6.1.3 manipulating genomes Flashcards

1
Q

what is synthetic biology

A

creation of artificial biological parts or redesigning of existing ones

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2
Q

what is computational biology

A

using of computer-based techniques like computational models, large datasets, and bioinformatics to understand biological processes

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3
Q

what is bioinformatics

A

using software to analyse biological data like DNA sequences

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4
Q

enzymes used in isolating genes

A
  • reverse transcriptase
  • restriction endonuclease
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5
Q

reverse transcriptase

A

makes complimentary DNA (cDNA) using an mRNA sequence

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6
Q

restriction endonuclease

A

cuts DNA on the sugar-phosphate backbone at a specific base sequence

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7
Q

restriction site

A

place where DNA is cut by restriction endonuclease

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8
Q

palindrome sequence

A

restriction sites are cut in a staggered ‘palindromic’ way

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9
Q

What is gel electrophoresis?

A

Used by scientists to sort DNA strands according to length

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10
Q

What acts as a filter in gel electrophoresis

A

The gel - it acts as a sponge with small holes in it

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11
Q

What is agarose

A

A dried powder made of seaweed

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12
Q

What role does the electric current play in gel electrophoresis

A

Makes DNA move

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13
Q

Which direction do DNA fragments migrate in gel electrophoresis

A

From the negative pole to the positive pole

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14
Q

In what order do DNA fragments migrate towards positive pole

A

Shorter fragments move through holes in gel move quickly than long strands

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15
Q

What is the purpose of the loading buffer in gel electrophoresis

A

Lets electrical charges flow through the gel

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16
Q

What is the name of

17
Q

What is the purpose of the loading buffer

A

Lets electrical charges flow through the gel

18
Q

What is the name of the holes that DNA is loaded into

19
Q

What does the ‘DNA size standard’ contain

A

DNA strands of known length

20
Q

How do you know when the current is running gel electrophoresis

A

Air bubbles come out of electrodes at both ends of electrophoresis box

21
Q

What is used to stain DNA and why in gel electrophoresis

A
  • Ethidium bromide
    Binds to DNA and shows up under fluorescent light
22
Q

Why is it important to avoid contact with ethidium bromide

A

Binds to DNA and damages cells

23
Q

What is polymerase chain reaction

A

Used to amplify (clone) DNA samples

24
Q

Thermocycler

A

Adjusts temperature during PCR

25
Primer
Short sequences on DNA that are complementary to the bases at the start of the region to be copied
26
Taq polymerase
DNA polymerase that can survive at high temperatures
27
What are the 3 stages of PCR
1. Denaturation 2. Annealing 3. Extension
28
Denaturation
At 92°C DNA strands are separated by DNA helicase breaking H bonds
29
Annealing
At 55°C primers attach to DNA, act as starter sequence of double stranded DNA for polymerase, keeps DNA strands separated by preventing reformation of H bonds
30
Extension
At 72°C, Taq polymerase extends the sequence by joining free nucleosides in phosphodiester bonds, 2 chains produced by semi-conservative replication