Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes
| Autor: | Mariel C, Gerrard Wheeler, Cintia L, Arias, Verónica G, Maurino, Carlos S, Andreo, María F, Drincovich |
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| Rok vydání: | 2009 |
| Předmět: |
Base Sequence
Sequence Homology Amino Acid Arabidopsis Proteins Recombinant Fusion Proteins Green Fluorescent Proteins Molecular Sequence Data Arabidopsis Hydrogen-Ion Concentration Genes Plant Protein Structure Tertiary Enzyme Activation Isoenzymes Kinetics Cytosol Allosteric Regulation Fumarates Malate Dehydrogenase Catalytic Domain Malate Dehydrogenase (NADP+) Coenzyme A Amino Acid Sequence Allosteric Site DNA Primers |
| Zdroj: | The FEBS journal. 276(19) |
| ISSN: | 1742-4658 |
| Popis: | The Arabidopsis thaliana genome contains four genes encoding NADP-malic enzymes (NADP-ME1-4). Two isoenzymes, NADP-ME2 and NADP-ME3, which are shown to be located in the cytosol, share a remarkably high degree of identity (90%). However, they display different expression patterns and show distinct kinetic properties, especially with regard to their regulation by effectors, in both the forward (malate oxidative decarboxylation) and reverse (pyruvate reductive carboxylation) reactions. In order to identify the domains in the primary structure that could be responsible for the regulatory differences, four chimeras between these isoenzymes were constructed and analysed. All chimeric versions exhibited the same native structures as the parental proteins. Analysis of the chimeras constructed indicated that the region from amino acid residue 303 to the C-terminal end of NADP-ME2 is critical for fumarate activation. However, the region flanked by amino acid residues 303 and 500 of NADP-ME3 is involved in the pH-dependent inhibition by high malate concentration. Furthermore, the N-terminal region of NADP-ME2 is necessary for the activation by succinate of the reverse reaction. Overall, the results show that NADP-ME2 and NADP-ME3 are able to distinguish and interact differently with similar C(4) acids as a result of minimal structural differences. Therefore, although the active sites of NADP-ME2 and NADP-ME3 are highly conserved, both isoenzymes acquire different allosteric sites, leading to the creation of proteins with unique regulatory mechanisms, probably best suited to the specific organ and developmental pattern of expression of each isoenzyme. |
| Databáze: | OpenAIRE |
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