Characterization of angiotensin I-converting enzyme from anterior gills of the mangrove crab Ucides cordatus

Int J Biol Macromol. 2015 Mar:74:304-9. doi: 10.1016/j.ijbiomac.2014.12.036. Epub 2014 Dec 25.

Abstract

Angiotensin I-converting enzyme (ACE) is a well-known metallopeptidase that is found in vertebrates, invertebrates and bacteria. We isolated from the anterior gill of the crab Ucides cordatus an isoform of ACE, here named crab-ACE, which presented catalytic properties closely resembling to those of mammalian ACE. The enzyme was purified on Sepharose-lisinopril affinity chromatography to apparent homogeneity and a band of about 72 kDa could be visualized after silver staining and Western blotting. Assays performed with fluorescence resonance energy transfer (FRET) selective ACE substrates Abz-FRK(Dnp)P-OH, Abz-SDK(Dnp)P-OH and Abz-LFK(Dnp)-OH, allowed us to verify that crab-ACE has hydrolytic profile very similar to that of the ACE C-domain. In addition, we observed that crab-ACE can hydrolyze the ACE substrates, angiotensin I and bradykinin. The enzyme was strongly inhibited by the specific ACE inhibitor lisinopril (Ki of 1.26 nM). However, in contrast to other ACE isoforms, crab-ACE presented a very particular optimum pH, being the substrate Abz-FRK(Dnp)-P-OH hydrolyzed efficiently at pH 9.5. Other interesting characteristic of crab-ACE was that the maximum hydrolytic activity was reached at around 45°C. The description of an ACE isoform in Ucides cordatus is challenging and may contribute to a better understanding of the biochemical function of this enzyme in invertebrates.

Keywords: ACE isoform; Characterization; Crab gill; FRET peptides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors / pharmacology
  • Animals
  • Brachyura / enzymology*
  • Enzyme Activation / drug effects
  • Enzyme Stability / drug effects
  • Gills / enzymology*
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • Lisinopril / pharmacology
  • Peptidyl-Dipeptidase A / chemistry*
  • Peptidyl-Dipeptidase A / classification
  • Peptidyl-Dipeptidase A / genetics
  • Peptidyl-Dipeptidase A / isolation & purification
  • Peptidyl-Dipeptidase A / metabolism*
  • Phylogeny
  • Substrate Specificity
  • Temperature

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Lisinopril
  • Peptidyl-Dipeptidase A