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檀香醇生物合成的分子调控在檀香科植物中。

Molecular regulation of santalol biosynthesis in Santalum album L.

机构信息

Department of Biotechnology, Vittal Mallya Scientific Research Foundation, Bangalore 560076, India.

出版信息

Gene. 2013 Sep 25;527(2):642-8. doi: 10.1016/j.gene.2013.06.080. Epub 2013 Jul 13.

Abstract

Santalum album L. commonly known as East-Indian sandal or chandan is a hemiparasitic tree of family santalaceae. Santalol is a bioprospecting molecule present in sandalwood and any effort towards metabolic engineering of this important moiety would require knowledge on gene regulation. Santalol is a sesquiterpene synthesized through mevalonate or non-mevalonate pathways. First step of santalol biosynthesis involves head to tail condensation of isopentenyl pyrophosphate (IPP) with its allylic co-substrate dimethyl allyl pyrophosphate (DMAPP) to produce geranyl pyrophosphate (GPP; C10 - a monoterpene). GPP upon one additional condensation with IPP produces farnesyl pyrophosphate (FPP; C15 - an open chain sesquiterpene). Both the reactions are catalyzed by farnesyl diphosphate synthase (FDS). Santalene synthase (SS), a terpene cyclase catalyzes cyclization of open ring FPP into a mixture of cyclic sesquiterpenes such as α-santalene, epi-β-santalene, β-santalene and exo bergamotene, the main constituents of sandal oil. The objective of the present work was to generate a comprehensive knowledge on the genes involved in santalol production and study their molecular regulation. To achieve this, sequences encoding farnesyl diphosphate synthase and santalene synthase were isolated from sandalwood using suppression subtraction hybridization and 2D gel electrophoresis technology. Functional characterization of both the genes was done through enzyme assays and tissue-specific expression of both the genes was studied. To our knowledge, this is the first report on studies on molecular regulation, and tissue-specific expression of the genes involved in santalol biosynthesis.

摘要

檀香醇是檀香木中存在的一个生物勘探分子,对该重要部分进行代谢工程的任何努力都需要了解基因调控。檀香醇是通过甲羟戊酸或非甲羟戊酸途径合成的倍半萜烯。檀香醇生物合成的第一步涉及异戊烯基焦磷酸(IPP)与其烯丙基辅酶二甲烯丙基焦磷酸(DMAPP)的头对头缩合,生成香叶基焦磷酸(GPP;C10 - 单萜烯)。GPP 再与 IPP 缩合一次,生成法呢基焦磷酸(FPP;C15 - 开链倍半萜烯)。这两个反应都由法尼基二磷酸合酶(FDS)催化。檀香烯合酶(SS)是一种萜烯环化酶,催化开环 FPP 环化成混合的环状倍半萜烯,如α-檀香烯、表-β-檀香烯、β-檀香烯和外-佛手柑烯,它们是檀香油的主要成分。本工作的目的是生成涉及檀香醇生产的基因的综合知识,并研究它们的分子调控。为了实现这一目标,使用抑制差减杂交和 2D 凝胶电泳技术从檀香木中分离出编码法尼基二磷酸合酶和檀香烯合酶的序列。通过酶测定和两个基因的组织特异性表达研究了两个基因的功能特征。据我们所知,这是关于檀香醇生物合成中涉及的基因的分子调控和组织特异性表达的首次报道。

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