Literature DB >> 6268636

Purification and characterization of rat liver alpha-N-acetylglucosaminyl phosphodiesterase.

A Varki, S Kornfeld.   

Abstract

In an earlier report we described the identification of an alpha-N-acetylglucosaminyl phosphodiesterase that is capable of cleaving the outer phosphodiester-linked alpha-N-acetylglucosamine residues present on the high mannose oligosaccharides of newly synthesized lysosomal enzymes (Varki, A., and Kornfeld, S. (1980) J. Biol. Chem. 255, 8398-8401). We have now purified this enzyme 1800-fold with a 24% yield from rat liver, using subcellular fractionation, differential extraction with Triton X-10, DEAE-cellulose chromatography, heparin-Sepharose chromatography, concanavalin A-Sepharose affinity chromatography, and gel filtration on Sephacryl S-300. The purified preparation is free of lysosomal alpha-N-acetylglucosaminidase. The enzyme exhibited a single form on both the ion exchange and gel filtration steps. It has a broad pH optimum between 6.0-8.0 and is unaffected by divalent cations or reducing agents. The enzyme cleaves alpha-N-acetylglucosamine residues from five different locations on the high mannose oligosaccharide. In the case of molecules with one phosphodiester, the rate of cleavage is not affected by the size of the underlying oligosaccharide or the presence or absence of an asparagine-linked peptide. Molecules with two phosphodiesters are cleaved in a nonrandom manner. The enzyme has no activity toward p-nitrophenyl-alpha-N-acetylglucosamine but is capable of cleaving phosphodiester-linked N-acetylglucosamine in molecules such as UDP-N-acetylglucosamine, indicating that it can only hydrolyze N-acetylglucosamine residues that are alpha-linked to a phosphate group.

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Year:  1981        PMID: 6268636

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  24 in total

1.  Lysosomal hydrolase mannose 6-phosphate uncovering enzyme resides in the trans-Golgi network.

Authors:  J Rohrer; R Kornfeld
Journal:  Mol Biol Cell       Date:  2001-06       Impact factor: 4.138

2.  Properties of N-acetylglucosamine 1-phosphotransferase from human lymphoblasts.

Authors:  L Little; M Alcouloumre; A M Drotar; S Herman; R Robertson; R Y Yeh; A L Miller
Journal:  Biochem J       Date:  1987-11-15       Impact factor: 3.857

Review 3.  Trafficking of lysosomal enzymes in normal and disease states.

Authors:  S Kornfeld
Journal:  J Clin Invest       Date:  1986-01       Impact factor: 14.808

4.  Characterization of the mannose 6-phosphate-dependent pathway of lysosomal enzyme routing in an invertebrate.

Authors:  V Alvarez; A J Parodi; R Couso
Journal:  Biochem J       Date:  1995-09-01       Impact factor: 3.857

5.  The overexpressed human 46-kDa mannose 6-phosphate receptor mediates endocytosis and sorting of beta-glucuronidase.

Authors:  H Watanabe; J H Grubb; W S Sly
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

6.  Identification of a variant of mucolipidosis III (pseudo-Hurler polydystrophy): a catalytically active N-acetylglucosaminylphosphotransferase that fails to phosphorylate lysosomal enzymes.

Authors:  A P Varki; M L Reitman; S Kornfeld
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

Review 7.  A role for inherited metabolic deficits in persistent developmental stuttering.

Authors:  Changsoo Kang; Dennis Drayna
Journal:  Mol Genet Metab       Date:  2012-07-28       Impact factor: 4.797

8.  Mice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity.

Authors:  Marielle Boonen; Peter Vogel; Kenneth A Platt; Nancy Dahms; Stuart Kornfeld
Journal:  Mol Biol Cell       Date:  2009-08-26       Impact factor: 4.138

Review 9.  Strategies for carbohydrate recognition by the mannose 6-phosphate receptors.

Authors:  Nancy M Dahms; Linda J Olson; Jung-Ja P Kim
Journal:  Glycobiology       Date:  2008-07-11       Impact factor: 4.313

10.  Demonstration of the heterozygous state for I-cell disease and pseudo-Hurler polydystrophy by assay of N-acetylglucosaminylphosphotransferase in white blood cells and fibroblasts.

Authors:  A Varki; M L Reitman; A Vannier; S Kornfeld; J H Grubb; W S Sly
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

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