Nucleic Acids

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    • There are two types of nucleic acids - Deoxyribonucleic acids and ribonucleic acids.
    • Monomers of nucleic acids are called nucleotides.
    • RNA has similarities with DNA but differs in its sugar component (deoxyribose vs ribose), presence of uracil instead of thymine, and single strandedness.
    • The structure of DNA consists of four bases (adenine, thymine, cytosine, guanine) arranged into complementary base pairs (A-T, C-G).
    • DNA Nucleotides consist of a phosphate group, a pentose sugar called deoxyribose and a nitrogenous base.
    • Overall, the DNA nucleotide is negatively charged due to:
      • The negatively charged phosphate group
      • Which is useful when DNA combines with positively charged histones in the nucleus to form new chromosomes.
    • Difference between DNA and RNA nucleotides include:
      • In DNA, there is only hydrogen attached at carbon 2 on the carbon ring, making it a deoxyribose sugar.
      • In RNA, there is a hydroxyl (OH) group attached on carbon 2 on the carbon ring, making it a ribose sugar.
      • DNA nucleotides may contain the bases - adenine, guanine, cytosine, thymine.
      • RNA nucleotides do NOT contain thymine, it's replaced with Uracil
    • Purine bases are adenine and guanine - they consist of 3 carbon rings.
    • Pyramidine bases are thymine, cytosine and uracil - they consist of 2 carbon rings.
    • Adenine and thymine form 2 hydrogen bonds.
    • Guanine and cytosine form 3 hydrogen bonds.
    • Polynuclotides are monomers of nucleotides that join together via condensation reaction, removing a water molecule, joined together through phosphodiester bonds.
    • How are polynucleotides formed?
      1. The phosphate group on carbon 5 of the pentose sugar of a nucleotide forms phosphodiester bond with the OH group at carbon 3 on the pentose sugar of another adjacent nucleotide, via condensation reaction, removing a water molecule.
      2. This forms a strong sugar phosphate backbone, with a nitrogenous base attached to each suagar.
    • Why are phosphodiester bonds very strong?
      To ensure that the genetic code is not broken down, preventing mutations.
    • How do DNA double helixes form?
      • Two anti-parallel strands of polynucleotides
      • Join together via hydrogen bonds between the complementary bases through complementary base pairing.
      • The anti-parallel strands then twist and coil around each other
      • Forming a DNA double helix.
    • Sugar phosphate backbone - function
      • It is a strong structure due to the strong phosphodiester bonds
      • This allows DNA to be stable and rigid, to prevent the genetic code from breaking down.
    • Double-helix - function
      • Contains sugar phosphate backbone outside with strong phosphodiester bonds
      • Contains weak hydrogen bonds between the nitrogenous bases on the inside
      • The sugar phosphate backbone protects the weak hydrogen bonds on the inside, preventing the genetic code from breaking down.
    • Weak hydrogen bonds - function
      • Allows DNA helicase to break the bonds between complementary bases to be used for replication.
    • DNA is large and compact - function
      • This means it stores more genetic information
      • Therefore more of it can combine with histones to form more of the stable chromosome.
    • DNA has complementary bases - function
      • This allows identical copies of it to be made, with the correct genetic information.
    • DNA Purification Step 1 with reasons

      Grind sample with water - to break the cell wall of the plant cell.
    • DNA Purification STEP 2 with reasons

      Add the ground sample to a test tube and add detergent - this breaks down the cell membrane and the nuclear envelope, which releases DNA from the nucleus.
    • DNA Purification STEP 3 with reasons
      Add the enzyme protease into it - this breaks down the proteins, histones, that are combined with DNA.
    • DNA Purification STEP 4 with reasons

      Add drops of ethanol - this causes DNA to precipitate as a white solid
    • DNA purification STEP 5 with reasons

      Remove the precipitate of DNA by wrapping it around a glass rod
    • Semi-conservative replication STEP 1

      DNA helicase unzips the double helix by breaking the hydrogen bonds between the complementary bases.
      Leaving with two separate strands of DNA with exposed bases.
    • Semi-conservative replication STEP 2

      Free DNA nucleotides in the nucleus pair up with the complementary bases by a process of complementary base pairing.
      They form hydrogen bonds between the complementary bases.
      Adenine pairs up with thymine, Guanine pairs up with cytosine.
    • Semi-conservative replication STEP 3

      The enzyme DNA polymerase then joins the free nucleotides together via condensation reaction, producing phosphodiester bonds between them, this process is also known as polymerisation (making a polymer).
      A sugar phosphate backbone is now formed, which is very strong and rigid.
    • Semi-conservative replication STEP 4

      The strands then twist and coil around each other, forming a double helix structure of DNA.

      This leaves us with two identical DNA molecules.
    • Why is this called Semi-conservative

      This is because in the new DNA molecule, one of the strands is an old/original template, and the other is the new template.
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