Carbohydratemolecules contain the elements carbon, hydrogen and oxygen.
In the human body, carbohydrates are brokendown by enzymes in the mouth and small intestine.
Carbohydrates can be classed into different groups (monosaccharides, disaccharides and polysaccharides) depending on their complexity.
Monosaccharides:
Are simplesugars that consists of a singlemonomer unit e.g. glucose or fructose.
Glucosemolecules contain lots of energy which can be released in respiration by breaking the bondsbetween the carbonatoms.
A disaccharide is made when twomonosaccharidesjointogether.
Maltose is formed from twoglucose molecules.
Sucrose is formed from oneglucose and onefructosemolecule.
A polysaccharide is formed when lots of monomer units jointogether in longchains to form a polymer.
Starch, glycogen or cellulose are all formed when lots of glucose molecules jointogether.
Polysaccharides are insoluble and therefore useful as storagemolecules.
Animo acids in proteins: (Part 1)
Proteins are polymers formed from longchains of monomers called amino acids joined together.
Amino acids contain carbon, nitrogen, hydrogen and oxygenatoms.
Just 20 different standard amino acids make up all the proteins found in the human body (although many more amino acids occur in nature).
Animo acids in proteins: (Part 2)
Amino acids can be arranged in any order, resulting in hundreds of thousands of differentproteins.
Examples of proteins include enzymes, haemoglobin, ligaments and keratin.
In the human body, proteins that we ingest are brokendown into the constituent amino acids.
Enzymes in the stomach and smallintestine break down the protein.
These amino acids can then be used in the synthesis of newproteins.
Amino acids join together to form proteins:
Here it is, but in a picture form.
Protein shape:
Different proteins have differentamino acidsequences resulting in the peptide chainfolding into different shapes.
The function of a protein is determined by its shape.
Even a small difference in the amino acid sequence will result in a completely differentprotein being formed.
In this way, every protein has a unique3-D shape that enables it to carryout its function.
Fatty acids and glycerol in lipids:
Lipids (fats and oils) are made up of triglycerides.
Their basic unit is oneglycerolmoleculechemicallybonded to threefattyacidchains.
Lipids contain carbon, hydrogen and oxygenatoms.
Unlike carbohydrates and proteins, they don't form polymers (they don't form a longchain of repeating sub-units).
Lipids are divided into fats (solids at room temperature)and oils (liquids at room temperature).
In the human body lipids are brokendown by enzymes called lipases in the smallintestine.
The structure of a triglyceride:
Here it is, but in a picture.
Benedict's test (reducingsugars):
A wide range of biologicalmolecules can be tested for using simple chemical tests.
This allows the biologicalmolecules within a sample (such as a food substance) to be determined.
Reducing sugars include simple sugars like glucose that are just made from one unit (monomer), and some sugars made from twounitsjoinedtogether like maltose.
The presence of reducing sugars can be tested for with a Benedict's test.
Test for a reducing sugar:
Add Benedict's reagent (which is blue) to the samplesolution in a testtube.
Heat in a waterbath that has been set at 75•C for 5 minutes.
Take the testtubeout of the waterbath and observe the colour.
A positivetest will show a colour change from blue to orange/dark red.
An orange/darkred precipitate (solid particles suspended in the solution) will form.
A negative test will remain blue.
The amount of colourchange is an indication of the amount of reducing sugar present.
From: blue → green → yellow → orange → red.
Diagram of testing for a reducing sugar:
Here it is, with annotations to.
Iodine test(starch):
We can use iodine to test for the presence or absence of starch in a food sample.
Add drops of iodinesolution to the food sample.
A positive test will show a colourchange from orange-brown to blue-black.
The colour remainsorange-brown if there is nostarch present.
Diagram on testing iodine for starch:
Here it is, with annotations to.
Biuret test (protein):
The biuret test can be used to identify if any protein is present in a sample.
Add drops of biuret solution (a mixture of sodium hydroxide and copper sulphate) to the food sample.
A positive test will show a colourchange from blue to violet / purple.
If there is noproteinpresent, the solution will stay blue.
Diagram on testing Biuret for protein:
Here it is, with annotations to.
Emulsion test (lipids):
An emulsion test can be used to identify if any lipids are present in a sample.
Mix the food sample with 4cm3 of ethanol and shake.
Allow time for the sample to dissolve in the ethanol.
Strain the ethanol solution into anothertesttube.
Add the ethanolsolution to an equalvolume of colddistilled water (4cm3).
A positive test will show a cloudyemulsionforming.
The morelipid is present, the stronger the milky colour will be.
Diagram on testing emulsion for lipids:
Here it is, with annotations to.
Food test results table:
Here it is...
Practical investigation safety tips:
If you were carrying out these tests you should try to identify the main hazards and think of ways to reduceharm.
Biuret solution contains copper (II) sulfate which is dangerous particularly if it gets in the eyes, so always wear goggles.
Iodine is also an irritant to the eyes.
Sodiumhydroxide in biuret solution is corrosive, if any chemicals get onto your skinwash your hands immediately.
Ethanol is highlyflammable; keep it away from any Bunsenburner.
The Bunsenburner itself is a hazard due to the openflame.