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Compartment-specific energy requirements of photosynthetic carbon metabolism in Camelina sativa leaves
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk kemi och biofysik.
Department of Energy, Plant Research Laboratory, Michigan State University, MI, East Lansing, United States; Department of Biochemistry and Molecular Biology, Michigan State University, MI, East Lansing, United States; Plant Resilience Institute, Michigan State University, MI, East Lansing, United States.
2022 (Engelska)Ingår i: Planta, ISSN 0032-0935, E-ISSN 1432-2048, Vol. 255, nr 5, artikel-id 103Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Main conclusion: The oxidative pentose phosphate pathway provides cytosolic NADPH yet reduces carbon and energy use efficiency. Repressing this pathway and introducing cytosolic NADPH-dependent malate dehydrogenase may increase crop yields by ≈5%.

Abstract: Detailed knowledge about plant energy metabolism may aid crop improvements. Using published estimates of flux through central carbon metabolism, we phenotype energy metabolism in illuminated Camelina sativa leaves (grown at 22 °C, 500 µmol photons m−2 s−1) and report several findings. First, the oxidative pentose phosphate pathway (OPPP) transfers 3.3% of the NADPH consumed in the Calvin–Benson cycle to the cytosol. NADPH supply proceeds at about 10% of the rate of net carbon assimilation. However, concomitantly respired CO2 accounts for 4.8% of total rubisco activity. Hence, 4.8% of the flux through the Calvin–Benson cycle and photorespiration is spent on supplying cytosolic NADPH, a significant investment. Associated energy requirements exceed the energy output of the OPPP. Thus, autotrophic carbon metabolism is not simply optimised for flux into carbon sinks but sacrifices carbon and energy use efficiency to support cytosolic energy metabolism. To reduce these costs, we suggest bioengineering plants with a repressed cytosolic OPPP, and an inserted cytosolic NADPH-dependent malate dehydrogenase tuned to compensate for the loss in OPPP activity (if required). Second, sucrose cycling is a minor investment in overall leaf energy metabolism but a significant investment in cytosolic energy metabolism. Third, leaf energy balancing strictly requires oxidative phosphorylation, cofactor export from chloroplasts, and peroxisomal NADH import. Fourth, mitochondria are energetically self-sufficient. Fifth, carbon metabolism has an ATP/NADPH demand ratio of 1.52 which is met if ≤ 21.7% of whole electron flux is cyclic. Sixth, electron transport has a photon use efficiency of ≥ 62%. Last, we discuss interactions between the OPPP and the cytosolic oxidation–reduction cycle in supplying leaf cytosolic NADPH.

Ort, förlag, år, upplaga, sidor
Springer-Verlag New York, 2022. Vol. 255, nr 5, artikel-id 103
Nyckelord [en]
ATP/NADPH ratio, Bioenergetics, Energy metabolism, Glucose-6-phosphate shunt, Oxidative pentose phosphate pathway, Sucrose cycling
Nationell ämneskategori
Botanik
Identifikatorer
URN: urn:nbn:se:umu:diva-194330DOI: 10.1007/s00425-022-03884-5ISI: 000781939100001PubMedID: 35415783Scopus ID: 2-s2.0-85128126841OAI: oai:DiVA.org:umu-194330DiVA, id: diva2:1655952
Tillgänglig från: 2022-05-04 Skapad: 2022-05-04 Senast uppdaterad: 2022-05-04Bibliografiskt granskad

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