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水杨酸诱导的AtAACT和AtMVD表达上调增强了白蚁伞中三萜生物合成。

Salicylic acid-induced upregulation of AtAACT and AtMVD expression enhances triterpene biosynthesis in Athelia termitophila.

作者信息

Hu Fangcheng, Fang Yonggang, Xing Lianxi

机构信息

College of Life Sciences, Northwest University, Xi'an, 710069, China.

Shaanxi Key Laboratory for Animal Conservation (Northwest University), Xi'an, 710069, China.

出版信息

World J Microbiol Biotechnol. 2025 Feb 27;41(3):87. doi: 10.1007/s11274-025-04301-1.

Abstract

Triterpenoids exhibit great potential in the food and pharmaceutical industries and are the predominant secondary metabolites of Athelia termitophila (TMB). AtAACT catalyzes the conversion of acetyl-CoA and acetoacetate in mevalonate biosynthesis, while AtMVD catalyzes the decarboxylation of mevalonate diphosphate, producing key precursors essential for triterpenoid synthesis. To augment the biosynthesis of TMB triterpenes, we cloned the AtAACT and AtMVD genes into plasmids, which were subsequently used to transform Escherichia coli. The resulting bacterial strains were used for sequencing and bioinformatic analyses to elucidate the encoded amino acid sequences. Furthermore, salicylic acid (SA) was employed as an elicitor to enhance triterpene biosynthesis in TMB. The SA treatment was initiated on the 6th day of incubation and maintained continuously across all time points (36, 48, and 60 h and others), achieving a maximal triterpene concentration of 41.83 ± 0.5 mg/100 mL, corresponding to a 26% increase compared to the uninduced group. Comparative transcriptomic analysis showed that the expression of AtAACT and AtMVD was significantly upregulated in the SA-treated group compared to the control. This upregulation underscores the crucial roles of these genes in facilitating triterpene biosynthesis in TMB. Furthermore, qPCR temporal profiling revealed that AtAACT achieved peak transcript levels at 36 h post-induction, whereas AtMVD peaked at 48 h. This study provides an effective strategy to enhance TMB triterpene content and offers new insights into the mechanisms of SA-treated triterpene biosynthesis.

摘要

三萜类化合物在食品和制药行业具有巨大潜力,是嗜白蚁阿氏菌(TMB)的主要次生代谢产物。AtAACT催化甲羟戊酸生物合成中乙酰辅酶A和乙酰乙酸的转化,而AtMVD催化甲羟戊酸二磷酸的脱羧反应,产生三萜类化合物合成所必需的关键前体。为了增加TMB三萜类化合物的生物合成,我们将AtAACT和AtMVD基因克隆到质粒中,随后用于转化大肠杆菌。所得菌株用于测序和生物信息学分析,以阐明编码的氨基酸序列。此外,水杨酸(SA)被用作诱导剂,以增强TMB中三萜类化合物的生物合成。SA处理在培养的第6天开始,并在所有时间点(36、48和60小时及其他时间点)持续进行,三萜类化合物的最大浓度达到41.83±0.5mg/100mL,与未诱导组相比增加了26%。比较转录组分析表明,与对照组相比,SA处理组中AtAACT和AtMVD的表达显著上调。这种上调突出了这些基因在促进TMB中三萜类化合物生物合成中的关键作用。此外,qPCR时间分析表明,AtAACT在诱导后36小时达到转录水平峰值,而AtMVD在48小时达到峰值。本研究提供了一种提高TMB三萜类化合物含量的有效策略,并为SA处理的三萜类化合物生物合成机制提供了新的见解。

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