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FRNSC 420 - EXAM 4 PRACTICE QUESTIONS AND ANSWERS (100% PASS)

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FRNSC 420 - EXAM 4 PRACTICE QUESTIONS AND ANSWERS (100% PASS) positive allosteric regulation - Answer️️ -binding of a regulatory molecule to an enzyme induces a conformation change, increasing the enzyme's affinity for a substrate - proteins are activators = enhance RNAP binding and/or ind...

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  • August 31, 2024
  • 30
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • FRNSC421W /FRNSC 420
  • FRNSC421W /FRNSC 420
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©PREP4EXAMS2024/2025 REAL EXAMS DUMP Wednesday, August 7, 2024 9: 33 PM



FRNSC 420 - EXAM 4 PRACTICE QUESTIONS AND
ANSWERS (100% PASS)


positive allosteric regulation - Answer✔️✔️-binding of a regulatory molecule to an
enzyme induces a conformation change, increasing the enzyme's affinity for a
substrate

- proteins are activators = enhance RNAP binding and/or induce conformational
change, can change binding constant (KB) or rate constant (kf), lowers activation
energies

negative allosteric regulation - Answer✔️✔️-bound regulatory molecule must
release to induce the conformation change necessary for substrate to bind an
enzyme

- proteins are repressors = block RNAP binding or escape

allosteric regulation of Cdk - Answer✔️✔️-replication initiation in eukaryotes

- Cdk is inactive when not bound to cyclin, with helices blocking its active site;
when Cdk is inactive, helicases are readily loaded onto DNA

- cyclin binds to Cdk to induce a conformational change that exposes its active site

- active site is phosphorylated by kinase CAK; when activated, Cdk will
phosphorylate Cdc6/Cdt1 in the eukaryotic PIC

- phosphorylation activates loaded helicases and prevents others from loading,
allowing for the unwinding of DNA and subsequent initiation of replication




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effects of binding constants on promoters - Answer✔️✔️-promoter/RNAP
interaction strength can be determined by the amount of the holoenzyme needed to
occupy ½ of the promoter

- KB = [RP]/[R][P]

- equilibrium in bound & unbound RNAP is [RP]/[R][P] = 1

- from that, you get KB = 1/[R], shows KB when ½ of the promoter is occupied

- when KB is large, less holoenzyme is needed to bind ½ of the promoter =
stronger RNAP/promoter interaction

- when KB is smaller, more holoenzyme needed = weaker

- also dependent on rate constant k, where larger k = quicker conversion

allosteric regulation of glnA - Answer✔️✔️-RNAP is pre-bound to glnA (glutamine
synthetase gene, involved nitrogen metabolism) in the closed complex

- RNAP has a σ⁵⁴ factor = unable to unwind DNA, must be activated

- activator is NtrC, binds 4 sites at ~150 bps upstream from promoter

- IHF contains pseudo-loops which bind DNA and bend it 180⁰, facilitating
interaction between NtrC and the σ⁵⁴ factor

- NtrC utilizes ATPase activity; energy from ATP hydrolysis induces a
conformational change in RNAP to 'open' it

- process is regulated by environmental conditions in the cell; NtrC can only bind
to DNA in low nitrogen levels

- NtrC is phosphorylated by kinase NtrB, which induces a conformational change
in NtrC to expose its DNA-binding domain

- only then it can bind DNA and activate transcription



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promoter spacing in merT - Answer✔️✔️-protein MerR controls the expression of
the merT gene, expression is activated in the presence of mercury (Hg)

- MerR binds sequence between -35 and -10 regions of the merT promoter opposite
to RNAP (contains σ⁷⁰) for simultaneous binding

- spacing between the -35 and -10 elements is ~19 bps, much larger than the usual
15-17 bps; elements are unaligned on DNA, facing opposite sides of the helix

- without Hg, MerR binds to lock this conformation in position; structural
distortion prevents RNAP from transcribing the gene

- when bound to Hg, MerR undergoes a conformational change that allows for
DNA to twist at the center of the promoter

- new configuration allows for the -35 and -10 elements to align with one another

catabolite repression - Answer✔️✔️-in E. coli, presence of glucose causes the down
regulation of operons whose products participate in the metabolism of other carbon
sources

- glucose is preferred carbon source in E. coli

- when lactose is absent, the lac repressor will remain bound to the lac operator,
only dissociating when lactose is present = basal transcription

- through induction (activation), transcription of the lac operon is further activated
in the presence of lactose when glucose is absent entirely

operons - Answer✔️✔️-cluster of coordinated, regulated genes; contain:

- structural genes that encode enzymes

- regulatory genes that encode repressors or activators

- regulatory sites (promoters, operators, binding sites)



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