bio paper 1 module 2 Flashcards
Describe the structure of ATP and ADP
-phosphorylated nucleotides
-nucleotide derivative of adenine
-ATP has 3 inorganic (tri) phosphate groups
-ADP only has 2 (di)
Describe the structure of DNA
-molecule twists to form double helix of 2 deoxyribose polynucleotide strands (2 sugar phosphate backbones)
-H bonds form between complimentary base pairs on strands that run antiparallel
Identify features of the genetic code
-non-overlapping: each triplet is only read once
-degenerate: more than one triplet codes for the same amino acid
-universal: same bases and sequences used by all species
What does transcription produce and where does it occur?
-produces mRNA
-occurs in nucleus
Outline the process of transcription
-RNA polymerase binds to promoter region of gene
-section of DNA uncoils into 2 strands with exposed bases. antisense strand acts as a template
-free nucleotides are attracted to their complimentary bases
-RNA polymerase joins adjacent nucleotides to form phosphodiester bonds
What happens after a strand of DNA is transcribed?
-RNA polymerase detaches at terminator region
-H bonds reform and DNA rewinds
-splicing removes introns from pre-mRNA in eukaryotic cells
-mRNA moves out of the nucleus via the nuclear pores and attaches to a ribosome
What does translation produce and where does it occur?
-produces proteins
-occurs in cytoplasm on ribosomes (which are made of proteins and rRNA
Outline the process of translation
-ribosome moves along mRNA until start codon
-tRNA anticodon attaches to complimentary bases on mRNA
-condensation reactions between amino acids and tRNA form peptide bonds, requires energy from ATP hydrolysis
-process continues to form polypeptide chain until stop codon is reaches
Explain the induced fit model of enzyme action
-shape of active site is not directly complimentary to substrate + is flexible
-conformational change enables ES complexes to form when substrate adsorbs
-this puts strain on substrate bonds, lowering activation energy
-bonds in enzyme product complex are weak so product desorbs
Explain the lock and key model of enzyme action
-suggests that active site has a rigid shape determined by tertiary structure so only complimentary to 1 substrate
-formation of ES complex lowers activation energy
-bonds in enzyme product complex are weak so product desorbs
How does substrate/enzyme conc affect rate of reaction
-rate increases proportionally to substrate conc
-rate levels off when maimum no. of ES complexes form at any given time
How does temp affect the rate of enzyme-controlled reactions?
-rate increases as KE increases and peaks at optimum temp
-above optimum ionic + H bonds in tertiary structure break= active site no longer complimentary to substrate= denatured
Equation for Q10
R2/R1
How does pH affect rate of reaction?
-enzymes has a narrow optimum pH range
-outside range H+/OH- ions interact with H-bonds + ionic bonds in tertiary structure= denature
What are inactive precursors?
-to prevent damage to cells, some enzymes in metabolic pathways are synthesised as inactive precursors e.g. proteases
-one part of precursor acts as an inhibitor. ES complexes form when it is removed
Suggest how a student could produce a desired conc of solution from a stock solution
Outline what happens during prophase
1.chromosomes condense becoming visible (X shaped)
2.centrioles move to opposite poles of cells (animal cells) + mitotic spindle forms
3.nuclear envelope + nucleolus break down= chromosomes free in cytoplasm