Increased sedoheptulose-1,7-bisphosphatase content in Setaria viridis does not affect C4 photosynthesis

Author:

Ermakova Maria12ORCID,Lopez-Calcagno Patricia E34ORCID,Furbank Robert T1ORCID,Raines Christine A3ORCID,von Caemmerer Susanne1ORCID

Affiliation:

1. Centre of Excellence for Translational Photosynthesis, Division of Plant Science, Research School of Biology, The Australian National University , Canberra 2600 , Australia

2. School of Biological Sciences, Monash University , Melbourne, Victoria 3800 , Australia

3. School of Biological Sciences, University of Essex , Colchester CO4 3SQ , UK

4. School of Natural and Environmental Sciences, Newcastle University , Newcastle NE1 7RU , UK

Abstract

Abstract Sedoheptulose-1,7-bisphosphatase (SBPase) is one of the rate-limiting enzymes of the Calvin cycle, and increasing the abundance of SBPase in C3 plants provides higher photosynthetic rates and stimulates biomass and yield. C4 plants usually have higher photosynthetic rates because they operate a biochemical CO2-concentrating mechanism between mesophyll and bundle sheath cells. In the C4 system, SBPase and other enzymes of the Calvin cycle are localized to the bundle sheath cells. Here we tested what effect increasing abundance of SBPase would have on C4 photosynthesis. Using green foxtail millet (Setaria viridis), a model C4 plant of NADP-ME subtype, we created transgenic plants with 1.5 to 3.2 times higher SBPase content compared to wild-type plants. Transcripts of the transgene were found predominantly in the bundle sheaths suggesting the correct cellular localization of the protein. The abundance of ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit was not affected in transgenic plants overexpressing SBPase, and neither was leaf chlorophyll content or photosynthetic electron transport parameters. We found no association between SBPase content in S. viridis and saturating rates of CO2 assimilation. Moreover, a detailed analysis of CO2 assimilation rates at different CO2 partial pressures, irradiances, and leaf temperatures showed no improvement of photosynthesis in plants overexpressing SBPase. We discuss the potential implications of these results for understanding the role of SBPase in regulation of C4 photosynthesis.

Funder

Australian Research Council Centre

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

Reference53 articles.

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5. Chloroplast sedoheptulose 1,7-bisphosphatase: evidence for regulation by the ferredoxin/thioredoxin system;Breazeale;Zeitsch Naturforsch C,1978

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