Differential regulation by phytochrome of the appearance of plastidic and cytoplasmatic isoforms of glutathione reductase in mustard (Sinapis alba L.) cotyledons

An increase of glutathione reductase (GR; EC 1.6.4.2) activity during the transformation of mustard (Sinapis alba L.) cotyledons from storage organs to photosynthetically competent leaves was previously found to be controlled by light acting via phytochrome (Drumm, H., Mohr, H., Z. Naturforsch. 28c 559–563, 1973). Two isoforms of GR could be separated by disc electrophoresis. In the present study we have applied ionexchange chromatography to separate isoforms of GR during the development of the cotyledons. Furthermore, the technique of in situ photooxidation of plastids was used to distinguish between plastidic and cytoplasmatic isoforms. The isoform GR₂ is the plastidic enzyme, as shown by its sensitivity to photooxidative treatment, while GR₁ is a cytoplasmatic protein not affected by photooxidative treatment of plastids. Both isoforms are promoted by phytochrome but with different time courses. The appearance of GR₁ is independent of the integrity of the plastids, as one might expect. However, unexpectedly, the phytochrome-mediated re-appearance of GR₂ after a photooxidative treatment is much less affected by photooxidative destruction of the plastids, i.e. by the lack of a particular plastidic factor, than was to be expected from previous experience with typical plastidic proteins. An interpretation of this finding must await measurements at the level of GR₂ mRNA.Abbreviations c continuous - D darkness - FR far-red light (3.5 W·m^-2) - FPLC fast protein liquid chromatography - GR glutathione reductase (EC 1.6.4.2) - NF Norflurazon - R fed light (6.8 W·m^-2) - = Pfr/Ptot wavelength-dependent photoequilibrium of the phytochrome system