Lab 5 Flashcards

1
Q

What is the purpose of restriction enzymes?

A

To protect bacteria from invading foreign DNA by digesting the foreign DNA at a specific recognition nucleotide sequence (6bps).

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2
Q

What do restriction digests require?

A
  1. DNA
  2. Restriction enzymes
  3. Buffer
  4. Water
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3
Q

What is the purpose of the buffer in a restriction digest?

A

To maintain an optimal pH of the solution for the enzyme.

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4
Q

What is the purpose of the water in the restriction digest?

A

Provides volume and allows easier mixing of the DNA and buffer.

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5
Q

Why is the concentration of DNA in the sample good to know for restriction digests?

A

Allows us to know the amount of restriction enzymes required for complete digestion of the DNA.

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6
Q

What is one unit (U) of restriction enzyme activity?

A

The amount of restriction enzyme needed to completely digest (cut) one microgram (ug) of substrate DNA in one hour at the optimum temperature of the enzyme (around 37).

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7
Q

How is enzymatic activity of restriction enzymes measured?

A

Units of their activity; ability to cut DNA.

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8
Q

What does excess of enzyme result in?

A

Incomplete or non-specific digestion of DNA.

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9
Q

What is electrophoresis?

A

Charged molecules migrate in an electrical field.

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10
Q

What is the rate of migration determined by?

A

The size of the molecules and their electrical charge.

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11
Q

How does the migration rate of DNA molecules relate to their molecular weight?

A

Inversely proportional

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12
Q

What is the purpose of ethidium bromide or GelRed?

A

Intercalate with DNA to allow the bands to be observed under UV light.

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13
Q

Where does the DNA move to in gel electrophoresis?

A

Move to the anode (positive charged pole; red) since it has a negative charge.

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14
Q

Where does the loading dye move in gel electrophoresis?

A

Move to the anode (positive charged pole; red) since it has a negative charge.

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15
Q

Where does the GelRed or ethidium bromide move in gel electrophoresis?

A

Move to the cathode (negative charged pole; black).

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16
Q

Why is a DNA ladder added?

A

Estimates the sizes of your bands.

17
Q

What restriction enzymes are used in lab 5 experiment?

A

Xbal (cuts at T-A) and NotI (cuts at G-C).

18
Q

Where will the restriction enzymes cut the blue colony (without the insert)?

A

Cut at MCS

19
Q

How many bands does the blue colony produce?

A

1

20
Q

Where will the restriction enzymes cut the white colony (with the insert)?

A

Cut at MCS

21
Q

How many bands does the white colony produce?

A

2 - one regular DNA and the other is the insert itself.

22
Q

Why are the restriction enzymes added last?

A

Added to the sample at which it has an optimal reaction condition.

23
Q

What does loading dye do?

A

Adds weight to your DNA samples, making them dense so they can sink to the bottom of the wells.

24
Q

Why are there multiple bands for the uncut DNA?

A

Multiple cloning site so plasmid DNA might be supercoiled, nicked, or linear.

25
Q

Why does the supercoiled DNA travel faster and farther down?

A

Since it’s tightly wrapped, it experiences less friction.

26
Q

Why does the nicked DNA travel slower and smaller distances?

A

Open circular plasmids cause more friction.