VL 2 (Petra Wendler) Flashcards

1
Q

Name the three Steps of energy extraction.

A

1. Step : digestion of
- fat –> fatty acids and glycerin
- Polysaccheride –> Glucose and diffrent Sugars
- Proteins –> amino acid

2. Step: Production of Acetyl-CoA

3.Step: complete oxidation of Acetyl-group to Co2
Acetyl-Coa –> Krebs cycle –8e—> oxidative phosphorylierung –> ATP

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2
Q

Explain catabolism and anabolism

A

Catabolism:
- breakdown of complex molecules into simpler substances, to release energy and provide building blocks for anabolism.
- Key Processes: Glycolysis, Krebs Cycle, Fatty Acid Oxidation, Protein Degradation.
(Example: Digesting food to produce energy)

Anabolism:
- synthesis of complex molecules from simpler substances, to build and maintain structures in cells and tissues.
- Key Processes: Protein Synthesis, DNA Replication, Photosynthesis, Cell Division.
(Example: Creating new proteins or forming glucose in photosynthesis)

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3
Q

What is the diffrence between phototrophic organisms and chemotrophic organisms?

A

Phototrophic organisms: get energy from sunlight

Chemotrophic organisms: get energy through oxidation of nutrients

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4
Q

Properties of metabolic reactions:

A
  1. Many metabolic reactions are near-equilibrium reactions (ΔG ≈ 0).
  2. Irreversible metabolic reactions take place far away from equilibrium (ΔG &laquo_space;0).
  3. Enzymes accelerate adjustment of the equilibration without changing its position.
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5
Q

Thermodynamik pricipal in metabolism

A
  1. Many metabolic reactions are near-equilibrium reactions (ΔG ≈ 0).
  2. Irreversible metabolic reactions take place far away from equilibrium (ΔG &laquo_space;0).
  3. Enzymes accelerate adjustment of the equilibration without changing its position.

Properties of metabolic pathways:
1. Metabolic pathways consist of sever

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6
Q

Gibbs free Energy

A
  • Gibbs free energy is determined by concentration of reaction partners
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7
Q

What is an exergonic and endergonic reaction?

A

exergonic: If ΔG < 0, direction of reaction is A + B → C + D (right)
–> concentration of reaction partners > 1 ([A][B] < [C][D])

endergonic: If ΔG > 0, direction of reaction is C + D → A + B (order increases) (left)
–> concentration of reaction partners < 1 ([A][B]> [C][D])

equilibrium: If ΔG = 0, the reaction is in equilibrium
–> concentration of reaction partners = 1 ([A][B]= [C][D])

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8
Q

How is the high phosphorylation potential of ATP achieved?

A
  1. Resonance stabilization of ADP and Pi
  2. Electrostatic repulsion of the 4 negative charges at ATP
  3. Stabilisation through hydration of ADP and Pi
  4. Gain in entropy

ATP + H20 <–> ADP + Pi
ΔG0‘ = -30,6 kJ/mol

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9
Q

Wjat is the active carrier of C2-Fragments?

A

Coenzyme A

Acetyl-CoA + H2O Acetat <–> CoA + H+
ΔG0‘ = -31,4 kJ/mol

Unlike oxygen esters, thioesters are not stabiliized by resonance structures
–> high acetyl group transfer potential

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10
Q

Activated electron carrier for oxidation?

A

NAD+ Nicotinamideadeninedinucleotide

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11
Q

What is the actrivated electron carrier for oxidation?

A

FAD Flavineadeninedinucleotide

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12
Q

What is the activated electron carrier for reductive biosynthesis?

A

NADPH Nicotineamideadeninedinucleotidephosphat

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13
Q

Carrier molecules in metabolism

A
  1. In the absence of catalysts, carriers are kinetically very stable.
    This allows enzymes to control the flow of free energy.
  2. The exchange of activated groups is carried out by a small set of carrier molecules in metabolism.
    Modular construction is economical and elegant.
  3. Many carriers are based on watersoluble vitamins:
    * FADH and FMN: Vitamin B2 (Riboflavin)
    * NADH, NADPH: Vitamin B3 (Niacin)
    * Coenzyme A: Vitamin B5 (Pantothenate)
  4. NAD+/NADH+: in catabolic processes; NADP+/NADPH+: in anabolic processes
  5. ATP, NADH, CoA, FAD all contain an ADP
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14
Q

Glykolysis

A
  1. Glucose –> Hexokinase
  2. Glucose 6-phosphate –> Phosphohexose isomerase
  3. Fructose 6-phosphate –> Phospho fructokinase-1
  4. Fructose 1,6-bisposphate –> Aldolase
  5. Glyceraldehyd 3-phosphate + Dihydroxyacetone phosphate –> Triose phosphate isomerase
  6. Glyceraldehyd 3-phosphate –> Glyceraldehye 3-phosphate dehydrognease
  7. 1,3-Bisphosphoglycerate –> Phosphoglycerate kinase
  8. 3-phosphoglycerate –> Phosphoglycerarte mutase
  9. 2-Phosphoglycerate –> Enolase
  10. Phosphoenolpyruvat –> Pyruvate kinase
  11. Pyruvat
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15
Q

Glykolysis in general

A
  • Thermodynamically open system: equilibrium
  • hexokinase,phosphofructokinase and pyruvate kinase have significantly negative ΔGphysiol
    –> Speed-determining steps for steady state
    –> Regulation of metabolic pathways at pacemaker reactions (allosteric)
  • Flow of intermediates is constant in steady state. Synthesis and degradation are in balance
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16
Q

What is Gluconeogenesis and where does it takes place?

A
  • in liver and guts
  • Formation of glucose from non carbohydrates (lactate, amino acids, glycerol) via pyruvate to keep blood sugar levels constant
  • Relevant in periods of hunger
  • The organism can not produce glucose from acetyl-co !!!
  • Exergonic reactions of glycolysis are bypassed by other reactions
  • Gluconeogenesis requires 3 cell compartments: cytosol, mitochondria, ER
  • The path from pyruvate to glucose costs more energy than the pathway from glucose to pyruvate supplies
17
Q

Glucolysis vs. Gluconeogensis

A

Glycolysis:
Glc + 2NAD+ + 2 ADP + 2Pi →
2 Pyruvate + 2 NADH + 2H+ + 2ATP + 2H2O

Glycolysis produces two molecules of pyruvate from one molecule of glucose, producing 2 ATP and 2 NADH.

Glyconeogenesis:
2 Pyruvate + 2 NADH + 4ATP + 2GTP + 6H2O → Glucose + 2NAD+ + 2H+ + 4ADP + 2GDP + 6Pi

Gluconeogenesis produces one molecule of glucose from two molecules of pyruvate, consuming two NADH, 4ATP and 2GTP. It is not just the reverse of glycolysis

18
Q

What happens with Pyruvate?

A
  • Pyruvate needs to be further processed to regenerated NAD+ and maintain redox balance
  1. Acetaldehyd –> Ethanol
  2. Lactat
  3. Acetyl-CoA
19
Q

What is the: Pentose phosphate pathway?

A
  • Takes place in all cells; serves changing cellular needs
  • Supplies riboses for DNA and RNA
  • Delivers NADPH/H+ as a hydrogen transporter for anabolic processes (fatty acid
    biosynthesis, peroxide poisoning, glutathione regeneration, …)
  • A maximum of 10% of the glucose molecules go into pentose phosphate pathway
  • Divided into 2 sections

The pentose phosphate pathway provides reduction equivalents for biosyntheses as NADPH and pentoses

20
Q

NADH vs. NADPH

A

NADH:
* is used to produce ATP in the respiratory chain
* is predominantly oxidized (NAD +) as needed in glycolysis

NADPH:
* serves for reductive biosynthesis in
- Liver: biosynthesis of cholesterol and fatty acid
- Adipose tissue: fatty acid biosynthesis
- Breast tissue: biosynthesis of milk fats
- Adrenal Bark: Biosynthesis of Steroids from Cholesterol
- Testes / ovaries: production of sex organs from cholesterol
* Protects the erythrocyte membrane and liver cells from cell toxins
* is preferably present in the reduced form (NADPH / H +)

21
Q

Acetyl-CoA: interface of ATP generation

A
  • Smallest common product of degradation of amino acids, fatty acids and carbohydrates
  • takes C2-molecules into Krebs cycle
  • produced in mitochondrium
22
Q

What is the Pyruvate-dehydrognease complex?

A
  • Localised in mitochondrial matrix
  • Catalyses the oxidative decarboxylation of pyruvate
    to acetyl-CoA
  • is a multi enzyme complex:
    –> 3 enzymes (E1, E2, E3)
    –> 5 coenzymes:
  • Thiaminepyrophosphate (vitamine B1),
  • Liponamide,
  • Coenzyme A (vitamine B5),
  • FAD (vitamine B2),
  • NAD+ (vitamine B3)
23
Q

What is the interim balance?

A

2x ATP glycolysis
2x ATP citric acid cycle

2x NADH/H+ glycolysis
2x NADH/H+ pyruvate dehydrogenase
6x NADH/H+ citric acid cycle
2x FADH2 citric acid cycle

1 glucose -> 6 CO2 + 4 ATP + 10 NADH/H+ + 2 FADH2