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Summary for GCSE AQA biology paper 1 (. With important notes)

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This is the ultimate £2.50 Investment for your Grade 9. THIS IS A SUMMARY (3 sheets) What is inside? Units 1-4 Complete: Every sub-topic from Cell Biology to Bioenergetics. The "Required Practical" Bible: Full methods and the "hidden" variables examiners ask about. Triple-Only Exclusives: Monoclonal Antibodies, Aseptic Technique, and Oxygen Debt mechanics. Grade 9 Keywords: Master the use of terms like "complementary," "hybridoma," "turgid," and "metabolism." Math for Biology: Step-by-step Magnification, Binary Fission, and Inverse Square Law calculations. This guide is built for Active Recall. Stop reading; start mastering.

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1. Cell Structure & Microscopy

Prokaryotes vs. Eukaryotes

Prokaryotes (Bacteria): These are significantly smaller than eukaryotic cells. Their genetic
material is not enclosed in a nucleus. It consists of a single DNA loop, and they may also contain
one or more small rings of DNA called plasmids. They lack mitochondria and chloroplasts.

Eukaryotes (Animal & Plant): These cells contain their genetic material (DNA) enclosed within a
nucleus. They feature specialized membrane-bound organelles like mitochondria and (in plants)
chloroplasts.

Sub-cellular Structures (Mark-Scheme Vocabulary)

Nucleus: Contains chromosomes made of DNA molecules; controls cell activities.

Mitochondria: Site of aerobic respiration. You must state that this "releases energy" for the cell.

Ribosomes: The site of protein synthesis.

Chloroplasts: Found in green parts of plants; contain chlorophyll to absorb light for
photosynthesis.

Cell Wall: Made of cellulose in plants and algae, which strengthens the cell and provides
structural support.

Microscopy Calculations

Formula: Magnification = \frac{\text{Image Size}}{\text{Actual Size}}

Key Distinction: Electron microscopes have a much higher magnification and resolution than
light microscopes. This allows biologists to study cells in much finer detail, seeing internal
structures like ribosomes.

Unit Conversion: Always convert mm to \mu m by multiplying by 1000 before calculating.

2. [Triple Only] Culturing Microorganisms

Aseptic Technique (The "How" and "Why")

To grow pure cultures and prevent the growth of unwanted pathogens:

Sterilization: Petri dishes and culture media must be sterilized before use to kill existing bacteria.

Inoculation: The inoculating loop must be sterilized by passing it through a Bunsen burner flame.

Incubation: In schools, cultures should be incubated at a maximum of 25°C. This prevents the
growth of harmful pathogens that thrive at human body temperature (37°C).

Sealing: The lid of the Petri dish should be secured with adhesive tape to prevent
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