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来自大麦(Hordeum vulgare L.)的木葡聚糖木葡糖基转移酶在其受体结合位点结合寡聚和多聚木葡聚糖分子。

Xyloglucan xyloglucosyl transferases from barley (Hordeum vulgare L.) bind oligomeric and polymeric xyloglucan molecules in their acceptor binding sites.

作者信息

Vaaje-Kolstad Gustav, Farkas Vladimir, Hrmova Maria, Fincher Geoffrey B

机构信息

Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, 1432 As, Norway.

出版信息

Biochim Biophys Acta. 2010 Jul;1800(7):674-84. doi: 10.1016/j.bbagen.2010.04.001. Epub 2010 Apr 11.

Abstract

BACKGROUND

Xyloglucan xyloglucosyl transferases (EC 2.4.1.207), known as xyloglucan endotransglycosylases (XETs) use a disproportionation reaction mechanism and modulate molecular masses of xyloglucans. However, it is not known precisely how these size modulations and transfer reactions occur with polymeric acceptor substrates.

METHODS

cDNAs encoding three barley HvXETs were expressed in Pichia pastoris and reaction mechanism and molecular properties of HvXETs were investigated.

RESULTS

Significant differences in catalytic efficiencies (k(cat)*K(m)(-)(1)) were observed and these values were 0.01, 0.02 and 0.2 s(-)(1)*mg(-)(1)*ml for HvXET3, HvXET4 and HvXET6, respectively, using tamarind xyloglucan as a donor substrate. HPLC analyses of the reaction mixtures showed that HvXET6 followed a stochastic reaction mechanism with fluorescently or radioactively labelled tamarind xyloglucans and xyloglucan-derived oligosaccharides. The analyses from two successive reaction cycles revealed that HvXET6 could increase or decrease molecular masses of xyloglucans. In the first reaction cycle equilibrium was reached under limiting donor substrate concentrations, while xyloglucan mass modulations occurred during the second reaction cycle and depended on the molecular masses of incoming acceptors. Deglycosylation experiments indicated that occupancy of a singular N-glycosylation site was required for activity of HvXET6. Experiments with organic solvents demonstrated that HvXET6 tolerated DMSO, glycerol, methanol and 1,4-butanediol in 20% (v/v) concentrations.

CONCLUSIONS

The two-phase experiments demonstrated that large xyloglucan molecules can bind in the acceptor sites of HvXETs.

GENERAL SIGNIFICANCE

The results characterise donor and acceptor binding sites in plant XET, report that HvXETs act on xyloglucan donor substrates adsorbed onto nanocrystals and that HvXETs tolerate the presence of organic solvents.

摘要

背景

木葡聚糖木葡糖基转移酶(EC 2.4.1.207),即木葡聚糖内转糖基酶(XETs),采用歧化反应机制并调节木葡聚糖的分子量。然而,尚不清楚这些大小调节和转移反应是如何在聚合受体底物上发生的。

方法

在毕赤酵母中表达编码三种大麦HvXETs的cDNA,并研究HvXETs的反应机制和分子特性。

结果

观察到催化效率(k(cat)*K(m)(-)(1))存在显著差异,以罗望子木葡聚糖作为供体底物时,HvXET3、HvXET4和HvXET6的这些值分别为0.01、0.02和0.2 s(-)(1)*mg(-)(1)*ml。对反应混合物的HPLC分析表明,HvXET6对荧光或放射性标记的罗望子木葡聚糖和木葡聚糖衍生的寡糖遵循随机反应机制。对两个连续反应循环的分析表明,HvXET6可以增加或降低木葡聚糖的分子量。在第一个反应循环中,在供体底物浓度有限的情况下达到平衡,而木葡聚糖的质量调节发生在第二个反应循环中,并取决于进入受体的分子量。去糖基化实验表明,HvXET6的活性需要一个单一N-糖基化位点的占据。有机溶剂实验表明,HvXET6在20%(v/v)浓度下能耐受二甲基亚砜、甘油、甲醇和1,4-丁二醇。

结论

两阶段实验表明,大木葡聚糖分子可以结合在HvXETs的受体位点上。

一般意义

这些结果表征了植物XET中的供体和受体结合位点,报告了HvXETs作用于吸附在纳米晶体上的木葡聚糖供体底物,并且HvXETs能耐受有机溶剂的存在。

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