Department of Plant Biology, University of Minnesota, St. Paul, MN 55108-1095, USA.
J Biol Chem. 2012 Aug 31;287(36):30296-304. doi: 10.1074/jbc.M112.372888. Epub 2012 Jul 17.
Plant sucrose transporters (SUTs) are H(+)-coupled uptake transporters. Type I and II (SUTs) are phylogenetically related but have different substrate specificities. Type I SUTs transport sucrose, maltose, and a wide range of natural and synthetic α- and β-glucosides. Type II SUTs are more selective for sucrose and maltose. Here, we investigated the structural basis for this difference in substrate specificity. We used a novel gene shuffling method called synthetic template shuffling to introduce 62 differentially conserved amino acid residues from type I SUTs into OsSUT1, a type II SUT from rice. The OsSUT1 variants were tested for their ability to transport the fluorescent coumarin β-glucoside esculin when expressed in yeast. Fluorescent yeast cells were selected using fluorescence-activated cell sorting (FACS). Substitution of five amino acids present in type I SUTs in OsSUT1 was found to be sufficient to confer esculin uptake activity. The changes clustered in two areas of the OsSUT1 protein: in the first loop and the top of TMS2 (T80L and A86K) and in TMS5 (S220A, S221A, and T224Y). The substrate specificity of this OsSUT1 variant was almost identical to that of type I SUTs. Corresponding changes in the sugarcane type II transporter ShSUT1 also changed substrate specificity, indicating that these residues contribute to substrate specificity in type II SUTs in general.
植物蔗糖转运蛋白(SUTs)是质子偶联的摄取转运蛋白。I 型和 II 型(SUTs)在系统发育上相关,但具有不同的底物特异性。I 型 SUT 运输蔗糖、麦芽糖以及广泛的天然和合成的α-和β-葡萄糖苷。II 型 SUT 对蔗糖和麦芽糖的选择性更高。在这里,我们研究了这种底物特异性差异的结构基础。我们使用了一种称为合成模板改组的新型基因改组方法,将 62 个差异保守的氨基酸残基从 I 型 SUT 引入到水稻的 II 型 SUT OsSUT1 中。当在酵母中表达时,对 OsSUT1 变体运输荧光香豆素β-葡萄糖苷 Esculin 的能力进行了测试。使用荧光激活细胞分选(FACS)对荧光酵母细胞进行了选择。发现 OsSUT1 中存在于 I 型 SUT 中的五个氨基酸的取代足以赋予 Esculin 摄取活性。这些变化聚集在 OsSUT1 蛋白的两个区域:在第一个环和 TMS2 的顶部(T80L 和 A86K)以及 TMS5(S220A、S221A 和 T224Y)。该 OsSUT1 变体的底物特异性几乎与 I 型 SUTs 相同。甘蔗 II 型转运蛋白 ShSUT1 中的相应变化也改变了底物特异性,表明这些残基通常有助于 II 型 SUT 的底物特异性。