CAPE Biology Unit 1 study materials
CAPE Biology Unit 1 study resources

CAPE Biology Unit 1 cheat sheet

CAPE Biology Unit 1 · Keep the key ideas within reach.

Quick reference

Module 1: Cell Structure, Function and Transport

  • Prokaryotic cells lack membrane-bound organelles and a true nucleus; their DNA is a circular chromosome in a nucleoid region, and they may carry plasmids, 70S ribosomes, and a peptidoglycan wall.

  • Eukaryotic organelles: nucleus (chromatin, nucleolus), rough ER (ribosome-studded, protein synthesis), smooth ER (lipid synthesis, detoxification), Golgi (modification and packaging), lysosomes (hydrolytic enzymes), mitochondria (aerobic respiration), chloroplasts (photosynthesis).

  • Endosymbiotic theory evidence: mitochondria and chloroplasts have double membranes, circular DNA, 70S ribosomes, and divide independently of the cell.

  • Magnification = image size / actual size; keep units consistent (convert µm to mm by multiplying by 1000).

  • Resolution is the ability to distinguish two close points; electron microscopes have higher resolution than light microscopes because of shorter electron wavelength.

  • Diffusion is passive movement down a concentration gradient; rate increases with steeper gradient, higher temperature, larger surface area, and shorter distance.

  • Osmosis is diffusion of water across a selectively permeable membrane from higher to lower water potential; water potential of pure water at atmospheric pressure is 0 kPa.

  • Active transport moves substances against a concentration gradient using ATP and carrier proteins; it is saturable and inhibited by metabolic poisons.

  • Fluid mosaic model: phospholipid bilayer with embedded proteins, cholesterol, and glycoproteins; membrane fluidity depends on phospholipid tail saturation and cholesterol content.

Quick reference

Module 2: Biological Molecules and Enzymes

  • Carbohydrates: monosaccharides (glucose, fructose), disaccharides (maltose, sucrose, lactose) joined by glycosidic bonds, polysaccharides (starch, glycogen, cellulose) joined by glycosidic bonds.

  • Starch is a storage polysaccharide of alpha-glucose (amylose unbranched, amylopectin branched); glycogen is more highly branched for rapid glucose release; cellulose is beta-glucose chains with 1,4 bonds forming microfibrils.

  • Proteins are polymers of amino acids joined by peptide bonds; primary structure is amino acid sequence, secondary is alpha-helix or beta-pleated sheet held by hydrogen bonds, tertiary is 3D folding via ionic, hydrogen, disulfide, and hydrophobic interactions, quaternary is multiple polypeptide chains.

  • Lipids: triglycerides are glycerol plus three fatty acids joined by ester bonds; saturated fatty acids lack double bonds, unsaturated have C=C double bonds; phospholipids are amphipathic with a hydrophilic head and hydrophobic tails.

  • Benedict's test: reducing sugars give a brick-red precipitate on heating; non-reducing sugars require prior acid hydrolysis and neutralisation.

  • Biuret test: proteins give a purple colour; iodine test: starch gives blue-black; emulsion test: lipids give a cloudy white emulsion with ethanol and water.

  • Enzymes are biological catalysts that lower activation energy; they are specific to their substrate at the active site.

  • Factors affecting enzyme activity: temperature (denaturation above optimum), pH (changes ionisation of active site), substrate concentration (rate plateaus at Vmax), enzyme concentration, and inhibitors.

  • Competitive inhibitors bind the active site and are overcome by increasing substrate concentration; non-competitive inhibitors bind elsewhere and change enzyme shape, so they are not overcome by more substrate.

Quick reference

Module 3: Genetics, Variation and Classification

  • DNA is a double helix of nucleotides (deoxyribose, phosphate, nitrogenous base); adenine pairs with thymine (two hydrogen bonds), guanine with cytosine (three hydrogen bonds).

  • DNA replication is semi-conservative: helicase unwinds, each strand acts as template, DNA polymerase adds complementary nucleotides, and each daughter molecule has one old and one new strand.

  • Transcription produces mRNA from a DNA template in the nucleus; translation at ribosomes uses tRNA anticodons to add amino acids in the sequence specified by mRNA codons.

  • The genetic code is triplet, degenerate (multiple codons per amino acid), non-overlapping, and universal.

  • Mitosis produces two genetically identical diploid daughter cells for growth and repair; meiosis produces four genetically varied haploid cells for gamete formation.

  • Meiosis variation sources: independent assortment of homologous chromosomes in meiosis I and crossing over between non-sister chromatids.

  • Monohybrid cross ratios: F2 from heterozygous parents gives 3:1 phenotype and 1:2:1 genotype; test cross with a recessive homozygote reveals unknown genotype.

  • Codominance and incomplete dominance modify expected ratios; sex-linked traits show different inheritance patterns in males and females.

  • Classification hierarchy: domain, kingdom, phylum, class, order, family, genus, species; binomial nomenclature uses genus and species names in italics.