Mitochondria in photosynthetic cells: Coordinating redox control and energy balance

Author:

Igamberdiev Abir U1ORCID,Bykova Natalia V2ORCID

Affiliation:

1. Department of Biology, Memorial University of Newfoundland , St. John's, NL A1C 5S7 , Canada

2. Morden Research and Development Centre, Agriculture and Agri-Food Canada , Morden, MB R6M 1Y5 , Canada

Abstract

Abstract In photosynthetic tissues in the light, the function of energy production is associated primarily with chloroplasts, while mitochondrial metabolism adjusts to balance ATP supply, regulate the reduction level of pyridine nucleotides, and optimize major metabolic fluxes. The tricarboxylic acid cycle in the light transforms into a noncyclic open structure (hemicycle) maintained primarily by the influx of malate and the export of citrate to the cytosol. The exchange of malate and citrate forms the basis of feeding redox energy from the chloroplast into the cytosolic pathways. This supports the level of NADPH in different compartments, contributes to the biosynthesis of amino acids, and drives secondary metabolism via a supply of substrates for 2-oxoglutarate-dependent dioxygenase and for cytochrome P450-catalyzed monooxygenase reactions. This results in the maintenance of redox and energy balance in photosynthetic plant cells and in the formation of numerous bioactive compounds specific to any particular plant species. The noncoupled mitochondrial respiration operates in coordination with the malate and citrate valves and supports intensive fluxes of respiration and photorespiration. The metabolic system of plants has features associated with the remarkable metabolic plasticity of mitochondria that permit the use of energy accumulated during photosynthesis in a way that all anabolic and catabolic pathways become optimized and coordinated.

Funder

Natural Sciences and Engineering Research Council of Canada

Agriculture and Agri-Food Canada

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

Reference134 articles.

1. Nitric oxide coordinates growth, development, and stress response via histone modification and gene expression;Ageeva-Kieferle;Plant Physiol,2021

2. The internal rotenone-insensitive NADPH dehydrogenase contributes to malate oxidation by potato tuber and pea leaf mitochondria;Agius;Physiol Plant,1998

3. The occurrence and control of nitric oxide generation by the plant mitochondrial electron transport chain;Alber;Plant Cell Environ,2017

4. The flexibility of metabolic interactions between chloroplasts and mitochondria in Nicotiana tabacum leaf;Alber;Plant J,2021

5. Engineering strategies to boost crop productivity by cutting respiratory carbon loss;Amthor;Plant Cell,2019

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