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36 Cards in this Set

  • Front
  • Back
1st law of thermodynamics
Energy cannot be created or destroyed
2nd law of thermodynamics
Energy transformation is not 100% efficient, and usable energy is lost, while entropy increases
Gibbs Free Energy Equation
∆G=∆H-T∆S
+∆G = endergonic, anabolism
-∆G = exergonic, catabolism
Gibbs free energy needed to reach equilibrium
∆G = ∆G˚ +RT ln ([C][D]/[A][B])
∆G˚ = ∆G when reactants and products in 1 molar quantities
Equilibrium Constant
Keq = ([C][D]/[A][B])
∆G'˚ and K'eq
∆G˚ and Keq at pH = 7 and T = 37˚C
K'eq > 1; ∆G'˚< 0
K'eq = 1; ∆G'˚= 0
K'eq < 1; ∆G'˚> 0
5 Characteristics of Metabolism
1. Irreversible
2. Independent Catabolic and Anabolic pathways
3. First committed step
4. Regulated (usually through enzymes)
5. Specific cellular locations
5 reactions in Metabolism
1. Make or break carbon bonds
2. Internal rearrangement, isomerization, elimination
3. Free radical reaction
4. Group transfer reaction
5. Oxidation-Reduction reaction
ATP Hydrolysis
- H2O hydrolyzes ATP
- Phosphate group stabilized by resonance
- ATP and ADP stabilized by Mg2+
Human's Daily ATP
- Take in 11,700 kJ of food
- 50% efficiency, 5860 kJ to ATP
- 50 kJ/ATP = 117 moles ATP/day
- 50 g of ATP in body; so each one recycled 1300x
ATP Generation Mechanisms
1. Substrate-Level Phosphorylation
2. Oxidative Phosphorylation
3. Photophosphorylation
Substrate-Level Phosphorylation
Transfer of high energy PO4- group from compound to ADP
- Different Energy per compound
- ex: PEP, Creatine Phosphate
Oxidative-Phosphorylation
ATP created from proton gradient created by transfer of electrons in an electron transport chain
- Triggered by compounds
Photophosphorylation
ATP created from proton gradient created by transfer of electrons in an electron transport chain
- Triggered by sunlight
Carbohydrates/Saccharides
- Formula = (CH2O)n
- Act as Structural Elements or Energy Sources
- Can exist in many "isomeric forms"
Monosaccharide
- Simple sugars with 3-7 Carbon Atoms
- Many Types:
- Aldose: Contains aldehyde group
- Ketose: Contains ketose group
Monosaccharide Cyclization
- Occurs in pentoses and hexoses
- Carbonyl group -> Anomeric Carbon
- Carbonyl Oxygen -> hydroxyl group (determines whether the sugar is alpha or beta)
- Different side as CH2OH? alpha
- Same side? beta
Oligosaccharides
Typically 2-10 molecules
Bound by glycosidic bonds (dehydration)
Usually found covalently bound to proteins or lipids on cell surface to act as recognition signals
Polysaccharides
10-infinite number of molecules
Bound through dehydration (glycosidic bonds)
Different locations of binding lead to differences in starch, glycogen, or cellulose
- alpha cyclic sugars makes alpha glycosidic linkage
- beta sugar makes beta linkage
Molecular Binding of Cellulose vs Starch vs Glycogen
Cellulose -> B 1,4 linkages (linear)
Starch and Glycogen -> A 1,4 linkages
- A 1,6 linkages allow branching
- C1 = Anomeric carbon
- Glycogen is higher branched than starch
3 Great Characteristics of Glucose
1. complete oxidation -> ∆G'˚ = -2,840 kJ/mole
2. Can be stored as large quantities of hexose units, controlling blood sugar levels and allowing easy transition to ATP
3. Versatile Precursor to many biosynthetic reactions
4 major fates of glucose
1. Synthesis of complex polysaccharides (for ECM and cell wall)
2. Storage as glucose polymers (for storage)
3. Oxidation to ribose 5-phosphate (via pentose phosphate pathway, for DNA)
4. Oxidation to pyruvate via glycolysis (for ATP)
Two Glycolitic Stages
1. Preparatory Phase
2. Energy Conserving Stage (payout)
- Takes 10 Reactions
- Process turns Glucose -> (2) 3 carbon pyruvic acid + ATP + NADH
Glytolitic Stage 1: Preparatory Phase
2 ATP's are invested
Glucose -> Fructose 1,6 biphosphate (F-1,6-BP)
then F-1,6-BP -> (2) triose glcyeraldehyde 3-phosphate (GAP)
Glytolitic Stage 2: Energy Conserving Stage
(2) GAP -> (2) Pyruvate + 4 ATP + 2NADH
Feeder Pathways from Storage
Starch or Glycogen feed into glycolysis 2 steps
1. Phospholytic cleavage of terminal glucose --> glucose 1-phosphate
2. Phosphoglucomutase converts glucose 1-phosphate into glucose 6-phosphate
Feeder Pathways from ingestion
Ingested polysaccharides broken down by intestinal hydrolytic enzymes -> monosaccharides
- Leads to variety of D-Hexoses; which can be phosphorylated into G6P, F6P, or F1P
- Galactose 1P and Glucose 1P require nucleotide derived UDP
3 Pyruvate Fates
1. 2 Ethanol + CO2 (fermentation in yeast)
- Makes alchohol
2. 2 Acetyl CoA (aerobic)
3. Lactate (anerobic)
- cheese/yogurt
Regeneration of NADH
Glycolytic oxidation of glyceraldehyde uses NAD+ as electron acceptor. O2 takes this electron back to regenerate NAD+; but in anaerobic conditions, an organic molecule (i.e. lactate,ethanol) accepts this electron
Metabolic Regulation Tactics
1. Altering enzyme activity
2. Using equilibrium and mass action
3. Have tissue specific isozymes of enzymes (same enzyme, different tissue, different rate)
4. Responding to energy (ATP/ADP) ratios (most enzymes need full ATP saturation)
AMP-Activated ATP Kinase (AMPK)
When [ATP]/[AMP] decreases, triggers AMPK to increase ATP.
- Activated by low ratio, exercise, SNS, or hormones
- When active, phosphorylates proteins and shifts metabolism away from energy (ATP) consumption
- Ex: Makes brain hungry, increases fatty acid oxidation
AMP Production
AMP produced by:
1. ATP hydrolyzed to ADP
2. 2 ADP converted to 1 ATP and 1 AMP
4 ways of regulating glycolysis and glyconeogenesis
1. Allosteric Activation/Inhibition (intracellular)
2. Reversible Phosphorylation
3. Regulating Expression of Genes (via T-factors)
4. Signal Transduction Events
Allosteric Regulation in PFK and FBPase
PFK = ATP + F6P -> ADP + F1,6P -> Glycolysis
FBPase = F1,6P + H2O -> F6P + Pi -> Gluconeogenesis
F26BP activates PFK, inhibits FBPase
- Contains Kinase group and Phosphotase group
- F26BP increases glycolysis
Insulin activates PFK, glucagon activates FBPase
Reversible Phosphorylation of Pyruvate Kinase
Phosphorylated P-Kinase is less active
- Becomes phosphorylated in presence of ATP
Insulin Gene Regulation
Insulin attaches to a receptor that goes on to downregulate genes for gluconeogenic enzymes