Summary

These notes cover topics such as phosphagens, energy-rich molecules in animal muscle, fire flashes (ATP reactions), equilibrium constants and actual free-energy change, and more. Various diagrams and chemical equations help to illustrate concepts.

Full Transcript

Phosphagens: Energy-rich storage molecules in animal muscle Phosphocreatine (PC) and phosphoarginine (PA) are phosphoamides Have higher group-transfer potentials than ATP Produced in muscle during times of ample ATP Used to replenish ATP when needed via creatine kinase reactio...

Phosphagens: Energy-rich storage molecules in animal muscle Phosphocreatine (PC) and phosphoarginine (PA) are phosphoamides Have higher group-transfer potentials than ATP Produced in muscle during times of ample ATP Used to replenish ATP when needed via creatine kinase reaction Fire flashes: glowing reports of ATP From chemical energy into light energy. An pyrophosphate cleavage of ATP to form luciferyl adenylate. In the presence of O2 and luciferase, the luciferin undergoes a multiple step oxidative decarboxylation to oxyluciferin and accompanied by remission of light. Equilibrium Constants and Actual Free-Energy Change For real-life situation in cell biology we will use the ΔG’ For the reaction: aA + bB cC + dD ΔG’ = ΔGo’ + RT ln ([C]c[D]d/[A]a[B]b) Is a function of reactant and product concentrations and of the tempreture The actual free energy of ATP hydrolysis is very diffrent Phosphorylation potential Reaction coupling ΔG1 = 13.8 kJ/mol and ΔG2 = -30.5 kJ/mol Chemical logic and common biochemical Reactions □ Cells have the capacity to carry out thousands of specific (Enzyme catalyzed reactions) □ On the enzyme active sites (Breaking and Forming of the new bonds) ✔Reactions in living cells includes: -Oxidation-reduction (Dehydrogenases) -Group transfer reactions (Kinases) -H2O addition/removal (Hydrolases) -Formation double bond (Lyases) -Isomerization (Isomerases) -Make and break C-C bonds (Ligases) Cells need energy to do all their biological work To generate and maintain its highly ordered structure (biosynthesis of macromolecules). To generate motion (mechanical work). To generate concentration and electrical gradients across cell membranes (active transport). To generate heat and light. The Free Energy of ATP Energy from oxidation of metabolic fuels is largely recovered in the form of ATP high-energy phosphoanhydride bonds □ Charge repulsion □ Resonance stabilization □ High Entropy Hydrolysis of phosphoenolpyruvate (PEP) Catalyzed by pyruvate kinase, this reaction is followed by spontaneous tautomerization of the product. Pyruvate, tautomerization is not possible in PEP, and thus the products of hydrolysis are stabilized relative to reactants. Phosphagens: Energy-rich storage molecules in animal muscle High-energy phosphate compound Phosphocreatine (PC) and phosphoarginine (PA) Have higher group-transfer potentials than ATP Produced in muscle during times of ample ATP Used to replenish ATP when needed via Creatine and arginine kinase reaction Phosphoryl-Group Transfer Phosphoryl-group-transfer potential - the ability of a compound to transfer its phosphoryl group Energy-rich or high-energy compounds have group transfer potentials equal to or greater than that of ATP Low-energy compounds have group transfer potentials less than that of ATP Phosphoryl-Group Transfer Larg free enrgy change that company ATP hydrolysis High-energy phospahte compound 1 cal = 4.184 J ATP provides energy by group transfers, Not by simple hydrolysis --- in two steps A phosphoryl group is first transferred from ATP to glutamate Glutamine The phosphoryl displaced by NH3group is synthase released and as Pi ATP can carry energy from high-energy phosphate compounds produced by catabolism to compounds such as glucose, converting them into more active forms Nucleophilic displacement reaction of ATP Thioesters---Hydrolysis of acetyl-coenzyme A Acetyl-CoA is a thioester with a large, negative, standard free energy of hydrolysis. Thioesters contain a sulfur atom in the position occupied by an oxygen atom in oxygen esters. NADH and NADPH act with dehydrogenases as soluble electron carriers From vitamin niacin (source of the nicotinamide) NADH absorb at 340 nm. Most dehydrogenase that use NAD or NADP bind the cofactor in the conserved protein domain Vit-B3 What are the effects of Niacin Deficiency? Dermatitis Diarrhea Dementia death Structure of oxidized and reduced FAD and FMN Flavin Nucleotides are tightly bound in flavoproteins. Accepts 1 or 2 electrons

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