• Medientyp: E-Artikel
  • Titel: Malate decarboxylases: evolution and roles of NAD(P)-ME isoforms in species performing C4and C3photosynthesis
  • Beteiligte: Maier, Alexandra; Zell, Martina B.; Maurino, Veronica G.
  • Erschienen: Oxford University Press, 2011
  • Erschienen in: Journal of Experimental Botany
  • Sprache: Englisch
  • DOI: 10.1093/jxb/err024
  • ISSN: 0022-0957; 1460-2431
  • Schlagwörter: BIOCHEMISTRY, MOLECULAR BIOLOGY, AND BIOTECHNOLOGY PERSPECTIVES
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  • Beschreibung: <p>In the C 4 pathway of photosynthesis two types of malate decarboxylases release CO 2 in bundle sheath cells, NADP-and NAD-dependent malic enzyme (NADP-ME and NAD-ME), located in the chloroplasts and the mitochondria of these cells, respectively. The C 4 decarboxylases involved in C 4 photosynthesis did not evolve de novo; they were recruited from existing housekeeping isoforms. NADP-ME housekeeping isoforms would function in the control of malate levels during hypoxia, pathogen defence responses, and microspore separation, while NAD-ME participates in the respiration of malate in the tricarboxylic acid cycle. Recently, the existence of three enzymatic NAD-ME entities in Arabidopsis, occurring by alternative association of two subunits, was described as a novel mechanism to regulate NAD-ME activity under changing metabolic environments. The C 4 NADP-ME is thought to have evolved from a C 3 chloroplastic ancestor, which in turn would have evolved from an ancient cytosolic enzyme. In this way, the C 4 NADP-ME would have emerged through gene duplication, acquisition of a new promoter, and neofunctionalization. In contrast, there would exist a unique NAD-ME in C 4 plants, which would have been adapted to perform a dual function through changes in the kinetic and regulatory properties of the C 3 ancestors. In addition to this, for the evolution of C 4 NAD-ME, insertion of promoters or enhancers into the single-copy genes of the C 3 ancestors would have changed the expression without gene duplication.</p>
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