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鉴定和功能分析两个与催化茶树()中()-3-己烯醛还原为()-3-己烯醇有关的醇脱氢酶基因。

Identification and Functional Analysis of Two Alcohol Dehydrogenase Genes Involved in Catalyzing the Reduction of ()-3-Hexenal into ()-3-Hexenol in Tea Plants ().

机构信息

State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei 230036, China.

Henan Key Laboratory of Tea Plant Biology, Xinyang Normal University, Xinyang 464000, China.

出版信息

J Agric Food Chem. 2022 Feb 16;70(6):1830-1839. doi: 10.1021/acs.jafc.1c06984. Epub 2022 Feb 3.

Abstract

Alcohol dehydrogenase (ADH) is a vital enzyme in the biosynthesis pathway of six-carbon volatiles in plants. However, little is known about its functions in tea plants. Here, we identified two genes ( and ). An protein expression assay showed that both CsADH1 and CsADH2 proteins can catalyze the reduction of ()-3-hexenal into ()-3-hexenol. Subcellular localization revealed that both CsADH1 and CsADH2 proteins were predominantly localized in the nucleus and cytosol. had high transcripts in young stems in autumn, while showed extremely high expression levels in stems and roots. The expression of was mainly downregulated under ABA treatment, while and transcripts were significantly lower under MeJA treatment at 12 and 24 h. Under cold treatment, transcripts first decreased and then increased, while demonstrated an almost opposite expression pattern. Notably, was significantly upregulated under simulated invasion. Gene suppression by antisense oligonucleotides (AsODNs) demonstrated that AsODN_ treatment significantly reduced transcripts and the abundance of ()-3-hexenol products. The results indicate that the two genes may play an important role in response to (a)biotic stresses and in the process of ()-3-hexenol biosynthesis.

摘要

醇脱氢酶(ADH)是植物六碳挥发物生物合成途径中的一种重要酶。然而,关于其在茶树中的功能知之甚少。在这里,我们鉴定了两个基因(和)。CsADH1 和 CsADH2 蛋白的表达分析表明,这两种蛋白都能催化()-3-己烯醛还原为()-3-己烯醇。亚细胞定位表明,CsADH1 和 CsADH2 蛋白主要定位于细胞核和细胞质。在秋季的幼茎中具有高转录本,而在茎和根中则表现出极高的表达水平。ABA 处理下的表达主要下调,而 MeJA 处理 12 和 24 h 时和的转录本显著降低。冷处理下,转录本先下降后上升,而则表现出几乎相反的表达模式。值得注意的是,在模拟病原菌入侵下,表达显著上调。反义寡核苷酸(AsODN)的基因抑制表明,AsODN_处理显著降低了的转录本和()-3-己烯醇产物的丰度。结果表明,这两个基因可能在应对(生物)胁迫和()-3-己烯醇生物合成过程中发挥重要作用。

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