Biology

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    • All life on Earth shares a common chemistry. This provides indirect evidence for evolution.
    • Despite their great variety, the cells of all living organisms contain only a few groups of carbon based (organic) compounds that interact in similar ways.
    • Carbohydrates
      Commonly used by cells as respiratory substrates. They also form structural components in plasma membranes and cell walls.
    • Monomers
      Small identical or similar molecules which can be condensed (joined/linked together) to make larger molecules called polymers.
    • Polymers
      Large molecules made from joining many (3 or more) identical or similar monomers together.
    • Monomer linking into polymers
      1. Condensation reaction
      2. Removal of one water molecule
      3. Forms a bond
    • Polymer breakdown into monomers
      1. Hydrolysis reaction
      2. Addition of one water molecule
      3. Breaks the bond between two monomers
    • Carbohydrate structure

      Elements: Carbon, Hydrogen, Oxygen
      Ratio of H:O is 2:1
      Generic formula: (CH2O)n when n=3 to 7
    • Monosaccharides
      Carbohydrate monomers that can join together in condensation reactions to create disaccharides and polysaccharides
    • Monosaccharides
      • Glucose, galactose, fructose
    • Alpha glucose

      Chemical formula: C6H12O6
      Structure shown with carbon atoms numbered
    • Bonds between glucose molecules often refer to the carbon atom the bond attaches to, e.g. 1-4 glycosidic bond.
    • Condensation reaction between monosaccharides
      1. Two monosaccharides (glucose) join
      2. Forms a disaccharide (maltose)
      3. Releases one water molecule
    • Glycosidic bond

      Bond that forms between monosaccharides in a condensation reaction
    • Disaccharides
      • Maltose, lactose, sucrose
    • Hydrolysis of disaccharides
      1. Disaccharide (maltose) + water
      2. Yields two monosaccharides (glucose)
      3. Glycosidic bond is broken
    • Carbohydrates
      • Monosaccharides
      • Disaccharides
      • Polysaccharides (starch, glycogen, cellulose)
    • Starch
      • Long, linear chains of alpha glucose
      Coils into a helix
      Compact structure good for storage
      Insoluble so doesn't affect water potential
      Large so can't diffuse out of cells
    • Amylopectin
      • Branched chain of alpha glucose
      1. 4 and 1-6 glycosidic bonds
      Large surface area for rapid hydrolysis by enzymes
      Insoluble so doesn't affect water potential
      Large so can't diffuse out of cells
    • Glycogen
      • Similar to starch but with shorter chains and more branching
      Larger surface area for rapid hydrolysis into glucose
      Stored in muscles and liver
      Insoluble so doesn't affect water potential
    • Alpha glucose is the monomer found in starch and glycogen. Beta glucose is the monomer found in cellulose.
    • Cellulose
      • Long, straight, unbranched chains of beta glucose
      Every other beta glucose rotates 180 degrees
      Chains held together by hydrogen bonds to form microfibrils/macrofibrils
      Provides strength and support to plant cell walls
    • The structure of cellulose
      Is related to its role in providing strength and support to plant cell walls
    • Hydrogen bonds are important in cellulose molecules as they hold the chains/cellulose molecules together, providing strength and rigidity.
    • Benedict's test for reducing sugars

      Add Benedict's solution, heat to 95°C
      Colour change to green/yellow/orange/red precipitate indicates reducing sugars
    • If no colour change in Benedict's test, could indicate presence of non-reducing sugars.
    • Benedict's test for non-reducing sugars

      If no change in Benedict's test for reducing sugars, then heat the solution further
    • Two reducing sugar solutions (A and B) have an enzyme added
      After 20 minutes, solution B had twice as much precipitate as A
    • Precipitate
      Shows reducing sugar present
    • Benedict's test for reducing sugars
      1. 2 different reducing sugar solutions (A & B) of the same concentration have an enzyme added
      2. Solution B had twice as much precipitate than A after 20 minutes
    • Suggest why solution B had twice as much precipitate than A after 20 minutes
    • Benedict's test for Non-Reducing Sugar

      Sucrose is the only NR sugar you need to know however there are others
    • Steps to show a non-reducing sugar is present
      1. Heat a sample with acid for a few minutes to hydrolyse the glycosidic bonds
      2. Neutralise the solution with an alkali
      3. Heat again with Benedict's reagent
      4. Brick red precipitate shows a positive result
    • The Benedict's test is only a semi-quantitative test for sugars
    • Colorimeter
      Quantitative test that measures the intensity of light transmitted through a solution/sample
    • Standardising the method for colorimeter
      1. Shake samples before testing
      2. Zero the colorimeter before use
      3. Use the same filter throughout
      4. Use same volume for each reading
    • Arbitrary unit (AU)

      Unit used to measure absorbance in a colorimeter
    • Producing a calibration curve for an unknown reducing sugar
      1. Make up known concentrations of the sugar
      2. Carry out Benedict's test on each sample
      3. Measure absorbance/transmission with colorimeter
      4. Plot calibration curve with concentration on X axis and absorbance/transmission on Y
      5. Find unknown concentration from calibration curve
    • Testing for starch
      1. Add potassium iodide (KI) solution
      2. Blue-black colour indicates presence of starch
    • Triglycerides
      Storage molecules made from glycerol and 3 fatty acids
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