Analysis of enzyme-catalyzed nucleotide modification by aldose reductase
Conference
·
· Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:6079690
Homogeneous bovine kidney aldose reductase catalyzes two reactions in addition to the normal aldehyde-dependent oxidation of NADPH. First, adduct formation between the oxidized nucleotide and the oxidized substrate is observed during turnover due to initial formation of a reversible E:NADP/sup +/:R-CHO ternary complex, which subsequently reacts to give the covalent complex (E:NADP/sup +/-R-CHO). The reaction is enzyme-catalyzed with substantial enhancement of both the pseudo-first order rate constant and the overall K/sub eq/ relative to the reaction with free NADP/sup +/ in aqueous buffer. Analysis of the concentration dependence and time-course for reversible dead-end and covalent complex formation are described for several aldehyde and nucleotide substrates. Non-linear time courses for aldehyde reduction and substrate inhibition by the aldehyde substrate in initial velocity studies are completely accounted for by this mechanism, thereby eliminating a simple Dalziel-type explanation for the substrate activation by aldehyde which is also observed. Second, enzyme-catalyzed oxidation of NADPH occurs in the absence of aldehyde substrate with a rate equal to .03% of V/sub max/ for the normal reduction of glyceraldehyde. By 500 MHz /sup 1/H-NMR, the enzyme-catalyzed oxidation of (4-/sup 2/H)NADPH appears to be greater than 95% stereospecific. Spectroscopic evidence for a similar oxidation reaction is observed for the covalent E:NADP/sup +/-R-CHO adduct with glyceraldehyde, but not with glycolaldehyde.
- Research Organization:
- Research Institute of Scripps Clinic, La Jolla, CA
- OSTI ID:
- 6079690
- Report Number(s):
- CONF-870644-
- Conference Information:
- Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 46:6
- Country of Publication:
- United States
- Language:
- English
Similar Records
Characterization of WY 14,643 and its Complex with Aldose Reductase
Aldose and aldehyde reductases : structure-function studies on the coenzyme and inhibitor-binding sites.
Chemical modification of human muscle aldose reductase by pyridoxal 5'-phosphate
Journal Article
·
Mon Oct 10 00:00:00 EDT 2016
· Scientific Reports
·
OSTI ID:1378554
Aldose and aldehyde reductases : structure-function studies on the coenzyme and inhibitor-binding sites.
Journal Article
·
Fri Sep 03 00:00:00 EDT 1999
· Mol. Vision
·
OSTI ID:942680
Chemical modification of human muscle aldose reductase by pyridoxal 5'-phosphate
Conference
·
Fri May 01 00:00:00 EDT 1987
· Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
·
OSTI ID:6073544
Related Subjects
550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BODY
CATTLE
COENZYMES
COMPLEXES
DEUTERIUM
DOMESTIC ANIMALS
ENZYMES
HYDROGEN ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KIDNEYS
KINETICS
LIGHT NUCLEI
MAMMALS
METABOLISM
NADP
NUCLEI
NUCLEOTIDES
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
ORGANS
OXIDOREDUCTASES
REACTION KINETICS
RUMINANTS
STABLE ISOTOPES
SUBSTRATES
TRACER TECHNIQUES
VERTEBRATES
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BODY
CATTLE
COENZYMES
COMPLEXES
DEUTERIUM
DOMESTIC ANIMALS
ENZYMES
HYDROGEN ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KIDNEYS
KINETICS
LIGHT NUCLEI
MAMMALS
METABOLISM
NADP
NUCLEI
NUCLEOTIDES
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
ORGANS
OXIDOREDUCTASES
REACTION KINETICS
RUMINANTS
STABLE ISOTOPES
SUBSTRATES
TRACER TECHNIQUES
VERTEBRATES