A chromogenic substrate for a β-xylosidase-coupled assay of α-glucuronidase

被引:41
作者
Biely, P
Hirsch, J
la Grange, DC
van Zyl, WH
Prior, BA
机构
[1] Slovak Acad Sci, Inst Chem, Bratislava 84238, Slovakia
[2] Univ Stellenbosch, Dept Microbiol, ZA-7602 Matieland, South Africa
关键词
alpha-glucuronidase; beta-xylosidase; enzyme assay; chromogenic substrate; 4-nitrophenyl glycoside; aldobiuronic acid;
D O I
10.1006/abio.2000.4810
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
4-Nitrophenyl 2-(4-O-methyl-alpha -D-glucopyranuronosyl)-beta -D-xylopyranoside obtained on deesterification of 4-nitrophenyl 2-O-(methyl 4-O-methyl-alpha -D-glucopyranosyluronate)-beta -D-xylopyranoside (Hirsch et at, Carbohydr. Res. 310, 145-149, 1998) was found to be an excellent substrate for the measurement of hemicellulolytic alpha -glucuronidase activity, A new precise alpha -glucuronidase assay was developed by coupling the alpha -glucuronidase-catalyzed formation of 4-nitrophenyl beta -D-xylopyranoside with its efficient hydrolysis by beta -xylosidase. A recombinant strain of Saccharomyces cerevisiae, harboring and expressing the beta -xylosidase gene xlnD of Aspergillus niger under control of the alcohol dehydrogenase II promoter on a multicopy plasmid, was used as a source of beta -xylosidase, The activity values of beta -xylosidase in the assay required to achieve a steady-state rate of 4-nitrophenol formation shortly after starting the alpha -glucuronidase reaction were obtained both experimentally and by calculation using the kinetics of coupled enzyme reactions, (C) 2000 Academic Press.
引用
收藏
页码:289 / 294
页数:6
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