Wang Zhikai, Zhou Guoying, Chen Jungang, Miao Xinyu, Xia Yandong, Du Zhuang, Liu Junang
Key Laboratory of National Forestry and Grassland Administration for Control of Diseases and Pests of South Plantation, Central South University of Forestry and Technology, Changsha, China.
Key Laboratory of Cultivation and Protection for Non-Wood Forest Trees, Central South University of Forestry and Technology, Changsha, China.
PLoS One. 2024 Dec 26;19(12):e0316178. doi: 10.1371/journal.pone.0316178. eCollection 2024.
Agarwood is a precious resinous heartwood highly valued for its cultural, religious, and medicinal significance. With the increasing market demand, natural agarwood resources are rapidly depleting, making the development of effective artificial induction methods for agarwood highly significant. This study aims to explore the feasibility of using callus tissue to assess the ability of fungi to induce agarwood formation. We selected two fungi isolated from Aquilaria sinensis, W-1 (Podospora setosa) and W-15 (Alternaria alstroemeriae), and used the known agarwood-inducing fungi YMY (Pestalotiopsis sp.) as a positive control, by treating A. sinensis callus with their fermented filtrates. The experimental results showed that W-1 and W-15 treatments significantly enhanced the activity of Superoxide dismutase (SOD) and Peroxidase (POD) in the callus tissue and upregulated the expression of 3-hydroxy-3-methylglutaryl-CoA synthase (HMGS), 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR), and sesquiterpene synthase (ASS-1). GC-MS analysis further confirmed that the contents of sesquiterpenes and aromatic compounds in A. sinensis treated with W-1 and W-15 were significantly elevated, suggesting that these fungi possess the capacity to induce the formation of agarwood. This study demonstrates that using callus tissue to screen fungi capable of inducing agarwood is feasible and effective, providing new insights for screening fungi resources that efficiently induce agarwood formation in the future.
沉香是一种珍贵的含树脂心材,因其文化、宗教和药用价值而备受珍视。随着市场需求的增加,天然沉香资源正在迅速枯竭,因此开发有效的沉香人工诱导方法具有重要意义。本研究旨在探讨利用愈伤组织来评估真菌诱导沉香形成能力的可行性。我们从白木香中分离出两种真菌,W-1(柄孢壳菌)和W-15(六出花链格孢),并以已知的沉香诱导真菌YMY(拟盘多毛孢属)作为阳性对照,用它们的发酵滤液处理白木香愈伤组织。实验结果表明,W-1和W-15处理显著提高了愈伤组织中超氧化物歧化酶(SOD)和过氧化物酶(POD)的活性,并上调了3-羟基-3-甲基戊二酰辅酶A合酶(HMGS)、1-脱氧-D-木酮糖-5-磷酸还原异构酶(DXR)和倍半萜合酶(ASS-1)的表达。气相色谱-质谱联用(GC-MS)分析进一步证实,经W-1和W-15处理的白木香中倍半萜和芳香化合物的含量显著升高,表明这些真菌具有诱导沉香形成的能力。本研究表明,利用愈伤组织筛选能够诱导沉香的真菌是可行且有效的,为今后筛选高效诱导沉香形成的真菌资源提供了新的见解。