Galicia PAU Biology cheat sheet
Galicia PAU Biology · Keep the key ideas within reach.
Module 2: Biomolecules - Water, Carbohydrates, Lipids, Proteins and Enzymes
Condensation forms glycosidic, ester and peptide bonds; hydrolysis reverses them.
Reducing-sugar test interpretation requires suitable assay conditions and controls; hydrolysis can change sucrose test results.
Cellulose = β-1,4 glucose, straight H-bonded microfibrils; starch and glycogen = α-glucose.
Triglyceride = glycerol + 3 fatty acids; phospholipid = phosphate head + 2 tails, amphipathic.
Enzymes lower activation energy; specificity comes from active-site shape.
Simple reversible competition increases apparent Km without changing Vmax; pure noncompetitive inhibition lowers Vmax without changing Km.
Module 1: Cell Biology - Ultrastructure, Membranes and Cell Division
Prokaryotes lack a membrane-bound nucleus; bacterial peptidoglycan walls are not universal and archaeal walls differ.
Fluid mosaic membranes contain a lipid bilayer and proteins; sterol and carbohydrate composition depends on the cell.
Facilitated diffusion is passive; primary active transport may use ATP directly and secondary transport uses a gradient.
Water potential ψ = ψs + ψp; water moves from higher (less negative) to lower ψ.
Mitosis (P-M-A-T) after S-phase replication maintains chromosome number.
Cytokinesis: cleavage furrow in animals, cell plate in plants.
Module 3: Genetics - DNA, Gene Expression, Meiosis and Inheritance
A–T has 2 hydrogen bonds, G–C has 3; strands are antiparallel with 3′–5′ phosphodiester bonds.
Semi-conservative replication: helicase, DNA polymerase (5′→3′), ligase on the lagging strand.
The standard code is triplet and degenerate, nearly universal; AUG is a common start codon with biological exceptions.
Meiosis I separates homologues; crossing over in prophase I produces recombinants.
A test cross is with a homozygous recessive to reveal an unknown genotype.
Informative linked-locus crosses often give excess parentals; recombination percentage approximates short map distances, not all intervals exactly.
Metabolismo celular: catabolismo y anabolismo, respiración, fotosíntesis, enzimas
En modelos simples: competitivo reversible aumenta Km aparente sin cambiar Vmax; no competitivo puro baja Vmax sin cambiar Km.
Glucólisis en el citosol: 2 ATP netos, 2 NADH y 2 piruvato por glucosa.
Krebs: por vuelta 3 NADH, 1 FADH₂, 1 ATP y 2 CO₂; dos vueltas por glucosa.
Cadena respiratoria: quimiosmosis, ATP sintasa y O₂ como aceptor final de electrones.
Fase luminosa produce ATP y NADPH; el O₂ viene de la fotólisis del agua.
Ciclo de Calvin: RuBisCO fija CO₂ y consume ATP y NADPH para sintetizar glúcidos.
Scientific Inquiry, Methodology, and the Nature of Science
Hypothesis = testable prediction; theory = broad supported explanation; law = consistent regularity.
Independent variable is manipulated; dependent is measured; controls are held constant.
Random assignment supports experimental causal inference; an observed association alone does not establish causation.
Accuracy = closeness to truth; precision = repeatability.
Replication and sample size reduce the influence of random chance.
Microbiología, inmunología y biotecnología: virus, bacterias, respuesta inmunitaria, aplicaciones biotecnológicas
Los virus son acelulares; los ciclos lítico y lisogénico son modelos de determinados bacteriófagos, no de todos los virus.
Retrovirus: retrotranscriptasa convierte ARN en ADN e integra el provirus.
Muchas bacterias tienen peptidoglicano; pared, plásmidos y otros rasgos deben comprobarse en cada organismo.
Linfocitos B → células plasmáticas → anticuerpos; CD4 ayudan y CD8 citotóxicos matan células infectadas.
La memoria adaptativa puede acelerar la respuesta; el predominio de IgG depende del contexto de la respuesta sistémica.
PCR: N0 por 2^n solo con duplicación ideal; en el mismo gel, ADN lineal pequeño suele migrar más lejos.
Biotechnology: interpreting DNA evidence and model controls
PCR copies a selected DNA region; ideal N0 times 2^n requires perfect doubling.
Positive, no-template and extraction controls test different potential failures.
DNA fragment length is not the same as nucleotide sequence identity.
Genomic DNA presence does not by itself establish gene expression.
A genetic change requires suitable evidence before its phenotype is inferred.