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Fig 10.5 Overview of catabolic pathways Prentice Hall c2002 Chapter 11
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Fig 11.1 Catabolism of glucose via glycolysis and the citric acid cycle NADH NADH, FADH2 Prentice Hall c2002 Chapter 11
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Net reaction of glycolysis
Converts: 1 glucose pyruvate + Two molecules of ATP are produced Two molecules of NAD+ are reduced to NADH Glucose + 2 ADP + 2 NAD+ + 2 Pi 2 Pyruvate + 2 ATP + 2 NADH + 2 H+ + 2 H2O Prentice Hall c2002 Chapter 11
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Glycolysis can be divided into two stages
Hexose stage: 2 ATP are consumed per glucose Triose stage: 4 ATP are produced per glucose Net: 2 ATP produced per glucose x2 Prentice Hall c2002 Chapter 11
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Table 11.1 Prentice Hall c2002 Chapter 11
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1 2 Fig 11.2 Transfer of a phosphoryl group from ATP to glucose
enzyme: hexokinase 1 Isomerization of glucose 6-phosphate to fructose 6-phosphate enzyme: glucose 6-phosphate isomerase 2 Prentice Hall c2002 Chapter 11
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Transfer of a second phosphoryl group from ATP to fructose 6-phosphate
enzyme: phosphofructokinase-1 3 Carbon 3 – Carbon 4 bond cleavage, yielding two triose phosphates enzyme: aldolase 4 Prentice Hall c2002 Chapter 11
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Prentice Hall c2002 Chapter 11
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Prentice Hall c2002 Chapter 11
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Enzyme 1. Hexokinase Transfers the g-phosphoryl of ATP to glucose C-6 oxygen to generate glucose 6-phosphate Mechanism: attack of C-6 hydroxyl oxygen of glucose on the g-phosphorous of MgATP2- displacing MgADP- Fig 11.3 Prentice Hall c2002 Chapter 11
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2. Glucose 6-Phosphate Isomerase
Converts glucose 6-phosphate (an aldose) to fructose 6-phosphate (a ketose) Enzyme converts glucose 6-phosphate to open chain form in the active site Fig 11.4 Prentice Hall c2002 Chapter 11
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3. Phosphofructokinase-1 (PFK-1)
Catalyzes transfer of a phosphoryl group from ATP to the C-1 hydroxyl group of fructose 6-phosphate to form fructose 1,6-bisphosphate (F1,6BP) PFK-1 is metabolically irreversible and a critical regulatory point for glycolysis in most cells (PFK-1 is the first committed step of glycolysis) Prentice Hall c2002 Chapter 11
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4. Aldolase Aldolase cleaves the hexose fructose 1,6-bisphosphate into two triose phosphates: glyceraldehyde 3-phosphate and dihydroxyacetone phosphate Prentice Hall c2002 Chapter 11
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5. Triose Phosphate Isomerase
Conversion of dihydroxyacetone phosphate into glyceraldehyde 3-phosphate Prentice Hall c2002 Chapter 11
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Fig 11.6 Fate of carbon atoms from hexose stage to triose stage
Prentice Hall c2002 Chapter 11
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6. Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDH)
Conversion of glyceraldehyde 3-phosphate to 1,3-bisphosphoglycerate (1,3BPG) Molecule of NAD+ is reduced to NADH Prentice Hall c2002 Chapter 11
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Mechanism of Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDH)
Fig 11.7 Mechanism of Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDH) Prentice Hall c2002 Chapter 11
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Fig 11.7 (continued) (3) (2) Prentice Hall c2002 Chapter 11
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Fig 11.7 (continued) Prentice Hall c2002 Chapter 11
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Box 11.2 Arsenate (AsO43-) poisoning
Arsenate can replace Pi as a substrate for glyceraldehyde 3-phosphate dehydrogenase Arseno analog which forms is unstable Prentice Hall c2002 Chapter 11
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7. Phosphoglycerate Kinase
Uses uses the high-energy phosphate of 1,3-bisphosphoglycerate to form ATP from ADP Transfer of phosphoryl group from the energy-rich 1,3-bisphosphoglycerate to ADP yields ATP and 3-phosphoglycerate Prentice Hall c2002 Chapter 11
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8. Phosphoglycerate Mutase
Catalyzes transfer of a phosphoryl group from one part of a substrate molecule to another Reaction occurs without input of ATP energy Prentice Hall c2002 Chapter 11
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9. Enolase: 2-phosphoglycerate to phosphoenolpyruvate (PEP)
Elimination of water (dehydration) yields PEP PEP has a very high phosphoryl group transfer potential because it exists in its unstable enol form Prentice Hall c2002 Chapter 11
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10. Pyruvate Kinase Metabolically irreversible reaction
Prentice Hall c2002 Chapter 11
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Fates of pyruvate For centuries, bakeries and breweries have exploited the conversion of glucose to ethanol and CO2 by glycolysis in yeast Prentice Hall c2002 Chapter 11
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Metabolism of Pyruvate
1. Aerobic conditions: pyruvate is oxidized to acetyl CoA, which enters the citric acid cycle for further oxidation 2. Anaerobic conditions (microorganisms): pyruvate is converted to ethanol 3. Anaerobic conditions (muscles, red blood cells): pyruvate is converted to lactate Prentice Hall c2002 Chapter 11
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Fig 11.10 Three major fates of pyruvate Prentice Hall c2002 Chapter 11
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Fig 11.11 Two enzymes required: (1) Pyruvate decarboxylase
(2) Alcohol dehydrogenase Anaerobic conversion of pyruvate to ethanol (yeast - anaerobic) Prentice Hall c2002 Chapter 11
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Reduction of Pyruvate to Lactate (muscles - anaerobic)
Muscles lack pyruvate dehydrogenase and cannot produce ethanol from pyruvate Muscle lactate dehydrogenase converts pyruvate to lactate This reaction regenerates NAD+ for use by glyceraldehyde 3-phosphate dehydrogenase in glycolysis Lactate formed in skeletal muscles during exercise is transported to the liver Liver lactate dehydrogenase can reconvert lactate to pyruvate Lactic acidosis can result from insufficient oxygen (an increase in lactic acid and decrease in blood pH) Prentice Hall c2002 Chapter 11
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Reduction of pyruvate to lactate
Glucose + 2 Pi ADP3- 2 Lactate- + 2 ATP H2O Prentice Hall c2002 Chapter 11
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Metabolically Irreversible Steps of Glycolysis
Enzymes not reversible: Reaction 1 - hexokinase Reaction 3 - phosphofructokinase Reaction 10 - pyruvate kinase These steps are metabolically irreversible, and these enzymes are regulated All other steps of glycolysis are near equilibrium in cells and not regulated Prentice Hall c2002 Chapter 11
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Regulation of Glycolysis
1. When ATP is needed, glycolysis is activated Inhibition of phosphofructokinase-1 is relieved. Pyruvate kinase is activated. 2. When ATP levels are sufficient, glycolysis activity decreases Phosphofructokinase-1 is inhibited. Hexokinase is inhibited. Prentice Hall c2002 Chapter 11
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Glucose transport into the cell
Fig 11.13 Glucose transport into the cell Prentice Hall c2002 Chapter 11
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Fig 11.14 Regulation of glucose transport
Glucose uptake into skeletal and heart muscle and adipocytes by GLUT 4 is stimulated by insulin Prentice Hall c2002 Chapter 11
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Regulation of Hexokinase
Hexokinase reaction is metabolically irreversible Glucose 6-phosphate (product) levels increase when glycolysis is inhibited at sites further along in the pathway Glucose 6-phosphate inhibits hexokinase. Prentice Hall c2002 Chapter 11
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Regulation of Phosphofructokinase-1 (PFK-1)
ATP is a substrate and an allosteric inhibitor of PFK-1 High concentrations of ADP and AMP allosterically activate PFK-1 by relieving the ATP inhibition. Elevated levels of citrate (indicate ample substrates for citric acid cycle) also inhibit Phospofructokinase-1 Prentice Hall c2002 Chapter 11
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Fig 11.16 Regulation of Phosphofructokinase-1 by ATP and AMP
AMP relieves ATP inhibition of PFK-1 Prentice Hall c2002 Chapter 11
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Regulation of PFK-1 by Fructose 2,6-bisphosphate (F2,6BP)
Fructose 2,6-bisphosphate is formed from Fructose 6-phosphate by the enzyme phosphofructokinase-2 (PFK-2) Fig Fructose 2,6-bisphosphate Prentice Hall c2002 Chapter 11
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Formation and hydrolysis of Fructose 2,6-bisphosphate
Prentice Hall c2002 Chapter 11
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Fig. 11.18 Effect of glucagon on liver glycolysis Prentice Hall c2002
Chapter 11
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Regulation of Pyruvate Kinase (PK)
Pyruvate Kinase is allosterically activated by Fructose 1,6-bisphosphate, and inhibited by ATP The hormone glucagon stimulates protein kinase A, which phosphorylates Pyruvate Kinase, converting it to a less active form. Prentice Hall c2002 Chapter 11
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Other Sugars Can Enter Glycolysis
Glucose is the main metabolic fuel in most organisms Other sugars convert to glycolytic intermediates Fructose and sucrose (contains fructose) are major sweeteners in many foods and beverages Galactose from milk lactose (a disaccharide) Mannose from dietary polysaccharides, glycoproteins Prentice Hall c2002 Chapter 11
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Fructose Is Converted to Glyceraldehyde 3-Phosphate
Fig 11.21 Prentice Hall c2002 Chapter 11
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Galactose is Converted to Glucose 1-Phosphate
Prentice Hall c2002 Chapter 11 Fig 11.22
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Mannose is Converted to Fructose 6-Phosphate
Prentice Hall c2002 Chapter 11
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Formation of 2,3-Bisphosphoglycerate in Red Blood Cells
2,3-Bisphosphoglycerate (2,3BPG) allosterically regulates hemoglobin oxygenation (red blood cells) Erythrocytes contain bisphosphoglycerate mutase which forms 2,3BPG from 1,3BPG In red blood cells about 20% of the glycolytic flux is diverted for the production of the important oxygen regulator 2,3BPG Prentice Hall c2002 Chapter 11
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Fig 11.24 Formation of 2,3BPG in red blood cells Prentice Hall c2002
Chapter 11
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Feed-forward activation
Feedback inhibition Product of a pathway controls the rate of its own synthesis by inhibiting an enzyme catalyzing an early step Feed-forward activation Metabolite early in the pathway activates an enzyme further down the pathway Prentice Hall c2002 Chapter 11
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