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鉴定和表征沉香属植物中的一种新型倍半萜合酶:沉香形成的重要基因。

Identification and characterization of a novel sesquiterpene synthase from Aquilaria sinensis: An important gene for agarwood formation.

机构信息

State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangdong Institute of Microbiology, Guangzhou 510070, China.

Sun Yat-Sen University Cancer Center; State key Laboratory of Oncology in South China; Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, China; Guangdong Pharmaceutical University, Guangzhou 510006, China.

出版信息

Int J Biol Macromol. 2018 Mar;108:884-892. doi: 10.1016/j.ijbiomac.2017.10.183. Epub 2017 Nov 2.

Abstract

Sesquiterpene synthases are key enzymes for biosynthesis of sesquiterpene compounds and are important for agarwood formation in Aquilaria sinensis.The As-sesTPS gene encoding a novel sesquiterpene synthase was expressed in Escherichia coli strain BL21 (DE3) as an inclusion body and purified by Ni affinity chromatography. The molecular weight of the protein was lower than the theoretical value. Amino acid sequencing results indicated that the 27.2kDa-recombinant protein was a truncated sesquiterpene synthase from chemically induced A. sinensis. After refolding, the truncated As-SesTPS protein catalyzed the conversion of farnesyl pyrophosphate (FPP) to nerolidol which is a characteristic component of agarwood. The optimal reaction pH for the As-SesTPS protein was 8.0, and the optimal temperature was 30°C. The values of Km and Vmax of As-SesTPS protein towards FPP were 0.0548mM, 42.83μmol/mg.min, respectively. The results of qPCR and iTRAQ demonstrated the much higher expression level of As-SesTPS gene in agarwood than that in whitewood. This study provides a foundation for elucidating the mechanism of agarwood formation in A. sinensis and the potential of the novel gene for improving the quality of artificial agarwood.

摘要

倍半萜合酶是倍半萜类化合物生物合成的关键酶,对沉香(Aquilaria sinensis)的形成起着重要作用。本研究从白木香(Aquilaria sinensis)中克隆了一个新型倍半萜合酶基因 As-sesTPS,并在大肠杆菌 BL21 (DE3)中表达为包涵体,经 Ni 亲和层析柱纯化。该蛋白分子量低于理论值,氨基酸测序结果表明,该 27.2kDa 的重组蛋白是一种化学诱导的白木香倍半萜合酶的截短体。经复性后,该截短体 As-SesTPS 蛋白能催化法呢基焦磷酸(FPP)转化为沉香醇,后者是沉香的特征成分。As-SesTPS 蛋白的最适反应 pH 为 8.0,最适温度为 30°C。该蛋白对 FPP 的 Km 和 Vmax 值分别为 0.0548mM 和 42.83μmol/mg.min。qPCR 和 iTRAQ 结果表明,As-SesTPS 基因在沉香中的表达水平明显高于白木香。本研究为阐明沉香形成的机制以及该新型基因在提高人工沉香质量方面的潜力提供了依据。

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