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After Digestion And Absorption
Of Food What Next?
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General Overview Of Metabolism (Carbohydrate, Protein, Fat)
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Carbohydrate Chemistry and Metabolism
By Gladys Kaba
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Outline Carbohydrate chemistry
Summary of digestion and absorption of carbohydrates. General overview of metabolism
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Outline 4. Carbohydrate Metabolism Glycolysis TCA cycle
Gluconeogenesis Metabolism of (Fructose, galactose, Mannose) PPP Glycogenesis and Glycogenolysis
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After Digestion And Absorption Of Carbohydrates What Next?
Carbohydrate Metabolism (Glucose)
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We eat food containing carbohydrates
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General Overview Of Metabolism (Carbohydrate, Protein, Fat)
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Overview Of Carbohydrate Metabolism
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(1) Glycolysis - Summary
glycolysis occurs in the cytosol Glucose (6C) 2 ATP 4 ADP 2 ADP 4 ATP Location Of Glycolytic Enzymes? 2 NAD 2 NADH + H 2 Pyruvate (3C)
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Functions/Importance Of Glycolysis
Glycolysis Provides Energy Glycolysis Provides Substrate for Oxidation Intermediates Products are used in Other Pathways 2,3-bisphosphoglycerate, fatty acid and cholesterol synthesis Alanine, glycerol 3-phosphate
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Cells With Special Needs Of Glycolysis
Erythrocytes (Red blood cells) Lens and cornea of the eye Cells in brain cells
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Physiological And Pathophysiological Conditions with special need for Glycolysis
Fed State Exercising muscles Cancer cells-----Warburg effect
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Phosphofructokinase-1
Fructose 6-phosphate Glucose Glucose 6-phosphate Phosphohexose isomerase Hexokinase Phosphofructokinase-1 Fructose 1,6- bisphosphate Pyruvate kinase Phosphoenolpyruvate Pyruvate 2-Phosphoglycerate Phosphoglycerate mutase Glyceraldehyde 3-phosphate dehydrogenase 1,3-Bisphosphoglycerate Phosphoglycerate kinase 3-Phosphoglycerate
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Glycolysis Regulation
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Abnormalities Associated with Glycolytic pathway
Affected Glycolytic enzyme/reaction Genetic Deficiencies of Glycolysis pyruvate kinase phosphoglycerate kinase
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Toxin affecting Glycolytic pathway
Mercury Arsenic
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After Glycolysis What next after?
Lactate (anaerobic) Glucose → 2 Pyruvate Acetyl-CoA (TCA cycle)
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1. Conversion of pyruvate to Acetyl CoA aerobic conditions
Location Of Pyruvate Dehydrogenase ?
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Glycolysis cytoplasm Glucose Pyruvic acid Acetyl-CoA mitochondrion
Kreb’s Cycle Glucose Glycolysis cytoplasm Pyruvic acid Acetyl-CoA mitochondrion Citric Acid Cycle Electron Transport ATP Production
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Carbohydrate, protein, and Fat Metabolism
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Kreb’s Cycle Aka Tricarboxylic Acid Cycle TCA Cycle Citric Acid Cycle Location Of Pyruvate Dehydrogenase And The TCA-cycle Enzymes?
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Main Function of the Kreb’s cycle
Oxidative process 3 NADH FADH2 GTP X 2 per glucose 6 NADH 2 FADH2 2 GTP All ultimately turned into ATP (oxidative phosphorylation/ electron transport chain)
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Total Energy per glucose
A) Cytosol Glycolysis 2 NADH 2 ATP B) Mitochondrion Pyruvate dehydrogenase --Krebs 6 NADH 2 FADH2 2 GTP
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Abnormalities / Diseases Associated With PDH And The TCA Cycle
Genetic Deficiency of Pyruvate Dehydrogenase 2) Genetic Diseases of the TCA Cycle : Fumarase deficiency Succinate dehydrogenase α-ketoglutarate dehydrogenase
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Abnormalities / Diseases Associated With PDH And The TCA Cycle
3) Thiamine Deficiency -- classical beriberi, Pyuvate Dehydrogenase α-ketoglutarate Dehydrogenase
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Regulation of the Tricarboxylic Acid Cycle?
About half page to be submitted next Wednesday before The class. Students Review Question? Additional questions would be sent through the on Thursday.
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After Glycolysis What next after?
Lactate (anaerobic) Glucose → 2 Pyruvate Acetyl-CoA (TCA cycle)
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(Anaerobic conditions)
2. Conversion To Lactate (Anaerobic conditions) (oxidized) (reduced)
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Cori cycle Lactate can be transported by blood
Exercising muscles and the Cori Cycle Lactate can be transported by blood to liver and used in gluconeogenesis
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How do cytosolic/cytoplasmic NADH get into the mitochondrial?
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How do cytosolic/cytoplasmic NADH get into the mitochondrial?
glycerol 3-phosphateshuttle - NADH as FADH malate-aspartate shuttle- NADH as NADH
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The malate-aspartate shuttle.
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Overview Of Carbohydrate Metabolism
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Gluconeogenesis non-carbohydrate precursors are converted to glucose.
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Gluconeogenesis Is Active
Tissues In Which Gluconeogenesis Is Active liver Renal Cortex
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Functions and importance
Gluconeogenesis Maintaining the blood glucose in the fasted state But the brain, red blood cells, and renal medulla, rely on glycolysis for ATP.
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Physiological Conditions In Which Gluconeogenesis Is Especially Active
fasted state, when stored as glycogen is depleted plasma concentration of glucose decline
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Physiological Conditions In Which Gluconeogenesis Is Especially Active
During prolonged physical exercise. important in the neonate. (the first few hours after delivery).
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Gluconeogenesis starting material lactate, pyruvate, Oxaloacetate
glycerol Some amino acids propionic acid ( oxidation of odd-chain fatty acids and branched methyl fatty acids)
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Biochemical Reactions Of Gluconeogenesis
Most are the same as glycolysis, But in the opposite direction, With some few exceptions
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Phosphofructokinase-1
Fructose 6-phosphate Glucose Glucose 6-phosphate Phosphohexose isomerase Hexokinase Phosphofructokinase-1 Fructose 1,6- bisphosphate Pyruvate kinase Phosphoenolpyruvate Pyruvate 2-Phosphoglycerate Phosphoglycerate mutase Glyceraldehyde 3-phosphate dehydrogenase 1,3-Bisphosphoglycerate Phosphoglycerate kinase 3-Phosphoglycerate
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Three Physiologically Irreversible Steps Glycolysis And Gluconeogenesis Are Different
Glucokinase/Hesosekinase ---glucose 6-phosphatase phosphofructokinase- 1 --fructose 1,6-bisphosphatase,
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Three Physiologically Irreversible Steps Glycolysis And Gluconeogenesis Are Different
3. pyruvate kinase A) Pyruvate carboxylase B) Phosphoenolpyruvate carboxykinase
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Localization of Gluconeogenesis
Most Of The Enzymes Are Found In The Cytosol, But Pyruvate Carboxylase----- Mitochondria Glucose 6-phosphatase------ Lumen Of The Endoplasmic Reticulum
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Regulation of gluconeogenesis
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General Overview Of Metabolism (Carbohydrate, Protein, Fat)
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