生物
相思
基因
生物化学
生物合成
突变
同步
遗传学
植物
基因组
突变体
作者
Fengqi Li,Chunyan Wu,Youssef Dewer,Yan Liang,Jing‐Jiang Zhou,Chen Luo,Guirong Wang
摘要
Abstract BACKGROUND The irregular acyclic homoterpenes 4,8‐dimethyl‐1,3,7‐nonatriene (DMNT) and 4,8,12‐trimethyl‐1,3,7,11‐tridecatetraene (TMTT) are key volatile compounds involved in various chemical ecological interactions, particularly contributing to plant defense against phytophagous insects. However, the genomic basis and evolutionary history of homoterpene biosynthesis in legumes remain largely unexplored, limiting our understanding of their functional diversification and ecological roles. RESULTS Using a yeast expression system, we identified two novel, tandemly duplicated cytochrome P450 genes, PlCYP82D47‐like and PlCYP82D47 , involved in DMNT and TMTT biosynthesis in lima bean ( Phaseolus lunatu s). PlCYP82D47‐like catalyzes the conversion of ( E )‐nerolidol and ( E , E )‐geranyllinalool to DMNT and TMTT, respectively, while PlCYP82D47 specifically converts ( E )‐nerolidol to DMNT. Evolutionary analysis revealed syntenic tandem duplicates of these genes in lima bean, cotton, and Arabidopsis , suggesting a conserved genomic architecture for DMNT/TMTT biosynthesis among dicotyledonous plants and implying potential gene loss events in this genomic region. Computational modeling identified residues L324 and L505 as critical for substrate recognition by PlCYP82D47 . Site‐directed mutagenesis and in vitro enzymatic assays confirmed that substitutions at these residues significantly reduced catalytic activity. CONCLUSION Our findings provide new insights into the enzymatic and evolutionary basis of homoterpene biosynthesis in legumes and offer promising targets for future metabolic engineering applications. © 2025 Society of Chemical Industry.
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