拟南芥转酮醇酶蛋白AtTKL1的同源建模及与α-三联噻吩结合作用分析  

Homologous Modeling of Transketolase At TKL1 and Its Combination withα-Terthienyl in Arabidopsis Thaliana

作　　者：赵斌[1,2] 霍静倩[1] 邢继红 齐萌[1] 张金林[1,2] 董金皋 

机构地区：[1]河北农业大学植物保护学院 [2]真菌毒素与植物分子病理学实验室,保定071000

出　　处：《高等学校化学学报》2015年第4期682-686,共5页Chemical Journal of Chinese Universities

基　　金：国家自然科学基金(批准号:31171877);河北省自然科学基金(批准号:C2012204006)资助~~

摘　　要：以玉米转酮醇酶(1ITZ)的晶体结构为模板,对拟南芥转酮醇酶(At TKL1)的三维结构进行模拟和优化.利用生物信息学方法,确定其氨基酸结合位点为His143,Gly234,Asn263,Arg434,Ser461,Gln488,Phe515,His539,Asp547和Arg598,催化氨基酸位点为His103和His340.通过分子模拟确定α-三联噻吩与At TKL1的活性口袋可有效结合,且At TKL1的催化位点和结合位点为其与α-三联噻吩结合的关键位点.利用荧光猝灭光谱技术确定At TKL1与α-三联噻吩之间存在结合作用;酶活力检测结果表明加入α-三联噻吩后转酮醇酶蛋白的活性降低,进一步验证了At TKL1与α-三联噻吩之间的相互作用.Transketolase is the key enzyme of photosynthesis pathways. It is of great importance for herbicide seeking through new herbicidal substance targeting transketolase. In this study,homologous protein of transketolase was obtained through Modeler and optimized using Amber12,its binding sites of pivotal amino acids were identified with bioinformatics tools. Interaction between At TKL1 and α-terthienyl finally got verified by spectroscopy and enzyme activity analysis. The three dimensional frame model of transketolase protein At TKL1 in Arabidopsis thaliana was homologically modeled according to Maize transketolase protein 1ITZ,revised by dynamic molecular methods. With bioinformatics tools, the sites in At TKL1 were determined, His143,Gly234,Asn263,Arg434,Ser461,Gln488,Phe515,His539,Asp547 and Arg598 for binding,His103 and His340 for catalysis. The molecular docking of At TKL1 and α-terthienyl was performed by computer simulation,and the results confirmed the perfect match of α-terthienyl with active cleavage of At TKL1. The binding sites His143 and Gly234,and the catalytic sites His103 and His340 were the responsible binding sites ofα-terthienyl. Prokaryotic expression of the protein and fluorescence quenching spectroscopy have verified the combination of α-terthienyl and At TKL1. The reduction on the activity of transketolase treatmented withα-terthienyl gave a further confirmation about the interaction between At TKL1 and α-terthienyl. The results will contribute to exploiting new efficient and low toxic herbicides.

关 键 词：转酮醇酶 α-三联噻吩 同源建模 分子对接 

分 类 号：O629.7[理学—有机化学]