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CARBOHYDRATE METABOLISM

CARBOHYDRATE METABOLISM. Mia Kusmiati Departemen Biokimia FK UNISBA. Carbohydrates. Carbohydrates are called carbohydrates because they are essentially hydrates of carbon (i.e. they are composed of carbon and water and have a composition of (CH 2 O) n.

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CARBOHYDRATE METABOLISM

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  1. CARBOHYDRATE METABOLISM Mia Kusmiati Departemen Biokimia FK UNISBA

  2. Carbohydrates • Carbohydrates are called carbohydrates because they are essentially hydrates of carbon (i.e. they are composed of carbon and water and have a composition of (CH2O)n. • The major nutritional role of carbohydrates is to provide energy and digestible carbohydrates provide 4 kilocalories per gram. No single carbohydrate is essential, but carbohydrates do participate in many required functions in the body.

  3. Carbohydrate Metabolism

  4. Glucose transport

  5. Glycolysis What is glycolysis?  Ten step metabolic pathway to convert glucose into two molecules of pyruvate and two molecules each of NADH and ATP.  All carbohydrates to be catabolized must enter the glycolytic pathway. - Glycolysis is central in generating both energy and metabolic intermediaries.

  6. The Glycolysis Pathway • Major anaerobic pathway in all cells • NAD+ is the major oxidant • Requires PO4 • Generates 2 ATP’s per glucose oxidized • End product is lactate (mammals) or ethanol (yeast) • Connects with Krebs cycle via pyruvate

  7. Phase I. Energy Investment. 1- Glucose is phosphorylated. Glucose enters a cell through a specific glucose transport process. It is quickly phosphorylated at the expense of an ATP. The investment of an ATP here is called “priming.” Enzymes = hexokinase or glucokinase 2. Isomerization of glucose 6-phosphate Enzyme = phosphoglucoisomerase

  8. glucose 6-phosphate fructose 6-phosphate aldose to ketose isomerization reversible, G= 1.7 kJ/mole

  9. 3- Second phosphorylation Enzyme = phosphofructokinase ATP ADP fructose 1,6 bisphosphate • second ATP investment • highly exergonic, essentially • irreversible, G°´= -14.2 kJ/mole • - highly regulated, modulating carbon • flux through glycolysis in response • to energy and carbon requirements

  10. 4- Cleavage to two triose phosphates Enzyme = aldolase HC=O H2COP HCOH O=C HCOP + CH2OH H glyceraldehydedihydroxyacetone 3-phosphate phosphate where P = phosphate cleaves a 6C sugar to 2 3C sugars G°´= +23.8 kJ/mole, driven by next Rx.

  11. 5-Isomerization of Dihydroxyacetone phosphate Enzyme = triose-phosphate isomerase H2C-OH C=O CH2-O- P dihydroxyacetone glyceraldehyde phosphate 3-phosphate

  12. 5-Isomerization of Dihydroxyacetone phosphate Enzyme = triose-phosphate isomerase H2C-OH C=O CH2-O- P dihydroxyacetone glyceraldehyde phosphate 3-phosphate

  13. allows interconversion of two triosephosphate products of aldolase cleavage only glyceraldehyde 3-phosphate canbe used further in glycolysis.  aldose-ketose isomerization similar to phosphoglucoisomerase rxn allows dihydroxyacetone phosphateto be metabolized asglyceraldehyde 3-phosphate reversible,G°´= +7.5 kJ/mole. This is important in gluconeogenesis

  14. **************************************** End of First Phase:  Production of two glyceraldehyde 3-phosphate molecules from one glucose molecule with the expenditure of two ATPs.  Therefore: the energy yields of the following steps are multipled by two. ***************************************** Second Phase:

  15. 6- Oxidation of glyceraldehyde 3-phosphate Enzyme= glyceraldehyde-3-phosphate dehydrogenase O HOPO OH NAD NADH O OPOH C=O O- HCOH H2C O- P + glyceraldehyde 3-phosphate 1,3 bisphosphoglycerate -addition of phosphate, oxidation, production of NADH, formation of high energy compound

  16. 7- Transfer of phosphate to make ATP Enzyme = phosphoglycerate kinase O=C-O- P O=C-OH P HC-OH + P HC-OH +P H2C-O-P P H2C-O-P P Adenosine Adenosine 1,3PG ADP 3-phosphoglycerate ATP - first substrate level phosphorylation, yielding ATP - 2 1,3 bis PG yield 2 ATPs, thus so far ATP yield = ATP input - high free energy yield, G°´=-18.8kJ/mole drives several of the previous steps.

  17. 8- Phosphate shift setup Enzyme= phosphoglycerate mutase - shifts phosphate from position 3 to 2 - reversible, ΔG = + 4.6 kJ/mole

  18. 9- Generation of second very highenergy compound Enzyme = enolase -- little energy change in this reaction, ΔG = +1.7 kJ/mole because the energy is locked into enolphosphate

  19. 10- Final generation of ATP • Enzyme = pyruvate kinase • P • O H ADP ATP O • -OOC-C=CH -OOC-C-CH3 • phosphoenolpyruvate pyruvate • second substrate levelphosphorylation • yielding ATP • - highly exergonic reaction, • irreversible, ΔG = -31.4 kJ/mole.

  20. Regulation of Glycolysis • 6-phosphofructokinase-1 Allosteric enzyme negative allosteric effectors Citrate , ATP Positive allosteric effectors AMP, fructose1,6-bisphosphate, fructose2,6-bisphosphate Changes in energy state of the cell (ATP and AMP)

  21. Regulation of Glycolysisfig.6-4

  22. Pyruvate Kinase Allosteric enzyme Inhibited by ATP. Isoenzyme in liver activated by fructose 1,6 bisphosphate inhibited by alanine Regulated by phosphorylation and dephosphorylation Hexokinase Different isoenzymes Hexokinase IV glucose 6-phosphate is an allosteric inhibitor promote biosynthesis Regulation of Glycolysis

  23. The Significance of Glycolysis • Glycolysis is the emergency energy-yielding pathway • Main way to produce ATP in some tissues red blood cells, retina, testis, skin, medulla of kidney • In clinical practice

  24. Aerobic Oxidation of Glucose • Glucose oxidation • Oxidation of glucose to pyruvate in cytosol • Oxidation of pyruvate to acetylCoA in mitochondria • Tricarboxylic acid cycle and oxidative phosphorylation

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