Regulation of Rubisco activation in antisense plants of tobacco containing reduced levels of Rubisco activase
โ Scribed by Edward T. Hammond; T. John Andrews; Keith A. Mott; Ian E. Woodrow
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 360 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0960-7412
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โฆ Synopsis
Summary
Following an increase in photon flux density (PFD), ribulose bisphosphate carboxylase/oxygenase (Rubisco) undergoes a slow activation which substantially limits the rate of photosynthesis. This activation process is mediated in part by Rubisco activase. Antisense DNA plants of tobacco were used to quantify the degree to which activase limits Rubisco activation. Reductions in leaf activase content caused proportional reductions in the rate of Rubisco activation following a PFD increase from 110 to 1200 ฮผmol m^โ2^ sec^โ1^. This was the case for activase levels up to and slightly beyond normal wildโtype activase levels. Activase therefore has a flux control coefficient of unity with respect to the Rubisco activation flux. Such a high control coefficient has rarely been measured for any metabolic system, and this is the highest control coefficient measured for an important photosynthetic flux. In contrast, the rate of Rubisco inactivation in leaves following a drop in PFD of 1200 to 110 ฮผmol m^โ2^ sec^โ1^ was unchanged by a 60% reduction in activase levels. Despite the high degree of control that activase exerts over the rate of activation, and thus nonโsteadyโstate photosynthesis, it was shown that steadyโstate photosynthesis was largely unaffected by activase concentration until it was reduced below approximately 15% of the wildโtype level. The significance of these results and their implications for published models of Rubisco activation are discussed.
๐ SIMILAR VOLUMES
Deletions in the spinach rubisco activase (Rca) promoter in transgenic tobacco were analyzed to define the regions necessary for conferring fight-inducible and fissue-specifc expression. Transgenic plants were constructed with Bal 31 deletions of the Rca promoter fused to the coding region of the ba