» Articles » PMID: 35904136

Enhanced Abundance and Activity of the Chloroplast ATP Synthase in Rice Through the Overexpression of the AtpD Subunit

Overview
Journal J Exp Bot
Specialty Biology
Date 2022 Jul 29
PMID 35904136
Authors
Affiliations
Soon will be listed here.
Abstract

ATP, produced by the light reactions of photosynthesis, acts as the universal cellular energy cofactor fuelling all life processes. Chloroplast ATP synthase produces ATP using the proton motive force created by solar energy-driven thylakoid electron transport reactions. Here we investigate how increasing abundance of ATP synthase affects leaf photosynthesis and growth of rice, Oryza sativa variety Kitaake. We show that overexpression of AtpD, the nuclear-encoded subunit of the chloroplast ATP synthase, stimulates both abundance of the complex, confirmed by immunodetection of thylakoid complexes separated by Blue Native-PAGE, and ATP synthase activity, detected as higher proton conductivity of the thylakoid membrane. Plants with increased AtpD content had higher CO2 assimilation rates when a stepwise increase in CO2 partial pressure was imposed on leaves at high irradiance. Fitting of the CO2 response curves of assimilation revealed that plants overexpressing AtpD had a higher electron transport rate (J) at high CO2, despite having wild-type-like abundance of the cytochrome b6f complex. A higher maximum carboxylation rate (Vcmax) and lower cyclic electron flow detected in transgenic plants both pointed to an increased ATP production compared with wild-type plants. Our results present evidence that the activity of ATP synthase modulates the rate of electron transport at high CO2 and high irradiance.

Citing Articles

Enhancing Photosynthesis and Plant Productivity through Genetic Modification.

Nazari M, Kordrostami M, Ghasemi-Soloklui A, Eaton-Rye J, Pashkovskiy P, Kuznetsov V Cells. 2024; 13(16.

PMID: 39195209 PMC: 11352682. DOI: 10.3390/cells13161319.


Physiological, transcriptomic and metabolomic insights of three extremophyte woody species living in the multi-stress environment of the Atacama Desert.

Gajardo H, Morales M, Larama G, Luengo-Escobar A, Lopez D, Machado M Planta. 2024; 260(3):55.

PMID: 39020000 DOI: 10.1007/s00425-024-04484-1.


Structure, Regulation, and Significance of Cyanobacterial and Chloroplast Adenosine Triphosphate Synthase in the Adaptability of Oxygenic Photosynthetic Organisms.

Yi S, Guo X, Lou W, Mao S, Luan G, Lu X Microorganisms. 2024; 12(5).

PMID: 38792770 PMC: 11124002. DOI: 10.3390/microorganisms12050940.


Chloroplast ATP synthase: From structure to engineering.

Ruhle T, Leister D, Pasch V Plant Cell. 2024; 36(10):3974-3996.

PMID: 38484126 PMC: 11449085. DOI: 10.1093/plcell/koae081.


Conspicuous chloroplast with light harvesting-photosystem I/II megacomplex in marine Prorocentrum cordatum.

Kalvelage J, Wohlbrand L, Senkler J, Schumacher J, Ditz N, Bischof K Plant Physiol. 2024; 195(1):306-325.

PMID: 38330164 PMC: 11181951. DOI: 10.1093/plphys/kiae052.


References
1.
Lyska D, Meierhoff K, Westhoff P . How to build functional thylakoid membranes: from plastid transcription to protein complex assembly. Planta. 2012; 237(2):413-28. PMC: 3555230. DOI: 10.1007/s00425-012-1752-5. View

2.
Simkin A, McAusland L, Lawson T, Raines C . Overexpression of the RieskeFeS Protein Increases Electron Transport Rates and Biomass Yield. Plant Physiol. 2017; 175(1):134-145. PMC: 5580758. DOI: 10.1104/pp.17.00622. View

3.
von Ballmoos C, Cook G, Dimroth P . Unique rotary ATP synthase and its biological diversity. Annu Rev Biophys. 2008; 37:43-64. DOI: 10.1146/annurev.biophys.37.032807.130018. View

4.
Davis G, Kramer D . Optimization of ATP Synthase c-Rings for Oxygenic Photosynthesis. Front Plant Sci. 2020; 10:1778. PMC: 7003800. DOI: 10.3389/fpls.2019.01778. View

5.
Engelbrecht S, Schurmann K, Junge W . Chloroplast ATP synthase contains one single copy of subunit delta that is indispensable for photophosphorylation. Eur J Biochem. 1989; 179(1):117-22. DOI: 10.1111/j.1432-1033.1989.tb14528.x. View