Zettl R, Schell J, Palme K
Max-Planck-Institut für Züchtungsforschung, Cologne, Federal Republic of Germany.
Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):689-93. doi: 10.1073/pnas.91.2.689.
We used 5-azido-[7-3H]indole-3-acetic acid (5-azido-[7-3H]IAA), a photoaffinity analogue of the plant hormone indole-3-acetic acid (IAA), to search for auxin-binding proteins in Arabidopsis thaliana membranes. We identified an auxin-binding protein with a molecular mass of 24 kDa (Atpm24) in microsomes as well as in plasma membrane vesicles. Atpm24 was solubilized by 1% Triton X-100 and partially purified. A cDNA clone (Atpm24.1) corresponding to Atpm24 was isolated. The amino acid sequence predicted from the Atpm24.1 cDNA contains 212 amino acid residues with a relative molecular mass of 24,128 Da. Data base searches revealed that the predicted protein has homology to glutathione S-transferases (GSTs; EC 2.5.1.18). When Atpm24.1 was expressed in Escherichia coli, we found a high level of GST activity in the bacterial extracts. We have analyzed the substrate specificity of this protein and found that cumene hydroperoxide and trans-stilbene oxide but not trans-cinnamic acid or IAA-CoA were substrates. A role for this GST in physiological processes of plants is discussed.
我们使用5-叠氮基-[7-³H]吲哚-3-乙酸(5-叠氮基-[7-³H]IAA),一种植物激素吲哚-3-乙酸(IAA)的光亲和类似物,来寻找拟南芥膜中的生长素结合蛋白。我们在微粒体以及质膜囊泡中鉴定出一种分子量为24 kDa的生长素结合蛋白(Atpm24)。Atpm24用1% Triton X-100溶解并部分纯化。分离出了与Atpm24对应的cDNA克隆(Atpm24.1)。从Atpm24.1 cDNA预测的氨基酸序列包含212个氨基酸残基,相对分子质量为24,128 Da。数据库搜索显示,预测的蛋白质与谷胱甘肽S-转移酶(GSTs;EC 2.5.1.18)具有同源性。当Atpm24.1在大肠杆菌中表达时,我们在细菌提取物中发现了高水平的GST活性。我们分析了该蛋白的底物特异性,发现氢过氧化异丙苯和反式氧化芪是底物,而反式肉桂酸或IAA-CoA不是底物。讨论了这种GST在植物生理过程中的作用。