Guo Lu, Liu Yuan-Gen, Fu Ying-Wen, Wang Yu-Yan, Wang Hao-Jin, Zhu Shu-Mei, He Qi-Zhi, Zhang Dong-Xue, Zhu Shan-Shan, Wang Si-Xian, Tong Tian, Dong Xu-Jie, Wang Xiao-Ling, Liu Yong-Nan, Liu Gao-Qiang
Hunan Provincial Key Laboratory of Forestry Biotechnology and International Cooperation Base of Science and Technology Innovation on Forest Resource Biotechnology, Central South University of Forestry and Technology, Changsha, China.
Hunan University of Humanities, Science and Technology, Loudi, China.
NPJ Sci Food. 2025 Mar 26;9(1):44. doi: 10.1038/s41538-025-00407-w.
Treatment with C18:1 and C18:2, but not C18:0, increased the triterpenoid content of the medicinal fungus Sanghuangporus lonicericola. We identified 413 terpenoids, including 210 volatile terpenoids. Eight upregulated terpenoids, including 3,13,15-trihydroxyoleanane-12-one, dulcioic acid and serrat-14-ene-3,20,24,29-tetrol, were shared between the C18:1 and C18:2 treatments but not the C18:0 treatment. The C18:1 and C18:2 treatments increased the levels of 12 and 7 odour-related terpenoids, respectively, and increased the level of alpha-farnesene (herbal odour). Gene set enrichment analysis revealed that compared with C18:0, C18:1 and C18:2 produced stronger activation of the terpenoid biosynthesis, fatty acid degradation, and MAPK signalling pathways and stronger inhibition of basal transcription factors at both the transcript and protein levels. Finally, two-way orthogonal partial least squares analysis revealed that gene and protein expression in the identified pathways was correlated with levels of unsaturated fatty acid-induced terpenoid metabolites. Together, our integrated multiomics data revealed the key pathways involved in unsaturated fatty acid-induced terpenoid biosynthesis in S. lonicericola.
用C18:1和C18:2而非C18:0处理,可提高药用真菌忍冬桑黄的三萜含量。我们鉴定出413种萜类化合物,其中包括210种挥发性萜类化合物。在C18:1和C18:2处理组中共有8种上调的萜类化合物,包括3,13,15 - 三羟基齐墩果烷 - 12 - 酮、甜菊酸和锯齿鲨烯 - 14 - 烯 - 3,20,24,29 - 四醇,但C18:0处理组中没有。C18:1和C18:2处理分别使12种和7种与气味相关的萜类化合物水平升高,并使α - 法尼烯(草药气味)水平升高。基因集富集分析显示,与C18:0相比,C18:1和C18:2在转录本和蛋白质水平上对萜类生物合成、脂肪酸降解和MAPK信号通路产生更强的激活作用,并对基础转录因子产生更强的抑制作用。最后,双向正交偏最小二乘法分析表明,所鉴定途径中的基因和蛋白质表达与不饱和脂肪酸诱导的萜类代谢产物水平相关。总之,我们的综合多组学数据揭示了忍冬桑黄中不饱和脂肪酸诱导的萜类生物合成所涉及的关键途径。