Mitochondria and peroxisomes Flashcards

1
Q

Mitochondrial replacement therapy [2 marks]

A
  • Healthy ovum is enucelated first

- Nucleus of healthy ovum replaced by nucleus of mother (with defective mitochondria)

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2
Q

Structure of mitochondria [5 marks]

A
  • Double membrane
  • Gel-like, viscous matrix (due to reduced water content)
  • Inner membrane folds to form cristae
  • Inner membrane is impermeable to passage of ions and small molecules
  • Outer membrane contains porins
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3
Q

Where does the citric acid cycle occur? [1 mark]

A

Mitochondrial matrix

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4
Q

Purpose of cirstae

A
  • Increases surface area for enzymes involved in ATP synthesis
  • Sites of oxidative phsophorylation
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5
Q

Why do mitochondria associate with microtubules? [1 marks]

A

Allow even distribution of mitochondria across the cell

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6
Q

Why do mitochondria change their morphology? [1 marks]

A

To suit a cell’s need

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7
Q

How do mitochondria change their morphology? [3 marks]

A
  • Fuse together
  • Form elongated, dynamic tubular networks
  • Networks are evenly distributed across the cytoplasm
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8
Q

When do mitochondria change their morphology? [4 marks]

A
  • During apoptosis (due to proteins released from them)
  • Calcium transfer
  • Cell cycle
  • Starvation
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9
Q

What happens to mitochondria during starvation? [2 marks]

A
  • They become stretched out (due to fusion)

- May protect against autophagy

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10
Q

Nuclear pathway (of protein synthesis) [4 marks]

A

Genomic DNA → RNA → precursor protein → imported protein

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11
Q

Mitochondrial pathway (of protein synthesis) [3 marks]

A

Organelle DNA → RNA → Protein synthesised in organelle

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12
Q

Where are mitochondrial DNA (mtDNA) present and how do they arise? [2 marks]

A
  • Present in matrix

- Inherited cytoplasmically from the mother

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13
Q

mtDNA structure [3 marks]

A
  • Circular chromosomes

- Has almost 17,000 base pairs

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14
Q

Mitochondrial stop codon [2 marks]

A
  • AGA/AGG

- In the nucleus, this forms arginine

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15
Q

Mitochondria functions [5 marks]

A
  • Breakdown of fatty acids to acetyl CoA (in the matrix)
  • Decarboxylation of pyruvate (in matrix)
  • Oxidation phosphorylation
  • Thermogenesis
  • Important in apoptosis
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16
Q

Causes of beriberi disease [2 marks]

A
  • Caused by a deficiency of thiamine (vitamin B1)

- Thiamine pyrophosphate is a prosthetic group for pyruvate dehydrogenase and α-ketoglutarate dehydrogenase

17
Q

Effects of beriberi [4 marks]

A
  • High serum levels of substrates
  • DUE TO LACK OF ATP: damage to peripheral nervous system, limb pain, muscle weakness, distorted skin sensations
  • Enlarged heart (for compensation)
  • Insufficient cardiac output
18
Q

Peroxisome structure [4 marks]

A
  • Single membrane
  • Crystalloid core (due to high concentration of proteins)
  • Rich in concentrated enzymes
  • Have no DNA or ribosomes
19
Q

Where do peroxisome come from? [1 mark]

A

From precursor vesicles that pinch off from ER

20
Q

How are proteins made for the peroxisomes made and imported? [3 marks]

A
  • Encoded in the nucleus
  • Translated in the cytoplasm
  • Imported into the peroxisomes
21
Q

How do peroxisomes replicate? [1 mark]

A

Fission

22
Q

What do enzymes for peroxisomes do? [2 marks]

A
  • Break down purines (AMP, GMP) into uric acid

- oxidise substrates and form H2O2

23
Q

What are peroxisomes important for? [1 mark]

A

Important for the synthesis of some lipids

24
Q

What happens to hydrogen peroxide? [1 mark]

A

Broken down by catalase to form water and oxygen