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豌豆 SAD 短链脱氢酶/还原酶:醌还原、组织分布和异源表达。

The pea SAD short-chain dehydrogenase/reductase: quinone reduction, tissue distribution, and heterologous expression.

机构信息

Akademin för Naturvetenskap och Teknik och Centrum för Livsvetenskap , Orebro Universitet, S-70182 Orebro, Sweden.

出版信息

Plant Physiol. 2011 Apr;155(4):1839-50. doi: 10.1104/pp.111.173336. Epub 2011 Feb 22.

Abstract

The pea (Pisum sativum) tetrameric short-chain alcohol dehydrogenase-like protein (SAD) family consists of at least three highly similar members (SAD-A, -B, and -C). According to mRNA data, environmental stimuli induce SAD expression. The aim of this study was to characterize the SAD proteins by examining their catalytic function, distribution in pea, and induction in different tissues. In enzyme activity assays using a range of potential substrates, the SAD-C enzyme was shown to reduce one- or two-ring-membered quinones lacking long hydrophobic hydrocarbon tails. Immunological assays using a specific antiserum against the protein demonstrated that different tissues and cell types contain small amounts of SAD protein that was predominantly located within epidermal or subepidermal cells and around vascular tissue. Particularly high local concentrations were observed in the protoderm of the seed cotyledonary axis. Two bow-shaped rows of cells in the ovary and the placental surface facing the ovule also exhibited considerable SAD staining. Ultraviolet-B irradiation led to increased staining in epidermal and subepidermal cells of leaves and stems. The different localization patterns of SAD suggest functions both in development and in responses to environmental stimuli. Finally, the pea SAD-C promoter was shown to confer heterologous wound-induced expression in Arabidopsis (Arabidopsis thaliana), which confirmed that the inducibility of its expression is regulated at the transcriptional level.

摘要

豌豆四聚体短链醇脱氢酶样蛋白(SAD)家族至少由三个高度相似的成员(SAD-A、-B 和 -C)组成。根据 mRNA 数据,环境刺激会诱导 SAD 的表达。本研究旨在通过研究 SAD 蛋白的催化功能、在豌豆中的分布以及在不同组织中的诱导情况来对其进行表征。在使用一系列潜在底物的酶活性测定中,SAD-C 酶被证明能够还原缺乏长疏水烃尾的一或二环成员醌。使用针对该蛋白的特异性抗血清进行的免疫测定表明,不同的组织和细胞类型含有少量的 SAD 蛋白,主要位于表皮或表皮下细胞以及血管组织周围。在种子子叶轴的原表皮中观察到特别高的局部浓度。在卵巢中呈弓状排列的两排细胞和面向胚珠的胎盘表面也表现出相当数量的 SAD 染色。紫外线-B 辐射导致叶片和茎部的表皮和表皮下细胞的染色增加。SAD 的不同定位模式表明其在发育和对环境刺激的反应中都具有功能。最后,证明豌豆 SAD-C 启动子可在拟南芥(Arabidopsis thaliana)中赋予异源的伤诱导表达,这证实了其表达的诱导是在转录水平上受到调控的。

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Short-chain dehydrogenases/reductases (SDR): the 2002 update.短链脱氢酶/还原酶(SDR):2002年更新版
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Short-chain dehydrogenases/reductases (SDRs).短链脱氢酶/还原酶(SDRs)
Eur J Biochem. 2002 Sep;269(18):4409-17. doi: 10.1046/j.1432-1033.2002.03130.x.

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