Biotechnology Flashcards

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1
Q

What is does PCR stand for?

A

Polymerase Chain Reaction

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2
Q

What are the steps involved in PCR?

A
  • Denaturation
  • Annealing
  • Elongation

Remember 3 letters and three steps

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3
Q

Can you descrbe the process of denaturation?

A
  • Helicase separates the two strands of DNA to be copied
  • Temperatures of approximately 94-96ºC to bek the hydrogen bonds
  • This separates the strands but does not disrupt each individual strand

H96S: high on 96 to separate

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4
Q

Can you describe the process of annealing?

A
  • Annealing is when the temperature is decrease to 50-60ºC
  • Short strands of DNA called primers bind to the single DNA strands
  • Primers are complementary at the end of the DNA strand

primers need 60 to complement each other

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5
Q

Can you describe the process of elongation?

A
  • Similar to DNA transcription, taq polymerase joins new, complementary nucleotides
  • continues section where the primer was placed
  • Temperature rises to 72ºC, the optimal temperature of taq polymerase to start binding

taq polymerase loves 72

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6
Q

Why is taq polymerase used during PCR?

A
  • comes from the heat-loving bacterium, Thermus aquaticus
  • does not denature when exposed to high heat, therefore it is preferrable

love the heat

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7
Q

What is the function of gel electrophoresis?

A
  • separate DNA strands based on their lenghts
  • DNA is placed inside semi-solid gels, immersed in electrolyte solution
  • DNA is negative and moves towards the positive electrode
  • The larger the DNA strand, the slower it will travel.
  • The results look similar to barcodes or ladders

SEPLL

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8
Q

How are DNA ladders used to compare the sample DNA?

A
  • the ladder contains DNA with the known lengths
  • determine the length of DNA from the sample
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9
Q

What is the purpose of a primer?

A

It used as a starting point for DNA synthesis.

the prime for time!

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10
Q

What are the uses of gel electrophoresis?

A
  • hereditary diseases
  • paternity tests
  • forensics/ crime scenes
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11
Q

What is DNA sequencing?

A
  • by comparing how DNA sequences change and mutations can be detected
  • many diseases can be detected by this

e.g sickle cell anemia, cystic fibrosis, some cancers

NOTE: also used in paternity tests and compare species to track evolutionary changes.

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12
Q

Ethical considerations involved with genetic information

A

Autonomy

Equity

Privacy

Confidentiality

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13
Q

Define restriction enzyme

A

Enzymes that cut DNA across the double helix.
* each restriction enzyme has specific recognition site (DNA sequence) which it will cut.

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14
Q

Define DNA sequencing

A

Determines the precise order of nucleotides (phosphate and sugar molecule with nitrogen base) in a sample of DNA.

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15
Q

Describe comparative genomics

A

Comparative genomics is a new field of biological research in which the genome sequences of different species are compared.

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16
Q

What is the result of comparing the genome of different species?

A
  • provides effective means of studying evolutionary changes
  • helping to identity preserved genes and those which give organisms their unique characteristics.
17
Q

Describe the sticky end restriction enzymes

A
  • DNA cut is staggered
  • Sticky end is a stretch of unpaired nucleotides overhanging
  • exposed strand can only re-join to DNA with complimentary based pairs
  • Can be from a different organism

STICKY IS GAY

18
Q

Describe the blunt end restriction enzymes

A
  • no overhangs
  • cuts straight across DNA
  • terminates in base pair

BLUNT IS STRAIGHT

19
Q

How is bioinformatics useful?

A
  • assist evolutionary biologist in tracing the evolution of a large number of organisms by measuring changes in DNA
  • Done instead of traditional methods e.g., physical taxonomy, physiological observations
  • recent development allows researchers to compare entire genomes.