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Glycolysis. Anaerobic degradation of glucose to yield lactate or ethanol and CO 2. Learning Objectives. Sequence of Reactions Metabolites Enzymes Enzyme Mechanisms Energetics Regulation. Overview of Glycolysis. Glucose (C 6 ) —> 2 Pyruvate (C 3 ) 2 ADP + 2 P i —> 2 ATP.
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Glycolysis Anaerobic degradation of glucose to yield lactate or ethanol and CO2
Learning Objectives • Sequence of Reactions • Metabolites • Enzymes • Enzyme Mechanisms • Energetics • Regulation
Overview of Glycolysis Glucose (C6) —> 2 Pyruvate (C3) 2 ADP + 2 Pi —> 2 ATP
Glycolysis Figure 15-1
Summary of Stage I Glucose + 2 ATP ——> 2 GA3P + 2 ADP + 2 H+
Stage II of Glycolysis(Energy Recovery) Substrate Level Phosphorylation
Stage II of Glycolysis(Energy Recovery) 3PGA —> Serine, Cysteine and Glycine PEP —> Aromatic Amino Acids
Stage II of Glycolysis(Energy Recovery) Substrate Level Phosphorylation Pyruvate —> Alanine
Summary of Stage II 2 GA3P + 2 NAD+ + 4 ADP + 2 Pi 2 Pyruvate + 2 NADH + 2 H+ + 4 ATP
Summary of Glycolysis Glucose + 2 NAD+ + 2 ADP + 2 Pi 2 Pyruvate + 2 NADH + 2 H+ + 2 ATP NOTE: NAD+ must be regenerated!
Hexokinase(First Use of ATP) NOTE: Lack of Specificity
Role of Mg2+ Page 489
Substrate-induced Conformational Changes in Yeast Hexokinase Figure 15-2
Results of Conformational Change • Exclusion of water • Increased nucleophilicity of CH2OH • Proximity effect
Regulation of Hexokinase Inhibition by glucose-6-P Impermeability
Hexokinase versus Glucokinase • Hexokinase (all tissues) • Non-specific • KM = ~100 µM • Inhibited by glucose-6-P • Glucokinase (primarily in liver) • Specific • KM = ~10 mM • Not inhibited by glucose-6-P
Functional Rationale • Most tissues: metabolize blood glucose which enters cells • Glc-6-P impermeable to cell membrane • Product inhibition • Liver: maintain blood glucose • High blood glucose: glycogen • Low blood glucose: glycolysis
Hexokinase versus Glucokinase Figure 22-4
Metabolism of Glucose-6-P Regulation!
Reaction Mechanism of Phosphoglucose Isomerase(Substrate Binding) Figure 15-3 part 1
Reaction Mechanism of Phosphoglucose Isomerase(Acid-Catalyzed Ring Opening) Figure 15-3 part 2
Reaction Mechanism of Phosphoglucose Isomerase(Formation of cis-enediolate Intermediate) Figure 15-3 part 3
Reaction Mechanism of Phosphoglucose Isomerase(Proton Transfer) Figure 15-3 part 4
Reaction Mechanism of Phosphoglucose Isomerase(Base-Catalyzed Ring Closure) Figure 15-3 part 5
Reaction Mechanism of Phosphoglucose Isomerase(Product Release) Figure 15-3 part 1
Phosphofructokinase(Second Use of ATP) NOTE: bisphosphate versus diphosphate
Characteristics of Reaction Catalyzed by PFK • Rate-determining reaction • Reversed by Fructose-1,6-bisphosphatase • Mechanism similar to Hexokinase
Regulatory Properties of PFK • Main control point in glycolysis • Allosteric enzyme • Positive effectors • AMP • Fructose-2,6-bisphosphate • Negative effectors • ATP • Citrate
-D-Fructose-2,6-Bisphosphate Page 558
Mechanism of Base-Catalyzed Aldol Cleavage NOTE: requirement for C=O at C2 Rationale for Phosphoglucose Isomerase Figure 15-4
Enzymatic Mechanism of Aldolase(Substrate Binding) Figure 15-5 part 1
Enzymatic Mechanism of Aldolase(Schiff Base (imine) Formation) Figure 15-5 part 2
Enzymatic Mechanism of Aldolase(Aldol Cleavage) Figure 15-5 part 3
Enzymatic Mechanism of Aldolase(Tautomerization and Protonation) Figure 15-5 part 4
Enzymatic Mechanism of Aldolase(Schiff Base Hydrolysis and Product Release) Figure 15-5 part 5
Transition State Analog Inhibitors ofTriose Phosphate Isomerase Part 494
Schematic Diagram of the First Stage of Glycolysis Figure 15-7
Summary of Stage I Glucose + 2 ATP ——> 2 GA3P + 2 ADP + 2 H+
Enzymatic Mechanism ofGlyceraldehyde-3-P Dehydrogenase(Substrate Binding) Figure 15-9 part 1