Control of synthesisde novoof ascorbate oxidase in the mustard seedling (Sinapis albaL.) by phytochrome
β Scribed by G. J. Acton; H. Drumm; H. Mohr
- Publisher
- Springer-Verlag
- Year
- 1974
- Tongue
- English
- Weight
- 860 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0032-0935
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β¦ Synopsis
Density-labelling with deuterium oxide has been used to distinguish preexisting from newly made ascorbate oxidase (EC 1.10.3.3) molecules in cotyledons of the mustard seedling (Sinapis alba L.). The time course of the change in bandwidth of isopycnically banded enzyme, taken together with the accompanying shifts in density, showed that the enzyme was synthesized de novo, was continuously turning over, and had a halt-life of about 1.25 days in darkness. Phytochrome-mediated increases in enzyme activity were accompanied by (i) a faster rate of labelling and (ii) faster progression of the profile to that of a uniformly labelled population, than in dark controls run in parallel. The conclusion is drawn, that phytochrome regulates the rate of synthesis de novo of the protein moiety of ascorbate oxidase in the mustard seedling.
π SIMILAR VOLUMES
Nitrite reductase (NIR; EC 1.7.7.1) is a central enzyme in nitrate assimilation and is localized in plastids. The present study concerns the regulation of the appearance of NIR in cotyledons of the mustard (Sinapis alba L.) seedling. It was shown that light exerts its positive control over the nitra
Control of the appearance of ascorbate peroxidase (EC 1.11.1.11) in mustard seedling cotyledons by phytochrome and photooxidative treatments
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