Essential Arginine Residues in the Nitrate Uptake System from Corn Seedling Roots
Open Access
- 1 October 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 94 (2) , 745-751
- https://doi.org/10.1104/pp.94.2.745
Abstract
Three dicarbonyl reagents were used to demonstrate the presence of an essential arginine residue in the NO3− uptake system from corn seedling roots (Zea mays L., Golden Cross Bantam). Incubation of corn seedlings with 2,3-butanedione (0.125-1.0 millimolar) and 1,2-cyclohexanedione (0.5-4.0 millimolar) in the presence of borate or with phenylglyoxal (0.25-2.0 millimolar) at pH 7.0 and 30°C resulted in a time-dependent loss of NO3− uptake following pseudo-first-order kinetics. Second-order rate constants obtained from slopes of linear plots of pseudo-first-order rate constants versus reagent concentrations were 1.67 × 10−2, 0.68 × 10−2, and 1.00 × 10−2 millimolar per minute for 2,3-butanedione, 1,2-cyclohexanedione, and phenylglyoxal, respectively, indicating the faster rate of inactivation with 2,3-butanedione at equimolar concentration. Double log plots of pseudo-first-order rate constants versus reagent concentrations yielded slope values of 1.031 (2,3-butanedione), 1.004 (1,2-cyclohexanedione), and 1.067 (phenylglyoxal), respectively, suggesting the modification of a single arginine residue. The effectiveness of the dicarbonyl reagents appeared to increase with increasing medium pH from 5.5 to 8.0. Unaltered Km and decreased Vmax in the presence of reagents indicate the inactivation of the modified carriers with unaltered properties. The results thus obtained indicate that the NO3− transport system possesses at least one essential arginine residue.Keywords
This publication has 25 references indexed in Scilit:
- Modification of an essential arginine residue associated with the plasma membrane ATPase of red beet (Beta vulgaris L.) storage tissueArchives of Biochemistry and Biophysics, 1989
- New evidence for the essential role of arginine residues in anion transport across the red blood cell membraneBiochimica et Biophysica Acta (BBA) - Biomembranes, 1987
- Characterization of an essential arginine residue in the plasma membrane H+-ATPase of Neurospora crassa.Journal of Biological Chemistry, 1986
- Anion transport in red blood cells and arginine-specific reagents. Interaction between the substrate-binding site and the binding site of arginine-specific reagentsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1985
- Irreversible inactivation of red cell chloride exchange with phenylglyoxal, and arginine-specific reagent.The Journal of general physiology, 1982
- Arginyl residues and anion binding sites in proteinsMolecular and Cellular Biochemistry, 1979
- An essential arginyl residue in yeast hexokinaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1979
- Arginyl Residues: Anion Recognition Sites in EnzymesScience, 1977
- Essential arginyl residues in mitochondrial adenosine triphosphatase.Journal of Biological Chemistry, 1976
- The Reaction of Phenylglyoxal with Arginine Residues in ProteinsJournal of Biological Chemistry, 1968