Wang Honggang, Yu Luyao, Li Shuangshuang, Wang Jin, Cheng Wenjing, Zhu Siqing, Shi Feng, Tai Yuling, Yuan Yi
School of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Plant Mol Biol. 2025 Jul 7;115(4):83. doi: 10.1007/s11103-025-01606-5.
German chamomile (Matricaria chamomilla L.) is a traditional aromatic medicinal plant, its flower contains volatile aromatic oil (essential oil). The main sesquiterpene components of the essential oil are (E)-β-farnesene, chamazulene, and α-bisabolol, these components have significant medicinal value and are used in food, cosmetics, and pharmaceuticals. However, the German chamomile genome has not yet been cataloged in any database; consequently, research on the intricate regulatory network and interaction mechanisms among proteins in German chamomile remains limited. Furthermore, no study has thus far developed a yeast cDNA library for German chamomile. Therefore, we constructed a homogenized yeast cDNA library using different tissues of German chamomile, this yeast cDNA library had a titer of 1.444 × 10 colony-forming units/mL, an average insert size of > 1,000 bp, and a positive rate of 100%. In addition, 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate synthase (HDS) that interacted with Hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase (HDR) involved in the final step of the methylerythritol 4-phosphate (MEP) pathway was verified through the yeast two-hybrid (Y2H) assay and bimolecular fluorescence complementation (BiFC). At the same time, the expression pattern and function of McHDS were further analyzed. In conclusion, we successfully constructed a yeast cDNA library of German chamomile for the first time, and McHDS interacting with McHDRa/b was successfully screened, providing a reliable theoretical foundation for investigating the molecular mechanism of its coordination with McHDRa/b to regulate the biosynthesis of (E)-β-farnesene in German chamomile. Which lays the groundwork for our comprehensive understanding of the protein interaction network involved in sesquiterpene synthesis of German chamomile.
德国洋甘菊(母菊)是一种传统的芳香药用植物,其花朵含有挥发性芳香油(精油)。该精油的主要倍半萜成分是(E)-β-法尼烯、天蓝烃和α-红没药醇,这些成分具有重要的药用价值,可用于食品、化妆品和药品中。然而,德国洋甘菊的基因组尚未在任何数据库中编目;因此,对德国洋甘菊中蛋白质之间复杂的调控网络和相互作用机制的研究仍然有限。此外,迄今为止,还没有针对德国洋甘菊开发酵母cDNA文库的研究。因此,我们利用德国洋甘菊的不同组织构建了一个均一化酵母cDNA文库,该酵母cDNA文库的滴度为1.444×10菌落形成单位/毫升,平均插入片段大小大于1000 bp,阳性率为100%。此外,通过酵母双杂交(Y2H)分析和双分子荧光互补(BiFC)验证了与参与甲基赤藓糖醇4-磷酸(MEP)途径最后一步的羟基-2-甲基-2-(E)-丁烯基4-二磷酸还原酶(HDR)相互作用的1-羟基-2-甲基-2-(E)-丁烯基4-二磷酸合酶(HDS)。同时,进一步分析了McHDS的表达模式和功能。总之,我们首次成功构建了德国洋甘菊的酵母cDNA文库,并成功筛选出与McHDRa/b相互作用的McHDS,为研究其与McHDRa/b协同调节德国洋甘菊中(E)-β-法尼烯生物合成的分子机制提供了可靠的理论基础。这为我们全面了解德国洋甘菊倍半萜合成中涉及的蛋白质相互作用网络奠定了基础。