nucleic acids Flashcards

1
Q

define nucleic acids

A

large polymeric molecules:

- limited number of repeating units that are covalently linked to form long chains

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2
Q

difference between RNA and DNA

A

RNA: ribonucleic acid (most abundant, several functions, extremely unstable - hydrolyses quickly)
DNA: deoxyribonucleic acid (storage genetic information)

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3
Q

what is a nucleotide?

A
  • basic components of DNA and RNA
  • energy currency (ATP)
  • hormone-like functions (cAMP) in regulation of metabolism
  • components of coenzymes
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4
Q

what are the main components of nucleotides?

A

one or more phosphate groups (3’ or 5’), strong acid
- more phosphates can be linked together via phosphoanhydric bonds
ribose or deoxyribose
nitrogenous base (heterocyclic compound with nitrogen with basic properties) linked to C1 atom via beta-N-glycosidic linkage

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5
Q

biological nucleotides

A

pentose D-ribose

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6
Q

DNA

A

pentose D-2’-deoxyribose

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7
Q

nucleosides and the work of adenosine

A

breakdown and synthesis intermediate of nucleotides and nucleic acids

  • no phosphate ester (ribose/deoxyribose + base)
  • found in metabolism reactions
  • ex. adenosine -> neurotransmitter regulating sleep/wake cycle binding to specific neuronal adenosine receptors
    - adenosine levels increase during the day and decrease during sleep
    - when bound to receptor induces sleep
    - antagonist of adenosine: caffeine (natural alkaloid found in plants) binds to receptor without activating it
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8
Q

properties of nitrogenous bases

A
  • planar
  • aromatic
  • heterocyclic derived from purine/pyrimidine
  • acidity: phosphate groups are ionised, first ionisation is strong ad following are less acidic due to charge repulsion (more negative charges)
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9
Q

describe the bond in nitrogenous bases

A

high energy phosphoanhydric bonds -> hydrolysis releases -31 kJ/mol

  • anhydride bonds causes high energy
  • ATP reacts with water in presence of Mg+ (acts as catalist) -> free phosphate groups can stabilise the charge by resonance, creating low energy compounds
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10
Q

mechanism of polymerisation

A
  • each nucleotide has free phosphoric acid functional group and 1/2 alcohol functions (-OH)
  • acids and alcohols can condense to form esters and release water to create oligonucleotides (many nucleotides linked together)
    - delta G-> +25 kJ/mol
    • unfavourable in aqueous solutions
    • can be synthesised through activation of individual nucleotides
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11
Q

oligonucleotides

A
  • linked through phosphodiester bonds between 3’ hydroxyl of nucleotides N and the 5’ phosphate of nucleotide N+1
  • 5’ to 3’ polarity of chain -> looking in 5’ to 3’ direction atoms are different than 3’ to 5’ direction
  • primary structure: sequence of nucleotides linked by phosphodiester bonds -> sequence nitrogenous bases
  • can be synthesised in lab
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12
Q

structure of DNA

A

winds as double helix (2 chains)
- right handed (due to chirality)
the two chains have opposite polarity -> one is 5’->3’ the other 3’->5’
- backbone is deoxyribose+phosphate groups, outside of molecule (exposed to water since phosphate fives hydrophobic properties)
- bases are inside the structure (shielded from solvent)
- interact through N bonds (A-T, G-C)
- sequence is not restricted (can be changed and adapted to carry genetic information without changing overall structure)

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13
Q

base pairing in DNA

A
  • carry genetic information
  • double helix allows for semi-conservative replication
    • one filament is template for synthesis of the opposite
  • bases inside the helix are paired with specific hydrogen bonding pattern
    • A–T (2H bonds)
    • G—C (3H bonds)
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14
Q

biological synthesis of DNA

A
  • condensation of 2 nucleotides is disfavoured by the positive free-energy variation between reactants and products
    • use of (deoxy)nucleotides triosphates
    • anhydrid is used as it is more reactive
    • ergonic reaction that releases energy
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15
Q

structure and synthesis of RNA

A
  • pentose
  • bases A U G C can be modified after synthesis of nucleic acid
  • mostly single-stranded but forms helix structures by pairing different parts of same molecule (fold other making H bonds)
  • genetic material for viruses
  • high turnover in cells -> easily hydrolysed in process catalysed by ribonuclease
  • synthesis in most organisms is catalysed by DNA-dependent RNA polymerase
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