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一种用于β-葡萄糖醛酸酶的荧光底物:在荧光测定、聚丙烯酰胺凝胶和组织化学分析中的应用。

A fluorogenic substrate for beta-glucuronidase: applications in fluorometric, polyacrylamide gel and histochemical assays.

作者信息

Zhou M, Upson R H, Diwu Z, Haugland R P

机构信息

Molecular Probes, Inc., Eugene OR 97402, USA.

出版信息

J Biochem Biophys Methods. 1996 Dec 30;33(3):197-205. doi: 10.1016/s0165-022x(96)00026-7.

Abstract

We have developed a fluorogenic substrate, ELF-97 beta-D-glucuronide, that provides significant advantages over existing substrates in detecting beta-glucuronidase activity. ELF-97 beta-D-glucuronide allows the detection of enzymatic activity in situ, yielding a hydrolytic product that exhibits maximal fluorescence within the physiological pH range. This substrate yields a hydrolytic product that demonstrates a more than 100 nm Stokes shift, which minimizes interference from autofluorescence in plant tissue. With the commercial enzyme, ELF-97 beta-D-glucuronide can detect less than 2 x 10(-4) U/ml of beta-glucuronidase activity in solution, and 5 x 10(-4) U per lane in polyacrylamide gels. Assays using transgenic Arabidopsis, whole leaf extracts of GUS-positive, but not GUS-negative plans, show significant GUS activity upon incubation with ELF-97 beta-D-glucuronide. Furthermore, the ability of this substrate to form insoluble precipitates at the sites of enzymatic activity makes it suitable for in situ localization of GUS activity in tissue samples of higher plants.

摘要

我们开发了一种荧光底物ELF-97β-D-葡萄糖醛酸苷,与现有底物相比,它在检测β-葡萄糖醛酸酶活性方面具有显著优势。ELF-97β-D-葡萄糖醛酸苷能够原位检测酶活性,产生一种在生理pH范围内呈现最大荧光的水解产物。该底物产生的水解产物具有超过100 nm的斯托克斯位移,可将植物组织中自发荧光的干扰降至最低。使用商业酶时,ELF-97β-D-葡萄糖醛酸苷能够检测溶液中低于2×10⁻⁴ U/ml的β-葡萄糖醛酸酶活性,以及聚丙烯酰胺凝胶中每条泳道5×10⁻⁴ U的活性。使用转基因拟南芥进行的检测表明,与ELF-97β-D-葡萄糖醛酸苷孵育后,GUS阳性而非GUS阴性植株的全叶提取物显示出显著的GUS活性。此外,这种底物在酶活性位点形成不溶性沉淀的能力使其适用于高等植物组织样本中GUS活性的原位定位。

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