Abstract

Nitrate reductase (NR), a committed enzyme in nitrate assimilation, is involved in the generation of nitric oxide (NO) in plants. In wheat leaf segments exposed to sodium nitroprusside (SNP) or S-nitrosoglutathione (GSNO), NR activity was significantly reduced to different degrees between 3 and 21h, whereas its activity was partially recovered when the NO scavenger cPTIO was used. At 21h, NR activity decreased from 38% with 10μM SNP to 91% with 500μM SNP, respect to the C values. S-nitrosoglutathione reduced NR activity between 18% and 26% only at 3h. When added directly to the incubation solution, NR activity was quickly and strongly inhibited more than 90% by 10 or 50μM SNP, whereas 10μM GSNO reduced the enzyme activity an average of 50%, at 30min of incubation. l-NAME and d-arginine (nitric oxide synthase (NOS) inhibitors) increased NR activity by 14% and 52% respectively, at 21h of exposure, leading us to suppose that endogenous NOS-dependent NO formation could also be modulating NR activity. NR protein expression was not affected by 10 or 100μM SNP at 3 or 21h of incubation, whereas nitration of tyrosines was not detected in the NR protein. Nitrates, which content increased along the time in the tissues, could be exerting a role in this regulation.

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