Molecular Microbiology-2: Applications in research, diagnostics, Micro molecular lab expt Flashcards

1
Q

Mutagenesis Studies

A
  • discover if by mutating a gene, the protein function is disrupted and how?
  • investigate active site in protein
  • essential gene?
  • make protein work in different way
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2
Q

Plasmids

A
  • plasmids can be made artificially-genetic engineering
  • replicate independently of host chromosome
  • double stranded DNA and circular
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3
Q

Experiment mutagenesis of plasmid DNA containing ‘pink’ gene

A

Aims:

  1. Transform plasmid DNA that has been mutated into E. coli
  2. Examine colonies on LB plates containing antibiotic kanamycin - which colonies have been mutated?
  3. Plate out single colonies from this plate
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4
Q

Plasmid DNA

A

mCherry gene–> pink protein that makes bacterial colony pink

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5
Q

E.coli mutator strain

A
  • low mutation rate in microbes
  • increased mutation rate due to mutation in DNA replication and repair systems
  • example: Mutations in DnaQ gene-encodes subunit of DNA polymerase III-reduces proofreading capacity –> increased mutation
  • use these bacterial mutator strains for random mutation of DNA- study function of gene products
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6
Q

Study of mutagenised DNA with mCherry plasmid

A

E.coli mutator strain + mCherry plasmid
–>
mutated plasmids + wild type plasmids

Pink colonies = functional mCherry gene
White colonies = non-functional mCherry gene

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7
Q

Transformation procedure:

A

CaCl2 -> E.coli + mutated plasmid vector

–> 42degrees –> 37degrees

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8
Q

Selection using kanamycin

A
  • kanamycin=is an aminoglycoside antibiotic, inhibits bacterial protein synthesis
  • resistance gene inactivates kanamycin by modifying the structure
  • only E.coli that contains plasmid with resistance gene will survive and grow into a colony
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9
Q

Small subunit ribosomal RNA (SSUrRNA) gene analysis:

A

16S in prokaryotes

18S in eukaryotes

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10
Q

PCR of 16S ribosomal RNA gene

A
  • denaturation (95)
  • primers stick to conserved regions
  • Taq polymerase extends the sequence to make new template (72)
  • 25-35 repeated cycles makes copies of original cDNA so there is enough to sequence
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11
Q

LUCA

A

-last universal common ancestor

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12
Q

Molecular diagnostics

A

-microbial identification
-what causes the disease and where did it come from
methods include:
-PCR
-real-time-quantitative PCR
-sequencing ribosomal RNA genes or species specific genes
-whole genome sequencing

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13
Q

MRSA sequencing study

A

1/100 people carry MRSA on their skin without knowing

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14
Q

Methods:

A
  • cultures bacteria on selective medium
  • antimicrobial susceptibility testing
  • next generation sequencing (Illumina)
  • bioinformatics : DNA sequence alignment alignment -SNPs
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15
Q

MRSA sequencing study results

A

-contains genes for Panton-Valentine leukocidin-toxin causing necrotic lesions

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16
Q

Molecular mechanisms of human infectivity of African trypanosomes

A
  • what T.b gambiense genes are involved in human infectivity?
  • what SNPs are present in field isolates of trypanosomes
  • T.b.gambiense + T.b.rhodesiense = HAT (human infective)
  • T.b.brucei = cannot survive human serum