CARBOHYDRATE
METABOLISM
Underline option are answers
1. Gluconeogenesis:
a) Is favoured when isulin
concentration is high
b) Occurs in the liver during prolonged fasting
c) Allows skeletal muscle to produce glucose for export to blood for use by the CNS
d) Is stimulated by high levels of
glucose-6-phosphate
e) Uses Acetyl CoA as substrate
2. Glucose-6-phosphate
dehydrogenase:
a) Is the key enzyme in glycogenesis
b) Is activated by high levels of NADP+
c) Catalyzes conversion G6P to
fructose-6-phosphate
d) Is important in muscle during
exercise
e) Not found in RBC's
3. In the TCA cycle:
a) 3
ATP's are produced by substrate-level phosphorylation
b) Oxygen is directly involved
c) All reactions are reversible
d) Succinyl CoA is
the precursor for Heme synthesis
e) Oxaloacetate is converted to pyruvate
4. The following can be synthesized
from glucose in the human body:
a) Ribose and lactate
b)
Lactose and cellulose
c)
Sucrose and ribulose
d) Cellulose and fructose
e) Fatty acid sucrose
5. Glucose-6-phosphate
deficiency:
a) Is known as Von Gierke's disease
b) Is
associated with hypoglycemia in the fed state
c) Inhibits the last step of
glycogenolysis and gluconeogenesis in the liver
d) Is associated with hyperuricemia
e) B is the only
wrong statement
6. In glycogenesis:
a) ATP is required
b) Phosphoglucomutase catalyses irreversible
step
c) Glucose residues are added to
the reducing end of glycogen d) Glycogen synthase is the
key enzyme
e) 2 ATP molecules are consumed
7. In galactosemia:
a) Treatment
involves restriction of glucose in diet
b) The liver function
can be seriously affected
c) Galactose is deposited in
tissues
d) Galactose is readily converted
to glucose
e) Galactosuria is the most serious
manifestation
8. Uncoupling of oxidative
phosphorylation:
a) Decreases the oxygen consumption
b) Releases heat only
c)
Occurs during hypoxia
d) Causes a buildup of NADH
e) Produces more ATP
9. The enzyme not involved
in glycolyisis is:
a)
Aldolase
b)
Endolase
c) Pyruvate kinase
d) Phosphoglycerate mutase
e) Alpha
phosphoglycerate dehydrogenase
10. Which of the following is not a
glycolytic intermediate?
a) Glucose-6-phosphate
b) Fructose-6-phosphate
c) Dihydroxyacetone phosphate
d) Pyruvate
e)
Glycerol-3-phosphate
11. Which site utilizes glucose as
an energy source exclusively in all conditions:
a) Brain
b) Muscle
c) Liver
d) Fat cell
e) Erythrocyte
12. The following agent interferes
with oxidative phosphorylation:
a) Cyanide inhibits
NADH-dehydrogenase
b) Carbon monoxide inhibits
Coenzyme Q
c) Rotenone enhances electron transfer
d) Oligomyein inhibits electron
transfer
e) Dintrophenol
uncouples phosphorylation from electron transfer
13. The following compounds are
part of the pyruvate dehydrogenase complex:
a) Thiamin
diphosphate
b) Lipoamide
c) CoA
d) NAD+
e) All of the above
14. UDP-G:
a) Is derived from vitamin B1
b) Is a
substrate for the enzyme glycogen phosphorylase
c) Is
intermediate in glycerophospholipid synthesis
d) Is not required for normal
galactose metabolism
e) Can be formed from UDP-Galactose
15. Glycogen phosphorylase:
a) Is a
mitochondrial enzyme
b) Is
activated by dephosphorylation
c) Acts by the same mechanism as
intestinal amylase
d) Produces uridine diphosphate
from glycogen
e) Produces
glucose-1-phosphate
16. Fructose 2,6 bisphosphate:
a) Is
a glycolytic intermediate
b) Activates
phosphofructokinase 1
c) Is synthesized by
phopshofuctokinase 1
d) Enhances fructose 1,6
bisphosphate
e) Level in the liver is increased
by glucagon
17. Pyruvate carboxylase:
a) Converts
acetyl CoA to pyruvate
b) Requires carnitine
c) Converts pyruvate to oxaloacetate
d) Is activated by high fructose
1,6 bisphosphate
e) Requires pyridoxal phosphate
18. In glycogen storage
diseases:
a) Von Gierke's disease is type III
b) Hypoglycemia
is the main feature of type V
c) Type
II is associated with glucose 6 phosphatase deficiency
d) Type IV is called
Andersen's disease
e) Hepatomegally is the main
feature of all types
19. Which of the following
statements about galactosemia is correct:
a)
Treatment involves restriction of glucose in the diet
b) A
deficiency of glucokinase is the major case
c) Is treated by
elimination of galactose from the diet
d) Can be treated by restricting
sucrose in the diet
e) Is inherited as autosomal
dominant character
20. Glucose-6-phosphate
dehydrogenase:
a) Is
the key enzyme in glycogenesis
b) Deficiency can
cause hemolytic anemia
c) Catalyses conversion of G6P to
fructose-6-phosphate
d) Is important in muscles during
exercise
e) Is not found in RBC's
21. Synthesis of glucose from pyruvate
by gluconeogenesis in the liver:
a) Occurs
exclusively in the cytosol
b) Is inhibited during prolonged
fasting
c) Requires participation of
biotin
d) Requires lactate as intermediate
e) Occurs exclusively in the
mitochondrion
22. In the TCA cycle:
a) Four NADH molecules are produced
b) Substrate-level phosphorylation occur by the action of sccinyl
CoA
thiokinase
c) The
reactions can proceed in the absence of molecular oxygen
d) Fumarase reactions occur immediately after
isocitrate dehydrogenases
reactions
e) Glutamate dehydrogenase is a key
enzyme
23. In fructose
metabolism:
a)
Deficiency of hexokinase results in fructosuria
b)
Glucokinase is the major enzyme
c) Fructokinase
phosphorylates fructose
d) Fructose 6 phosphate is produced
by fructokinase
e) Aldolase A is the key enzyme
24. Oxidation of glucose by red
blood cells gives:
a) Lactate
+ NADH+H
b) 36 ATP molecules per molecule of glucose
c) Lactate and NAD+
d) Carbon dioxide and water
e) 2 NADPH
25. The pentose phosphate pathway:
a) Produces
ATP
b) Is a mitochondrial pathway
c) Is important for reductive
biosynthesis
d) Is least active in the liver
e) Is inhibited by high glucose
levels
26. The following agent
interferes with oxidative phosphorylation:
a) Carbon monoxide inhibits
cytochrome reductase
b) Cyanide inhibits
NADH-dehydrogenase
c) Rotenone enhances electron
transfer
d) Oligomyein inhibits electron
transfer and phosphorylation
e) Dintrophenol
enhances ATP synthesis
27. UDP-Glucose:
a) Is indirectly involved in
bilirubin conjugation
b) Is a
substrate for the enzyme 4-epimerase in lactating mammary gland
c) Is
intermediate in sphingolipid synthase
d) Is required for galactose
metabolism
e) All of the above
28. Glycogen synthesis:
a) Is a mitochondrial
pathway
b) Is activated during the fasting
state
c) Occurs in the
liver and muscle
d) Produces uridine diphosphate
from glycogen
e) All of the above
29. Pyruvate is:
a) Converted to acetyl CoA by
pyruvate carboxylase
b) Four-carbon
compound
c)
Converted to oxaloacetate by pyruvate dehydrogenase complex
d) Converted to
alanine by transamination
e) Intermediate in the TCA cycle
30. In glycogen storage diseases:
a) Fatigability and muscle cramps
are main features of Von Geirke's disease
b)
Hypoglycemia is the main feature of type V
c) Type
II is associated with glucose 6 phosphatase deficiency
d) Type IV is called
Andersen's disease
e) Hepatomegally is the main
feature of all types
31. The following enzyme
would be impaired in biotin deficiency:
a)
Fructose 1,6-bisphosphate
b)
Pyruvate kinase
c) PEP carboxykinase
d) Pyruvate carboxylase
e) Malate dehydrogenase
32. The following statement about
the pentose phosphate pathway is correct:
a) Pentoses
can be formed both oxidatively and non-oxidant
b) This pathway is
important to fatty acid synthesis because it produces
equivalents
c) Fructose 6 phosphate can be used
to make ribose-5-phosphate d) Glyceraldehyde-3-phosphate can be used to make dinitrophenol
e) All of the above are correct
33. The following is caused by
deficiency in aldolase B:
a) Hereditory fructose intolerence
b) Jaundice
c) Hypoglycemia
d) Catarct
e) Ataxia
34. The rate of glycolysis in the
liver is increased by:
a) Insulin
b) ATP
c)
Citrate
d) NADH
e) Glucose
6-phosphate
35. The preparative step
of glycolysis involves the following:
a) ATP
synthesis at the substrate level
b) The
incorporation of Pi into a triose phosphate
c) The reduction of
NAD+ to NADH
d) The formation of
1,3-bisphosphoglycerate
e) Formation of triose phosphates
from a hexose diphosphorase
36. The following is present in the
liver, but is absent in muscles:
a) Pyruvate
carboxylase
b) Glycogen synthase
c) Lactate dehydrogenase
d) Pyruvate dehydrogenase
e)
Glucose-6-phosphatase
37. The following enzyme utilizes
FAD as a coenzyme:
a) Malate
dehydrogenase
b) Aconitase
c) Succinate dehydrogenase
d) Isocitrate dehydrogenase
e) Lactate dehydrogenase
38. A patient complaining
of painful cramps in the legs during exercise and has easy fatigability, the
most likely cause is:
a) Diabetes mellitus
b) Deficiency of
glucose-5-phosphatase
c) Deficiency of the
debranching enzyme or muscle phosphorylase d) Defective glycogen
synthesis
e) Over-storage of glycogen
39. Malonate inhibits
succinate dehydrogenase because:
a) Binds irreversibly to the active
site
b)
Covalently modifies the enzyme
c)
Resembles succinate but cannot react
d) Displaces he FAD coenzyme
e) Chelates a metal
ion required by the enzyme
40. In oxidative phosphorylation:
a) An electrochemical
potential is created across the inner mitochondrial
membrane
b) ATP is synthesized from ADP and
Pi
c) Protons are pumped
into the interspace between the inner and outer
mitochondrial membranes
d) The energy released from the
electron flow is directly used for synthesis of
ATP
e) D is incorrect
41. Phosphofructokinase-1:
a) Is activated by high level of
ATP
b)
Catalyzes the only irreversible reaction in glycolysis
c) Is activated by the high level of AMP
d) Converts fructose 1-phosphate to
fructose 1,6-bisphosphate
e) Is costimulated with fructose
1,6 bisphosphatase
42. In gluconeogenesis:
a) Pyruvate
is converted to acetyl CoA
b) Valine and Leucine are
substrates
c) Energy consumption
is high
d) Insulin is needed to enhance the
synthesis of glucose
e) Acetyl CoA is a substrate
43. Glycogen synthesis:
a) Is
typically the reverse of glycogenolysis
b) Is mitochondrial pathway
c) Is very active in adipose tissue
d) Requires uridine
diphosphate-glucose as intermediate
e) Is activated by adrenaline
44. Galactosemia:
a) Causes mental retardation
b) Can cause liver failure
c) Is caused by deficiency of
galactose-1-phosphate uridyl transferase d)
Can be treated by restricting galactose from the diet
e) All of the above
is correct
45. The following can be
obtained from the TCA cycle intermediates:
a) Fatty acids and glucose
b)
Cholesterol and ketone bodies
c) Heme
and glutamine
d) A, B and C are
correct
e) Only B is correct
46. The tissue which can
metabolize normally glucose, fatty acids and ketone bodies for ATP production
is:
a) Liver
b) Skeletal muscle
c)
Brain
d) Red blood cell
e) All of the above
47. All of the following
compounds are part of the pyruvate dehydrogenase complex except:
a) Thiamine
diphosphate
b) Lipoamide
c) Biotin
d) FAD
e) NAD+
48. Which of the following
glycolytic intermediates is a close precursor to TAG:
a) Glucose
6 phosphate
b) Fructose 6 phosphate
c) Dihydroxyacetone
phosphate
d) Pyruvate
e) 3-phosphoglycerate
49. The carbon skeleton of glucose
can participate in the synthesis of:
a) Purine
ring
b) Fatty acid
c) Glutamine
d) Pyrimidine ring
e) All of the above
is correct
50. The following agent
interferes with oxidative phosphorylation:
a) Cyanide inhibits
NADH-dehydrogenase
b) Carbon monoxide inhibits
coenzyme Q
c) Rotenone enhances electron
transfer
d) Oligomyein
inhibits electron transfer
e) Dintrophenol uncouples
phosphorylation from electron transfer
51. In oxidative phosphorylation:
a) Ubiquinone transfers electrons
from complex I to complex II
b) Dinitrophenol inhibits the flow
of electrons
c) The electrons transported from
one FADH2 to oxygen will produce 3 ATP's d) Complex IV
contains copper
e) Complex III is called cytochrome
oxidase
52. In galactosemia:
a) Cataract results
from accumulation of galactose in the lens
b) The liver function can be
seriously affected as a result of phosphate
depletion
c) Galactose is deposited in
tissues
d) Galactose is readily converted
to glucose
e) Galactosuria is the most serious
manifestation
53. The pyruvate dehydrogenase
complex defect is mainly manifestd in the following condition:
a) Beriberi
b)
Pellagra
c)
Pernicious Anemia
d) Scurvy
e) Rickets
54. The committed step in
glycolysis is catalyzed by:
a) Hexokinase
b) Phosphofructokinase-1
c)
Pyruvate kinase
d) Phosphoglycerate mutase
e) Glyceraldehyde 3 phosphate
dehydrogenase
55. The following agent
interferes with oxidative phosphorylation:
a) Cyanide inhibits
NADH-dehydrogenase
b) Carbon monoxide inhibits
Coenzyme Q
c) Rotenone enhances electron
transfer
d) Cyanide inhibits cytochrome
oxidase
e) Oligomycin
inhibits electron transfer
56. The pyruvate dehydrogenase
complex:
a)
Requires pyridoxal phosphate
b) Is inactive when thiamin is deficient
c)
Deficiency results in pernicious anemia
d) Catalyses a carboxylation
reaction
e) Is a key enzyme in the red blood
cell
57. Activation of
phophofructokinase-1 in the liver:
a)
Inhibits hexokinase
b)
Enhances gluconeogenesis
c)
Enhances the activity of pyruvate kinase
d) Occurs as a result of high
glucagons/insulin ratio
e) Results in accumulation
of fructose-6-phosphate
58. Which of the following
cells utilize glucose, fatty acid and ketone bodies as fuels:
a) Neuron
b) Myocyte
c) Hepatocyte
d) Adipocyte
e) Erythrocyte
59. Glycogen phosphorylase:
a) Is activated by insulin
b) Is
activated by dephosphorylation
c) Requires inorganic phosphate
d) Produces uridine diphosphate
glucose from glycogen
e) Is a key enzyme in
gluconeogenesis
60. In oxidative
phosphorylation:
a) Ubiquinone transfers electrons
from complex I to complex II
b)
Dinitrophenol inhibits the flow of electrons
c) The
electrons transported from one FADH2 to oxygen will produce 3 ATP
d) A decrease in oxygen supply
increases the flow of the electrons through the
complexes
e) An increase in the
rate of ATP synthesis will decrease electron transport
61. Glycogen:
a) Is found in liver and
muscle
b) Is a branched polysaccharide
formed from glucose
c) Is responsible for maintenance
of blood glucose level between meals d) Excessively deposits in liver of von Geirk's disease patient
e) All of the above
is correct
62. Fructose:
a) Enters directly into glycolysis as Fructose-6-phosphate in the
liver
b) Is
isomerized to glucose before catabolism
c) Is a
potent lipogenic factor
d) Is produced from lactose
e) Is a non-reducing sugar
63. Hypoglycemia can
result from:
a)
Deficiency of debranching enzyme (Cori's disease)
b)
Deficiency in glucose-6-phosphatase
c)
Defects in beta oxidation in the liver
d) Insulin overdose
e) All of the above is
correct
64. The common features of
glycolysis and the PPP include:
a) Both pathways produce
carbon dioxide
b) Both pathways use NAD as
coenzyme
c) Both pathways are mitochondrial
d) Both pathways produce ATP
e) Both pathways
occur in RBC's
65. Gluconeogenesis:
a) Is
the reversal of glycolysis
b) Is active during prolonged fasting
c)
Requires participation of carnitine
d) Uses acetate as substrate
e) Is very active in the fed state
66. Galactosemia:
a) Is
caused by increased galactose intake
b) Can
be avoided by using sucrose-free diet
c) Is
associated with hypoglycemia
d) Results from
galactose-1-phosphate uridyl transferase deficiency e) Is a genetic disorder caused by lactase deficiency
67. Hereditary fructose
intolerance:
a) Is always associated with
hypoglycemia
b) Results from fructokinase
deficiency
c) Results from
aldose b deficiency
d) Results in accumulation of
fructose-6-phosphate
e) Can be treated by restriction of
lactose in the diet
68. Muscle glycogen:
a)
Accumulates in lysosomes in Pomp's disease
b) Is
largely depleted by marathon running
c)
Provides phosphohexoses for muscular glycolysis
d) Provides most of glucose in the
blood
e) A, B and C are
correct
69. An enzyme that
produces non-mitochondrial NADH is:
a)
Alpha-ketoglutarate dehydrogenase
b) Glyceraldehyde 3 phosphate dehydrogenase
c)
Succinate dehydrogenase
d) 6-phophogluconate dehydrogenase
e) 3-HMG CoA synthase
70. Glycerol-3-Phosphate:
a) Is
produced by reduction of dihydroxyacetone phosphate
b) Is
precursor of phosphatidic acid
c) Can
be produced by glycerol kinase
d) Is intermediate in TAG synthesis
e) All of the above
is correct
71. The following agent interferes
with oxidative phosphorylation:
a)
Cyanide inhibits NADH dehydrogenase
b)
Carbon monoxide inhibits coenzyme Q
c)
Rotenone enhances electron transfer
d) Oligomycin inhibits complex I
e) Dinitrophenol
uncouples phosphorylation from electron transfer
72. In the fed state:
a) Glucose is
converted to glycogen and stored in skeletal muscle
b) Adipose tissue converts
triglycerides to glucose
c) Amino acids are transaminated to
form ketone bodies
d) Glycogen stores in liver are
depleted
e) Glycogen phosphorylase is in the
active form
73. Twenty four hours after a meal,
the primary source of glucose carbons for the brain is:
a)
Skeletal muscle protein
b)
Glycerol from adipose tissue
c) Dietary
glucose
d) Muscle glycogen
e) Both A and B are
correct
74. Activity of the
following enzyme is expected to increase in the fed-state:
a)
Lactate dehydrogenase
b) Glucose 6-Phosphate dehydrogenase
c)
Glucose 6-Phosphatase
d) Glycogen phosphorylase
e) PEP carboxykinase
75. The following enzymes are
absent in muscles but are present in the liver:
a)
Pyruvate carboxylase and citrate synthase
b) Glucose-6-phosphatase and glycerol kinase
c)
Lactate dehydrogenase and isocitrate dehydrogenase
d) Pyruvate dehydrogenase and
beta-ketothiolase
e) Glycogen synthase and 3HMG CoA
synthase
76. Concerning inhibition
of the electron transport chain:
a)
Cyanide inhibits NADH dehydrogenase
b)
Carbon monoxide inhibits coenzyme Q
c)
Rotenone enhances electron transfer
d) Oligomycin inhibits complex I
e) Dinitrophenol
uncouples phosphorylation from electron transfer
77. Liver glycogen synthase and
PFK-1:
a) Are
activated simultaneously in the fed state
b)
PFK-1 is activated before glycogen synthase
c) Both
are allosteric enzymes
d) Both are activated by insulin
e) All of the above is correct
78. Insulin activates PFK-1
in the liver by:
a) Increasing the level of AMP
b)
Phosphorylation
c)
Increasing the level of fructose 2,6 bisphosphate
d) Inhibiting fructose 1,6
bisphosphatase
e) None of the above
79. Metabolism of the
major fuels mostly culminate in:
a)
Glucose 6 phosphate
b)
Pyruvate
c)
Oxaloacetate
d) Acetyl CoA
e) Fumerate
80. In the liver during
the fed state:
a) Glucokinase indirectly enhances uptake of glucose
b)
Hexokinase is inhibited
c)
Glucose 6 phosphate dehydrogenase is very active
d) Glycogen phosphorylase is
dephosphorylated
e) All of the above is correct
81. Glycerol 3 phosphate
dehydrogenase:
a) Converts glycerol 3 phosphate to DHAP in the fed state
b)
Converts DHAP to glycerol 3 phosphate in the fasting state
c)
Catalyses a reversible reaction
d) Is an allosteric enzyme
e) Is a glycolytic enzyme
82. Liver enzymes which are active
in the fed state include:
a) Glycerol kinase
b) PEP
carboxykinase
c) Pyruvate kinase
d) Glucose 6 phosphatase
e) Glycogen phosphorylase
83. Insulin:
a) Activates acetyl CoA carboxylase
b)
Causes the phosphorylation of acetyl CoA carboxylase
c)
Stimulates lipolysis
d) Inhibits the formation of
malonyl CoA
e) Inhibits fatty acid synthesis in
adipose cells
84. Insulin exerts its
effect on target tissue through:
a) Enhancing tyrosine synthesis
b) Binding
tyrosine kinase receptor
c)
Increasing phosphorylation of all cellular proteins
d) Increasing intracellular cAMP
e) Inhibition of protein kinase C
85. Glucagon:
a) Is a
steroid hormone
b)
Binds intracellular receptors
c)
Mimic all actions of epinephrine
d) Enhances glycogenolysis in the liver
e) Is transcriptional enhancer
86. Hypoglycemia:
a) Is caused by hyperinsulinemia
b) Is
prominent feature of DKA
c)
Enhances release of glucagon
d) Affects the brain seriously
e) B is the only wrong statement
88. In Diabetes Mellitus:
a) Type II is more common than type one
b) Type
I is more serious than type II
c) Type
I is called insulin dependent
d) DKA is usually associated with
type I
e) All of the above is correct
89. Glucose alanine cycle:
a)
Serves to carry amino groups from the skeletal muscle to the liver
b)
Requires participation of gluconeogenesis in the liver
c)
Provides the working muscle with glucose made by the liver
d) Requires participation of
transamination reactions in both the skeletal
muscle and the liver
e) All of the above is correct
90. Lactate is increased in the
blood:
a)
During sleep
b)
During exercise
c) In
Von Gierke's disease
d) Thiamin deficiency
e) B, C and D are correct
91. Glucose, fatty acids and ketone
bodies are normally oxidized for ATP production by:
a)
Liver
b)
Skeletal muscle
c)
Brain
d) Red blood cell
e) All of the above is correct
92. During prolonged starvation,
all of the following tissues can use fuels other than glucose except:
a) Red
blood cells
b)
Muscle
c)
Brain
d) Kidney
e) Adipose tissues
93. The enzyme which is not involved
in glycolysis is:
a)
Aldolase
b)
Enolase
c) Pyruvate kinase
d) Phosphoglycerate mutase
e) Alpha phosphoglycerate
dehydrogenase
94. Activation of
phosphofructokinase-1 in the liver:
a) Inhibits
hexokinase
b)
Enhances gluconeogenesis
c) Enhances the activity of
pyruvate kinase
d) Occurs as a result of high
glucagons/insulin ratio
e) Results in accumulation of
fructose 6 phosphate
95. Which of the following
glycolytic intermediates is converted to a precursor of TAG synthesis:
a) Glucose
6 phosphate
b) Fructose 6 phosphate
c) Dihydroxyacetone phosphate
d) Pyruvate
e) PEP
96. Human liver usually produces
glucose during prolonged fasting from:
a) Palmitic
acid and alanine
b) Glycerol and
lactate
c) Leucine and Serine
d) Galactose and fructose
e) Lactate and acetyl CoA
97. The Electron Transport
Chain:
a) Produces
ATP at substrate level
b) Produces 3 ATP's per FADH2
c) Gets NADH and FADH2
from beta oxidation and TCA cycle d)
Occurs in the mitochondrial matrix
e) Is inhibited by carnitine
98. The Hexose Monophosphate Shunt:
a) Is
the same as PPP
b) Releases CO2
c) Produces NADPH
d) Is active in the adrenal cortex
e) All of the above
is correct
99. Phosphofructokinase-1:
a) Allosteric
enzyme
b) Activated by ATP
c) Catalyses a reversible step
d) Produces fructose 2,6
bisphosphate
e) All of the above is correct
100. Type 1 glycogen
storage disease:
a) Is
known as Cori's disease
b) Is associated with cardiomegally
c) Causes hyperglycemia
d) Is known as McArdle's disease
e) None of the above
101. In the TCA cycle:
a) Malate
dehydrogenase catalyzes a reversible reaction
b) Malonate is an intermediate
c) Two ATP molecules are produced
d) All reactions are reversible
e) All intermediates are
phosphorylated
102. In gluconeogenesis:
a) Lactate
comes from the RBC's and the brain
b) Glycerol is produced from TAG in
the adipose tissue
c) Linolenic acid is a substrate
d) The rate of glucose production
increases during the fed state
e) B is the only correct answer
103. Glycogenolysis:
a) Is
synthesis of glucose from non carbohydrates
b) Produces fructose 1 phosphate
c) Is a cytosolic pathway
d) Is active in the fed state
e) Require glycogen synthase
104. In galactosemia:
a) Galactosuria
is the most serious maifestation
b) Cataract results from
accumulation of galactose in the lens
c) Galactose is converted to
galactitol
d) The liver function can be
seriously affected as a result of phosphate
depletion
e) Both C and D are correct
105. Oxidative PPP:
a) Needs
F6P as Substrate
b) Is activated by high levels of
NAP+
c) Catalyzes conversion of G6P to
F6P
d) Is important in muscle during
exercise
e) Is active in the fasting state
106. The TCA Cycle:
a) Provides
Acetyl CoA for Ketone Body Synthesis
b) Is inactive in the absence of
Oxygen
c) Converts all amino acids to
Glucose by Gluconeogenesis
d) Is blocked by excessive
Beta-Oxidation
e) Can convert Oxaloacetate to
Pyruvate
107. Glucose-6-Phosphatase
Deficiency:
a) Is
known as Von Gierke's Disease
b) Is associated with Hypoglycemia
c) Inhibits Glycogenolysis &
Gluconeogenesis in the liver
d) Is associated with Hyperuricemia
e) All of the above is correct
108. The following is required in
both Glycogenesis and Glycogenolysis:
a) CTP
b) Phosphoglucomutase
c) Glucose residues are added to
the reducing end of Glycogen d) Glycogen
Synthase
e) Insulin
109. The Liver:
a) Has
a high capacity for Fatty Acid Oxidation
b) Can produce Glucose from
Glycerol
c) Is the only site for Ketogenesis
d) Activates acetoacetate to
acetoacetyl CoA
e) D is the only wrong answer
110. In the fed state, glucose
reaching the liver has the following fates:
a) Is
converted into Glycogen
b) May be converted into
Triacylglycerols
c) Is oxidized to produce ATP
d) Is oxidized via PPP to generate
ribose and NADPH
e) All of the above is correct
111. In the well-fed state:
a) There
is high glucose level in the portal blood
b) There is high chylomicrons in
the portal blood
c) Hexokinase is very active in the
liver
d) Lipogenesis is active only in
adipose tissue
e) The liver converts Lactate to
Fatty Acids
112. The following liver enzymes
have decreased concentration in the fasting state:
a) G-6-Phosphatase
b) Phosphoenolpyruvate
Carboxykinase
c) F1,6-Bisphosphate
d) G-6-P Dehydrogenase
e) Pyruvate Carboxylase
113. Metabolism of major fuels
(glucose, fatty acids, amino acids) mostly culminate in:
a) Glucose-6-Phosphate
b) Pyruvate
c) Oxaloacetate
d) Acetyl CoA
e) Fumerate
114. In the fed state, glucose
reaching the liver has the following fates:
a) Is
converted into Glycogen
b) May be converted into Triacylglycerols
c) Is oxidized to produce ATP
d) Is oxidized via PPP to generate
ribose and NADPH
e) All of the above is correct
115. Glycogen synthesis:
a) Is a reversible pathway
b) Is a mitochondrial pathway
c) Is activated during the fasting
state
d) Occurs in the
liver and muscle
e) Produces Uridine Diphosphate
from Glycogen
116. Fructose 2,6 bisphosphate:
a) Is
not a glycolytic intermediate
b) Activates phosphofructokinase 1
c) Is synthesized by
phopshofuctokinase 2
d) Inhibits fructose 1,6 bisphosphate
e) All of the above
is correct
117. In glycogen storage
diseases:
a) Fatigability and muscle cramps
are main features of Von Geirke's disease
b)
Hypoglycemia is the main feature of type V
c) Type II is
associated with glucose 6 phosphatase deficiency
d) Type IV is due to
deficiency of the branching enzyme
e) Hepatomegally is the main
feature of all types
118. The following enzyme requires
biotin as a coenzyme:
a)
Fructose 1,6-bisphoshate
b)
Pyruvate kinase
c) PEP carboxykinase
d) Pyruvate carboxylase
e) Malate dehydrogenase
119. All the following
enzymes are present in the liver and muscle except:
a)
Pyruvate Carboxylase
b)
Glycogen Synthase
c) Lactate
Dehydrogenase
d) Pyruvate Dehydrogenase
e) Glucose-6-Phosphatase
120. The Pyruvate Dehydrogenase
Complex:
a) Requires
pyridoxal phosphate
b) Deficiency results in pernicious
anemia
c) Is inactive when Vitamin B1 is
deficient
d) Catalyzes a carboxylation
reaction
e) Is a key enzyme in the Red Blood
Cell
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