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枯草芽孢杆菌果聚糖蔗糖酶中果糖基转移的结构框架。

Structural framework of fructosyl transfer in Bacillus subtilis levansucrase.

作者信息

Meng Guoyu, Fütterer Klaus

机构信息

School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.

出版信息

Nat Struct Biol. 2003 Nov;10(11):935-41. doi: 10.1038/nsb974. Epub 2003 Sep 28.

Abstract

Many bacteria and about 40,000 plant species form primary carbohydrate reserves based on fructan; these polymers of beta-D-fructofuranose are thought to confer tolerance to drought and frost in plants. Microbial fructan, the beta(2,6)-linked levan, is synthesized directly from sucrose by levansucrase, which is able to catalyze both sucrose hydrolysis and levan polymerization. The crystal structure of Bacillus subtilis levansucrase, determined to a resolution of 1.5 A, shows a rare five-fold beta-propeller topology with a deep, negatively charged central pocket. Arg360, a residue essential for polymerase activity, lies in a solvent-exposed site adjacent to the central pocket. Mutagenesis data and the sucrose-bound structure of inactive levansucrase E342A, at a resolution of 2.1 A, strongly suggest that three conserved acidic side chains in the central pocket are critical for catalysis, and presumably function as nucleophile (Asp86) and general acid (Glu342), or stabilize the transition state (Asp247).

摘要

许多细菌和大约40000种植物以果聚糖为基础形成主要的碳水化合物储备;这些β-D-呋喃果糖的聚合物被认为能赋予植物耐旱和耐寒能力。微生物果聚糖,即β(2,6)-连接的左聚糖,由蔗糖蔗糖酶直接从蔗糖合成,该酶能够催化蔗糖水解和左聚糖聚合。枯草芽孢杆菌蔗糖蔗糖酶的晶体结构,分辨率为1.5埃,显示出罕见的五重β-螺旋桨拓扑结构,带有一个深的、带负电荷的中央口袋。Arg360是聚合酶活性所必需的残基,位于与中央口袋相邻的溶剂暴露位点。诱变数据以及失活的蔗糖蔗糖酶E342A在2.1埃分辨率下的蔗糖结合结构,强烈表明中央口袋中的三个保守酸性侧链对催化至关重要,可能作为亲核试剂(Asp86)和广义酸(Glu342)发挥作用,或稳定过渡态(Asp247)。

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