10. ATP synthase is a key enzyme of mitochondrial energy conversion. Mitochondrial ATP synthase deficiency is due to a mutation in a gene important for the formation of a subunit in the ATP synthase complex, seen in the illustration below. Scientists could use cells with this gene mutation to investigate which of the following questions? (LS1-7) * Inner mitochondrial membrane PYRUVATE GLYCOLYSS ODATION CITRIC ACO CYCLE ODATIVE PHOSPHORYL ATION ATP synthase Protein complex of electron carriers Intermembrane• space Inner mitochondrial membrane FADH, FAD 2 H* + ½02 H,0 NADH NAD ADP + P ATP (carrying electrons from food) Mitochondrial matrix Oxidative phosphorylation What effect does the mutation have on the movement of electrons between the electron carriers of the electron transport chain? What effect does the mutation have on the amount of ATP synthesized during cellular respiration? What effect does the mutation have on the number of protons pumped into the intermembrane space of the mitochondria? What effect does the mutation have on the number of water molecules formed at the end of the electron transport chain?

Biochemistry
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ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Reginald H. Garrett, Charles M. Grisham
Chapter21: Photosynthesis
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Problem 5P: The Relative Efficiency of ATP Synthesis in Noncyclic versus Cyclic Photophosphorylation If...
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10. ATP synthase is a key enzyme of mitochondrial energy conversion.
Mitochondrial ATP synthase deficiency is due to a mutation in a gene
important for the formation of a subunit in the ATP synthase complex,
seen in the illustration below. Scientists could use cells with this gene
mutation to investigate which of the following questions? (LS1-7) *
Inner
mitochondrial
membrane
PYRUVATE
GLYCOLYSIS ODATION
ACO
CYCLE
OXIDATIVE
PHOSPHORYL-
ATION
ATP
synthase
Protein complex
of electron
Intermembrane-
space
carriers
III
Inner
mitochondrial
membrane
FADH, FAD
2 H* + ½02
H,0
NAD
NADH
(carrying electrons
from food)
ADP + O
АТР
Mitochondrial
matrix
Oxidative phosphorylation
What effect does the mutation have on the movement of electrons between the
electron carriers of the electron transport chain?
What effect does the mutation have on the amount of ATP synthesized during cellular
respiration?
What effect does the mutation have on the number of protons pumped into the
intermembrane space of the mitochondria?
What effect does the mutation have on the number of water molecules formed at the
end of the electron transport chain?
Transcribed Image Text:10. ATP synthase is a key enzyme of mitochondrial energy conversion. Mitochondrial ATP synthase deficiency is due to a mutation in a gene important for the formation of a subunit in the ATP synthase complex, seen in the illustration below. Scientists could use cells with this gene mutation to investigate which of the following questions? (LS1-7) * Inner mitochondrial membrane PYRUVATE GLYCOLYSIS ODATION ACO CYCLE OXIDATIVE PHOSPHORYL- ATION ATP synthase Protein complex of electron Intermembrane- space carriers III Inner mitochondrial membrane FADH, FAD 2 H* + ½02 H,0 NAD NADH (carrying electrons from food) ADP + O АТР Mitochondrial matrix Oxidative phosphorylation What effect does the mutation have on the movement of electrons between the electron carriers of the electron transport chain? What effect does the mutation have on the amount of ATP synthesized during cellular respiration? What effect does the mutation have on the number of protons pumped into the intermembrane space of the mitochondria? What effect does the mutation have on the number of water molecules formed at the end of the electron transport chain?
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