BTL2 flashcards
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32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Michaelis-Menten equation
- v = Vmax[S]/(Km + [S]). It describes enzyme velocity as a function of substrate concentration, with Vmax at saturation and Km at half-maximal velocity.
- Gibbs free energy change
- ΔG = ΔH − TΔS. A negative ΔG indicates a spontaneous (exergonic) reaction; a positive value indicates a nonspontaneous (endergonic) reaction requiring energy input.
- Competitive inhibition kinetics
- An inhibitor binds the enzyme active site, competing with substrate. Apparent Km increases while Vmax is unchanged, because high substrate can overcome inhibition.
- Fluid mosaic model
- Describes membranes as a phospholipid bilayer with embedded integral proteins, peripheral proteins, cholesterol, and glycoproteins, all able to move laterally within the membrane.
- Net ATP from glycolysis
- Per glucose molecule, glycolysis consumes 2 ATP and produces 4 ATP, giving a net gain of 2 ATP plus 2 NADH and 2 pyruvate molecules.
- G2/M checkpoint
- A cell cycle control point that verifies DNA replication is complete and damage is repaired before the cell enters mitosis, preventing propagation of mutations.
- Semiconservative replication
- Each new DNA double helix contains one original parental strand and one newly synthesized strand, as demonstrated by the Meselson-Stahl density gradient experiment.
- PCR thermal cycling steps
- Denaturation near 95 degrees Celsius separates strands, annealing near 55-65 degrees Celsius binds primers, and extension near 72 degrees Celsius lets thermostable polymerase synthesize DNA.
- Dihybrid cross ratio
- For two independently assorting heterozygous genes (AaBb x AaBb), the F2 phenotypic ratio is 9:3:3:1, reflecting independent assortment of alleles.
- Nonsense mutation
- A base substitution that converts a codon into a stop codon, causing premature termination of translation and usually producing a truncated, nonfunctional protein.
- Frameshift mutation
- Insertion or deletion of nucleotides not in multiples of three shifts the reading frame, altering all downstream codons and typically destroying protein function.
- DNA polymerase directionality
- DNA polymerase adds nucleotides only to the 3' end, so synthesis proceeds 5' to 3'. The lagging strand is synthesized discontinuously as Okazaki fragments later joined by ligase.
- Restriction endonuclease function
- Enzymes that recognize specific palindromic DNA sequences and cleave them, often producing sticky ends useful for inserting fragments into cloning vectors.
- Gram stain principle
- Gram-positive cells retain crystal violet due to thick peptidoglycan and appear purple; Gram-negative cells have thin peptidoglycan and an outer membrane, decolorize, and stain pink.
- Bacterial growth curve phases
- Lag phase precedes exponential (log) growth, then stationary phase balances growth and death, and finally death phase reduces viable cell numbers as nutrients deplete.
- Antibody structure
- Two heavy and two light chains linked by disulfide bonds; variable regions form the antigen-binding site, while constant regions define isotype and effector function.
- Innate versus adaptive immunity
- Innate immunity is rapid, nonspecific, and lacks memory; adaptive immunity is slower, antigen-specific, and produces memory B and T cells for faster secondary responses.
- CD8 cytotoxic T cells
- T lymphocytes recognizing antigen presented on MHC class I molecules; they kill virus-infected and tumor cells by releasing perforin and granzymes.
- Primary versus secondary response
- The primary response produces mainly IgM first, then IgG; the secondary response is faster, larger, and dominated by IgG due to memory B cells.
- Sterilization versus disinfection
- Sterilization destroys all microorganisms including endospores; disinfection reduces pathogenic organisms on surfaces but may not eliminate spores or all viruses.
- Viral replication requirement
- Viruses lack ribosomes and metabolic machinery, so they are obligate intracellular parasites that replicate only inside a host cell using host biosynthetic pathways.
- Monod growth kinetics
- μ = μmax·S/(Ks + S) relates specific growth rate to limiting substrate concentration; Ks is the substrate concentration supporting half-maximal growth rate.
- Fed-batch culture
- A bioprocess where nutrients are added during the run without removing culture fluid, avoiding substrate inhibition and extending product formation time.
- CRISPR-Cas9 editing
- A guide RNA directs Cas9 nuclease to a complementary target sequence, creating a double-strand break repaired by error-prone NHEJ or homology-directed repair.
- Sandwich ELISA
- An assay using a capture antibody bound to a plate and a detection antibody that binds a different epitope of the same antigen, giving high sensitivity.
- Recombinant protein workflow
- Cloning the gene into an expression vector, transforming a host cell, selecting transformants, inducing expression, and purifying the target protein by chromatography.
- Dissolved oxygen control
- In bioreactors, agitation and aeration rates are adjusted to keep dissolved oxygen above the critical level needed for microbial respiration and product formation.
- Affinity chromatography
- A purification method using a specific ligand immobilized on a resin to bind the target protein selectively, which is then eluted by changing buffer conditions.
- kLa oxygen transfer coefficient
- A volumetric mass transfer coefficient describing oxygen transfer from gas bubbles to liquid; it is matched during scale-up to preserve dissolved oxygen availability.
- Transformation in cloning
- Introduction of recombinant plasmid DNA into competent bacterial cells, often by heat shock or electroporation, followed by selection on antibiotic media.
- SDS-PAGE protein analysis
- Electrophoresis that denatures proteins with SDS, giving a uniform negative charge, so migration depends on molecular mass and purity can be assessed.
- Enzyme-linked immunosorbent assay
- An antibody-based assay detecting antigen or antibody through enzyme-linked colorimetric signal, available in direct, indirect, sandwich, and competitive formats.