Chapter 2 Biological Molecules Flashcards
(46 cards)
Benedict’s test for reducing sugars
Equal volume of sample being tested and Benedict’s solution, mixed and heated in a water bath.
- POSTIVE: green, yellow, orange, brick-red ( depending on amount of reducing sugar present )
- NEGATIVE: solution remains blue
Iodine test for starch
Using a pipette, add few drops of iodine solution to the sample.
- POSTIVE: sample will turn blue-black
- NEGATIVE: remains orange-brown
Emulsion test for lipids
Add equal volume of sample, ethanol and distilled water, shake.
- POSTIVE: forms a white, milky emulsion
- NEGATIVE: remains clear
Biuret test for proteins
Equal volume of sample and biuret solution, mix.
- POSTIVE: purple
- NEGATIVE: remains blue
Test to identify the presence of
non-reducing sugars
Hydrochloric aid is added to hydrolyse the sugar in the sample in a ratio of 1:2, and heated. Sodium hydroxide is added to make the solution alkaline. Benedict’s test is carried out.
- POSTIVE: green, yellow, orange, brick-red
- NEGATIVE: remains blue
Structure of α-glucose and β-glucose
Glucose has molecular formula C6H12O6
- α-glucose: The –OH on carbon 1 is below the ring
- β-glucose: The –OH on carbon 1 is above the ring
Define monomer
A simple molecule which is used as a basic building block for the synthesis of a polymer
Define polymer
A giant molecule made from many similar repeating subunits joined together in a chain, held together by covalent bonds
Define macromolecule
A large molecule formed due to polymerisation
Define monosaccharide
A molecule consisting of a single sugar unit with the general formula (CH2O)n
Define disaccharide
A sugar molecule consisting of two monosaccharides joined together by a glycosidic bond
Define polysaccharide
A polymer whose subunits are monosaccharides joined together by glycosidic bonds
Is sucrose a reducing sugar or non-reducing sugar?
Non-reducing sugar
Name some reducing sugars
- Glucose
- Fructose
- Maltose
Formation of a glycosidic bond
A C-O-C link formed when two monosaccharides undergo condensation reaction, releasing a water molecule.
Breakage of a glycosidic bond
- The breakage of a glycosidic bond occurs through hydrolysis
- Acid hydrolysis of sucrose breaks glycosidic bond to retrieve the monomers
What are the two components that make up starch?
Amylose and Amylopectin
Molecular structure of amylose
- α-1,4 glycosidic bond
- Helical and more compact
- Unbranching
Molecular structure of amylopectin
- α-1,4 and 1,6 glycosidic bonds
- Branched
Molecular structure of glycogen
Used for storage of energy in animal cells
- α-1,6 glycosidic bonds
- Branched
Molecular structure of cellulose
- Found in plant cell walls
- β-1,4 glycosidic bonds
- Alternate Beta glucose molecules are rotated 180° to form bonds
- 60-70 cellulose molecules tightly cross-linked to form bundles called microfibrils
- Microfibrils are held together in bundles called fibres by hydrogen bonds
Formation and molecular structure of triglycerides
- Forms by condensation of 3 fatty acids and a glycerol molecule, forming an ester bond
Unsaturated fatty acids
C=C bonds
Saturated fatty acids
C-C bonds