Chapter 3 Review Flashcards

1
Q

DNA is a polymer of

A

dNMPs

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2
Q

Pyrimidines include

A

cytosine, thymine and uracil

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3
Q

Purines include

A

adenine and guanine

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4
Q

Base + ribose =

A

nucleoside

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5
Q

Base + ribosome phosphate =

A

nucleotide

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6
Q

Of deoxyribose, phosphates will react with the ______ on the _____ carbon or the ____ carbon.

A

Alcohols ; 3’ or 5’

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7
Q

Spontaneous deamination leads to _______. Water spontaneously reacts with _________ to form _____.

A

Uracil; cytosine, uracil ; A PROTEIN LOOKING FOR URACIL CAN’T DISTINGUISH IF IT WAS SUPPOSED TO BE THERE OR IF IT’S A PRODUCT OF DEAMINATION.

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8
Q

Why are nucleotide sequences synthesized 5’ to 3’?

A

3’ always attacks the phosphate of the 5’ of the growing DNA chain.

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9
Q

Edwin Chargaff (1950s)

A

Equal # of A to T, and Equal # of G to C

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10
Q

Rosalind Franklin (1950s)

A
  • X-Ray diffraction of DNA

- The strong diffraction base on the reciprocal space was 1/d = 3.14 angstroms.

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11
Q

Jerry Donohue (1950s)

A
  • Bases can be in keto or enol state; HOWEVER, almost always in keto state.
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12
Q

Endonuclease

A

Cleaves a nucleic acid within the polypeptide strand; CUT DNA at certain sequences.

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13
Q

Exonuclease

A

Cleaves a nucleic acid by removing one of its terminal residues.

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14
Q

Restriction Endonuclease

A

A bacterial enzyme that recognizes a specific DNA sequence and cleaves the DNA as part of a restriction-modification system.

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15
Q

Modification Methylase

A

A bacterial enzyme that methylates a specific sequence of DNA as part of a restriction-modification system.

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16
Q

The bases primarily exist in their ____ form.

A

keto

17
Q

Why do G-C bonds have a higher melting temp. than A-T?

A

They have more hydrogen bonds than A-T

18
Q

What is necessary for replication?

A

Complimentary bases

19
Q

Transcription and Translation

A

DNA goes to transcription –> mRNA (codes for tRNAs) –> tRNA (translational RNA ; amino acids are attached to them) –> translation –> Bonds together to make a protein

20
Q

mRNA is short-lived because

A

it is “chewed up” and translated to become a protein.

21
Q

mRNA start codon

A

AUG

22
Q

mRNA stop codon

A

UAG

23
Q

Eukaryotes package DNA in

A

nucleosomes

24
Q

DNA is wrapped around _____ ; These then stack on top of each other to make ______

A

Histones; chromatin

25
Q

tRNA

A
  • reads three bases at a time

- hydrogen bonds (good because it is reversible)

26
Q

DNA Ligase

A

Adds phosphodiester bonds

27
Q

Template strand of DNA is being sequenced from

A

3’ to 5’

28
Q

Always read DNA strands from

A

5’ to 3’

29
Q

The two strands of DNA are ______ but each forms a right-handed helix

A

antiparallel

30
Q

The _________ occupy the core of the double helix .

A

aromatic bases

31
Q

The ____________ run along the periphery, thereby minimizing the repulsions between charged phosphate groups

A

sugar-phosphate chains

32
Q

The surface of the double helix contains two grooves of unequal width: the ______ and ______ grooves.

A

major and minor

33
Q

Each base is _________ to a base in the opposite strand to form a ______ base pair

A

Hydrogen bonded ; Planar

34
Q

Incoming dNTP is attacked at the _____ phosphate by the ____ hydroxyl of the growing DNA chain.

A

α ; 3’

35
Q

The direction of ribosome movement on the mRNA is

A

5’ to 3’

36
Q

Nucleotides participate in

A
  • oxidation-reduction reactions
  • Energy transfer
  • Intracellular signaling
  • biosynthetic reactions
37
Q

Stem-loop structure is the result of

A

RNA bases pairing with themselves.

38
Q

Molecular Cloning with Restriction Enzymes

A

The cloning vector and the foreign DNA are cut by the same restriction endonuclease –> The sticky ends of the vector and the foreign DNA fragments anneal and are covalently joined by DNA ligase –> Result: chimeric DNA containing a portion of the foreign DNA inserted into the vector

39
Q

Polymerase Chain Reaction (PCR)

A
  • An in vitro method for amplifying the amount of a particular DNA sequence.
    1. Separate strands by heating, cooling, and annealing primers
    2. Extend primers by DNA polymerase
    3. Repeat steps 1 & 2