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PMID: 6696771 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human aldehyde dehydrogenase: catalytic activity in oriental liver.

Biochemical and biophysical research communications ·Vol. 118 ·No. 1 ·1984-01-13 ·Pages 97-102

Ferencz-Biro K, Pietruszko R

Abstract

Population genetics followed by purification suggested that "null" mutation in the mitochondrial E2 isozyme of human aldehyde dehydrogenase (EC 1.2.1.3) occurred in the Oriental individuals who are sensitive to alcohol. This report demonstrates that the Oriental E2, thought to be a "null" mutant, is catalytically active and except for maximal velocity and isoelectric point, identical with Caucasian E2 isozyme. The data presented are not inconsistent with mutation but preclude active site of the enzyme as the point at which alteration has occurred; they are, however, inconsistent with "null" mutation.

MeSH Terms
Aldehyde Dehydrogenase Aldehyde Oxidoreductases/genetics,isolation & purification,metabolism Asians Humans Isoenzymes/genetics,isolation & purification,metabolism Mitochondria, Liver/enzymology Mutation Whites
Chemicals
Isoenzymes Aldehyde Oxidoreductases Aldehyde Dehydrogenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ferencz-Biro K
Pietruszko R
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1984-01-13
Pages
97-102
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NIAAA NIH HHS · AA00046 · United States
NIAAA NIH HHS · AA00186 · United States
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