分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Characterization of a γ-Humulene Synthase from Fungus Ascobolus immersus

Haichun Zeng, Jiatong Zeng, Yuxin Zhou, Beilin Meng, Li Rao

Journal:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY

IF:6.7

DOI:10.1021/acs.jafc.6c03126

PMID:42084954

Published:2026-05-05

research field:酶工程合成生物学真菌学天然产物化学生物化学

Abstract

γ-Humulene is an 11-membered macrocyclic sesquiterpene widely distributed in plants and valued for its diverse biological activities. However, no dedicated γ-humulene synthase has been identified to date. In this study, a sesquiterpene synthase (AiSTS) from the fungus Ascobolus immersus was identified and functionally characterized. In vivo heterologous expression and in vitro enzymatic assays demonstrated that AiSTS specifically catalyzes the conversion of (E,E)- farnesyl pyrophosphate ((E,E)-FPP) into γ-humulene. Furthermore, AiSTS also exhibits notable substrate promiscuity, accepting (E)-geranyl pyrophosphate ((E)-GPP) and (E,E,E)-geranylgeranyl pyrophosphate ((E,E,E)-GGPP) to generate diverse mono- and diterpene products. Site-directed mutagenesis revealed seven amino acid residues that are essential for enzyme folding, catalytic efficiency, and product selectivity. The discovery of AiSTS expands the repertoire of fungal terpene synthases and lays a solid foundation for enzyme engineering and sustainable microbial production of γ-humulene.

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