Practice Questions

62. The safe initiation of the intrinsic pathway of programmed cell death (apoptosis) is triggered by the release into the cytosol of the mitochondrial protein

A. ATP synthase subunit A
B. Cytochrome c
C. Succinate dehydrogenase
D. Malate dehydrogenase

Mitochondrial outer membrane permeabilization releases Cytochrome c into the cytosol, where it activates the apoptosome and executioner caspases.

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61. The high-rate generation of ATP across the inner mitochondrial membrane is directly powered by the immediate downstream action of the

A. Krebs cycle substrate levels
B. Proton electrochemical gradient
C. Oxygen consumption rate in the matrix
D. Acetyl-CoA supply line

The electron transport chain pumps protons into the intermembrane space, building a proton-motive force (proton electrochemical gradient) that drives ATP synthase mechanically.

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Cardiolipin is a double-phospholipid compound unique to the inner mitochondrial membrane that acts as an electrical insulator to block proton leakage.

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59. The chemical energy currency synthesized inside mitochondria via the process of oxidative phosphorylation is

A. Adenosine diphosphate
B. Adenosine triphosphate
C. Nicotinamide adenine dinucleotide
D. Guanosine triphosphate

Mitochondria are the powerhouses of the cell because they regenerate adenosine triphosphate (ATP) from ADP and inorganic phosphate.

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58. The unique characteristic that defines mitochondria as semi-autonomous organelles within eukaryotic cells is the presence of

A. A single lipid outer covering
B. Their own circular DNA and 70S ribosomes
C. An internal network of cisternae
D. Crystalline protein storage bodies

Mitochondria possess independent circular DNA genomes and bacterial-like 70S ribosomes, allowing independent transcription and translation of select proteins.

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The matrix is the gel-like central compartment of the mitochondrion where the Krebs cycle takes place. Stroma is found in chloroplasts.

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Cristae are folds of the inner mitochondrial membrane that house the respiratory chain and ATP synthase complexes.

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55. Sulfation modifications, which add sulfate groups to specific carbohydrate structures on newly made proteins, take place within the

A. Peroxisomal matrix
B. Golgi apparatus cisternae
C. Outer nuclear envelope fold
D. Lumen of the smooth ER

The sulfation of proteoglycans and proteins is a specialized maturation step carried out by sulfotransferase enzymes located in the trans-Golgi.

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54. In eukaryotic protein secretion, the localized fusion of secretory vesicles with the target membrane is coordinated by the structural interaction of

A. Importin and exportin heterodimers
B. Specific Rab GTPases and tethering proteins
C. Cardiolipin microdomains on the bilayer
D. Nuclear lamins complexed with actin filaments

Rab GTPases serve as molecular tags on transport vesicles, interacting with specific tethering complexes on target membranes to ensure docking accuracy.

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53. The precise mechanical mechanism by which COPI-coated vesicles selectively capture escaped ER-resident proteins within the Golgi stack relies on the

A. pH gradient altering the affinity of KDEL receptors for their cargo
B. Direct phosphorylation of cargo molecules by Golgi kinases
C. Electrical potential across the cis-Golgi membrane
D. Binding of clathrin heavy chains to the vesicle core

The Golgi has a slightly lower pH than the ER. This acidic environment increases the affinity of KDEL receptors for ER proteins, facilitating their capture into retrograde COPI vesicles.

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