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Metabolism -- ~ P Regulation. The Krebs Cycle. Take Home : Occurs in the mitochondrial matrix Rate is very dependent on the ratio of oxidized to reduced coenzyme Feed ins -- 2 C frags. . from carbohydrate and fat metabolism; Amino acid frags in other places.
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The Krebs Cycle • Take Home: • Occurs in the mitochondrial matrix • Rate is very dependent on the ratio of oxidized to reduced coenzyme • Feed ins -- 2 C frags.. from carbohydrate and fat metabolism; • Amino acid frags in other places
Energy Schematic of the ETS • Take Home • In inner membrane • Will maintain a favorable steady-state ratio of oxidized to reduced coenzyme if sufficient O2 is present to accept each electron produced in the Krebs and other reactions.
What Are the Means Used to Estimate Steady-State Metabolism?
Energetics of Aerobic Glycolysis The overall reaction (path does not matter): A distinct stoichiometry exists between all members of this process. This means that if we know carbohydrate is the fuel, then if we measure the change in one component of this reaction, we know the changes in all others.
How About Lipid? Once again, if we know that lipid (palmitic acid) is the fuel, we can measure one factor in the reaction and find all the others.
How do we know the fuel being used? You cannot tell simply from what the animal eats. There is a certain ratio of CO2 production to O2 consumption exists for different fuels. For carbs: Ratio is 1:1
The Ratio is Different In Palmitic Acid 16/23 = 0.7
How the Table Values For Energy EquivalenceWere Obtained – An example
Problem Suppose the following: What is the metabolic power (P)?
Phosphagen Cycle -- Phosphagen Buffer During High Demand This process is controlled by the amount of enzyme present (CK) and thermodynamically (amts. of reactants/products)
Review: Control of Metabolism [ATP] regulation is a problem given that demand can, especially in muscles, increase dramatically in a short period of time. The concept of pathway flux (overall rate -- mols/(product time) Equibrial and non-equilibrial reactions and control of flux PFK and glycogen phosphorylase as examples of non-equilibrial reactions. Inhibition and de-inhibition; activation.
Association/Dissociation Constants as Physiological Organizers The concept of Kd What should be the relative values of Kd for AMP and ATP on the regulatory sites of PFK? Where should the Kd for AMP and ATP be compared to normal “resting” concentrations of these substances?