Phaseolus vulgaris STP13.1 is an H+‐coupled monosaccharide transporter, present in source leaves and seed coats, with higher substrate affinity at depolarized potentials

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-04-22 DOI:10.1002/pld3.585
Joseph L. Pegler, John W. Patrick, Benjamin McDermott, Anthony Brown, Jackson M. J. Oultram, Christopher P. L. Grof, John M. Ward
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Abstract

Sugar transport proteins (STPs) are high‐affinity H+‐coupled hexose symporters. Recently, the contribution of STP13 to bacterial and fungal pathogen resistance across multiple plant species has garnered significant interest. Quantitative PCR analysis of source leaves, developing embryos, and seed coats of Phaseolus vulgaris L. (common bean) revealed that PvSTP13.1 was expressed in source leaves and seed coats throughout seed development. In contrast, PvSTP13.1 transcripts were detected at exceedingly low levels in developing embryos. To characterize the transport mechanism, PvSTP13.1 was expressed in Xenopus laevis oocytes, and inward‐directed currents were analyzed using two‐electrode voltage clamping. PvSTP13.1 was shown to function as an H+‐coupled monosaccharide symporter exhibiting a unique high affinity for hexoses and aldopentoses at depolarized membrane potentials. Specifically, of the 31 assessed substrates, which included aldohexoses, deoxyhexoses, fructose, 3‐O‐methyl‐D‐glucose, aldopentoses, polyols, glycosides, disaccharides, trisaccharides, and glucuronic acid, PvSTP13.1 displayed the highest affinity (K0.5) for glucose (43 μM), mannose (92 μM), galactose (145 μM), fructose (224 μM), xylose (1.0 mM), and fucose (3.7 mM) at pH 5.6 at a depolarized membrane potential of −40 mV. The results presented here suggest PvSTP13.1 contributes to retrieval of hexoses from the apoplasmic space in source leaves and coats of developing seeds.
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Phaseolus vulgaris STP13.1 是一种 H+ 偶联单糖转运体,存在于源叶和种皮中,在去极化电位时具有更高的底物亲和力
糖转运蛋白(STPs)是一种高亲和力的 H+ 偶联六糖合体。最近,STP13 对多种植物的细菌和真菌病原体抗性的贡献引起了人们的极大兴趣。对芸豆(Phaseolus vulgaris L.)的源叶、发育中的胚和种皮进行的定量 PCR 分析表明,PvSTP13.1 在源叶和种皮的整个种子发育过程中都有表达。相反,在发育中的胚中检测到的 PvSTP13.1 转录物水平极低。为了确定转运机制的特征,PvSTP13.1 在爪蟾卵母细胞中进行了表达,并使用双电极电压箝位分析了内向电流。研究表明,PvSTP13.1 是一种 H+ 耦合的单糖交感器,在去极化膜电位下对己糖和醛五糖具有独特的高亲和力。具体来说,在 31 种评估底物(包括醛己糖、脱氧己糖、果糖、3-O-甲基-D-葡萄糖、醛戊糖、多元醇、糖苷、二糖、三糖和葡萄糖醛酸)中,PvSTP13.在 pH 值为 5.6、去极化膜电位为 -40 mV 时,PvSTP13 对葡萄糖(43 μM)、甘露糖(92 μM)、半乳糖(145 μM)、果糖(224 μM)、木糖(1.0 mM)和岩藻糖(3.7 mM)的亲和力(K0.5)最高。本文介绍的结果表明,PvSTP13.1 有助于从源叶和发育中种子的颖壳中的质外空间回收己糖。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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