An ATP synthase harboring an atypical γ–subunit is involved in ATP synthesis in tomato fruit chromoplasts

Summary Chromoplasts are non‐photosynthetic plastids specialized in the synthesis and accumulation of carotenoids. During fruit ripening, chloroplasts differentiate into photosynthetically inactive chromoplasts in a process characterized by the degradation of the thylakoid membranes, and by the acti...

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Veröffentlicht in:The Plant journal : for cell and molecular biology 2013-04, Vol.74 (1), p.74-85
Hauptverfasser: Pateraki, Irini, Renato, Marta, Azcón‐Bieto, Joaquín, Boronat, Albert
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Renato, Marta
Azcón‐Bieto, Joaquín
Boronat, Albert
description Summary Chromoplasts are non‐photosynthetic plastids specialized in the synthesis and accumulation of carotenoids. During fruit ripening, chloroplasts differentiate into photosynthetically inactive chromoplasts in a process characterized by the degradation of the thylakoid membranes, and by the active synthesis and accumulation of carotenoids. This transition renders chromoplasts unable to photochemically synthesize ATP, and therefore these organelles need to obtain the ATP required for anabolic processes through alternative sources. It is widely accepted that the ATP used for biosynthetic processes in non‐photosynthetic plastids is imported from the cytosol or is obtained through glycolysis. In this work, however, we show that isolated tomato (Solanum lycopersicum) fruit chromoplasts are able to synthesize ATP de novo through a respiratory pathway using NADPH as an electron donor. We also report the involvement of a plastidial ATP synthase harboring an atypical γ–subunit induced during ripening, which lacks the regulatory dithiol domain present in plant and algae chloroplast γ–subunits. Silencing of this atypical γ–subunit during fruit ripening impairs the capacity of isolated chromoplast to synthesize ATP de novo. We propose that the replacement of the γ–subunit present in tomato leaf and green fruit chloroplasts by the atypical γ–subunit lacking the dithiol domain during fruit ripening reflects evolutionary changes, which allow the operation of chromoplast ATP synthase under the particular physiological conditions found in this organelle.
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During fruit ripening, chloroplasts differentiate into photosynthetically inactive chromoplasts in a process characterized by the degradation of the thylakoid membranes, and by the active synthesis and accumulation of carotenoids. This transition renders chromoplasts unable to photochemically synthesize ATP, and therefore these organelles need to obtain the ATP required for anabolic processes through alternative sources. It is widely accepted that the ATP used for biosynthetic processes in non‐photosynthetic plastids is imported from the cytosol or is obtained through glycolysis. In this work, however, we show that isolated tomato (Solanum lycopersicum) fruit chromoplasts are able to synthesize ATP de novo through a respiratory pathway using NADPH as an electron donor. We also report the involvement of a plastidial ATP synthase harboring an atypical γ–subunit induced during ripening, which lacks the regulatory dithiol domain present in plant and algae chloroplast γ–subunits. Silencing of this atypical γ–subunit during fruit ripening impairs the capacity of isolated chromoplast to synthesize ATP de novo. 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subjects Adenosine Triphosphate - biosynthesis
Amino Acid Sequence
ATP synthase
ATP synthase γ–subunit
chromoplast
chromorespiration
Fruit - enzymology
Fruit - genetics
fruit ripening
Gene Expression Regulation, Plant
Lycopersicon esculentum
Lycopersicon esculentum - enzymology
Lycopersicon esculentum - genetics
Molecular Sequence Data
NADP - metabolism
Oxygen - metabolism
Plant Proteins - genetics
Plant Proteins - metabolism
Plastids - enzymology
Proton-Translocating ATPases - antagonists & inhibitors
Proton-Translocating ATPases - genetics
Proton-Translocating ATPases - metabolism
Solanum
tomato
title An ATP synthase harboring an atypical γ–subunit is involved in ATP synthesis in tomato fruit chromoplasts
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