KA2 U1 Flashcards

1
Q

DNA consists of?

A

Units called nucleotides, twisted into a double stranded helix.

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2
Q

Nucleotides are made of 3 parts

A

•Deoxyribose sugar
•Phosphate
•base

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3
Q

Rulings of carbons attached to D and P

A

•Deoxyribose has in a nucleotide has a base attached to its carbon 1

•and a phosphate attached to its carbon 5

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4
Q

Nucleotides are joined by what to form a strand with sugar phosphate backbone

A

•Nucleotides are joined by their deoxyribose sugar and phosphate to form a strand with a sugar phosphate backbone

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5
Q

What does the sequence of DNA form

A

Genetic code

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6
Q

Based on opposite strands are held together by what?

A

•Weak hydrogen bonds between complementary base pairs

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7
Q

Anti parrarel structure

A

• the two DNA strands have their sugar phosphate backbones running opposite directions from each other

•this is a double stranded antiparrarek structure.

•Each strand has a deoxyribose sugar at 3 end and a phosphate at the 5 end

D3 P5

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8
Q

DNA replication is replicated using what enzyme

A

DNA polymerase

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9
Q

Why do primers need to start replacation

A

As they can only add nucleotides in one direction

To the 3 end of the new strand

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10
Q

A primer is what

A

A short strand of nucleotide

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11
Q

Where do primers bind

A

3end of the template DNA strands allowing DNA polymerase to add nucleotides

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12
Q

Stages of DNA replication

A

S1: DNA molecules unwinds

S2: Hydrogen bonds between base pairs break to from two template strands

S3: a primer binds to the 3 end of the originally template strand

S4: DNA polymerase enzyme adds nucleotides using complementary base pairing to the 3 end of the new strand

S5: this results in the leading strand replicating continually

S6: lagging strand nucleotides are added by DNA polymerase to form fragments

7 Ligase joins DNA fragments on the lagging strand to form a complete strand

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13
Q

What is PCR

A

A technique used to amplify specific target sequences of DNA

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14
Q

What does PCR USE to do this

A

Primers which are complementary to specific target sequences at the two end of DNA to be amplified

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15
Q

Stage1 PCR

A

DNA is heated between 92-98 degrease to seperate DNA strands

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16
Q

Stage 2 PCR

A

it’s then cooled between 50-65 degrees to allow primers to bind to target sequence

17
Q

Stage 3

A

It’s the heated between 70 and 80 degrease to allow heat tolerant DNA polymerase to replicate the region of DNA

18
Q

Stage 4

A

Two identical copies of DNA made after first cycle

Repeated cycles of heating and cooling amplify the target region of DNA and allow billions of copies to be produced

19
Q

Practical applications of PCR

A

•Solve crimes
•settle paternity suites
•diagnose paternity suits