12.1.2 - Pages 9-16
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- FrontATP synthesis reactionBackADP + Pi → ATP requires energy input
- FrontStandard free energy change of ATP formationBackΔG°' = +30.5 kJ/mol
- FrontEnergy requirement for ATP synthesisBackATP must be formed using another energy source
- FrontSubstrate-level phosphorylationBackFormation of ATP by direct transfer of a phosphate group from a substrate to ADP
- FrontElectron transport chain requirement in substrate-level phosphorylationBackNot required
- FrontExamples of substrate-level phosphorylation substratesBackPhosphoenolpyruvate, 1,3-bisphosphoglycerate, and succinyl-CoA
- FrontExample reaction of substrate-level phosphorylationBackPEP + ADP → pyruvate + ATP
- FrontLocation of substrate-level phosphorylationBackGlycolysis and TCA cycle
- FrontOxidative phosphorylationBackMain ATP production system in humans
- FrontFirst step of oxidative phosphorylationBackFuel molecules are oxidized
- FrontNAD⁺ reduction in oxidative phosphorylationBackNAD⁺ becomes NADH
- FrontRole of NADH in oxidative phosphorylationBackCarries electrons to the electron transport chain
- FrontFinal electron acceptor in oxidative phosphorylationBackOxygen
- FrontProton gradient formationBackOccurs across the mitochondrial membrane during electron transport
- FrontATP synthase functionBackSynthesizes ATP using the proton gradient
- FrontLocation of oxidative phosphorylationBackMitochondria
- FrontATP yield from oxidative phosphorylationBackProduces approximately 90% of ATP in aerobic cells
- FrontPhotosynthetic phosphorylationBackATP production driven by light energy
- FrontOrganisms performing photosynthetic phosphorylationBackPlants, algae, and cyanobacteria
- FrontEnergy source for photosynthetic phosphorylationBackLight
- FrontMechanism of photosynthetic phosphorylationBackLight drives electron flow creating a proton gradient used to synthesize ATP
- FrontRelevance of photosynthetic phosphorylation to humansBackNot relevant for human metabolism
- FrontRedox reactionsBackOxidation and reduction reactions that drive metabolism
- FrontOxidationBackLoss of electrons
- FrontReductionBackGain of electrons
- FrontOxidation in metabolismBackFuel molecules lose electrons during breakdown
- FrontReduction in metabolismBackElectron carriers gain electrons
- FrontExample of reductionBackNAD⁺ gains electrons to form NADH
- FrontCatabolism as an oxidative processBackFuel molecules lose electrons during breakdown
- FrontExample of catabolic oxidationBackGlucose is oxidized to carbon dioxide
- FrontElectron carriers in catabolismBackNAD⁺ and FAD accept electrons
- FrontNAD⁺ functionBackActs as an electron collector in metabolism
- FrontReduction of NAD⁺BackNAD⁺ + 2e⁻ + H⁺ → NADH
- FrontRole of NADHBackDelivers electrons to the electron transport chain
- FrontAnabolism as a reductive processBackBuilding molecules requires electron input
- FrontElectron donor in anabolismBackNADPH
- FrontExample of reductive biosynthesisBackFatty acid synthesis requires NADPH
- FrontCatabolism electron carrierBackProduces NADH
- FrontAnabolism electron carrierBackUses NADPH
- FrontConvergent pathwaysBackPathways where many different molecules are broken down into a few common intermediates
- FrontExample of carbohydrate convergenceBackGlucose → pyruvate → acetyl-CoA
- FrontExample of fat convergenceBackFatty acids → acetyl-CoA
- FrontExample of protein convergenceBackAmino acids → acetyl-CoA or TCA intermediates
- FrontMajor convergence moleculeBackAcetyl-CoA
- FrontRole of acetyl-CoABackCentral metabolic hub that enters the citric acid cycle
- FrontCitric acid cycleBackMetabolic pathway that processes acetyl-CoA
- FrontDivergent pathwaysBackPathways where a few starting molecules produce many different products
- FrontExample of divergence from acetyl-CoABackFatty acids, cholesterol, steroid hormones, and phospholipids
- FrontAmphibolic pathwaysBackPathways that function in both catabolism and anabolism
- FrontExample of amphibolic pathwayBackCitric acid cycle
- FrontCatabolic role of citric acid cycleBackBreaks down acetyl-CoA
- FrontAnabolic role of citric acid cycleBackProvides intermediates for synthesis of amino acids, glucose, and fatty acids
- FrontMetabolic pathwayBackA sequence of enzyme-catalyzed reactions converting substrates to products
- FrontRole of enzymes in pathwaysBackEach step is catalyzed by a specific enzyme
- FrontMultienzyme complexesBackGroups of physically connected enzymes that catalyze sequential reactions
- FrontExample of multienzyme complexBackPyruvate dehydrogenase complex
- FrontFunction of pyruvate dehydrogenase complexBackConverts pyruvate to acetyl-CoA
- FrontExample of multienzyme complexBackFatty acid synthase
- FrontFunction of fatty acid synthaseBackSynthesizes fatty acids
- FrontExample of multienzyme systemBackPyrimidine synthesis enzymes
- FrontFunction of pyrimidine synthesis enzymesBackProduce nucleotide bases
- FrontAdvantages of multienzyme complexesBackIncreased speed, substrate channeling, reduced diffusion loss, and improved regulation
- FrontSubstrate channelingBackDirect transfer of intermediates between enzymes without diffusion
- FrontCompartmentationBackSeparation of metabolic pathways into different cellular locations
- FrontCytosol locationBackFluid portion of the cell where certain pathways occur
- FrontCytosolic pathwaysBackGlycolysis, pentose phosphate pathway, and fatty acid synthesis
- FrontMitochondrial matrix locationBackInterior of mitochondria where specific pathways occur
- FrontMitochondrial pathwaysBackCitric acid cycle, oxidative phosphorylation, beta-oxidation, and ketone body formation
- FrontPathways requiring multiple compartmentsBackGluconeogenesis and urea cycle
- FrontPurpose of compartmentationBackPrevents pathway interference, allows regulation, and maintains distinct chemical environments
- FrontExample of compartment separationBackFatty acid synthesis and fatty acid breakdown occur in different compartments
- FrontIrreversible reactionsBackReactions with large negative ΔG that cannot easily run in reverse
- FrontRole of irreversible reactionsBackServe as key regulatory points in metabolic pathways
- FrontNon-reversibility of pathwaysBackAnabolic and catabolic pathways are not simple reversals of each other
- FrontBypassing irreversible stepsBackAlternate enzymes are used in opposing pathways
- FrontExample of pathway bypassBackGlycolysis irreversible steps are bypassed in gluconeogenesis
- FrontPurpose of bypass reactionsBackPrevents futile cycling
- FrontFutile cyclingBackSimultaneous forward and reverse pathway activity wasting energy
- FrontRegulation of metabolismBackControl of metabolic pathways to maintain balance and efficiency
- FrontMethods of metabolic regulationBackEnzyme amount, enzyme activity, and substrate availability
- FrontControl of enzyme amountBackRegulation through gene transcription affecting enzyme levels
- FrontEffect of increased enzyme concentrationBackIncreases pathway rate
- FrontControl of enzyme activityBackRegulation through activation or inhibition of enzymes
- FrontMechanisms of enzyme activity controlBackAllosteric regulation and covalent modification
- FrontControl of substrate availabilityBackAvailability of substrate determines whether reactions proceed
- FrontExample of substrate controlBackLow glucose levels slow glycolysis
- FrontFeedback inhibitionBackEnd product of a pathway inhibits an earlier step
- FrontMechanism of feedback inhibitionBackProduct binds to and inhibits an upstream enzyme
- FrontPurpose of feedback inhibitionBackPrevents overproduction of end products
- FrontAllosteric regulationBackRegulation of enzyme activity by binding at a site other than the active site
- FrontEffect of allosteric bindingBackChanges enzyme shape and activity
- FrontPhosphofructokinase (PFK)BackKey regulatory enzyme in glycolysis
- FrontActivators of PFKBackAMP and fructose-2,6-bisphosphate
- FrontInhibitors of PFKBackATP and citrate
- FrontEnergy status effect on PFKBackHigh energy inhibits glycolysis, low energy stimulates it
- FrontFructose-1,6-bisphosphataseBackKey regulatory enzyme in gluconeogenesis
- FrontActivator of fructose-1,6-bisphosphataseBackCitrate
- FrontInhibitors of fructose-1,6-bisphosphataseBackAMP and fructose-2,6-bisphosphate
- FrontReciprocal regulation of glycolysis and gluconeogenesisBackWhen one pathway is active, the other is suppressed
- FrontCovalent modificationBackRegulation of enzyme activity by addition or removal of chemical groups
- FrontCommon covalent modificationBackPhosphorylation
- FrontPhosphorylationBackAddition of a phosphate group to a protein
- FrontProtein kinaseBackEnzyme that catalyzes phosphorylation using ATP
- FrontPhosphorylation reactionBackProtein + ATP → phosphorylated protein + ADP
- FrontProtein phosphataseBackEnzyme that removes phosphate groups from proteins
- FrontDephosphorylation reactionBackPhosphorylated protein + H₂O → protein + Pi
- FrontEffect of phosphorylation on enzymesBackCan activate or inhibit enzyme activity
- FrontProcesses regulated by phosphorylationBackGlycogen metabolism, glycolysis, gluconeogenesis, and hormone signaling
- FrontHormonal control of metabolismBackHormones regulate pathways through signaling cascades
- FrontExamples of metabolic hormonesBackInsulin, glucagon, and epinephrine
- FrontPrinciple of metabolismBackOccurs through enzyme-controlled pathways
- FrontCatabolic outputsBackATP, NADH, and FADH₂
- FrontAnabolic inputsBackATP and NADPH
- FrontATP roleBackPrimary energy currency of the cell
- FrontProperties of metabolic pathwaysBackInterconnected, compartmentalized, and highly regulated
- FrontMain regulatory mechanismsBackAllosteric regulation, covalent modification, and feedback inhibition
- FrontAdditional regulation methodsBackControl of enzyme amount and substrate availability
- FrontCatabolism characteristicsBackOxidative, ATP-producing, and convergent
- FrontAnabolism characteristicsBackReductive, ATP- and NADPH-consuming, and divergent
- FrontTypes of ATP productionBackOxidative phosphorylation and substrate-level phosphorylation
- FrontKey metabolic regulatorsBackAllosteric effectors, phosphorylation, gene expression, and feedback inhibition
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