Molecular Identification and Functional Characterization of Arabidopsis thaliana Mitochondrial and Chloroplastic NAD+ Carrier Proteins

Ferdinando Palmieri(Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies), Benjamin Rieder(University of Kaiserslautern), Angela Ventrella(University of Bari Aldo Moro), Emanuela Blanco(University of Bari Aldo Moro), Phuc Thi(Max Planck Institute of Molecular Plant Physiology), Adriano Nunes‐Nesi(Max Planck Institute of Molecular Plant Physiology), A.Ulrike Trauth(University of Kaiserslautern), Giuseppe Fiermonte(Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies), Joachim Tjaden(University of Kaiserslautern), Gennaro Agrimi(University of Bari Aldo Moro), Simon Kirchberger(University of Kaiserslautern), Eleonora Paradies(University of Bari Aldo Moro), Alisdair R. Fernie(Max Planck Institute of Molecular Plant Physiology), H. Ekkehard Neuhaus(University of Kaiserslautern)
Journal of Biological Chemistry
September 12, 2009
Cited by 170Open Access
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Abstract

The Arabidopsis thaliana L. genome contains 58 membrane proteins belonging to the mitochondrial carrier family. Two mitochondrial carrier family members, here named AtNDT1 and AtNDT2, exhibit high structural similarities to the mitochondrial nicotinamide adenine dinucleotide (NAD(+)) carrier ScNDT1 from bakers' yeast. Expression of AtNDT1 or AtNDT2 restores mitochondrial NAD(+) transport activity in a yeast mutant lacking ScNDT. Localization studies with green fluorescent protein fusion proteins provided evidence that AtNDT1 resides in chloroplasts, whereas only AtNDT2 locates to mitochondria. Heterologous expression in Escherichia coli followed by purification, reconstitution in proteoliposomes, and uptake experiments revealed that both carriers exhibit a submillimolar affinity for NAD(+) and transport this compound in a counter-exchange mode. Among various substrates ADP and AMP are the most efficient counter-exchange substrates for NAD(+). Atndt1- and Atndt2-promoter-GUS plants demonstrate that both genes are strongly expressed in developing tissues and in particular in highly metabolically active cells. The presence of both carriers is discussed with respect to the subcellular localization of de novo NAD(+) biosynthesis in plants and with respect to both the NAD(+)-dependent metabolic pathways and the redox balance of chloroplasts and mitochondria.


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