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Development of a colourimetric assay for glycosynthases

机译:用于糖合作酶的Colouremetric测定的开发

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The synthesis of glycosidic structures by catalysis via glycosynthases has gained much interest due to the potential high product yields and specificity of the enzymes. Nevertheless, the characterisation and implementation of new glycosynthases is greatly hampered by the lack of high-throughput methods for reaction analysis and screening of potential glycosynthase variants. Fluoride detection, via silyl ether chemosensors, has recently shown high potential for the identification of glycosynthase mutants in a high-throughput manner, though limited by the low maximal detection concentration. In the present paper, we describe a new version of a glycosynthase activity assay using a silyl ether of p-nitrophenol, allowing fast reliable detection of fluoride even at concentrations of 4 mM and higher. This improvement of detection allows not only screening and identification but also kinetic characterisation of glycosynthases and synthetic reactions in a fast microtiter plate format. The applicability of the assay was successfully demonstrated by the biochemical characterisation of the mesophilic beta-glucosynthase of Abg-E358S (Rhizobium radiobacter) and psychrotolerant beta-glucosynthase BglU-E377A (Micrococcus antarcticus). The limitation of hyperthermophilic glycosidases as potential glycosynthases, when using glycosyl fluoride donors, was also illustrated by the example of the putative beta-galactosidase GalPf from Pyrococcus furiosus. (C) 2017 Elsevier B.V. All rights reserved.
机译:由于潜在的高产量和酶的特异性,通过糖合作酶的催化合成糖苷结构的合成。然而,通过缺乏用于反应分析和筛选潜在的糖合酶变体的高通量方法,极大地阻碍了新的糖合作酶的表征和实施。氟化物检测通过甲硅烷基醚化学传感器最近示出了高潜力以高通量方式鉴定糖合酶突变体,但通过低最大检测浓度的限制。在本文中,我们描述了使用对硝基苯酚的甲硅烷基醚的糖基合酶活性测定的新版本,即使在4mm和更高的浓度下也能够快速可靠地检测氟化物。这种检测的改善允许不仅筛选和鉴定,而且还可以以快速的微量滴定板格式的糖合作酶和合成反应的动力学表征。通过ABG-E358S(Rhizobium resibacter)和心肌缺陷β-葡萄糖合酶BGLU-E377A(Microcococcus Antarcticus)的生化表征成功证明了测定的适用性。通过来自Pyrococcus Furoiosus的推定β-半乳糖苷酶Galpf的实施例,还示出了当使用糖基氟化物供体时作为潜在的糖合作酶的超嗜热糖苷酶的限制。 (c)2017 Elsevier B.v.保留所有权利。

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