Observations of mitochondria within living cells have shown that:
mitochondria cannot fuse with one another.
their shape is
always cylindrical
they can exist as a highly branched,
interconnected tubular network.
they cannot split
apart.
they can exist as individual conical organelles.
they can exist as a highly branched, interconnected tubular network.
________ were responsible for the accumulation of significant levels
of atmospheric oxygen on Earth between 2.4 and 2.7 billion years ago.
Aerobic bacteria
Cyanobacteria
Plants
Anaerobic bacteria
Mitochondria
Cyanobacteria
The composition of the inner mitochondrial membrane is MOST like that of:
the outer mitochondrial membrane.
the plasma membrane of a
eukaryotic cell.
bacterial plasma membranes.
the nuclear
membrane.
the endoplasmic reticulum (ER).
bacterial plasma membranes.
Which of the following would NOT be found as part of the
mitochondrial matrix?
ribosomes larger than those in the cytoplasm of the
cell
circular DNA
enzymes
tRNAs
ribosomes smaller
than those in the cytoplasm of the cell
ribosomes larger than those in the cytoplasm of the cell
Each pair of electrons transferred from NADH to oxygen by means of
the electron-transport chain releases sufficient energy to drive the
formation of approximately how many molecules of ATP?
one
two
three
thirty-six
more than thirty-six
three
Which of the following are reduced coenzymes?
NADH and FADH2
NAD+ and FAD
ATP and GTP
coenzyme A and
TCA
NADP and FAD
NADH and FADH2
Anaerobic metabolism provides energy for muscle contraction when the
supply of ___________ is limited.
oxygen
ATP
creatine
glucose
glycogen
oxygen
During aerobic exercise, muscle fibers first use glycogen for energy
and then they switch to use of:
creatine phosphate.
free fatty
acids.
glucose.
lactic acid.
creatine.
free fatty acids.
In what form does a portion of the product of glycolysis enter the
TCA cycle?
acetyl CoA
pyruvate
NADH
glucose
citric acid
acetyl CoA
At the end of the electron transport chain, low-energy electrons are
transferred to ______, which is the terminal electron acceptor,
forming ______.
molecular oxygen (O2); glucose
water
(H2O); molecular oxygen (O2)
pyruvate;
lactate
molecular oxygen (O2); water
(H2O)
NAD+; NADH
molecular oxygen (O2); water (H2O)
Creatine phosphate can be used by a muscle fiber to generate:
myosin.
ADP.
ATP.
pyruvate.
free fatty acids.
ATP.
Which component involved in the Krebs (TCA) cycle is bound to the
inner mitochondrial membrane?
oxaloacetate
acetyl CoA
succinate
dehydrogenase
succinate
succinyl CoA
succinate dehydrogenase
To what is the 2-carbon fragment of acetyl CoA added to make citric
acid at the start of the Krebs cycle?
oxaloacetate
citric
acid
succinate
ketoglutarate
isocitric acid
oxaloacetate
Types of electron carriers found in the electron transport chain of
the inner mitochondrial membrane do NOT include:
flavoproteins.
cytochromes.
iron-sulfur proteins.
ubiquinone.
NAD.
NAD.
Which of the following statements is FALSE about cytochrome oxidase?
It is also known as complex IV in the electron transport
chain.
It acts as a proton pump.
Activity of the enzyme
leads to production of oxygen.
For every molecule of oxygen
reduced, eight protons move through the complex.
Translocation of
protons through the complex is coupled to conformational changes
generated by the release of energy that accompanies the transfer of electrons.
Activity of the enzyme leads to production of oxygen.
Which of the following is NOT a feature of oxidative phosphorylation?
direct transfer of phosphate from a substrate molecule to ADP,
also known as substrate-level phosphorylation).
an
electrochemical gradient across the inner mitochondrial
membrane.
transport of protons across the inner mitochondrial
membrane
NADH dehydrogenase.
cytochromes.
direct transfer of phosphate from a substrate molecule to ADP, also known as substrate-level phosphorylation)
If complex III were incorporated into an artificial lipid vesicle in
order to demonstrate its proton-translocating ability in isolation,
which of the following would be an appropriate electron donor?
flavoprotein
ubiquinone (UQ)
ubiquinol
(UQH2)
cytochrome c oxidase
succinate dehydrogenase
ubiquinol (UQH2)
If a cell did NOT have an electron transport chain, which mechanism
would have to account for its ATP production?
oxidative phosphorylation.
substrate-level
phosphorylation.
a proton pump
the TCA cycle
aerobic metabolism
substrate-level phosphorylation.
The oxygen in the blood is:
bound to hemoglobin.
dissolved in blood plasma.
bound
to hemoglobin and dissolved in blood plasma.
bound to the red
blood cell membrane.
mostly found in white blood cell cytoplasm.
bound to hemoglobin and dissolved in blood plasma.
There is a device made of a platinum contact and a silver contact
embedded in an electrolyte solution that creates a current when
voltage is placed across the contacts. The current is created by a set
of oxidation-reduction reactions involving oxygen, the two metals, and
chloride ions. The current is higher if more oxygen is present, so
this device can be used to determine the concentration of oxygen. What
is this device called?
a battery electrode
a Clark generator
an oxygen
meter
a Clark electrode
a pH electrode
a Clark electrode
What is a common use of a Clark-type transcutaneous oxygen sensor?
monitoring the concentration of oxygen in a blood sample from an
older person
monitoring blood oxygen levels in newborn babies in
the intensive care unit
measuring the oxygen exhaled by a
patient
measuring the oxygen content of the skin
measuring
the oxygen exhaled by a patient and oxygen content of the skin
monitoring blood oxygen levels in newborn babies in the intensive care unit
In a pulse oximeter, what light-emitting diodes are used to determine
blood oxygen?
one that emits red light at 660 nm and one that emits infrared
light
one that emits green light at 550 nm and one that emits
infrared light
one that emits red light at 660 nm and one that
emits ultraviolet light
one that emits green light at 550 nm and
one that emits ultraviolet light
one that emits blue light at 450
nm and one that emits infrared light
one that emits red light at 660 nm and one that emits infrared light
How does a pulse oximeter determine when a person’s heart beats?
It detects the peaks in redder deoxygenated blood that occur at
each heartbeat.
It detects the peaks in redder deoxygenated blood
that occur in between heartbeats.
It detects the peaks in redder
oxygenated blood that occur at each heartbeat.
It detects the
peaks in bluer oxygenated blood that occur in between
heartbeats.
It detects the peaks in bluer oxygenated blood that
occur at each heartbeat.
It detects the peaks in redder oxygenated blood that occur at each heartbeat.
Which one of the following can act as an “uncoupler” of glucose
oxidation and ADP phosphorylation?
cytochrome oxidase
dinitrophenol
copper
proton
pumps
heme groups
dinitrophenol
Maintenance of the proton-motive force requires that:
the mitochondrial matrix supplies electrons for passage down the
electron transport chain.
the inner mitochondrial membrane is
impermeable to protons.
the inner mitochondrial membrane is
impermeable to electrons.
the plasma membrane is impermeable to
protons.
protons remain lipid soluble.
the inner mitochondrial membrane is impermeable to protons.
The Fo portion of the ATP synthase:
contains a channel through which protons can move from the
intermembrane space to the mitochondrial matrix.
is composed of
different five polypeptides.
is located in the outer
mitochondrial membrane.
has the same structure in a wide variety
of different organisms.
all of these statements are true about
the Fo of mitochondrial ATP synthase.
contains a channel through which protons can move from the intermembrane space to the mitochondrial matrix.
The binding change mechanism of ATP production was proposed by:
Paul Boyer.
John Walker.
Masasuke Yoshida.
Efraim
Racker.
Humberto Fernandez-Moran.
Paul Boyer.
The F1 portion of mitochondrial ATP synthase:
is composed of four polypeptides.
is coded for by
mitochondrial DNA and synthesized in the matrix.
is located in
the outer mitochondrial membrane.
synthesizes ATP.
is a
protein that lacks quaternary structure.
synthesizes ATP.
Two types of biological structures that contain rotating parts are
ATP synthase and:
cytochrome c oxidase.
sperm cells.
bacterial
flagella.
invertebrate feeding structures.
the only rotating
structure in the biological world is ATP synthase.
bacterial flagella.
Which one of the following statements is FALSE regarding action of
the Fo portion of ATP synthase?
The c subunits are organized into a ring-shaped
complex.
Subunits of the c ring move successively past a
stationary a subunit.
The g subunit rotates at rates of
more than 100 revolutions per second.
The movement of electrons
through the membrane drives the rotation of the ring of c
subunits.
Rotation of the c ring of F0 leads
to the synthesis and release of ATP by catalytic subunits of the
F1 portion of the enzyme.
The movement of electrons through the membrane drives the rotation of the ring of c subunits.
ATP synthase is located:
in the plasma membrane.
in the outer membrane of the
mitochondrion.
in the matrix of the mitochondrion.
in the
inner membrane of the mitochondrion.
in the intermembrane space.
in the inner membrane of the mitochondrion.
According to the rotational catalysis model, _______ energy stored in
the proton gradient is transduced into ________ energy of a rotating
stalk, which is transduced into __________ energy stored in ATP.
mechanical; electrical; chemical
chemical; electrical;
mechanical
electrical; chemical; mechanical
electrical;
mechanical; chemical
chemical; mechanical; electrical
electrical; mechanical; chemical
Which of the following BEST describes the mechanism by which ATP is
synthesized by ATP synthase using the energy of proton movement?
Protons move through the Fo subunit and thereby allow
ADP and Pi to bind the enzyme.
Protons move through
the Fo subunit and rotate the γ subunit, inducing changes
in the conformation of the β subunit catalytic sites and allowing
formation and release of ATP.
Protons bind to the F1
subunit and electrostatically join ADP and Pi.
Protons
allow substrate-level phosphorylation to occur, much like that in
glycolysis.
Protons are channeled through the F1
subunit into the mitochondrial matrix where they release energy that
is captured by ADP.
Protons move through the Fo subunit and rotate the γ subunit, inducing changes in the conformation of the β subunit catalytic sites and allowing formation and release of ATP.
The three catalytic sites of ATP synthase ___________.
have different substrate binding affinities
have different
product binding affinities
at any one time are present in
different conformations
pass sequentially through their three
different conformations
All of these are correct.
All of these are correct.
Which of the following statements about mitochondrial diseases is TRUE?
Individuals with mutations in the same mitochondrial gene will
all exhibit the same disorder.
All mitochondrial diseases are
mild and are easily tolerated by the patient.
Oxygen radicals
formed in mitochondria cause an increased mutation rate in mtDNA
relative to nuclear DNA.
Scientists have described a clear
connection between mutations in mtDNA and aging.
Mitochondrial
diseases will always be inherited by offspring of the same father.
Oxygen radicals formed in mitochondria cause an increased mutation rate in mtDNA relative to nuclear DNA.
Which statement about the condition X-linked adrenoleukodystrophy
(X-ALD) is FALSE?
It was the topic of the movie Lorenzo's Oil.
It
has been successfully treated by bone marrow transplantation.
It
can cause damage to the myelin sheath covering neurons in the
brain.
It is being studied in a large-scale clinical
trial.
It will be inherited by female children only.
It will be inherited by female children only.
Peroxisomes:
may contain a dense crystalline core.
are found only in
reptilian and avian cells.
concentrate molecules of lithium
peroxide within the cell.
are only found in bacterial
cells.
produce ATP in the cell.
may contain a dense crystalline core.
Mitochondrial DNA:
is contributed to the fertilized egg by the sperm cell.
is
contributed to the offspring exclusively by the egg cell.
may
exhibit heteroplasmy, meaning that some mtDNA is contributed by the
mother and some is contributed by the father.
is not subject to
mutations because it is not replicated in the nucleus of the
cell.
inherited from the father often leads to mitochondrial disorders.
is contributed to the offspring exclusively by the egg cell.
Using differential centrifugation, you are trying to isolate
peroxisomes from a mixture of cellular organelles. After a few
centrifugation steps, you think you may have a relatively pure
suspension. How might you determine that your suspension does, indeed,
have peroxisomes?
Do an assay for the enzyme catalase.
Do an assay for the
enzyme succinate dehydrogenase.
Look in the microscope for an
organelle with a double membrane.
Assay your suspension for
nucleic acid.
Assay your suspension for H2O2.
Do an assay for the enzyme catalase.
Which of the following is a form of stored energy in plants?
starch
DNA
oils (triglycerides)
starch and oils (triglycerides)
proteins
starch and oils (triglycerides)
What is the main form of energy storage in seeds and crops like
soybeans, maize, and sunflowers?
starch
DNA
oils (triglycerides)
starch and oils (triglycerides)
proteins
DNA
What organelle converts citrate into glucose by a series of enzymes
of the glyoxylate cycle?
the nucleus
the glyoxysome
the peroxisome
the
endoplasmic reticulum
the lysosome
the glyoxysome
When a seed is maturing, triglycerides are synthesized. Where are
they stored?
peroxisomes
the nucleus
oil
bodies
lysosomes
the Golgi apparatus
oil bodies
Stored fat in seeds remains inert until:
seed germination
seed planting
seed
shedding
photosynthesis
aerobic respiration
seed planting
What is the name of the biochemical pathway in seeds that converts
citrate into glucose?
Krebs cycle
glycolysis
non-cyclic
photophosphorylation
glyoxylate cycle
electron transport
glyoxylate cycle
Which organelle below is not found in both plants and animals?
cell membrane
mitochondria
peroxisomes
glyoxysomes
vacuoles
glyoxysomes