biological molecules - nucleic acids and DNA Flashcards

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1
Q

what is the structure of a DNA nucleotide

A

a deoxyribose pentose sugar attached to a phosphate group (PO4 3-) and a nitrogenous base

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2
Q

what is the difference between DNA and RNA

A

DNA = deoxyribonucleic acid
RNA = ribonucleic acid

the pentose sugar in DNA is deoxyribose, in RNA it is ribose

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3
Q

what is the monomer unit for nucleic acids

A

nucleotides

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4
Q

what are the 5 nitrogenous bases

A

A - adenine
C - cytosine
G - guanine
T - thymine (DNA only)
U- uracil (RNA only)

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5
Q

what bonds are found in nucleic acids strands

A

phosphodiester bonds

these form between the phosphate group of carbon 5 and the OH group on carbon 3 of pentose sugar
formed in a condensation reaction
broken by hydrolysis

these form the sugar-phosphate backbone

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6
Q

what bonds are formed between bases

A

hydrogen bonds

A+T+U form 2 hydrogen bonds
C+G form 3 hydrogen bonds

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7
Q

what are the complementary base pairs

A

C+G
A+T in DNA / A+U in RNA

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8
Q

what are the 2 types of bases

A

purine and pyramidine

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9
Q

which bases are purine

A

A G

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10
Q

which bases are pyramidine

A

C U T

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11
Q

what is the difference between purine and pyramidine bases

A

purine bases are larger due to double C rings

pyramidine bases are smaller due to single C rings

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12
Q

how does complementary base pair bonding ensure 2 DNA strands are equidistant

A

purines bond with pyramidines

as purines are larger and pyramidines are smaller this ensures there is a constant distance between sugar-phosphate backbone

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13
Q

how are DNA/RNA sequences read

A

from 5’ to 3’

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14
Q

DNA strands are not described as parallel
- what are they described as and why

A
  • antiparallel
  • one strand runs from 5’ to 3’ and the other runs from 3’ to 5’
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15
Q

why are DNA strands antiparallel

A

one strand must be rotated 180 degrees to allow for hydrogen bonding between bases

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16
Q

outline the steps involved in DNA extraction with a plant sample

A
  • grind up sample using a pestle and mortar
  • mix sample with detergent
  • add salt
  • add protease
  • add ice cold ethanol down the side of the test tube
17
Q

why must the sample be ground during DNA extraction

A

to break down cell walls

18
Q

why is detergent added during DNA extraction

A

to break down cell membrane, releasing cell contents

19
Q

why is salt added during DNA extraction

A

neutralises charges on phosphates in DNA backbone + breaks hydrogen bonds between DNA and water, so it is less soluble

20
Q

why is protease added during extraction of DNA

A

breaks down histone proteins associated with DNA

21
Q

why is ice cold ethanol added during the extraction of DNA

A

this causes the DNA to form a white precipitate between the layer of the sample and the ethanol

ice cold as it helps to make DNA more insoluble

22
Q

why must the extraction of DNA be carried out at a low temperature

A

reduces the rate of enzyme controlled reactions that break down DNA

23
Q

why is it important that cell replication results in 2 genetically identical molecules of DNA

A

this ensures the continuation of a species

24
Q

why is DNA replication described as being semi conservative

A

each one of the 2 daughter DNA molecules contains one original strand and one newly synthesised strand

25
Q

outline the steps of DNA replication

A
  • DNA molecule unwinds and hydrogen bonds between bases are broken by DNA helicase, unzipping molecule
  • free floating nucleotides in the nucleoplasm pair up with bases on original DNA strands via complementary base pairing
  • DNA polymerase forms phosphodiester bonds, reforming sugar-phosphate backbone and molecules retwist to form double helix shapes
  • 2 new DNA molecules are produced
26
Q

what are 2 functions of DNA

A
  • storage and transfer of genetic information
  • protein synthesis
27
Q

what is the difference between deoxyribose and ribose

A

deoxyribose has no OH group on carbon 2

28
Q

why is DNA replication important

A

DNA needs to replicate for mitosis/meiosis

29
Q

what are 3 important features of the DNA code

A
  • degenerate
  • non-overlapping
  • universal
30
Q

what is a primer

A

a short piece of RNA or DNA with a complementary sequence to part of the DNA template

31
Q

what is the difference between the leading strand and the lagging strand

A

the leading strand is built continuously and the lagging strand is built discontinuously

32
Q

why is there 1 leading strand and 1 lagging strand

A

due to the antiparallel nature of DNA

33
Q

why are primers needed in DNA replication

A

DNA polymerase requires them in order to bind to the 3’ OH group and begin reforming the sugar-phosphate backbone

34
Q

what does the discontinuous building of the lagging strand lead to the production of

A

okazaki fragments

35
Q

what are 3 reasons that complementary base pairing important in DNA replication

A
  • reduces occurance of mutations
  • allows for the formation of hydrogen bonds that holds strands together
  • DNA is replicated without error
36
Q

what are 3 differences between DNA and RNA

A

DNA is double stranded, RNA is single stranded

DNA has ACTG, RNA has ACUG

DNA is too big to leave the nucleus, RNA is small enough to fit through nuclear pores

37
Q
A