Liu Dafeng, Li Na, Yu Feng, Du Yanyan, Song Hongjun, Yao Wenshuang
Xinjiang Key Laboratory of Lavender Conservation and Utilization, College of Biological Sciences and Technology, Yili Normal University, Yining 835000, China.
School of Life Sciences, Xiamen University, Xiamen 361102, China.
Curr Issues Mol Biol. 2025 Jul 4;47(7):517. doi: 10.3390/cimb47070517.
Lavender species hold substantial economic importance due to their widespread cultivation for essential oils (EOs). Lavender EOs contain terpenes essential for industries such as cosmetics, personal care, and pharmaceuticals. In the biosynthetic pathway of EOs, bornyl diphosphate synthase (LaBPPS) catalyzes the conversion of geranyl diphosphate (GPP) to bornyl diphosphate (BPP). However, the functional mechanisms of LaBPPS remain poorly understood. Here, we conducted mutational experiments based on the molecular docking results, and found that mutations at positions D356A, D360A, R497A, D501A, or E508A led to a 50- to 100-fold reduction in the activity. Deletion of region 1-58 (∆1-58) did not affect activity compared to the wild-type (WT) protein, while deletions of regions 1-74 or 59-74 (∆1-74 or ∆59-74) significantly decreased the activity. Conversely, deletion of residues 578-602 (∆578-602) dramatically increased the activity. The gene showed dramatically higher expression levels in flowers compared to other tissues (stems, leaves and roots), peaking at 8:00. Our results provide valuable insights into EO biosynthesis in lavender and suggest potential strategies for genetic engineering aimed at improving EO quality.
薰衣草属植物因其广泛种植用于提取精油(EOs)而具有重要的经济价值。薰衣草精油含有对化妆品、个人护理和制药等行业至关重要的萜类化合物。在精油的生物合成途径中,冰片基二磷酸合酶(LaBPPS)催化香叶基二磷酸(GPP)转化为冰片基二磷酸(BPP)。然而,LaBPPS的功能机制仍知之甚少。在此,我们基于分子对接结果进行了突变实验,发现D356A、D360A、R497A、D501A或E508A位点的突变导致活性降低了50至100倍。与野生型(WT)蛋白相比,缺失1 - 58区域(∆1 - 58)不影响活性,而缺失1 - 74或59 - 74区域(∆1 - 74或∆59 - 74)显著降低了活性。相反,缺失578 - 602残基(∆578 - 602)显著提高了活性。该基因在花中的表达水平明显高于其他组织(茎、叶和根),在8:00达到峰值。我们的结果为薰衣草精油生物合成提供了有价值的见解,并提出了旨在提高精油质量的基因工程潜在策略。