Biological Molecules

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Last updated 9:59 AM on 11/4/25
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41 Terms

1
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What are monomers and polymers?

Monomers - smaller, repeating molecules / units from which larger molecules / polymers are made

Polymers - molecules made from many (a large number of) identical / similar monomer molecules

2
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What happens in condensation reactions

● 2 molecules join together

Forming a chemical bond

Releasing a water molecule

3
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What happens in hydrolysis reactions

● 2 molecules separated

Breaking a chemical bond

Using a water molecule

4
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Give examples of polymers and the monomers from which they’re made

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5
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What are monosaccharides? Give 3 common examples

Monomers from which larger carbohydrates are made

● Glucose, fructose, galactose

6
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Describe the structure of α-glucose

Left - full structure, carbon atoms labelled

Right - simplified structure as in the specification to be memorised for exam

<p>● <strong>Left </strong>- full structure, carbon atoms labelled</p><p> </p><p>● <strong>Right </strong>- simplified structure as in the specification to be memorised for exam</p>
7
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Describe the difference between the structure of α-glucose and β-glucose

Isomers - same molecular formula but differently arranged atoms

OH group is below carbon 1 in α-glucose but above carbon 1 in β-glucose

8
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What are disaccharides and how are they formed?

Two monosaccharides joined together with a glycosidic bond

● Formed by a condensation reaction, releasing a water molecule

9
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List 3 common disaccharides & monosaccharides from which they’re made

Maltose = Glucose + glucose

Sucrose = Glucose + fructose

Lactose = Glucose + galactose

10
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Draw a diagram to show how two monosaccharides are joined together

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11
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What are polysaccharides and how are they formed?

Many monosaccharides joined together with glycosidic bonds

● Formed by many condensation reactions, releasing many water molecules

12
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Describe the basic function and structure of starch

Energy store in plant cells

Polysaccharide of α-glucose

● Some has 1,4-glycosidic bonds so is unbranched (amylose)

● Some has 1,4- and 1,6-glycosidic bonds so is branched (amylopectin)

<p><u>Energy store in plant cells</u></p><p></p><p>● <strong>Polysaccharide </strong>of <strong>α-glucose</strong></p><p>● Some has <strong>1,4-glycosidic bonds</strong> so is <strong>unbranched </strong>(amylose)</p><p>● Some has<strong> 1,4- and 1,6-glycosidic bonds</strong> so is <strong>branched </strong>(amylopectin) </p>
13
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Describe the basic function and structure of glycogen

Energy store in animal cells

Polysaccharide made of α-glucose

1,4- and 1,6-glycosidic bondsbranched

<p><u>Energy store in animal cells</u></p><p></p><p>● <strong>Polysaccharide </strong>made of <strong>α-glucose</strong></p><p>●<strong> 1,4-</strong> and <strong>1,6-glycosidic bonds</strong> → <strong>branched</strong></p>
14
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Explain how the structure of starch relates to its function - amylose

Helical compact for storage in cell

Large, insoluble polysaccharide molecule → can’t leave cell / cross cell membrane

Insoluble in water → water potential of cell not affected (no osmotic effect)

15
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Explain how the structure of glycogen relates to its function - and amylopectin

Branched compact / fit more molecules in small area

Branched → more ends for faster hydrolysis → release glucose for respiration to make ATP for energy release

Large, insoluble polysaccharide molecule → can’t leave cell / cross cell membrane

Insoluble in water → water potential of cell not affected (no osmotic effect)

16
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Describe the basic function and structure of cellulose

Function

● Provides strength and structural support to plant / algal cell walls

Structure

Polysaccharide of β-glucose

1,4-glycosidic bonds so forms straight, unbranched chains

● Chains linked in parallel by hydrogen bonds, forming microfibrils

17
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Explain how the structure of cellulose relates to its function

Every other β-glucose molecule is inverted in a long, straight, unbranched chain

Many hydrogen bonds link parallel strands (crosslinks) to form microfibrils (strong fibres)

● Hydrogen bonds are strong in high numbers

● So provides strength to plant cell walls

<p>● <strong>Every other</strong> β-glucose molecule is <strong>inverted</strong> in a long, straight, unbranched chain</p><p></p><p> </p><p>● <strong>Many </strong>hydrogen bonds link parallel strands (crosslinks) to form <strong>microfibrils </strong>(strong fibres)</p><p></p><p> </p><p>● Hydrogen bonds are strong in <strong>high numbers</strong></p><p></p><p> </p><p>● So provides <strong>strength </strong>to plant cell walls</p>
18
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Identify the reducing sugars

monosaccharides, maltose, lactose

19
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Describe the test for reducing sugars

1. Add Benedict’s solution (blue) to sample

2. Heat in a boiling water bath

3. Positive result = green / yellow / orange / red precipitate

20
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Identify non-reducing sugars

sucrose

21
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Describe the test for non-reducing sugars

1. Do Benedict’s test (as above) and stays blue / negative

2. Heat in a boiling water bath with acid (to hydrolyse into reducing sugars)

3. Neutralise with alkali (eg. sodium bicarbonate)

4. Heat in a boiling water bath with Benedict’s solution

5. Positive result = green / yellow / orange / red precipitate

22
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Suggest a method to measure the quantity of sugar in a solution

● Carry out Benedict’s test as above, then filter and dry precipitate

● Find mass / weight

23
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Suggest another method to measure the quantity of sugar in a solution

1. Make sugar solutions of known concentrations (eg. dilution series)

2. Heat a set volume of each sample with a set volume of Benedict’s solution for the same time

3. Use colorimeter to measure absorbance (of light) of each known concentration

4. Plot calibration curve - concentration on x axis, absorbance on y axis and draw line of best fit

5. Repeat Benedict’s test with unknown sample and measure absorbance

6. Read off calibration curve to find concentration associated with unknown sample absorbance

<p>1. Make sugar solutions of <strong>known concentrations</strong> (eg. dilution series) </p><p>2. <strong>Heat </strong>a set <strong>volume </strong>of each sample with a set <strong>volume </strong>of <strong>Benedict’s solution</strong> for the <strong>same time</strong> </p><p>3. Use <strong>colorimeter </strong>to measure <strong>absorbance </strong>(of light) of each known concentration </p><p>4. Plot <strong>calibration curve - concentration</strong> on <strong>x </strong>axis, <strong>absorbance </strong>on <strong>y </strong>axis and draw <strong>line of best fit</strong> </p><p>5. Repeat Benedict’s test with <strong>unknown sample</strong> and measure absorbance </p><p>6. <strong>Read off</strong> calibration curve to find concentration associated with unknown sample absorbance</p><p></p>
24
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Describe the biochemical test for starch

1. Add iodine dissolved in potassium iodide (orange / brown) and shake / stir

2. Positive result = blue-black

25
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Name two groups of lipid

Triglycerides and phospholipids.

26
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Describe the structure of a fatty acid (RCOOH)

Variable R-group - hydrocarbon chain (this may be saturated or unsaturated)

● -COOH = carboxyl group

27
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Describe the difference between saturated and unsaturated fatty acids

Saturated - no C=C double bonds in hydrocarbon chain → all carbons fully saturated with hydroge

Unsaturated - one or more C=C double bond in hydrocarbon chain (creating a bend / kink)

28
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Describe how triglycerides form

1 glycerol molecule and 3 fatty acids

3 condensation reactions

● Removing 3 water molecules

● Forming 3 ester bonds 

<p>● <strong>1 glycerol</strong> molecule and <strong>3 fatty acids</strong></p><p>● <strong>3 condensation</strong> reactions</p><p>● Removing <strong>3 water molecules</strong></p><p>● Forming <strong>3 ester bonds&nbsp;</strong></p>
29
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Explain how the properties of triglycerides are related to their structure

function = energy storage

● High ratio of C-H bonds to carbon atoms in hydrocarbon chain

○ So used in respiration to release more energy than the same mass of carbohydrates

Hydrophobic / non-polar fatty acids so insoluble in water (clump together as droplets, tails inwards)

○ So no effect on water potential of cell (or can be used for waterproofing)

30
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Describe the difference between the structure of triglycerides and phospholipids

One of the fatty acids of a triglyceride is substituted by a phosphate-containing group 

<p>One of the fatty acids of a triglyceride is substituted by a phosphate-containing group&nbsp;</p>
31
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Describe how the properties of phospholipids relate to their structure

Function: form a bilayer in cell membrane, allowing diffusion of lipid-soluble (non-polar) or very small substances and restricting movement of water-soluble (polar) or larger substances.

Phosphate heads are hydrophilic

Attracted to water so point to water (aqueous environment) either side of membrane

Fatty acid tails are hydrophobic

Repelled by water so point away from water / to interior of membrane

32
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Describe the test for lipids

1. Add ethanol, shake (to dissolve lipids), then add water

2. Positive result = milky white emulsion

33
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Describe / draw the general structure of an amino acid

COOH = carboxyl group

R = variable side chain / group

H2N = amine group

<p>● <strong>COOH</strong> = carboxyl group</p><p>● <strong>R </strong>= variable side chain / group</p><p>● <strong>H2N </strong>= amine group</p>
34
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How many amino acids are common in all organisms? How do they vary?

The 20 amino acids that are common in all organisms differ only in their side group (R).

35
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Describe how amino acids join together

Condensation reaction

● Removing a water molecule

● Between carboxyl / COOH group of one and amine / NH2 group of another #

● Forming a peptide bond

<p>● <strong>Condensation </strong>reaction </p><p>● Removing a <strong>water </strong>molecule </p><p>● Between <strong>carboxyl / COOH</strong> group of one and <strong>amine / NH2</strong> group of another #</p><p>● Forming a<strong> peptide bond</strong></p>
36
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What are dipeptides and polypeptides?

Dipeptide - 2 amino acids joined together

● Polypeptide - many amino acids joined together

A functional protein may contain one or more polypeptides.

37
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Describe the primary structure of a protein

Sequence of amino acids in a polypeptide chain, joined by peptide bonds

38
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Describe the secondary structure of a protein

● Folding (repeating patterns) of polypeptide chain eg. alpha helix / beta pleated sheets

● Due to hydrogen bonding between amino acids

● Between NH (group of one amino acid) and C=O (group)

39
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Describe the tertiary structure of a protein

3D folding of polypeptide chain

● Due to interactions between amino acid R groups (dependent on sequence of amino acids)

● Forming hydrogen bonds, ionic bonds and disulfide bridges

<p>● <strong>3D folding</strong> of polypeptide chain</p><p>● Due to <strong>interactions </strong>between amino acid <strong>R groups</strong> (dependent on sequence of amino acids)</p><p>● Forming <strong>hydrogen bonds</strong>,<strong> ionic bonds</strong> and <strong>disulfide bridges</strong></p><p></p>
40
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Describe the quaternary structure of a protein

More than one polypeptide chain

● Formed by interactions between polypeptides (hydrogen bonds, ionic bonds, disulfide bridges)

<p>● <strong>More than one polypeptide</strong> chain</p><p>● Formed by interactions <strong>between polypeptides</strong> (hydrogen bonds, ionic bonds, disulfide bridges)</p>
41
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Describe the test for proteins

1. Add biuret reagent (sodium hydroxide + copper (II) sulphate)

2. Positive result = purple / lilac colour (indicating presence of peptide bonds)