Carbohydrates Flashcards

1
Q
In what tissue do we find the enzyme glucose-6-phosphatase
Select one:
a. Muscle
b. Liver
c. Adipose, liver and muscle
d. Adipose tissue
A

b. Liver

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q
What type of carbohydrate is cellulose?
Select one:
a. A simple sugar
b. A disaccharide
c. A polysaccharide
d. A monosaccharide
A

c. A polysaccharide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q
Sucrose comprises of a
Select one:
a. a glucose and a glucose molecule
b. a glucose and a galactose molecule
c. a glucose and a fructose molecule
d. a fructose and a fructose molecule
A

c. a glucose and a fructose molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q
How is a polysaccharide made?
Select one:
a. dehydration synthesis
b. glycolysis
c. beta oxidation
d. hydrolysis
A

a. dehydration synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q
Ca++ and Mg+ contribute to regulation of PDH by activating ­­­­­­­­­­­­­­\_\_\_\_\_\_\_\_\_\_\_ and inhibiting \_\_\_\_\_\_\_\_\_.
Select one:
a. PDH phosphatase, PDH kinase 
b. PDH kinase, glycogen phosphorylase
c. PDH kinase, lactate dehydrogenase
d. PDH mutase, PDH kinase
A

a. PDH phosphatase, PDH kinase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q
How much glycogen can we store in our liver?
Select one:
a. 200 g
b. 400 g
c. 100 g
d. 10 g
A

c. 100 g

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q
What is McArdles disease?
Select one:
a. The inability to undertake glycogenolysis
b. Lack of glycogen stores in the muscle
c. Reduced blood glucose
d. The inability to undertake glycolysis
A

a. The inability to undertake glycogenolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q
For the average individual, how much glycogen can be stored in the muscle?
Select one:
a. 30 – 50 g
b. 800 – 1000 g
c. 80 – 100 g
d. 300 – 500 g
A

d. 300 – 500 g

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q
Glycogen is formed from glucose, catalysed by which enzyme?
Select one:
a. phosphofructokinase
b. Phosphorylase
c. Glycogen synthase 
d. phosphoglucomutase
e. Hexokinase
A

c. Glycogen synthase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q
Glycogen phosphorylase is inactivated by
Select one:
a. Intramuscular creatine kinase      
b. ATP
c. Ca++         
d. All of the above
A

b. ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
How long do glycogen stores last during hard exercise?
Select one:
a. 0.5-1 hour
b. 4-5 hours
c. 3-4 hours
d. 1-2 hours
A

d. 1-2 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
What does glycogen synthase do?
Select one:
a. Converts glycogen to glucose
b. Converts glucose to glycogen
c. Converts glucose to pyruvate
d. Converts pyruvate to lactate
A

b. Converts glucose to glycogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
The hormone that stimulates glycogenolysis and gluconeogenesis is:
Select one:
a. Glucagon 
b. Insulin
c. Somatostatin
d. Secretin
A

a. Glucagon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q
Glut4 translocation is stimulated by
Select one:
a. AMP and Acetyl CoA 
b. insulin and phosphate
c. ATP and Ca++ 
d. Ca++ and insulin
A

d. Ca++ and insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q
Phosphorylation of glucose to glucose-6-phosphate in the liver is catalysed by
Select one:
a. Phosphofructokinase
b. Myokinase
c. Glucokinase
d. Hexokinase
A

c. Glucokinase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q
Pyruvate dehydrogenase activity is not regulated by
Select one:
a. Acetyl CoA
b. ATP        
c. Citrate
d. NADH
A

c. Citrate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q
Pyruvate dehydrogenase is regulated by
Select one:
a. Allosteric regulation
b. Substrate availability
c. Product inhibition
d. All answers are correct
A

d. All

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q
Which hormone is responsible for the transport of glucose into cells?
Select one:
a. glucagon
b. insulin
c. catecholamine
d.  albumin
A

b. Insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Which of the following is true?
Select one:
a. Pyruvate can diffuse across membranes without a transporter
b. Pyruvate is present in the mitochondrial matrix only
c. Pyruvate is decarboxylated to acetyl-coA by PDH
d. Pyruvate is a two carbon molecule

A

c. Pyruvate is decarboxylated to acetyl-coA by PDH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q
During prolonged exercise blood glucose uptake by skeletal muscle is:
Select one:
a. 1g/min
b. 0.1g/min
c. 10g/min
d. 80g/min
A

a. 1g/min

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What effect would an increase in glycogenolysis have on glucose uptake and why?

A

 More glycogenolysis = increased glucose-6-phosphate
 Increased levels of glucose -6-phosphate inhibit the enzyme hexokinase.
 Glucose uptake will decrease because there is a large amount of glucose-6-phosphate.
 Therefore, there is less glucose uptake into the cell.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

During exercise PDH is activated, describe how.

A

 PDH active form can be activated by PDH phosphatase.
 You get more active PDH when there are large amounts of pyruvate, CoA and NAD+ (metabolites) and the product amounts are low: acetyl-CoA, NADH and CO2
 Calcium is also a stimulant as it is released during muscle contraction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What are the three main disaccharides, the monosaccharides that make them up and the enzymes which hydrolyze them.

A

 Maltose: glucose and glucose, hydrolyzed by maltase
 Lactose: glucose and galactose, hydrolyzed by lactase
 Sucrose: glucose and fructose, hydrolyzed by sucrase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the benefit of having different membrane transporters for glucose and fructose and what are they?

A

 Into the enterocytes: glut 2 or SGLT1: glucose, glut 5: fructose
 Into blood: glut2 for both
 Into the brain: glut 1
 Important to have both as it means that more ‘sugar’ can be absorbed than if they used the same transporter.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What are the two forms of starch in the human diet, what is their prevalence and how do they differ?
 Amylose (15-20% in diet) Amylose is straight chain and only has 1,4 bonds.  Amylopectin (80-85% in diet). Amylopectin is branched and has two types of bonds (1,4 and 1,6).
26
Which of the following cannot be formed from pyruvate in human beings? a. Glucose b. Fructose c. Lactic acid d. Linoleic acid
d. Linoleic acid
27
The series of reactions involving the conversion of glucose to pyruvate is known as
Glycolysis
28
Which of the following is a feature of aerobic metabolism? a. Little or no oxygen is consumed b. Lactic acid is a major byproduct c. Energy is produced more slowly than in anaerobic metabolism d. Pyruvate is converted to glucose by reverse glycolysis to yield a net of 2 ATPs
c. Energy is produced more slowly than in anaerobic metabolism
29
Your roommate is participating in a weightlifting course and complains of a burning pain during workouts. You explain to that the rapid breakdown of glucose in his muscles produces large amounts of pyruvate, which the muscle converts to.....
Lactate
30
Which of the following is not a possible fate of metabolized glucose? a. Urea b. Acetyl CoA c. Amino acids d. Muscle glycogen
Urea
31
Which of the following nutrients can be made from compounds composed of 2-carbon skeletons? a. Glucose b. Fructose c. Glycogen d. Fatty acids
d. Fatty acids
32
Which of the following is a possible fate of acetyl CoA? a. Degradation to urea b. Synthesis to glycerol c. Synthesis to fatty acids d. Degradation to ammonia
c. Synthesis to fatty acids
33
An immediate consequence of a cellular deficiency of oxaloacetate is a slowing of.....
The TCA Cycle
34
In addition to energy, what are the principal end products of cellular oxidation of carbohydrates?
Water and carbon dioxide
35
Which of the following products is not generated via the TCA cycle or electron transport chain? a. Water b. Energy c. Ammonia d. Carbon dioxide
c. Ammonia
36
Products from the electron transport chain pathway include all of the following except a. CO2. b. urea. c. water. d. energy.
b. urea.
37
Outline the metabolic fates of pyruvate (produced in glycolysis).
Converted to lactate in anaerobic conditions. Converted to acetyl CoA in aerobic conditions, and then metabolised to CO2 in the TCA cycle.
38
Total energy yield of one ATP? (aerobic)
30 ATP + 2 GTP
39
What ensures the TCA cycle is driven in the correct direction?
Three of the enzyme stages are irreversible.
40
What is the beta oxidation pathway?
Pathway for fatty acid metabolism.
41
Products of beta-oxidation?
>fatty acid CoA (which re-enters the pathway to be broken down further)... >...and acetyl CoA (which goes to the TCA cycle).
42
Which enzyme, involved in glycogen breakdown, is present in the liver but not in muscles?
glucose-6-phosphatase
43
Why is glucose-6-phosphatase not present in muscles?
The liver has this enzyme, and so can break down glucose-6-phosphatase into glucose, which can be released into the blood. Muscle cells cannot do this, and so do not contribute to blood glucose concentration..
44
Benefit of glycogen branching?
Allows enzymes to cleave off entire branches. Also more ends to cleave from, so faster release.
45
How does glycogenolysis continue in prolonged exercise, without the need for hormonal interaction?
ATP conc is reduced and AMP conc rises. AMP is an allosteric activator of glycogen phosphorylase. (ATP is an allosteric inhibitor, so when energy levels are high, glycogenolysis is inhibited).
46
What is gluconeogenesis, and where does it take place?
Synthesis of glucose from non-carbohydrate sources. Takes place in the liver, in periods of carbohydrate deprivation.
47
In gluconeogenesis, what can and cannot be used as the substrate?
Sources include lactate, glycerol, glucogenic amino acids (all except leu, lys). NOT FATTY ACIDS- because link reaction is completely irreversible.
48
Why is gluconeogenesis not simply the reversal of glycolysis?
There are 3 irreversible reactions in glycolysis that must be bypassed.
49
What type of oxidation is the most efficient way of using O2 to produce energy
Glucose oxidation
50
How much energy does 1 oxygen molecule burn
5 Kcals
51
Explain why we need to maintain glucose levels (for the brain)
glucose is the primary fuel source for brain cells, as well as neurotransmitter synthesis
52
Which glucose transporter is present in the blood-brain barrier? a. glut 1 b. glut 2 c. glut 4 d. glut 5
a. glut 1
53
Which glucose transporter is present in the neuron? a. glut 1 b. glut 2 c. glut 3 d. glut 5
c. glut 3
54
Which glucose transporter is present in the muscle cell? a. glut 1 b. glut 2 c. glut 4 d. glut 5
c. glut 4
55
which hormone causes glut 4 translocation in the muscle
insulin
56
Muscle contraction can also stimulate GLUT4 translocation to plasma membrane. What are the two suggested signals
Calcium | AMP
57
For storage, what is glucose-6-phosphate converted into
glucose-1- phosphate (G1P) by phophoglucomutase
58
What is the purpose of UDP glucose
to bind to pre-existing glycogen to release UDP
59
What can activate PKA to deactivate glycogen synthase (3 things)
Ca2+, Adrenaline and Glucagon
60
When glycogen synthase (inactive) is phosphorylated into its active form, what happens in terms of glucose/glycogen
G-6-P is converted into glycogen
61
When glycogen synthase (active) is dephosphorylated into its active form, what happens in terms of glucose/glycogen
Glycogen is converted to g-6-p
62
``` At rest, glucose uptake is: a. 0.1 g/min B. 1 g/min c. 0.5 g/min d. 100 g/min ```
a. 0.1 g/min
63
Liver glycogenolysis and glucose output is what during prolonged exercise: a. 10 g/min b. 1 g/min c. 2 g/min d. 0.1 g/min
b. 1 g/min
64
Why does liver glycogenolysis/glucose output increase during prolonged exercise?
* AMP- the more the more glycogenolysis | * Glycogen P is activated by the presence of Ca and adrenaline
65
Which of the following is true: a. When liver glycogen decreases, blood glucose decreases, so blood glucose uptake increases. b. When liver glycogen increases, blood glucose decreases, so blood glucose uptake decreases. c. When liver glycogen decreases, blood glucose increases, so blood glucose uptake increases. d. When liver glycogen decreases, blood glucose decreases, so blood glucose uptake decreases.
When liver glycogen decreases, blood glucose decreases, so blood glucose uptake decreases.
66
How long does the glycolytic flux remain elevated for, after exercise? a. 24 hours b. 48 hours c. 72 hours d. It's not raised in the first place
b. 48 hours
67
During exercise what does CHO oxidation increase up to roughly: a. 1 g/min b. 2 g/min c. 5 g/min d. 10 g/min
b. 2 g/min