Purification of Prolylcarboxypeptidase (Angiotensinase C).

Abstract

Prolylcarboxypeptidase (Angiotensinase C) was purified 247-fold from homogenized hog kidney cortex by the sequential application of ammonium sulfate precipitation, DEAE-Sephadex and hydroxyapatite column chromatographies. The enzyme was relatively heat stable and free of cathepsin A contamination. Disc gel electrophoresis revealed only a single band of protein indicating homogeneity. The molecular weight of the enzyme was estimated to be 210,000. The Km of prolylcarboxypeptidase with Bz-Pro-Phe substrate was 0.0013 M. After pretreatment with 2-mercaptoethanol, urea and SDS prolylcarboxypeptidase dissociated to subunits. (Author)

Document Details

Document Type
Technical Report
Publication Date
Mar 22, 1973
Accession Number
AD0758018

Entities

People

  • E. G. Erdos
  • G. Oshima
  • H. S. J. Yeh
  • T. Kakimoto

Organizations

  • University of Oklahoma Health Sciences Center

Tags

DTIC Thesaurus Topics

  • Analytical Chemistry Techniques
  • Chromatography
  • Column Chromatography
  • Contamination
  • Electrophoresis
  • Gel Electrophoresis
  • Homogeneity
  • Kidneys
  • Molecular Weight
  • Precipitation
  • Substrates

Fields of Study

  • Biology
  • Computer science

Readers

  • Molecular and Cellular Biochemistry