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Genome Mining and Screening for Secondary Metabolite Production in the Endophytic Fungus Dactylonectria alcacerensis CT-6

Qianliang MingDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaXiuning HuangDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaYimo HeDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaLingyue QinDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaYu TangDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaYanxia LiuDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaYuting HuangDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, ChinaHongwei ZhangDrug and Instrument Supervision and Inspection Station, 32339 Troops of the Chinese People’s Liberation Army, Lhasa 850015, ChinaPeng LiDepartment of Pharmacognosy, College of Pharmacy, Army Medical University, Chongqing 400038, China
2023en
ABI

Аннотация

Endophytic fungi are a treasure trove of natural products with great chemical diversity that is largely unexploited. As an alternative to the traditional bioactivity-guided screening approach, the genome-mining-based approach provides a new methodology for obtaining novel natural products from endophytes. In our study, the whole genome of an endophyte, Dactylonectria alcacerensis CT-6, was obtained for the first time. Genomic analysis indicated that D. alcacerensis CT-6 has one 61.8 Mb genome with a G+C content of 49.86%. Gene annotation was extensively carried out using various BLAST databases. Genome collinearity analysis revealed that D. alcacerensis CT-6 has high homology with three other strains of the Dactylonectria genus. AntiSMASH analysis displayed 45 secondary metabolite biosynthetic gene clusters (BGCs) in D. alcacerensis CT-6, and most of them were unknown and yet to be unveiled. Furthermore, only six known substances had been isolated from the fermented products of D. alcacerensis CT-6, suggesting that a great number of cryptic BGCs in D. alcacerensis CT-6 are silent and/or expressed at low levels under conventional conditions. Therefore, our study provides an important basis for further chemical study of D. alcacerensis CT-6 using the gene-mining strategy to awaken these cryptic BGCs for the production of bioactive secondary metabolites.

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