chapter 8 objectives Flashcards

1
Q

what is the griffith experiment; role in discovering DNA

A

s. pne could either be smooth with capsule (more virulent) or rough without capsule

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2
Q

contribution of oswald with streptococcus pneumoniae

A

found that animals survived when they targeted DNA and that DNA was key to transformation of rough to smooth

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3
Q

overview of hershey chase experiment

A

proved that dna was hereditary material becayse when bacteriophages infect host only their DNA enters cell

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4
Q

contributions of watson and crick

A

they founded the structure of DNA shape (double helix)

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5
Q

4 nitrogenous bases in rna

A

purines: adenine and guanine
pyrimidines: uracil, cytosine

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6
Q

sugar in rna

A

ribose

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7
Q

dna vs rna

A

function: molecule of inheritance (d) protein synthesis (r)
location: nucleiod (d) proteins (r)
bases: a,g,c,t (d) a,g,c,u (r)
sugar: deoxyribose, ribose
structure: double stranded vs single stranded

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8
Q

central dogma

A

DNA–> RNA–> proteins

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9
Q

why is dna semi conservative

A

one strand is used as a template, while the other remains as an original strand

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10
Q

2 types of bacterial dna replication

A

bidirectional replication:
rolling circle replication

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11
Q

steps of bacterial dna replication

A

topoismerases unwinds dna, helicases breaks down bonds, binding proteins keep strands apart, dna poly III adds nucleotides, rna primase adds primers, ligase brings together okazaki fragments

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12
Q

what direction does dna polymerase II read

A

it reads in a 3’ to 5’ direction

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13
Q

synthesis of leading/lagging strands during dna replication

A

leading strand is sythesized 5’ to 3’ while lagging strand is synthesized 3’ to 5’

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14
Q

enzymes and the role they play in dna replication

A

Helicase: unzipping the DNA helix
Gyrase: helping to untangle the DNA supercoils
Primase: synthesizing an RNA primer
DNA polymerase III: adding bases to new DNA chain; proofreading the chain for mistakes
DNA polymerase I: removing primer, closing gaps, repairing mismatches
Ligase: final binding of nicks in DNA during synthesis and repair
Topoisomerases I and II: supercoiling and untangling

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15
Q

structural/functional differences between rna and dna

A
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16
Q

transcription

A

dna–> rna
initiation: sigma determines transcription starting pt
elongation: sigma released, rna polymerase moves along strand
termination: termination sequence tells rna polymerase to stop adding

17
Q

three types of rna involved in traslation

A

mRNA, tRNA, rRNA

18
Q

wobble

A

multiple codons can code for the same amino acid because only the first two nucleotides are required to encode the correct amino acid, the third will not change its sense

19
Q

codon

A

3 bases that code for one amino acid

20
Q

anticodon

A

carried by tRNA and contains complementary nucleotides to the codon in mRNA

21
Q

three start and stop codons

A

start: AUG
stop: UAA, UAG, and UGA

22
Q

locations of promoter, start codon, and a/p sites during translation

A

promoter: DNA
start: on mRNA
A site: holds the next amino acid
P site: holds growing polypeptide chain

23
Q

transcription/translation bacteria vs. eukaryotic

A

eukaryotic: transcription happens in nucleus, separate process, translation on 80s ribosomes
bacteria: happens simultaneously in cytoplasm using 70s ribosomes