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A continuous microtiter plate assay for screening nucleotide sugar-synthesizing nucleotidyltransferases.

作者信息

Ritter J E, Berlin C, Elling L

机构信息

Institut für Enzymtechnologie, Heinrich-Heine-Universität Düsseldorf im Forschungszentrum Jülich, Germany.

出版信息

Anal Biochem. 1996 Feb 1;234(1):74-82. doi: 10.1006/abio.1996.0052.

DOI:10.1006/abio.1996.0052
PMID:8742085
Abstract

A continuous microtiter plate nucleotidyltransferase substrate screening assay (NUSSA) is described which allows the identification of nucleotide sugar-synthesizing enzyme activities. The assay is accomplished by the determination of the common product of these enzymes PPi with a PPi-dependent phosphofructokinase. A subsequent enzyme reaction cascade leads to the production of 2 mol NAD per mol PPi. PPi-dependent phosphofructokinase was purified from potato with respect to contaminating enzyme activities which would disturb NUSSA performance. NUSSA allows the quick, simultaneous, and comprehensive check of different sugar 1-phosphate and nucleoside triphosphate substrates using purified pyrophosphorylases or crude extracts of plants, microorganisms, and mammalian tissues. Moreover, NUSSA will assist to evaluate these enzymes for the synthesis of important nucleotide sugars which serve as substrates of glycosyltransferases in carbohydrate syntheses.

摘要

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引用本文的文献

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UDP-Sugar Producing Pyrophosphorylases: Distinct and Essential Enzymes With Overlapping Substrate Specificities, Providing Precursors for Glycosylation Reactions.UDP-糖生成焦磷酸化酶:具有重叠底物特异性的独特且必需的酶,为糖基化反应提供前体。
Front Plant Sci. 2019 Jan 4;9:1822. doi: 10.3389/fpls.2018.01822. eCollection 2018.
2
Substrate Specificity and Inhibitor Sensitivity of Plant UDP-Sugar Producing Pyrophosphorylases.植物UDP-糖生成焦磷酸化酶的底物特异性和抑制剂敏感性
Front Plant Sci. 2017 Sep 20;8:1610. doi: 10.3389/fpls.2017.01610. eCollection 2017.
3
A comparison of sugar indicators enables a universal high-throughput sugar-1-phosphate nucleotidyltransferase assay.
糖指标的比较可实现通用的高通量糖-1-磷酸核苷酸转移酶检测。
Anal Biochem. 2008 Jun 15;377(2):251-8. doi: 10.1016/j.ab.2008.03.018. Epub 2008 Mar 15.