Abstract
1. The effect of NH4+, Pi and K+ on phosphofructokinase from muscle and nervous tissues of a large number of animals was investigated. The activation of the enzyme from lobster abdominal muscle by NH4+ was increased synergistically by the presence of Pi or SO4(2-). In the absence of K+, NH4+ plus Pi markedly activated phosphofructokinase from all tissues studied. In the presence of 100 mM-K+, NH4+ plus Pi activated phosphofructokinase from nervous tissue and muscle of invertebrates and the enzyme from brain of vertebrates, but there was no effect of NH4+ plus Pi on the enzyme from the muscles of vertebrates. Nonetheless, NH4+ plus Pi increased the activity of vertebrate muscle phosphofructokinase in the presence of 50 mM-K+ at inhibitory concentrations of ATP, i.e. these ions de-inhibited the enzyme. In the absence of NH4+ plus Pi, K+ activated phosphofructokinase from vertebrate tissues at non-inhibitory ATP concentrations, but the effect was less marked with the enzyme from invertebrate tissues. Indeed, high concentrations of K+ (greater than 50 mM) caused inhibition of invertebrate tissue phosphofructokinase. Of the other alkali-metal ions tested, only Rb+ activated phosphofructokinase from lobster abdominal muscle and rat heart muscle. 2. The properties of lobster abdominal-muscle phosphofructokinase were studied in detail. This muscle was chosen as representative of invertebrate muscle because large quantities of tissue could be obtained from one animal and the enzyme was considerably more stable in tissue extracts than in extracts of insect flight muscle. In general, the properties of the enzyme from this tissue were similar to those of the enzyme from many other tissues: ATP concentrations above an optimum value inhibited the enzyme and this inhibition was decreased by raising the fructose 6-phosphate or the AMP concentration. In particular, NH4+ plus Pi activated the enzyme at noninhibitory concentrations of ATP and they also relieved ATP inhibition (see above). 3. It is suggested that increases in the concentration of NH4+ and Pi, under conditions of increased ATP utilization in certain muscles and/or nervous tissue, may play a part in the stimulation of glycolysis through the effects on phosphofructokinase (the effect may be a direct activation and/or a relief of ATP inhibition). Changes in the concentration of NH4+ and Pi are consistent with this theory in nervous tissue and the anaerobic type of muscles. The role of AMP deaminase in production of NH4+ from AMP in these tissues is discussed in relation to the control of glycolysis.
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Selected References
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- Abrahams S. L., Younathan E. S. Modulation of the kinetic properties of phosphofructokinase by ammonium ions. J Biol Chem. 1971 Apr 25;246(8):2464–2467. [PubMed] [Google Scholar]
- CURRIE R. D., WEBSTER H. L. Preparation of 5'-adenylic acid deaminase based on phosphate-induced dissociation of rat actomyosin-deaminase complexes. Biochim Biophys Acta. 1962 Oct 8;64:30–40. doi: 10.1016/0006-3002(62)90757-6. [DOI] [PubMed] [Google Scholar]
- Dalziel K. Kinetics of control enzymes. Symp Soc Exp Biol. 1973;27:21–48. [PubMed] [Google Scholar]
- Dydyńska M., Wilkie D. R. The chemical and energetic properties of muscles poisoned with fluorodinitrobenzene. J Physiol. 1966 Jun;184(3):751–769. doi: 10.1113/jphysiol.1966.sp007946. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Folbergrová J., Passonneau J. V., Lowry O. H., Schulz D. W. Glycogen, ammonia and related metabolities in the brain during seizures evoked by methionine sulphoximine. J Neurochem. 1969 Feb;16(2):191–203. doi: 10.1111/j.1471-4159.1969.tb05937.x. [DOI] [PubMed] [Google Scholar]
- Frenkel R. Control of reduced diphosphopyridine nucleotide oscillations in beef heart extracts. 3. Purification and kinetics of beef heart phosphofructokinase. Arch Biochem Biophys. 1968 Apr;125(1):166–174. doi: 10.1016/0003-9861(68)90651-6. [DOI] [PubMed] [Google Scholar]
- Garland P. B., Randle P. J. Regulation of glucose uptake by muscles. 10. Effects of alloxan-diabetes, starvation, hypophysectomy and adrenalectomy, and of fatty acids, ketone bodies and pyruvate, on the glycerol output and concentrations of free fatty acids, long-chain fatty acyl-coenzyme A, glycerol phosphate and citrate-cycle intermediates in rat heart and diaphragm muscles. Biochem J. 1964 Dec;93(3):678–687. doi: 10.1042/bj0930678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HOFSTEE B. H. Non-inverted versus inverted plots in enzyme kinetics. Nature. 1959 Oct 24;184:1296–1298. doi: 10.1038/1841296b0. [DOI] [PubMed] [Google Scholar]
- Judge W. J., Dawson J. Paleolndian settlement technology in new Mexico. Science. 1972 Jun 16;176(4040):1210–1216. doi: 10.1126/science.176.4040.1210. [DOI] [PubMed] [Google Scholar]
- KAHANA S. E., LOWRY O. H., SCHULZ D. W., PASSONNEAU J. V., CRAWFORD E. J. The kinetics of phosphoglucoisomerase. J Biol Chem. 1960 Aug;235:2178–2184. [PubMed] [Google Scholar]
- KARPATKIN S., HELMREICH E., CORI C. F. REGULATION OF GLYCOLYSIS IN MUSCLE. II. EFFECT OF STIMULATION AND EPINEPHRINE IN ISOLATED FROG SARTORIUS MUSCLE. J Biol Chem. 1964 Oct;239:3139–3145. [PubMed] [Google Scholar]
- KREBS H. A., WOODFORD M. FRUCTOSE 1, 6-DIPHOSPHATASE IN STRIATED MUSCLE. Biochem J. 1965 Feb;94:436–445. doi: 10.1042/bj0940436. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LOWRY O. H., PASSONNEAU J. V., HASSELBERGER F. X., SCHULZ D. W. EFFECT OF ISCHEMIA ON KNOWN SUBSTRATES AND COFACTORS OF THE GLYCOLYTIC PATHWAY IN BRAIN. J Biol Chem. 1964 Jan;239:18–30. [PubMed] [Google Scholar]
- MUNTZ J. A., HURWITZ J. The effect of ammonium ions upon isolated reactions of the glycolytic scheme. Arch Biochem Biophys. 1951 Jun;32(1):137–149. doi: 10.1016/0003-9861(51)90247-0. [DOI] [PubMed] [Google Scholar]
- MUNTZ J. A. Partial purification and some properties of brain phosphofructokinase. Arch Biochem Biophys. 1953 Feb;42(2):435–445. doi: 10.1016/0003-9861(53)90371-3. [DOI] [PubMed] [Google Scholar]
- MUNTZ J. A. The formation of ammonia in brain extracts. J Biol Chem. 1953 Mar;201(1):221–233. [PubMed] [Google Scholar]
- Newsholme E. A., Crabtree B. Metabolic aspects of enzyme activity regulation. Symp Soc Exp Biol. 1973;27:429–460. [PubMed] [Google Scholar]
- Newsholme E. A., Crabtree B. The role of fructose-1,6-diphosphatase in the regulation of glycolysis in skeletal muscle. FEBS Lett. 1970 Apr 2;7(2):195–198. doi: 10.1016/0014-5793(70)80155-7. [DOI] [PubMed] [Google Scholar]
- Newsholme E. A., Randle P. J. Regulation of glucose uptake by muscle. 7. Effects of fatty acids, ketone bodies and pyruvate, and of alloxan-diabetes, starvation, hypophysectomy and adrenalectomy, on the concentrations of hexose phosphates, nucleotides and inorganic phosphate in perfused rat heart. Biochem J. 1964 Dec;93(3):641–651. doi: 10.1042/bj0930641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newsholme E. A., Sugden P. H. The apparent inhibition of phosphofrunctokinase by reduced nicotinamide-adenine dinucleotide: a problem of coupled-enzyme assays. Biochem J. 1970 Oct;119(4):787–789. doi: 10.1042/bj1190787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newsholme E. A., Taylor K. Glycerol kinase activities in muscles from vertebrates and invertebrates. Biochem J. 1969 May;112(4):465–474. doi: 10.1042/bj1120465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Opie L. H., Mansford K. R., Owen P. Effects of increased heart work on glycolysis and adenine nucleotides in the perfused heart of normal and diabetic rats. Biochem J. 1971 Sep;124(3):475–490. doi: 10.1042/bj1240475. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PASSONNEAU J. V., LOWRY O. H. Phosphofructokinase and the Pasteur effect. Biochem Biophys Res Commun. 1962 Feb 20;7:10–15. doi: 10.1016/0006-291x(62)90134-1. [DOI] [PubMed] [Google Scholar]
- Passonneau J. V., Lowry O. H. The role of phosphofructokinase in metabolic regulation. Adv Enzyme Regul. 1964;2:265–274. doi: 10.1016/s0065-2571(64)80018-2. [DOI] [PubMed] [Google Scholar]
- REGEN D. M., DAVIS W. W., MORGAN H. E., PARK C. R. THE REGULATION OF HEXOKINASE AND PHOSPHOFRUCTOKINASE ACTIVITY IN HEART MUSCLE. EFFECTS OF ALLOXAN DIABETES, GROWTH HORMONE, CORTISOL, AND ANOXIA. J Biol Chem. 1964 Jan;239:43–49. [PubMed] [Google Scholar]
- Rolleston F. S., Newsholme E. A. Control of glycolysis in cerebral cortex slices. Biochem J. 1967 Aug;104(2):524–533. doi: 10.1042/bj1040524. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ronca-Testoni S., Raggi A., Ronca G. Muscle AMP aminohydrolase. 3. A comparative study on the regulatory properties of skeletal muscle enzyme from various species. Biochim Biophys Acta. 1970 Jan 14;198(1):101–112. doi: 10.1016/0005-2744(70)90038-0. [DOI] [PubMed] [Google Scholar]
- Sacktor B., Hurlbut E. C. Regulation of metabolism in working muscle in vivo. II. Concentrations of adenine nucleotides, arginine phosphate, and inorganic phosphate in insect flight muscle during flight. J Biol Chem. 1966 Feb 10;241(3):632–634. [PubMed] [Google Scholar]
- Sacktor B., Wormser-Shavit E. Regulation of metabolism in working muscle in vivo. I. Concentrations of some glycolytic, tricarboxylic acid cycle, and amino acid intermediates in insect flight muscle during flight. J Biol Chem. 1966 Feb 10;241(3):624–631. [PubMed] [Google Scholar]
- Sugden P. H., Newsholme E. A. Activities of hexokinase, phosphofructokinase, 3-oxo acid coenzyme A-transferase and acetoacetyl-coenzyme A thiolase in nervous tissue from vertebrates and invertebrates. Biochem J. 1973 May;134(1):97–101. doi: 10.1042/bj1340097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- UNDERWOOD A. H., NEWSHOLME E. A. PROPERTIES OF PHOSPHOFRUCTOKINASE FROM RAT LIVER AND THEIR RELATION TO THE CONTROL OF GLYCOLYSIS AND GLUCONEOGENESIS. Biochem J. 1965 Jun;95:868–875. doi: 10.1042/bj0950868. [DOI] [PMC free article] [PubMed] [Google Scholar]
