真菌中定制酶的基因组挖掘中的潜力。