Cao Peng-Fei, Wu Chen-Gao, Dang Zhi-Hao, Shi Liang, Jiang Ai-Liang, Ren Ang, Zhao Ming-Wen
College of Life Sciences, Nanjing Agricultural University, Nanjing, People's Republic of China; Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, Nanjing, Jiangsu, People's Republic of China.
Microbiology Department, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, Nanjing, Jiangsu, People's Republic of China.
Int J Med Mushrooms. 2017;19(1):65-73. doi: 10.1615/IntJMedMushrooms.v19.i1.70.
We demonstrate herein that salicylic acid (SA) can enhance ganoderic acid (GA) accumulation in the lingzhi or reishi medicinal mushroom Ganoderma lucidum. Following treatment with different concentrations of SA, the GA content was increased 22.72% to 43.04% compared with the control group. When the fungi were treated with 200 μmol/L SA at different times, the GA content was improved 10.21% to 35.24% compared with the control group. By choosing the optimum point based on response surface methodology, the GA content could be increased up to 229.03 μg/100 mg, which was improved 66.38% compared with the control group. When the fungi were treated with 200 μmol/L SA, the transcription levels of key genes in the GA biosynthesis pathway-squalene (SQ) synthase (sqs), lanosterol (Lano; osc), and hydroxy-3-methylglutaryl-coenzyme A reductase (hmgr)-were improved 119.6-, 3.2-, and 4.2-fold, respectively. In addition, following treatment with 100 μmol/L SA, the levels of Lano and SQ, which are intermediate metabolites of GA biosynthesis, were increased 2.8- and 1.4-fold, respectively. These results indicate that SA can regulate the expression of genes related to GA biosynthesis and increases the metabolic levels of Lano and SQ, thereby resulting in the accumulation of GA.
我们在此证明,水杨酸(SA)可增强灵芝药用蘑菇Ganoderma lucidum中灵芝酸(GA)的积累。用不同浓度的SA处理后,与对照组相比,GA含量增加了22.72%至43.04%。当在不同时间用200μmol/L SA处理真菌时,与对照组相比,GA含量提高了10.21%至35.24%。通过基于响应面法选择最佳点,GA含量可提高至229.03μg/100mg,与对照组相比提高了66.38%。当用200μmol/L SA处理真菌时,GA生物合成途径中的关键基因——鲨烯(SQ)合酶(sqs)、羊毛甾醇(Lano;osc)和3-羟基-3-甲基戊二酰辅酶A还原酶(hmgr)的转录水平分别提高了119.6倍、3.2倍和4.2倍。此外,用100μmol/L SA处理后,GA生物合成的中间代谢产物Lano和SQ的水平分别提高了2.8倍和1.4倍。这些结果表明,SA可以调节与GA生物合成相关的基因表达,并提高Lano和SQ的代谢水平,从而导致GA的积累。