Post RN - Biochemistry (Unit 8) Metabolism of Carbohydrates
AreeshaAhmad1
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34 slides
Jul 16, 2024
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About This Presentation
Metabolism of Carbohydrates
Size: 2.52 MB
Language: en
Added: Jul 16, 2024
Slides: 34 pages
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Biochemistry Lecture Post RN (Unit 8) Metabolism of Carbohydrates by, Miss Areesha Ahmad Lecturer
GLYCOGENESIS It is the process of storing excess glucose for use by the body at a later time in the form of glycogen . It is stored in the liver and muscle cells.
GLYCOGENOLYSIS The word lysis means break down. It is the process in which glycogen molecules breaks down into glucose molecules . The glycogen previously stored by the liver is broken down to glucose and dispersed throughout the body.
GLYCOLYSIS
GLUCONEOGENESIS Gluconeogenesis (abbreviated GNG ) is a metabolic pathway that results in the generation of glucose from non-carbohydrate carbon substrates such as pyruvate, lactate, glycerol . Glucose is the only energy source used by the brain . Gluconeogenesis meets the needs of the body for glucose when sufficient carbohydrate is not available from the diet or glycogen reserves .
R ole of oxidative glucose catabolism in the citric acid cycle Oxidative glucose catabolism can be divided into three main stages : Glycolysis: The breakdown of glucose into pyruvate. Citric Acid Cycle: The oxidation of acetyl-CoA derived from pyruvate. Oxidative Phosphorylation: The production of ATP through the electron transport chain and chemiosmosis . Glycolysis Location: Cytoplasm Process: Glucose (6-carbon molecule) is broken down into two molecules of pyruvate (3-carbon molecules). Outcome: Produces 2 ATP molecules, 2 NADH molecules, and 2 pyruvate molecules.
Transition to the Citric Acid Cycle Before entering the citric acid cycle, pyruvate undergoes a transition step : Pyruvate Decarboxylation: Each pyruvate molecule is transported into the mitochondria, where it is converted into acetyl-CoA by the pyruvate dehydrogenase complex. This reaction produces one molecule of NADH and releases one molecule of CO2 per pyruvate . Pyruvate+CoA+NAD +→Acetyl-CoA+CO2+ NADH Citric Acid Cycle (Krebs Cycle) Location: Mitochondrial matrix Primary Role: To oxidize acetyl-CoA to CO2 and capture high-energy electrons in the form of NADH and FADH2.
Steps of the Citric Acid Cycle Citrate Formation: Acetyl-CoA (2-carbon) combines with oxaloacetate (4-carbon) to form citrate (6-carbon). Acetyl-CoA+Oxaloacetate→Citrate 2. Isomerization to Isocitrate : Citrate is rearranged to form isocitrate . Citrate→ Isocitrate 3. Oxidative Decarboxylation to α- Ketoglutarate : Isocitrate is oxidized to α- ketoglutarate (5-carbon), producing NADH and releasing CO2 . Isocitrate+NAD + → α- Ketoglutarate+NADH+CO 2
4. Oxidative Decarboxylation to Succinyl -CoA: α- Ketoglutarate is further oxidized to succinyl -CoA (4-carbon), producing another NADH and releasing CO2. α- Ketoglutarate+NAD ++CoA→Succinyl-CoA+NADH+CO2 5. Conversion to Succinate: Succinyl -CoA is converted to succinate, producing ATP (or GTP) in the process. Succinyl-CoA→Succinate+ATP ( orGTP ) 6. Oxidation to Fumarate : Succinate is oxidized to fumarate , producing FADH2. Succinate+FAD→Fumarate+FADH2 7. Hydration to Malate: Fumarate is hydrated to malate.Fumarate+H2O→MalateFumarate+H 2 O→Malate Fumarate+H 2 O→ Malate 8. Oxidation to Oxaloacetate: Malate is oxidized to oxaloacetate, producing NADH.Malate+NAD +→ Oxaloacetate+NADHMalate+NAD + → Oxaloacetate+NADH
Products of the Citric Acid Cycle (per Acetyl-CoA ): 2 CO2 molecules: Released as waste products. 3 NADH molecules: High-energy electron carriers used in the electron transport chain. 1 FADH2 molecule: Another electron carrier for the electron transport chain. 1 ATP (or GTP) molecule: Direct energy currency of the cell. Regeneration of Oxaloacetate: Allows the cycle to continue.
Role in Energy Production The NADH and FADH2 produced in the citric acid cycle carry high-energy electrons to the electron transport chain (ETC) located in the inner mitochondrial membrane. Here, the electrons pass through a series of protein complexes, ultimately leading to the production of ATP through oxidative phosphorylation.