Revision Notes
OCR A Level Biology A: Nucleotides, ATP, DNA and replication (H420) – Revision Notes
Condensed revision notes on nucleotides, ATP, DNA structure, the DNA purification practical and semi-conservative replication for OCR A Level Biology A.
- Subject
- Biology
- Level
- A LEVELS
- Topic
- Nucleotides, ATP, DNA structure and semi-conservative replication
- Author
- Marlbridge Academic Team
- Updated
Aligned to OCR A Level Biology (H420), Version 4.1 (April 2026), for first assessment in 2025. Official specification .
Syllabus page (what it covers and how it is assessed): OCR A Level Biology.
Syllabus points this page covers
H420
- 2.1.3 Nucleotides and nucleic acids
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Condensed recall for OCR A Level Biology A (H420, Version 4.1, April 2026), section 2.1.3(a) to (e). For full explanations and worked examples use the study guide, then test yourself with the practice questions. Course pages: OCR A Level Biology hub and the printable checklist. If you are unsure where to start, take a free diagnostic. The genetic code, transcription and translation (2.1.3(f) and (g)) are not covered here.
2.1.3(a) Nucleotides: DNA against RNA
Each nucleotide is built from a five-carbon sugar, a phosphate and a base containing nitrogen. It is the monomer of nucleic acids.
| DNA | RNA | |
|---|---|---|
| Sugar | Deoxyribose | Ribose |
| Pyrimidines | Cytosine, thymine | Cytosine, uracil |
| Purines | Adenine, guanine | Adenine, guanine |
| Strands | Two, antiparallel, twisted | Usually one |
- Purines (A, G) have two rings. Pyrimidines (C, T, U) have one ring.
- Memory aid: “CUT the pyrimidines” (cytosine, uracil, thymine); “PURe As Gold” (adenine and guanine are purines).
- Deoxyribose has a hydrogen atom, not a hydroxyl group, on carbon 2′.
- Link to practical: OCR lists a modelling activity, investigating DNA structure using RasMol. Be able to read a molecular model.
2.1.3(b) Phosphodiester bonds
- Synthesis: condensation. 5′ phosphate of one nucleotide joins the 3′ hydroxyl of the next. One water is released per bond.
- Breakdown: hydrolysis. One water is used per bond.
- A chain of n nucleotides has n − 1 phosphodiester bonds.
- A double-stranded fragment of n base pairs has 2(n − 1) of them.
| Step | Method |
|---|---|
| 1 | Count nucleotides in one strand: n |
| 2 | Bonds in one strand = n − 1 |
| 3 | Multiply by 2 for a double helix |
| 4 | Water released or used = number of bonds |
Reminder: a 30-nucleotide chain has 29 bonds; a 30 base-pair fragment has 58.
2.1.3(c) ADP and ATP
| ADP | ATP | |
|---|---|---|
| Sugar | Ribose | Ribose |
| Base | Adenine | Adenine |
| Inorganic phosphates | 2 | 3 |
- Both are phosphorylated nucleotides.
- ATP + water → ADP + Pi releases energy (hydrolysis). ADP + Pi → ATP is phosphorylation.
- Describe ATP as a molecule that releases energy when hydrolysed, not as an energy “store” or “source of energy” without the reaction.
- Reminder calculation: a process needing 183 kJ per mole, when each mole of ATP supplies 30.5 kJ, needs at least 183 ÷ 30.5 = 6.0 mol of ATP.
2.1.3(d)(i) DNA structure
- Two polynucleotides; sugar-phosphate backbone on the outside, bases inside.
- Complementary base pairing: A to T with two hydrogen bonds; G to C with three.
- Each pair = one purine + one pyrimidine, so the width is constant.
- Antiparallel: one strand runs 5′ to 3′, the other 3′ to 5′.
- The twisting of the paired strands gives the double helix.
- Stability: many hydrogen bonds together hold the strands; the backbone is covalent.
- Weak individual hydrogen bonds allow the strands to separate for copying.
Method for hydrogen-bond questions: let a = A–T pairs and g = G–C pairs. Write a + g = total pairs and 2a + 3g = total hydrogen bonds. Solve together.
2.1.3(d)(ii) Practical: DNA purification by precipitation
| Reagent or step | Purpose |
|---|---|
| Mashing | Breaks up tissue and cell walls |
| Detergent | Dissolves phospholipids of membranes, releasing DNA |
| Salt | Masks the negative charge on phosphates so DNA clumps |
| Gentle warming | Helps detergent work; inactivates enzymes that digest DNA |
| Protease (optional) | Digests proteins bound to DNA |
| Filtering | Removes debris |
| Ice-cold ethanol layer | DNA is insoluble in ethanol and precipitates at the boundary |
| Glass rod | Spools the white strands |
Controlling variables when comparing tissues: same starting mass, same volumes, same temperature and times, same ethanol layering. Dependent variable: dried mass or length of DNA. The product is crude, with RNA and protein present.
2.1.3(e) Semi-conservative replication
Semi-conservative: each new molecule = one original strand + one new strand.
Steps:
- Helicase breaks hydrogen bonds between bases and unwinds the helix.
- Each strand is a template.
- Free nucleotides pair by complementary base pairing.
- DNA polymerase forms phosphodiester bonds, adding nucleotides at the 3′ end of the new strand.
- Two molecules, each hybrid of old and new.
- Accuracy: templates plus base pairing copy the sequence, conserving genetic information for daughter cells.
- Spontaneous mutation: random changes in base sequence that occur without a mutagen, for example a wrong nucleotide incorporated. They are random in place and time.
- At AS Level the specification does not require learners to distinguish between types of mutation.
Labelling reminder (¹⁵N heavy, ¹⁴N light): start with all-heavy; after one generation in light medium, all hybrid; after a second generation, half hybrid and half light. A conservative model predicts no hybrid band at generation one.
After n rounds from one molecule: 2ⁿ molecules, always only two containing an original strand.
Worked reminders
Yield from a purification
A sample of 15.0 g of tissue gives 4.5 mg of dried DNA.
- Yield = 4.5 ÷ 15.0 = 0.30 mg per g.
- Compare tissues by yield per gram, not by total mass, because the starting masses may differ.
- Percentage difference = (new − baseline) ÷ baseline × 100. State your baseline.
Hybrid DNA after switching medium
All-heavy bacteria (HH) are grown for one generation in light medium, then returned to heavy medium for one generation.
- After light medium: all HL.
- In heavy medium each HL splits into one HH and one HL.
- Result: half HH, half HL, no LL.
Expected mutations
Data supplied: 2.0 × 10⁶ base pairs and 1 × 10⁻⁹ errors per base pair per replication.
- Errors per replication = 2.0 × 10⁶ × 1 × 10⁻⁹ = 2.0 × 10⁻³.
- Across 10⁶ replications = 2.0 × 10³ errors.
- A rate that is tiny per replication still gives many errors in a large population.
Exam wording to use
| If the question says | Write |
|---|---|
| Describe the structure of DNA | Two antiparallel polynucleotides, sugar-phosphate backbone, complementary base pairs joined by hydrogen bonds, twisted into a double helix |
| Explain why replication is semi-conservative | Each new molecule contains one original template strand and one new strand |
| Explain the role of DNA polymerase | Joins free nucleotides by forming phosphodiester bonds on the new strand, using the template and complementary base pairing |
| Explain the role of helicase | Breaks hydrogen bonds between complementary bases so the strands separate and act as templates |
| Describe a spontaneous mutation | A random change in the base sequence that arises during replication without a mutagen |
Linking ideas across the unit
- ATP, ADP and the RNA adenine nucleotide share the same sugar and base, so you can compare them in one sentence.
- Phosphodiester bonds appear twice: in DNA synthesis by DNA polymerase and in the backbone of every polynucleotide.
- Hydrogen bonds appear twice: between complementary bases in the helix and, in replication, as the bonds helicase breaks.
- Precipitation in the practical works because of the same phosphate groups that make the backbone negatively charged.
- If a question gives numbers, write the equation you are using before you substitute, and give units.
Must-know distinctions
| Often confused | Difference |
|---|---|
| Phosphodiester bond / hydrogen bond | Covalent link between nucleotides in a strand / weak link between complementary bases across strands |
| Helicase / DNA polymerase | Breaks hydrogen bonds between bases / forms phosphodiester bonds between nucleotides |
| ADP / ATP | Two phosphates / three phosphates |
| Purine / pyrimidine | Two rings / one ring |
| Condensation / hydrolysis | Water released / water used |
Quick self-test
- Name the three components of a nucleotide.
- State one structural difference between ribose and deoxyribose.
- How many phosphodiester bonds join the nucleotides in a single strand of 48 nucleotides?
- How many phosphodiester bonds are there in a double-stranded fragment of 48 base pairs?
- How many hydrogen bonds join a G–C pair?
- State what is meant by antiparallel.
- A 12 base-pair fragment has 30 hydrogen bonds. How many are G–C pairs?
- Why is ice-cold ethanol added in DNA purification?
- Name the enzyme that breaks hydrogen bonds during replication.
- After four rounds of semi-conservative replication, how many molecules contain an original strand if you began with one molecule?
Answers
- A pentose sugar, a phosphate group and a nitrogenous base.
- Deoxyribose has hydrogen on carbon 2′ where ribose has a hydroxyl group (one fewer oxygen atom).
-
- 2 × 47 = 94.
- Three.
- The two strands run in opposite directions, 5′ to 3′ and 3′ to 5′.
- a + g = 12 and 2a + 3g = 30, so g = 30 − 24 = 6 G–C pairs (and 6 A–T pairs).
- DNA is soluble in water but not in ethanol, so it precipitates as strands at the boundary.
- Helicase.
- Two (out of 16 molecules).
Where marks are usually lost
- Writing “hydrogen bonds” when the bond between nucleotides in one strand is a phosphodiester bond.
- Counting nucleotides instead of bonds between them.
- Saying “thymine in RNA” or “ribose in DNA”.
- Describing helicase as “unzipping the DNA” without saying it breaks hydrogen bonds between bases.
- Leaving out complementary base pairing when explaining accurate copying.
- Calling mutations “caused by” a mutagen when the question says spontaneous.
- Explaining the purification steps without saying what each reagent does to the cell or the DNA.
- Quoting percentage change without stating which value is the baseline.
Official syllabus
OCR, Level 3 Advanced GCE in Biology A (H420), Version 4.1 (April 2026), first assessment 2025, section 2.1.3(a) to (e).
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