Kinetic rate assay of urinary N-acetyl-beta-D-glucosaminidase with 2-chloro-4-nitrophenyl-N-acetyl-beta-D-glucosaminide as substrate. 1988

J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
Central Clinical Laboratory, Yokosuka Kyosai Hospital, Japan.

In this new procedure for determining the activity of N-acetyl-beta-D-glucosaminidase (EC 3.2.1.30; NAG) in urine, a new synthetic substrate, 2-chloro-4-nitrophenyl-N-acetyl-beta-D-glucosaminide is used. No sample blank is required because the activity is determined kinetically. Very high precision is possible, with CVs of less than 3.8% both within-run and between-run. Glucose, ascorbic acid, bilirubin, bromosulfonphthalein, and phenosulfonphthalein do not interfere. The reference interval (mean +/- 2 SD) for healthy subjects was 1.9-11.1 U per gram of creatinine. NAG activity can be determined over a wide range (2-500 U/L) with high sensitivity. The method is suitable for use with various automated analyzers, and it should be useful for screening for renal diseases.

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D012016 Reference Values The range or frequency distribution of a measurement in a population (of organisms, organs or things) that has not been selected for the presence of disease or abnormality. Normal Range,Normal Values,Reference Ranges,Normal Ranges,Normal Value,Range, Normal,Range, Reference,Ranges, Normal,Ranges, Reference,Reference Range,Reference Value,Value, Normal,Value, Reference,Values, Normal,Values, Reference
D005944 Glucosamine 2-Amino-2-Deoxyglucose,Dona,Dona S,Glucosamine Sulfate,Hespercorbin,Xicil,2 Amino 2 Deoxyglucose,Sulfate, Glucosamine
D006596 Hexosaminidases Enzymes that catalyze the hydrolysis of N-acylhexosamine residues in N-acylhexosamides. Hexosaminidases also act on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES. Galactosaminidases,Hexosaminidase,Galactosaminidase,Glucosaminidase,Glucosaminidases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006863 Hydrogen-Ion Concentration The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH pH,Concentration, Hydrogen-Ion,Concentrations, Hydrogen-Ion,Hydrogen Ion Concentration,Hydrogen-Ion Concentrations
D000117 Acetylglucosamine The N-acetyl derivative of glucosamine. Acetyl Glucosamine,N-Acetyl Glucosamine,N-Acetyl-beta-D-Glucosamine,N-Acetylglucosamine,beta-N-Acetylglucosamine,2-Acetamido-2-Deoxy-D-Glucose,2-Acetamido-2-Deoxyglucose,N-Acetyl-D-Glucosamine,2 Acetamido 2 Deoxy D Glucose,2 Acetamido 2 Deoxyglucose,Glucosamine, Acetyl,Glucosamine, N-Acetyl,N Acetyl D Glucosamine,N Acetyl Glucosamine,N Acetyl beta D Glucosamine,N Acetylglucosamine,beta N Acetylglucosamine
D000118 Acetylglucosaminidase A beta-N-Acetylhexosaminidase that catalyzes the hydrolysis of terminal, non-reducing 2-acetamido-2-deoxy-beta-glucose residues in chitobiose and higher analogs as well as in glycoproteins. Has been used widely in structural studies on bacterial cell walls and in the study of diseases such as MUCOLIPIDOSIS and various inflammatory disorders of muscle and connective tissue. N-Acetyl-beta-D-glucosaminidase,Chitobiase,N,N-Diacetylchitobiase,N-Ac-beta-Glucosaminidase,NAGase,beta-D-Acetamido-2-Deoxyglucosidase,beta-D-N-acetylglucosaminidase,beta-N-Acetylglucosaminidase,N Ac beta Glucosaminidase,N Acetyl beta D glucosaminidase,N,N Diacetylchitobiase,beta D Acetamido 2 Deoxyglucosidase,beta D N acetylglucosaminidase,beta N Acetylglucosaminidase
D001322 Autoanalysis Method of analyzing chemicals using automation. Autoanalyses

Related Publications

J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
July 1996, Clinica chimica acta; international journal of clinical chemistry,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
January 2003, Journal of clinical laboratory analysis,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
May 1990, Chemical & pharmaceutical bulletin,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
December 1989, Analytical biochemistry,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
May 1991, Chemical & pharmaceutical bulletin,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
January 1965, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
February 1995, Nihon rinsho. Japanese journal of clinical medicine,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
November 2004, Nihon rinsho. Japanese journal of clinical medicine,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
August 1999, Nihon rinsho. Japanese journal of clinical medicine,
J Makise, and E Saito, and M Obuchi, and M Kanayama, and K Ichikawa, and K Harakawa, and K Yoshida
July 1981, Clinical chemistry,
Copied contents to your clipboard!