Biologcal Molecules - Carbohydrates Flashcards

1
Q

Carbohydrates are made up of what three elements?

A

Carbon
Hydrogen
Oxygen

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

What is carbohydrate structure based on?

A

Units, monomers, which can join together to form diners & polymers

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

What is the monomer (single unit) of carbohydrates?

A

The monosaccharide

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

Monomer =
Dimer =
Polysaccharide =

A

Monosaccharide
Disaccharide
Polymer

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

Explain sugars within carbohydrates

A

They are monosaccharides and disaccharides
Their characteristics is tasting sweet and being soluble in water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are complex carbohydrates within carbohydrates?

A

Polysaccharides
Their characteristics are being not sweet tasting and being insoluble in water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Give examples of monosaccharides

A

A glucose, B glucose, fructose, Ribose & deoxyribose

(Only need to fully know about A glucose and Ribose)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Why is glucose the most important carbohydrate in our bodies?

A

Because it is used by the cells as a respiratory substrate.
This means it is gradually broken down, inside cells, to release energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why is glucose an example of a hexose sugar?

A

Because it has 6 carbon atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the two isomers of glucose?

A

Alpha glucose and Beta glucose
(Fructose is also an isomer of glucose)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What’s an isomer?

A

Two molecules with the same molecular formula but differ structurally

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are the structural rules to remember or monosaccharides?

A
  • 6 carbon atoms
  • at carbon atom 1, hydrogen is Above for Alpha (whereas Beta hydrogen is Below)
  • Fructose is still a hexose even though it is not a “hexagon” based shape because it has 6 carbon atoms
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Why are glucose molecules polar & soluble in water ?

A

Due to the hydrogen bonds that form between the hydroxyl groups and water molecules.

The solubility in water is important because it means glucose is dissolved in the cytosol of the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are Penrose sugars & give examples

A

Sugars with 5 carbons

Very important ones are ribose and deoxyribose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Go draw the Alpha glucose structure

A

(Answer in biology book online)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Go draw the structure of ribose

A

(Answer in the biology book)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

where is ribose found?

A

In the RNA (ribonucleic acid)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What are the differences between ribose and deoxyribose?

A
  • when compared with deoxyribose it can be seen that there is a difference at carbon 2
  • deoxyribose has a hydrogen atom instead of a hydroxyl group at C2 - it has one less oxygen atom
  • compared to ribose it it deoxygenated - hence the term deoxyribose
  • deoxyribose is the sugar found in DNA : (deoxyribonucleic acid)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Give examples of hexose and the amount of carbon atoms

A

6 CARBON ATOMS

Alpha glucose
Beta glucose
Fructose
Galactose

20
Q

Give examples of pentose + amount of carbon atoms

A
  • ribose
  • deoxyribose
21
Q

Give examples of triode and the amount of carbon atoms

A
  • triose phosphate
  • glycerine 3 phosphate
22
Q

Why is glucose a monosaccharide?

A

As it cannot be broken down further by hydrolysis

23
Q

Monomers and monosaccharides can be joined to form what?

A

Diners & Disaccharides

24
Q

Explain a condensation reaction?

A
  • in order for the two monosaccharides to join together this way, a bond has to form
  • this bond is achieved when the hydroxyl group at carbon 1 of one monosaccharide and the hydroxyl group of carbon atom 4 of the other monosaccharide react together
  • between them, the two hydroxyl groups donate to hydrogen atoms, and one oxygen atom, the atoms combine together to make H2O water
25
Q

What does the 1-4 glycosidic bond mean?

A

It refers to the number of the carbon atom within the molecules between which the bond is formed

So carbon one of one glucose is joined to carbon four of the other glucose

26
Q

What happens in a condensation reaction?

A

Glycosidic (covalent) bond is formed

Water is eliminated (released)

27
Q

What happens in the hydrolysis reaction?

A
  • glycosidic (covalent) bond broken
  • water used up
28
Q

What are the disaccharides made of?

A

MALTOSE : a glucose + a glucose

SUCROSE : a glucose + fructose

LACTOSE : a glucose + galactose

29
Q

What’s sucrose?

A

A disaccharide which is made from monosaccharides which are different to one another is sucrose

30
Q

What are polysaccharides?

A

We have already seen that monosaccharides can undergo condensation reactions to become disaccharides

Further condensation reactions with more monosaccharides will build up a carbohydrate, polymer or polysaccharide

Important polysaccharides are : starch, glycogen, and cellulose 

31
Q

What is starch and what are the two types?

A

Starch is a polymer of glucose molecule made by plants

The two types of glucose polymers within starch are amylose and amylopectin

Many alpha glucose molecules can be joined by Glycosidic bonds to form two slightly different polysaccharides known collectively as starch .

32
Q

What are the features of amylose?

A
  • linear chains
  • coil up into a helix
  • helix maintained by hydrogen bonds
  • joined by 1-4 glycosidic bonds (no branches)
33
Q

What are the features of amylopectin?

A

Joined together by 1-4 glycosidic bonds with some branching achieved by 1-6 glycosidic bonds

34
Q

What is glycogen?

A

Is a polymer of glucose molecules made by animals

It was joined by a 1-4 glycosidic bonds with frequent branching achieved by a 1-6 glycosidic bonds

It is very similar to amylopectin in structure

35
Q

Glycogen is stored in liver / muscle cells

Why do we store it as glycogen instead of glucose?

A
  • it is insoluble, so it does not affect water potential of cells (doesn’t affect osmosis)
  • It is compact, so a lot of glucose can be stored in a small place
  • It is a branched molecule, so there’s a lot of “ends” where glucose can be quickly released when needed
36
Q

What is needed to convert glucose to glycogen and vice versa?

A

GLUCOSE TO GLYCOGEN:
Insulin is needed

GLYCOGEN TO GLUCOSE:
Glucagon is needed

Glucose is a soluble monosaccharide found in the blood
Glycogen is insoluble and found in the liver & muscle cells

37
Q

What is glucose?
And how do the levels in the blood work?

A
  • glucose is used as a respiratory substrate it is broken down during respiration to release energy
  • our diet supplies the respiratory substrate we require to stay alive. During digestion, the carbohydrate components of a diet, a broken down into simple sugars, including glucose.
  • Some of those glucose will be used up immediately within respiring cells. There must always be enough glucose in the blood sustain the respiring cells. (Particularly brain cells.)
  • However, too much glucose in blood is harmful to brain cells, the retinas, and the glomerulus (filtering unit within the kidney) so it is important to keep the levels of glucose in the blood within a range of narrow parameters
  • When blood glucose levels are high, for example, after carbohydrate rich meal, glucose is taken it out of the blood and converted into glycogen

When blood glucose levels are low, for example, after a timer fasting like sleep or after a long period of exercise, glycogen is broken down into glucose, which is then released into the bloodstream

38
Q

What is cellulose?

A

Selling those is made up of beta glucose molecules. This has implications on the orientation of the glucose molecules within the polysaccharide chain.

39
Q

Explain the structure of beta glucose on the polysaccharide chain

A

When beta glucose molecules which are orientated in the same way, I’m not place together. It is not possible to make a Glycosidic bond. This is because the two hydroxyl groups are not increase proximity with one another.

But when alternate beta glucose molecules are flipped over by 180°, then the two hydroxyl groups are brought together. Every other one is flipped over.

This allows condensation reactions to occur from Glycosidic bonds. These are 1-4 glycosidic bonds

40
Q

Explain how fibrils are made

A

Cellulose molecules do not coil. They live straight because the glucose monomers contains so many hydroxyl groups lots of hydrogen bonds form between neighbouring cellulose molecules.

This produces bundles of 60 to 70 cellulose molecules, laying side-by-side all held together by thousands of hydrogen bonds

These bundles are called fibrils

(Hydrogen bonds form in cross bridges between cellulose molecules)

41
Q

How are fibres made?

A

The cellulose molecules bundle together to make fibrils, these are maintained by hydrogen bonds

The fibrils bundle together to make fibres more hydrogen bonding maintains these. You can see the fibres in micrographs of cellulose cell walls.

42
Q

Why are cellulose fibres so strong?

A

They are very strong because of all the hydrogen bonds

The cellulose fibres are embedded in pectins to form the cell wall
(Proteins that act as a glue)

I live in criss-crossing, layers for extra strength from busting on water moves into it by osmosis - it has to be able to stand turgor pressure

43
Q

How are the cellulose fibres fully permeable?

A

There are gaps between the cellulose fibres, which account for it being fully permeable

44
Q

Why is cellulose difficult to digest?

A

Cellulose is difficult to digest because mamusia do not make the enzyme cellulase- this is the enzyme which is required to break beta 1-4 glycosidic bonds because 1-4 glycosidic bonds don’t fit through the amylase enzyme

45
Q

FOR AMYLOSE GIVE:

The monosaccharide from which it is formed

Types of glycosidic bonds

Overall shape

Solubility

Function

Hydrogen bonding within or between molecules

A

Alpha glucose

A 1-4

Helix

Insoluble

Energy store in plants

Hydrogen bonds between sugar units in the chain

46
Q

FOR CELLULOSE GIVE:

The monosaccharide from which it is formed

Types of glycosidic bonds

Overall shape

Solubility

Function

Hydrogen bonding within or between molecules

A
  • Beta glucose
  • B 1-4
  • straight chain
  • insoluble
  • forms cell walls
  • hydrogen bonds between sugar units in different chains
47
Q

FOR GLYCOGEN GIVE:

The monosaccharide from which it is formed

Types of glycosidic bonds

Overall shape

Solubility

Function

Hydrogen bonding within or between molecules

A
  • a glucose
  • a 1-4 with a 1-6 at branches
  • branched and slightly coiled
  • insoluble
  • an energy store in animal cells
  • some hydrogen bonds between sugar units in the chain