Dissemin is shutting down on January 1st, 2025

Published in

Wiley, FEBS Letters, 3(463), p. 382-386, 1999

DOI: 10.1016/s0014-5793(99)01625-7

Links

Tools

Export citation

Search in Google Scholar

Cloning and heterologous expression of NAD(P)H:quinone reductase ofArabidopsis thaliana, a functional homologue of animal DT-diaphorase

Journal article published in 1999 by Francesca Sparla ORCID, Gabriella Tedeschi, Paolo Pupillo, Paolo Trost
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

In higher plants, NAD(P)H:quinone reductase (NQR) is the only flavoreductase known to reduce quinone substrates directly to hydroquinones by a two-electron reaction mechanism. This enzymatic activity is believed to protect aerobic organisms from the oxidative action of semiquinones. For this reason plant NQR has recently been suggested to be related to animal DT-diaphorase. A cDNA clone for NQR of Arabidopsis thaliana was identified, expressed in Escherichia coli, purified and characterized. Its amino acid sequence was found related to a number of putative proteins, mostly from prokaryotes, with still undetermined function. Conversely, in spite of the functional homology, sequence similarity between plant NQR and animal DT-diaphorase was limited and essentially confined to the flavin binding site.