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 CITRIC ACO OKDATIVE PHOSPHORYL ATION GLYCOLYSIS ONDATION CYCLE ATP synthase Protein complex of electron carriers Intermembrane space Inner mitochondrial membrane FADH, FAD 2 H* + ½02 H,0 NADH NAD ADP + O 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
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
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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 CITRIC
ACO
OXIDATIVE
PHOSPHORYL-
ATION
GLYCOLYSIS ONDATION
ATP
synthase
Intermembrane
Protein complex
of electron
space
carriers
IV
Inner
mitochondrial
membrane
FADH, FAD
2 H* + ½02
H,0
NADH
NAD
ADP + O
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?
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 CITRIC ACO OXIDATIVE PHOSPHORYL- ATION GLYCOLYSIS ONDATION ATP synthase Intermembrane Protein complex of electron space carriers IV Inner mitochondrial membrane FADH, FAD 2 H* + ½02 H,0 NADH NAD ADP + O 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?
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