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诱导子对甜菊糖甙生物合成途径中甜菊的影响。

The effect of the elicitors on the steviol glycosides biosynthesis pathway in Stevia rebaudiana.

机构信息

Department of Agronomy and Plant Breading, Faculty of Agriculture and Natural Resource, University of Mohaghegh Ardabili, and Agricultural Biotechnology Research Institute of Iran (ABRII), Karaj, Iran.

Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research Education and Extension Organisation (AREEO), Karaj, Iran; and Corresponding author. Email:

出版信息

Funct Plant Biol. 2019 Aug;46(9):787-795. doi: 10.1071/FP19014.

Abstract

Stevia rebaudiana Bertoni has been promoted for having sweet leaves as well as pharmaceutical and industrial properties. The sweet taste of Stevia leaves is due to the presence of steviol glycosides (a group of diterpene glycosides) found in a small number of plants. In the biosynthetic pathway of steviol glycosides (SGs), 15 enzymes that express the genes are associated with these enzymes under the influence of the elicitors. Due to the individuality of the stevia and few studies on the biosynthesis pathway of SGs, this paper attempted to investigate the effects of some of the elicitors, including methyl jasmonate (MeJA), salicylic acid (SA), auxins (Aux), cytokinins (CKs), gibberellins (GAs) and its inhibitors including paclobutrazol (BPZ) and chloroquate (CCC)), on the responsible genes for the biosynthesis of SGs. Some of these elicitors, including MeJA, SA and GA have great potential in increasing secondary metabolites. Moreover, the biosynthetic pathway of GAs and SGs are shared till ent-kaurenoic acid (ent-KA) biosynthesis, which raises the question of whether this hormone and its inhibitors are effective in the SGs biosynthesis.

摘要

甜菊(Stevia rebaudiana Bertoni)因具有甜叶和药用及工业用途而受到推崇。甜菊叶的甜味源于存在于少数植物中的甜菊糖苷(二萜糖苷的一组)。在甜菊糖苷(SGs)的生物合成途径中,有 15 种酶在这些酶的表达基因下与这些酶相关联,这些酶受到诱导剂的影响。由于甜菊的个体性以及对 SGs 生物合成途径的研究较少,本文试图研究一些诱导剂(包括茉莉酸甲酯(MeJA)、水杨酸(SA)、生长素(Aux)、细胞分裂素(CKs)、赤霉素(GAs)及其抑制剂包括多效唑(BPZ)和氯喹啉酸(CCC))对 SGs 生物合成负责基因的影响。其中一些诱导剂,包括 MeJA、SA 和 GA,在增加次生代谢物方面具有很大的潜力。此外,GA 和 SGs 的生物合成途径在 ent-贝壳杉烯酸(ent-KA)的生物合成之前是共享的,这就提出了一个问题,即这种激素及其抑制剂是否对 SGs 的生物合成有效。

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