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. 1967 Sep;104(3):866–871. doi: 10.1042/bj1040866

Phosphoenolpyruvate carboxykinase and pyruvate carboxylase in developing rat liver

F J Ballard 1, R W Hanson 1
PMCID: PMC1271226  PMID: 6049928

Abstract

1. Phosphoenolpyruvate carboxykinase and pyruvate carboxylase were measured in foetal, newborn and adult rat liver extracts by a radiochemical assay involving the fixation of [14C]bicarbonate. 2. Pyruvate-carboxylase activity in both foetal and adult liver occurs mainly in mitochondrial and nuclear fractions, with about 10% of the activity in the cytoplasm. 3. Similar studies of the intracellular distribution of phosphoenolpyruvate carboxykinase show that more than 90% of the activity is in the cytoplasm. However, in the 17-day foetal liver about 90% of the activity is in mitochondria and nuclei. 4. Pyruvate-carboxylase activity in both particulate and soluble fractions is very low in the 17-day foetal liver and increases to near adult levels before birth. 5. Phosphoenolpyruvate-carboxykinase activity in the soluble cell fraction increases 25-fold in the first 2 days after birth. This same enzyme in the mitochondria has considerable activity in the foetal and adult liver and is lower in the newborn. 6. Kinetic and other studies on the properties of phosphoenolpyruvate carboxykinase have shown no differences between the soluble and mitochondrial enzymes. 7. It is suggested that the appearance of the soluble phosphoenolpyruvate carboxykinase at birth initiates the rapid increase in overall gluconeogenesis at this stage.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andrews P. Estimation of the molecular weights of proteins by Sephadex gel-filtration. Biochem J. 1964 May;91(2):222–233. doi: 10.1042/bj0910222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ashmore J., Wagle S. R., Uete T. Studies on gluconeogenesis. Adv Enzyme Regul. 1964;2:101–114. doi: 10.1016/s0065-2571(64)80008-x. [DOI] [PubMed] [Google Scholar]
  3. BALLARD F. J., OLIVER I. T. Appearance of fructose-1,6-diphosphatase in post-natal rat liver. Nature. 1962 Aug 4;195:498–499. doi: 10.1038/195498a0. [DOI] [PubMed] [Google Scholar]
  4. BALLARD F. J., OLIVER I. T. CARBOHYDRATE METABOLISM IN LIVER FROM FOETAL AND NEONATAL SHEEP. Biochem J. 1965 Apr;95:191–200. doi: 10.1042/bj0950191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BALLARD F. J., OLIVER I. T. Glycogen metabolism in embryonic chick and neonatal rat liver. Biochim Biophys Acta. 1963 Jun 4;71:578–588. doi: 10.1016/0006-3002(63)91130-2. [DOI] [PubMed] [Google Scholar]
  6. BUHLER D. R. A simple scintillation counting technique for assaying C1402 in a Warburg flask. Anal Biochem. 1962 Nov;4:413–417. doi: 10.1016/0003-2697(62)90143-4. [DOI] [PubMed] [Google Scholar]
  7. BUSCH H., HURLBERT R. B., POTTER V. R. Anion exchange chromatography of acids of the citric acid cycle. J Biol Chem. 1952 May;196(2):717–727. [PubMed] [Google Scholar]
  8. Ballard F. J., Hanson R. W. Changes in lipid synthesis in rat liver during development. Biochem J. 1967 Mar;102(3):952–958. doi: 10.1042/bj1020952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ballard F. J., Hanson R. W. The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate. J Lipid Res. 1967 Mar;8(2):73–79. [PubMed] [Google Scholar]
  10. Barritt G. J., Keech D. B., Ling A. M. Apparent co-operative effect of acetyl-CoA on sheep kidney pyruvate carboxylase. Biochem Biophys Res Commun. 1966 Aug 12;24(3):476–481. doi: 10.1016/0006-291x(66)90186-0. [DOI] [PubMed] [Google Scholar]
  11. Chang H. C., Lane M. D. The enzymatic carboxylation of phosphoenolpyruvate. II. Purification and properties of liver mitochondrial phosphoenolpyruvate carboxykinase. J Biol Chem. 1966 May 25;241(10):2413–2420. [PubMed] [Google Scholar]
  12. Dawkins M. J. Biochemical aspects of developing function in newborn mammalian liver. Br Med Bull. 1966 Jan;22(1):27–33. doi: 10.1093/oxfordjournals.bmb.a070432. [DOI] [PubMed] [Google Scholar]
  13. Exton J. H., Park C. R. The stimulation of gluconeogenesis from lactate by epinephrine, glucagon, cyclic 3',5'-adenylate in the perfused rat liver. Pharmacol Rev. 1966 Mar;18(1):181–188. [PubMed] [Google Scholar]
  14. FREEDMAN A. D., KOHN L. PYRUVATE METABOLISM AND CONTROL: FACTORS AFFECTING PYRUVIC CARBOXYLASE ACTIVITY. Science. 1964 Jul 3;145(3627):58–60. doi: 10.1126/science.145.3627.58. [DOI] [PubMed] [Google Scholar]
  15. HENNING H. V., SEUBERT W. ZUM MECHANISMUS DER GLUCONEOGENESE UND IHRER STEUERUNG. I. QUANTITATIVE BESTIMMUNG DER PYRUVATCARBOXYLASE IN ROHEXTRAKTEN DER RATTENLEBER. Biochem Z. 1964 Jul 29;340:160–170. [PubMed] [Google Scholar]
  16. HOLTEN D. D., NORDLIE R. C. COMPARATIVE STUDIES OF CATALYTIC PROPERTIES OF GUINEA PIG LIVER INTRA- AND EXTRAMITOCHONDRIAL PHOSPHOENOLPYRUVATE CARBOXYKINASES. Biochemistry. 1965 Apr;4:723–731. doi: 10.1021/bi00880a018. [DOI] [PubMed] [Google Scholar]
  17. Henning H. V., Stumpf B., Ohly B., Seubert W. On the mechanism of gluconeogenesis and its regulation. 3. The glucogenic capacity and the activities of pyruvate carboxylase and PEP-carboxylase of rat kidney and rat liver after cortisol treatment and starvation. Biochem Z. 1966 Apr 27;344(3):274–288. [PubMed] [Google Scholar]
  18. KEECH D. B., UTTER M. F. PYRUVATE CARBOXYLASE. II. PROPERTIES. J Biol Chem. 1963 Aug;238:2609–2614. [PubMed] [Google Scholar]
  19. KREBS H. A. RENAL GLUCONEOGENESIS. Adv Enzyme Regul. 1963;1:385–400. doi: 10.1016/0065-2571(63)90034-7. [DOI] [PubMed] [Google Scholar]
  20. Krebs H. A., Eggleston L. V. Metabolism of acetoacetate in animal tissues. 1. Biochem J. 1945;39(5):408–419. [PMC free article] [PubMed] [Google Scholar]
  21. Lardy H. A., Foster D. O., Shrago E., Ray P. D. Metabolic and hormonal regulation of phosphopyruvate synthesis. Adv Enzyme Regul. 1964;2:39–47. doi: 10.1016/s0065-2571(64)80004-2. [DOI] [PubMed] [Google Scholar]
  22. NORDLIE R. C., LARDY H. A. Mammalian liver phosphoneolpyruvate carboxykinase activities. J Biol Chem. 1963 Jul;238:2259–2263. [PubMed] [Google Scholar]
  23. Prinz W., Seubert W. Effect of insulin on pyruvate carboxylase in alloxan diabetic animals. Biochem Biophys Res Commun. 1964 Aug 11;16(6):582–585. doi: 10.1016/0006-291x(64)90196-2. [DOI] [PubMed] [Google Scholar]
  24. SHRAGO E., LARDY H. A., NORDLIE R. C., FOSTER D. O. METABOLIC AND HORMONAL CONTROL OF PHOSPHOENOLPYRUVATE CARBOXYKINASE AND MALIC ENZYME IN RAT LIVER. J Biol Chem. 1963 Oct;238:3188–3192. [PubMed] [Google Scholar]
  25. SPENCER A. F., LOWENSTEIN J. M. The supply of precursors for the synthesis of fatty acids. J Biol Chem. 1962 Dec;237:3640–3648. [PubMed] [Google Scholar]
  26. UTTER M. F., KEECH D. B. PYRUVATE CARBOXYLASE. I. NATURE OF THE REACTION. J Biol Chem. 1963 Aug;238:2603–2608. [PubMed] [Google Scholar]
  27. VILLEE C. A., HAGERMAN D. D. Effect of oxygen deprivation on the metabolism of fetal and adult tissues. Am J Physiol. 1958 Sep;194(3):457–464. doi: 10.1152/ajplegacy.1958.194.3.457. [DOI] [PubMed] [Google Scholar]
  28. WEBER G., CANTERO A. Glucose-6-phosphate utilization in hepatoma, regenerating and newborn rat liver, and in the liver of fed and fasted normal rats. Cancer Res. 1957 Nov;17(10):995–1005. [PubMed] [Google Scholar]
  29. YOUNG J. W., SHRAGO E., LARDY H. A. METABOLIC CONTROL OF ENZYMES INVOLVED IN LIPOGENESIS AND GLUCONEOGENESIS. Biochemistry. 1964 Nov;3:1687–1692. doi: 10.1021/bi00899a015. [DOI] [PubMed] [Google Scholar]

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