Chapter 3 - Carbohydrates Flashcards

(44 cards)

1
Q

What are carbohydrates?

A

Carbohydrates are molecules which consist only of carbon, hydrogen and oxygen and they are long chains of sugar units called saccharides. There are three types of saccharides - monosaccharides, disaccharides and polysaccharides.

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2
Q

Name 3 roles of carbohydrates

A
  1. Energy storage - sugars can be stored as complex carbohydrates (eg: starch or glycogen)
  2. Structural components - cellulose and chitin are used in cell walls
  3. Building blocks for biological molecules - deoxyribose and ribose can be used to make nucleic acids
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3
Q

What are monosaccharides?

A

Monosaccharides are the simplest form of carbohydrates, also known as ‘simple sugars’. Monosaccharides are soluble, sweet-tasting and are found in many foods such as fruits, vegetables, and grains.

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4
Q

What are monosaccharides’ general formula

A

They have the general formula (CH2O)n where ‘n’ can be any number from 3 to 7.

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5
Q

How are monosaccharides classified?

A

According to the number of carbon atoms in each molecule:
Eg: hexose sugars = 6 carbon atoms
pentose = 5 carbon atoms

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6
Q

Give 3 examples of a hexose sugar

A

Glucose
Fructose
Galactose

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7
Q

Give 2 examples of a pentose sugar

A

Ribose
Deoxyribose

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8
Q

What is glucose?

A

Glucose is a hexose (6-carbon) sugar with the formula C6H12O6.
The atoms in glucose can be arranged in two different ways.
This means that there are two isomers of glucose:
Alpha-glucose (α-glucose)
Beta-glucose (β-glucose)

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9
Q

What is an isomer?

A

When the atoms in the molecule can be arranged in 2 different ways

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10
Q

What is the difference between alpha glucose and beta glucose?

A

The hydroxyl group (OH group) on carbon 1 of alpha glucose is below, whereas on beta glucose its above.

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11
Q

What are 2 features of glucose that help it function?

A
  1. It is soluble - The hydroxyl groups can form hydrogen bonds with water, so it can be transported around organisms.
  2. Its bonds store lots of energy - This energy is released when the bonds are broken.
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12
Q

How are disaccharides formed?

A

When two monosaccharides join together.

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13
Q

Give 3 examples of disaccharides

A
  1. Maltose (found in grains and cereals)
  2. Sucrose (used as a transport sugar in plants)
  3. Lactose (the main carbohydrate found in milk)
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14
Q

What is maltose is made up of?

A

Glucose joined to glucose.

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15
Q

What is sucrose is made up of?

A

Glucose joined to fructose.

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16
Q

What is lactose is made up of?

A

Glucose joined to galactose

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17
Q

How are disaccharides created and broken down?

A

Disaccharides are created via condensation reactions, and broken down via hydrolysis reactions. These reactions involve the formation or the breakdown of a covalent bond known as a glycosidic bond.

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18
Q

Describe a condensation reaction

A

When two monosaccharides join, a hydroxyl group (OH) of one monosaccharide reacts with a hydroxyl group (OH) of another monosaccharide. This forms a glycosidic bond, and a water molecule (H2O) is released.
Most of the time the hydroxyl groups on carbons 1 and 4 are reacting together, so a 1-4 glycosidic bond forms, but they can also form between other carbons.

19
Q

Describe a hydrolysis reaction

A

When a water molecule (H2O) is added to a disaccharide, the glycosidic bond is broken to release the 2 monosaccharides.

20
Q

What are polysaccharides?

A

Polysaccharides are complex carbohydrates made up of many monosaccharides joined via glycosidic bonds.

21
Q

Give three examples of polysaccharides

A
  1. starch - amylose + amylopectin
  2. glycogen
  3. cellulose
22
Q

What is starch used by?

A

Plants to store excess glucose. This means that starch can be hydrolysed back into glucose when they require energy.

23
Q

Describe the structure of starch

A

Starch is made up of many alpha-glucose monomers joined via glycosidic bonds to form chains. Starch chains come in two forms: amylose and amylopectin.

24
Q

Describe the structure of amylose

A

Amylose is a long, unbranched chain of alpha-glucose joined by 1-4 glycosidic bonds. The angles of these bonds cause the chain to coil into a helix to make a compact structure.

25
Describe the structure of amylopectin
Amylopectin is a long, branched chain of alpha-glucose joined by both 1-4 and 1-6 glycosidic bonds. Its side branches allow enzymes to hydrolyse alpha-glucose monomers easily.
26
What are features of starch that help it to function as a store of energy?
1. Insoluble 2. Large 3. Many side branches 4. Coiled 5. Hydrolysis releases alpha-glucose monomers
27
How does being insoluble help starch?
It does not affect the water potential, so water does not enter cells by osmosis.
28
How does being large help starch?
It cannot diffuse out of cells
29
How does having many side branches help starch?
These allow enzymes to hydrolyse the glycosidic bonds easily to rapidly release glucose.
30
How does being coiled help starch?
This makes it compact so that a lot of glucose can be stored in a small space.
31
How does the fact that the hydrolysis reactions releases alpha-glucose monomers help starch?
These are readily used in respiration.
32
What is glycogen used by and why?
Animals to store excess glucose. This means that glycogen can be hydrolysed back into glucose when animals require energy.
33
Describe the structure of glycogen
Made up of many alpha-glucose monomers via 1-4 and 1-6 glycosidic bonds to form highly branched chains
34
How does it help glycogen that hydrolysis easily breaks the alpha glucose monomers easily?
These are readily used in respiration
35
How does it help glycogen that it is insoluble?
doesn't affect the water potential of cells
36
How does it help glycogen that its compact?
A lot of glucose can be stored in a small space
37
How does it help glycogen that it is highly branched (more than starch)?
enzymes can easily hydrolyse the glycosidic bonds to rapidly release glucose
38
How does it help glycogen that it is large?
it cannot diffuse out of cells
39
Describe the structure of cellulose
Formed many beta glucose monomers joined together with glycosidic bonds
40
Describe how the beta-glucose molecules react together to make cellulose
If two beta-glucose monomers line up next to each other, the hydroxyl groups on carbon 1 and carbon 4 are too far from each other to react. Therefore every other beta-glucose molecule is flipped upside down. This brings the hydroxyl groups (OH) close enough together to react.
41
Describe why cellulose is strong
Many beta-glucose monomers join together form long, straight, unbranched chains. The alternating inversion of the beta glucose molecules also allows for hydrogen bonds to form between individual chains. Although each hydrogen bond itself is relatively weak, the huge number of these bonds provides great strength to cellulose as a whole.
42
Describe how microfibrils are formed
Multiple cellulose chains become tightly cross linked via hydrogen bonds to form bundles called microfibrils.
43
Describe how macrofibrils are formed
These microfibrils join together to make macrofibrils which combine to make strong cellulose fibres in the plant cell wall.
44
Describe 3 adaptions of cellulose for its role
1. Long, straight, and unbranched chains - These provide rigidity to the cell wall. 2. Hydrogen bonds - These cross link the chains to add collective tensile strength. 3. Microfibrils - These provide additional strength.