A functional arginine residue in NADPH-dependent aldehyde reductase from pig kidney.

W S Davidson,T G Flynn

doi:10.1016/s0021-9258(18)50646-3

Abstract

Pig kidney aldehyde reductase is inactivated by 2,3-butanedione, phenylglyoxal, methylglyoxal, and 1,2-cyclohexanedione. 2,3-Butanedione caused the most rapid loss in enzyme activity, the rate of loss being proportional to the concentration of 2,3-butanedione. Neither D-glyceraldehyde nor pyridine 3-aldehyde, both substrates for this broadly specific enzyme, protected the enzyme from inactivation but 1 mM NADPH or NADP completely prevented the loss of activity by 2,3-butanedione suggesting the involvement of arginine in the binding of cofactor. Nicotinamide mononucleotide (NMN) (reduced form) offered no protection to inactivation whereas ADP-ribose phosphate gave complete protection indicating that it is the latter portion of NADPH which interacts with the essential arginine. Both NMN and ADP-ribose phosphate are competitive inhibitors of aldehyde reductase with respect to NADPH. Butanedione-modified aldehyde reductase could still bind to a blue dextran-Sepharose 4B column suggesting that the modified arginine did not bind NADPH. This was confirmed by fluorescence spectra which showed that chemically modified aldehyde reductase caused the same blue shift of NADPH fluorescence as did native aldehyde reductase. Of additional interest was the quenching of NADPH fluorescence by aldehyde reductase which, with one exception, is in contrast to the fluorescence behavior of all other oxidoreductases.

Highlights

2,3-Butanedione caused the most rapid loss in enzyme activity, the rate of loss being proportional to the concentration of 2,3-butanedione
Nicotinamide mononucleotide (NMN) offered no protection to inactivation whereas ADP-ribose phosphate gave complete protection indicating that it is the latter portion of NADPH which interacts with the essential arginine
The loss of no other amino acid was evident on amino acid analysis. These results indicate that there is one essential arginine residue per molecule of pig kidney aldehyde reductase, that this residue is the only one modified by 20 mu 2,3-butanedione and that it is protected from modification by NADPH

Summary

Introduction

2,3-Butanedione caused the most rapid loss in enzyme activity, the rate of loss being proportional to the concentration of 2,3-butanedione. When chemical modification of aldehyde reductase by 2,3-butanedione was carried out in the presence of these compounds only ADP-ribose phosphate was seen to protect the enzyme completely from inactivation (Fig. 5). These results indicate that there is one essential arginine residue per molecule of pig kidney aldehyde reductase, that this residue is the only one modified by 20 mu 2,3-butanedione and that it is protected from modification by NADPH.

Results

Conclusion