ch.11 Flashcards

(10 cards)

1
Q

Organisms Undergoing ATP Synthesis without Oxygen

A

Examples: Many bacteria, yeast, and muscle cells in animals can synthesize ATP in the absence of oxygen through anaerobic respiration or fermentation

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2
Q

Summary of Anaerobic Respiration

A

Definition: Anaerobic respiration is a process where cells generate ATP without oxygen by using an electron transport chain (ETC) with a different final electron acceptor.
Difference from Aerobic Respiration: Uses molecules other than oxygen (e.g., nitrate, sulfate) as final electron acceptors.
ETC: Yes, anaerobic respiration has an ETC, but with alternative electron acceptors.
Final Electron Acceptors: Commonly nitrate (NO₃⁻) or sulfate (SO₄²⁻), depending on the organism.

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3
Q

Summary of Fermentation

A

Definition: Fermentation is an anaerobic process that allows ATP production through glycolysis and regenerates NAD⁺ without using an ETC.
Goal: Regenerate NAD⁺ to allow continuous ATP production via glycolysis.
Types of Fermentation:
Alcohol Fermentation: Produces ethanol and CO₂.
Lactic Acid Fermentation: Produces lactic acid.
ATP Yield: 2 ATP per glucose molecule.
Oxygen Requirement: Does not require oxygen.

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4
Q

Alcohol and Lactic Acid Fermentation

A

Alcohol Fermentation:
Process: Pyruvate is converted to ethanol and CO₂.
Organisms: Yeasts and some bacteria.
Lactic Acid Fermentation:
Process: Pyruvate is reduced to lactic acid.
Organisms: Certain bacteria and muscle cells in animals.

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5
Q

Efficiency Ranking of ATP Production

A
  1. Aerobic Respiration: Most efficient (~30-32 ATP per glucose), fully oxidizing glucose.
  2. Anaerobic Respiration: Less efficient due to alternative electron acceptors, yields fewer ATP.
  3. Fermentation: Least efficient, producing only 2 ATP per glucose molecule, as it only uses glycolysis.
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6
Q

Alternative Organic Molecules in Cellular Respiration

A
  1. Carbohydrates (first choice for energy).
  2. Fats (second, broken down into glycerol and fatty acids).
  3. Proteins (used last, broken into amino acids).
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7
Q

Entry Points of Monosaccharides

A

Monosaccharides other than glucose (from disaccharides and polysaccharides) enter cellular respiration at glycolysis, after being converted into intermediates like glucose-6-phosphate.

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8
Q

Breakdown of Fats

A

Process:
Lipases: Enzymes that break fats into glycerol and fatty acids.
Beta-Oxidation: Fatty acids are broken down in mitochondria (and peroxisomes) to produce acetyl-CoA.
Entry Points:
Glycerol: Enters glycolysis as an intermediate.
Acetyl-CoA: Enters the citric acid cycle.

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9
Q

Breakdown of Proteins

A

Process:
Proteases/Peptidases: Break down proteins into amino acids.
Deamination: Removes amino groups from amino acids, converting them into intermediates.
Entry Points:
Deaminated Amino Acids: Enter glycolysis, pyruvate processing, or the citric acid cycle, depending on the specific amino acid.
Amino Group Removal: Excess amino groups are converted to urea in the liver and excreted by the kidneys in vertebrates.

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10
Q

Use of Cellular Respiration Intermediates in Biosynthesis

A

Examples of Anabolic Pathways:
Glucose: Provides building blocks for glycogen and starch.
Pyruvate: Used to synthesize amino acids.
Glycolysis Intermediates: Can form nucleotides and amino acids.
Acetyl-CoA: Used to build fatty acids and cholesterol.
Citric Acid Cycle Intermediates: Serve as precursors for amino acids, heme groups, and other biomolecules.

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