Chapter 13 - Bacterial Genome Flashcards

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1
Q

Briefly summarize the experiments of Griffith; Avery, MacLeod, and McCarty; and Hershey and Chase.

A
  • Griffith used mice
    • Avery, macleod, mccarty used enzymes to degrade protein, rna, and dna
      Hershey and chase used bacteriophages
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2
Q

Explain how protein was ruled out as the molecule of genetic information storage in each of the experiments performed by these important microbiologists

A
  • Griffith noticed that clean r strain became virulent only when put together with s strain. This suggested something is responsible for transformation
  • Avery and group noticed that transformation did not occur when dna was destroyed. Suggested dna carries genetic info
    Hershey and chase noticed that bacteriophage injected dna into cell not protein
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3
Q

What are nucleic acids? How do DNA and RNA differ in structure

A
  • Nucleic acids are macromolecules that store and transmit genetic info
  • Nucleic acids are composed of nucleotides
  • Nucleotides have a sugar, phosphate and nitrogenous base
    DNA and RNA
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4
Q

Outline the transcription cycle observed in bacteria. Which steps require the following: RNA polymerase core enzyme, sigma factor, and RNA polymerase holoenzyme?

A
  • Transcription is when RNA polymerase holoenzyme binds to promotor region of DNA. DNA unwinds and RNA polymerase synthesizes RNA nucleotides
  • Elongation is when RNA polymerase moves along template strand synthesizing in 5’ to 3’ direction. DNA unwinds infront of enzyme and newly synthesized RNA detaches behind enzyme
    Termination is when a termination sequence or Rho protein binds to RNA and RNA transcript is released and machinery disassembles
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5
Q

What is a consensus sequence? What happens at the –35 and –10 sequences during transcription initiation?

A
  • A consensus sequence is a sequence of DNA that represents the most common nucleotide patten found at a specific position in a set of related DNA sequences. Ex promotor regions
  • The -35 and -10 sequences are promotor sequences that are recognized by the sigma factor of RNA polymerase holoenzyme
  • The sequences act as initial binding sites for RNA polymerase holoenzyme
  • -35 sequence = recognition and binding of RNA polymerase
    -10 sequence = facilitates unwinding of DNA to start transcription
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6
Q

What is the difference between a codon and an anticodon?

A
  • A codon is a sequence of nucleotides on mRNA that encode info for the polypeptide chain. Written in 5’ to 3’ direction
    Anticodon is a sequence of nucleotides on tRNA that encode for the corresponding amino acid to the codon. Written in 3’ to 5’ direction
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7
Q

What is meant by code degeneracy (redundancy)? How does wobble help alleviate the energy cost exacted on a cell due to code degeneracy?

A
  • 1st and 2nd codon are most important
  • 3rd codon can be different and code for the same amino acid as long as first two are the same
  • 64 codons only 20 amino acids
    Wobble reduces energy cost because it allows one tRNA to recognize multiple codons
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8
Q

In which direction are polypeptides synthesized?

A
  • From the N terminus to the C terminus
  • N terminus is amino group
    C terminus is carboxyl group
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9
Q

Briefly describe the structure of transfer RNA and relate this to its function. How are amino acids activated for protein synthesis, and why is the specificity of the aminoacyl-tRNA synthetase reaction so important?

A

Key regions
1. Anticodon loop = 3 complementary bases to mRNA codon
2. Acceptor stem = 3’ (CCA) end where amino acid is attached
3. D and T loops = allow tRNA to interact w ribosomes and enzymes
4. Variable loop = add flexibility and diversity
Amino acid activation
- Aminoacyl tRNA synthetases catalyze a two step reaction that attach amino acid to tRNA molecule
- This reaction is important because each aminoacyl tRNA synthetase is specific to one amino acid and corresponding tRNA
Attaching the wrong amino acid result in incorrect protein synthesis

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10
Q

What roles do ribosomal RNAs have?

A
  • Provide structure for tRNA and mRNA interaction
  • Catalyze formation of peptide bonds using 23S rRNA
  • APE sites where tRNA binds
  • 16S rRNA aligns mRNA by recognizing shine dalgarno sequence
    Ensures translation is accurate between codons and anticodons
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