Nucleic Acids

Nucleic acids are large molecules located in cell nuclei.

  • Two main types: DNA (deoxyribose nucleic acid) and RNA (ribose nucleic acid); both play key roles in protein synthesis and the transfer of genetic information.

  • Provide the basis for hereditary material.

  • Elements contained: Carbon, Nitrogen, Oxygen, Phosphorus, Hydrogen.

  • Structure: Large polymers formed from many nucleotides (monomers) linked together in a chain.

Individual Nucleotide Structure
  • Pentose monosaccharide (sugar): Contains 55 carbon atoms.

  • Phosphate group: A negatively charged inorganic molecule (PO42−\text{PO}_4^{2-}).

  • Nitrogenous base: Complex organic molecule containing 11 or 22 carbon rings plus nitrogen.

Nucleotides
  • Linked together by condensation reactions to form polymers (polynucleotides).

  • Phosphodiester bonds: The phosphate group at the 5′5' carbon of the pentose sugar of one nucleotide forms a covalent bond with the hydroxyl (-OH\text{-OH}) group at the 3′3' carbon of the pentose sugar of an adjacent nucleotide.

  • Phosphodiester bonds form a long, strong sugar-phosphate backbone with a nitrogenous base attached to each sugar.

  • Phosphodiester bonds can be broken via hydrolysis (the reverse of condensation reactions), releasing individual nucleotides.

Deoxyribonucleic Acid (DNA)
  • Sugar in DNA: Deoxyribose (a sugar containing one less oxygen atom than ribose).

  • DNA consists of nucleotides with 44 different bases, divided into 22 main groups: Pyrimidines and Purines.

Pyrimidines
  • Smaller bases with single carbon-ring structures.

  • Thymine (T), Cytosine (C).

Purines
  • Larger bases with double carbon-ring structures.

  • Adenine (A), Guanine (G).

The Double Helix
  • DNA molecules vary in length from a few to millions of nucleotides.

  • Made up of 22 polynucleotide strands coiled into a double helix.

  • Held together by hydrogen bonds between complementary bases.

  • Each strand has a phosphate group (5′5') at one end and a hydroxyl group (3′3') at the other end.

  • Both strands run in opposite directions (antiparallel).

Base Pairing Rules
  • Adenine + Thymine: Form 22 hydrogen bonds and always pair with each other.

  • Cytosine + Guanine: Form 33 hydrogen bonds and always pair with each other (complementary base pairing).

  • A pyrimidine base always binds to a purine base, resulting in a constant distance between the DNA backbones (parallel polynucleotide chains).

  • Complementary base pairing means DNA always contains equal amounts of adenine and thymine, as well as equal amounts of cytosine and guanine.

  • The sequence of bases along a DNA strand carries the genetic information of an organism in the form of a code.

Ribonucleic Acid (RNA)
  • Plays an essential role in transferring genetic information from DNA to proteins that make up enzymes and body tissues.

  • DNA stores all genetic information of an organism but cannot supply this information directly to protein synthesis sites because eukaryotic chromosomes are very long molecules comprising hundreds of genes.

  • RNA transcribes (copies) a gene-sized section of DNA into a short messenger RNA (mRNA) molecule.

    • Individual mRNA molecules are much shorter than a DNA chromosome.

  • RNA nucleotides differ from DNA nucleotides:

    • Pentose sugar is ribose rather than deoxyribose.

    • Thymine (T) is replaced by Uracil (U).

  • RNA nucleotides form polymers via phosphodiester bonds formed in condensation reactions.

  • RNA polymers are small enough to leave the nucleus and travel to ribosomes, where they are central to protein synthesis.

  • After protein synthesis, RNA molecules are degraded in the cytoplasm; phosphodiester bonds are hydrolysed, releasing RNA nucleotides to be reused.

Thymine vs. Uracil
  • Both thymine and uracil are pyrimidines that form 22 hydrogen bonds with adenine, so base pairing rules still apply.

  • RNA nucleotides bind to DNA to make copies of particular sections of DNA.

DNA Extraction

DNA can be extracted from plant material using the following procedure:

  1. Grind sample in a mortar and pestle: Breaks down the cell wall.

  2. Mix sample with detergent: Breaks down the cell membrane, releasing cell contents into solution.

  3. Add salt: Breaks hydrogen bonds between DNA and water molecules.

  4. Add protease enzyme: Breaks down proteins associated with DNA in nuclei.

  5. Add a layer of alcohol (ethanol) on top of sample: Causes DNA to precipitate out of solution.

  6. Observe DNA: DNA appears as white strands forming between the sample layer and alcohol layer; can be collected by spooling it on a glass rod.