Cloning and characterization of human liver cytosolic β-glycosidase

M. De Graaf, I. C. Van Veen, I. H. Van der Meulen-Muileman, W. R. Gerritsen, H. M. Pinedo, H. J. Haisma

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Cytosolic β-glucosidase (EC 3.2.1.21) from mammalian liver is a member of the family 1 glycoside hydrolases and is known for its ability to hydrolyse a range of β-D-glycosides, including β-D-glucoside and β-D-galactoside. We therefore refer to this enzyme as cytosolic β-glycosidase. We cloned the cDNA encoding the human cytosolic β-glycosidase by performing PCR on cDNA prepared from total human liver RNA. Specific primers were based on human expressed sequence tags found in the expressed sequence tag database. The cloned cDNA contained 1407 nt with an open reading frame encoding 469 amino acid residues. Amino acid sequence analysis indicates that human cytosolic β-glycosidase is most closely related to lactase phlorizin hydrolase and klotho protein. The enzyme was characterized by using cell lysates of COS-7 cells transfected with a eukaryotic expression vector containing the cDNA. The biochemical, kinetic and inhibition properties of the cloned enzyme were found to be identical with those reported for the enzyme purified from human liver.

Original languageEnglish (US)
Pages (from-to)907-910
Number of pages4
JournalBiochemical Journal
Volume356
Issue number3
DOIs
StatePublished - Jun 15 2001
Externally publishedYes

Keywords

  • Glycoside
  • Mammalian
  • β-galactosidase
  • β-glucosidase

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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