Carbohydrate Metabolism Flashcards

(73 cards)

1
Q

Organic molecules made up of carbon, hydrogen and oxygen atoms are called?

A

Carbohydrates

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2
Q

The two major types of carbohydrates include both?

A

Simple sugars

Complex sugars

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3
Q

Simple sugars are made up of?

A

Glucose and fructose etc

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4
Q

Complex sugars are made up of?

A

Starch
Glycogen
Cellulose

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5
Q

The classification of carbohydrates are?

A

Monosaccharides
Disaccharides
Oligosaccharides
Polysaccharides

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6
Q

Complex sugars are also called?

A

Polysaccharides

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7
Q

Polysaccharides are made up of multiple?

A

Monosaccharides

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8
Q

The two major functions of polysaccharides are?

A

Serve as energy storage (starch and glycogen)

Serve as structural components (chitin & cellulose)

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9
Q

Salivary amylase digests polysaccharides into?

A

Smaller oligosaccharides

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10
Q

Maltose is broken down into__1__ & __2__ by __3__

A
  1. Glucose
  2. Glucose
  3. Maltase
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11
Q

Lactose is broken down into__1__ & __2__ by __3__

A
  1. Galactose
  2. Glucose
  3. Lactase
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12
Q

Sucrose is broken down into__1__ & __2__ by __3__

A
  1. Fructose
  2. Glucose
  3. Sucrase
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13
Q

Amylase is denatured in the stomach by?

A

HCl

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14
Q

The dietary carbohydrates are the?

A

Monosaccharides

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14
Q

The dietary carbohydrates are the?

A

Monosaccharides
Disaccharides
Polysaccharides

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15
Q

Three examples of Monosaccharides are?

A

Glucose
Fructose
Galactose

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16
Q

The process by which cells break down fuel molecules through different metabolic pathways to transfer their energy into high energy compounds is called?

A

Cellular respiration

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17
Q

Examples of high energy compounds are?

A
ATP
GTP
NADH
FADH2
NADPH
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18
Q

ATP means?

A

Adenosine-5-triphosphate

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19
Q

GTP means?

A

Guanosine-5-triphosphate

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20
Q

NADH means?

A

Reduced nicotinamide adenine dinucleotide

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21
Q

FADH2 means?

A

Reduced flavin adenine dinucleotide

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22
Q

NADPH means?

A

Reduced nicotinamide adenine dinucleotide phosphate

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23
Q

Why is glucose the body’s most readily available source of energy?

A

It is relatively rich in potential energy(energy stored in chemical bonds)
It supplies a huge array of metabolic intermediates for biosynthetic reactions
It can be used to produce ATP aerobically or anaerobically from its intercellular storage polymers

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24
Glucose has three major pathways of utilisation, namely?
Glucose to pyruvate(oxidation via glycolysis) Glucose to ribose-5-phosphate & NADH(oxidation via PPP) Glucose to polysaccharides
25
What stores excess glucose as glycogen in the liver?
Hepatocytes
26
In glycolysis, a molecule of glucose is converted into?
Two molecules of pyruvate
27
In glycolysis, some of the free energy released from glucose is conserved in the form of?
ATP | NADH
28
The two phases of glycolysis are?
Preparatory phase | Pay-off phase
29
In the preparatory phase of glycolysis, how many molecules of ATP are used?
2
30
In the pay-off phase of glycolysis, how many molecules of ATP are produced?
4
31
The net yield of glycolysis is?
2 ATP | 2 NADH
32
Examples of Phosphorylated derivatives of hexose sugars are?
D-fructose D-mannose D-galactose
33
Hexoses can enter into the glycolytic pathway by being converted into?
A Phosphorylated derivative
34
D-fructose is present in its free from in?
Fruits
35
D-fructose is formed from the ____ in the small intestine
Hydrolysis of sucrose
36
D-fructose is phosphorylated by__1__ to give__2__
1. Hexokinase | 2. fructose-6-phosphate
37
The metabolism of D-fructose occurs in the?
Muscle Kidney Liver
38
In the liver, fructose is phosphorylated by __1__ to give __2__
1. Fructokinase | 2. Fructose-1-phosphate
39
Fructose -1-phosphate is converted into __1__ & __2__ by Fructose -1-phosphate aldolase
1. Glyceraldehyde | 2. Dihydroxyacetone phosphate
40
Phosphorylated derivatives are also called?
Intermediates of the glycolytic pathway
41
Dihydroxyacetone phosphate is converted into __1__ by the glycolytic enzyme __2__
1. Glyceraldehyde-3-phosphate | 2. Triose phosphate isomerase
42
Glyceraldehyde is converted into glyceraldehyde-3-phosphate by?
ATP & triose kinase
43
Fructoses enter the glycolytic pathway at step ___ of glycolysis
5
44
Fructoses enter the glycolytic pathway as?
Fructose-6-phosphate and glyceraldehyde-3-phosphate
45
D-mannose can be found in?
Glycoproteins of food | Various polysaccharides
46
D-mannose is phosphorylated by __1__ to give __2__
1. Hexokinase | 2. Mannose-6-phosphate
47
Mannose-6-phosphate is isomerized by ___ to give fructose-6-phosphate
Phosphomannose isomerase
48
Mannose enters the glycolytic pathway at step __ of glycolysis
3
49
Mannose enters glycolysis as?
Fructose-6-phospate
50
Galactose is converted into glucose in the ____ pathway
Leloir
51
Galactose is converted into galactose -1-phosphate by?
Galactokinase
52
UDP galactose is converted into UDP glucose by?
UDP glucose epimerase
53
galactose -1-phosphate is converted into UDP galactose by?
Galactose-1-phosphate uridyltransferase
54
3 problems of galactose metabolism are?
Galactose-1-phosphate uridyltransferase deficiency Galactokinase deficiency Uridine diphosphate-galactose-4-epimerase deficiency
55
The inability of the body to use galactose to produce energy is called?
Galactosemia
56
Galactosemia is a rare disease in?
Infants
57
Classical Galactosemia is caused by the deficiency of?
Galactose-1-phosphate uridyltransferase
58
Galactosemia is inherited as ?
Autosomal recessive disorder
59
Mutation in the ___ on chromosome 9 is responsible for galactosemia
GALT gene
60
Increased galactose levels in the urine is called?
Galactosuria
61
Accumulated galactose is diverted for the production of___ by the enzyme aldol reductase
Galactitol
62
Galactitol has been implicated in the development of?
Cataract
63
Galactitol and galactose-1-phosphate accumulation in body tissues leads to ___ in their functions
Impairment
64
Four clinical symptoms of galactosemia are?
Jaundice Mental retardation Weight loss(infants) Cataract (severe cases)
65
The diagnosis of galactosemia is done by measuring galactose-1-phosphate uridyltransferase activity in the?
Erythrocytes
66
The treatment of galactosemia is carried out by?
Supplying diet lacking in galactose and lactose
67
Galactokinase deficiency or GALK is caused by?
Mutation of GALK1 gene
68
GALK symptom is?
Cataract
69
GALK is treated by?
Eating food lacking galactose and lactose
70
Uridine diphosphate galactose-4-epimerase deficiency (GALE) symptoms are?
Cataracts Liver disease Kidney problems
71
GALE is caused by?
Mutation in GALE gene
72
Non- classical galactosemia is caused by?
Deficiency of UDP galactose-4-epimerase