The DOI matches its Crossref record, with a small difference in title or year; 17 of the 17 references it cites were found in a registry or an index.
Role of Oxalacetate in the Regulation of Mammalian Succinate Dehydrogenase
Open accessAbstract
Abstract In most procedures for the isolation of membrane-bound or soluble succinate dehydrogenase, the enzyme is obtained largely in the deactivated form. As judged by the quantity of oxalacetate enzymatically determined in perchlorate extracts, the deactivated form contains tightly bound oxalacetate in 1:1 proportion to the enzyme (equated with histidyl flavin content) in particles. A somewhat lower ratio has been obtained for soluble preparations of the enzyme. The oxalacetate is bound very tightly: it is not displaced by succinate or malonate in the cold, nor released by precipitation or gel exclusion of the enzyme, and it does not react with malate dehydrogenase. It is released, however, on denaturation of the enzyme with perchloric acid or under conditions which favor conversion of the enzyme to the activated form. If the enzyme is freed from oxalacetate by activation with bromide and gel exclusion, treatment of the oxalacetate-free fully active enzyme with very low concentrations of l- or d-malate or oxalacetate leads to deactivation and concomitant formation of tightly bound oxalacetate in the same molar ratio found in the enzyme as isolated from heart mitochondria. Dissociation of the complex formed in this manner requires the same experimental conditions as those needed for dissociation of the complex as found in the isolated enzyme. The activation energies for activation and for release of oxalacetate are the same but vary with the type of activator used. The first order rate constant for activation by a variety of agents is about twice that measured for the dissociation of tightly bound oxalacetate. Moreover, with some activators oxalacetate release shows a considerable lag behind recovery of catalytic activity. It is suggested that the presence of oxalacetate in the deactivated enzyme is not the cause of its lack of catalytic activity but a consequence of the deactivated conformation. Further observations are described which suggest that a deactivation-activation cycle may also occur in the absence of oxalacetate.
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“Besides a direct competition between succinate and malate, it has been observed that complex II can oxidize malate to the enol form oxaloacetate [67,68], which binds to the dicarboxylate binding site with high affinity [66].”
From Differential effects of complex II on mitochondrial ROS production and their relation to cardioprotective pre- and postconditioning (2013) · cites this paper as [67]
Citations
Cites
WILLIAMSON, J. R., & Corkey, B. E. (1969) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(69)13072-4 · Cited by 867
Dynamics of energy‐transducing membranes
Baum, H. (1975) · FEBS Letters · doi:10.1016/0014-5793(75)81015-5 · Cited by 348
Batch purification of ovomucoid and characterization of the purified product
Davis, J. G., Mapes, C. J., & Donovan, J. W. (1971) · Biochemistry · doi:10.1021/bi00777a006 · Cited by 270
Succinate dehydrogenase. I. Purification, molecular properties, and substructure
Hatefi, Y., & Davis, K. A. (1971) · Biochemistry · doi:10.1021/bi00789a014 · Cited by 254
Taborsky, G. (1973) · Elsevier eBooks · doi:10.1016/b978-0-120-68960-6.x5001-1 · Cited by 175
Studies on the Respiratory Chain-linked Reduced Nicotinamide Adenine Dinucleotide Dehydrogenase
Ringler, R. L., Minakami, S., & Singer, T. P. (1963) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)81338-2 · Cited by 157
Energy Metabolism and the Regulation of Metabolic Processes in Mitochondria
(1972) · Elsevier eBooks · doi:10.1016/b978-0-12-487850-1.x5001-5 · Cited by 152
Studies on Succinate Dehydrogenase
Kimura, T., HAUBER, J., & Singer, T. P. (1967) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99466-4 · Cited by 99
Control of succinate dehydrogenase in mitochondria
Gutman, M., Kearney, E. B., & Singer, T. P. (1971) · Biochemistry · doi:10.1021/bi00801a025 · Cited by 97
Self-citationSuccinate dehydrogenase. II. Enzymic properties
Hatefi, Y., Hanstein, W. G., Davis, K. A., & Ghalambor, M. A. (1971) · Biochemistry · doi:10.1021/bi00789a015 · Cited by 84
Research works printed but not linked: 4
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- Coles, 1972, Physiol. Chem. Phys., 4, 301
- Wojtczak, 1969, Bio chim. Biophys. Ada, 191, 10
- Vinogradov, 1973, Abstracts, 9th International Congress of Biochemistry, 110
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Items 101–101 of 101
Oxaloacetate inhibition of succinate dehydrogenase: mechanism and physiological implications
Sivitz, W. I., & Yu, L. P. (2026) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00200.2026
Metadata
- Authors
- Ackrell, B. A. C., Kearney, E. B., & Mayr, M.
- Affiliations
- San Francisco VA Medical Center (US)
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1974-04
- Volume
- 249
- Issue
- 7
- Pages
- 2021-2027
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1558696651
- Cited by
- 102
- References
- 17
- Citations by year
- 2026: 1 · 2025: 1 · 2021: 3 · 2020: 3 · 2019: 3 · 2017: 1 · 2016: 2 · 2015: 2 · 2014: 2 · 2013: 4 · 2012: 6
- FWCI
- 3.64
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Biochemical Acid Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Keywords
- succinate dehydrogenase, oxaloacetate, enzyme inactivation, enzyme activation, heart mitochondria, enzyme conformation, malate, enzyme regulation
- MeSH terms
- Allosteric Regulation, Animals, Bromides, Catalysis, Cattle, Electron Transport, Enzyme Activation, Flavins, Histidine, Hydrogen-Ion Concentration, Kinetics, Malates, Malonates, Mitochondria, Muscle, Myocardium, Osmolar Concentration, Oxaloacetates, Protein Binding, Protein Conformation, Solubility, Succinate Dehydrogenase, Thermodynamics
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