chapter 3 p2 Flashcards
- Carbohydrates
contain the elements carbon, hydrogen, and oxygen.
Carbohydrate literally means hydrated carbon’ (carbon and water).
The elements in carbohydrates usually appear in the ratio Cx (H20)y - This is known as the general formula of carbohydrates.
Carbohydrates are also known as saccharides or sugars.
monosaccharides:
- A single sugar unit
examples include glucose, fructose, and ribose.
When two monosaccharides link together they form a disaccharide, for example lactose and sucrose.
polysaccharide
When two or more (usually many more) monosaccharides are linked they form a polymer
- e.g Glycogen, cellulose, and starch
Glucose:
- The basic building blocks, or monomers, of some biologically important large carbohydrates are glucose molecules, which have the chemical formula C6H12O6
- Glucose is a monosaccharide composed of six carbons and therefore is a hexose monosaccharide (hexose sugar)
- In molecular diagrams the cardons are numbered clockwise beginning with the carbon on the right (clockwise) of the oxygen atom within the ring.
- There are two structural variations of the glucose molecule, alpha (a) and beta (3) glucose, in which the OH (hydroxyl) group on carbon 1 is in opposite positions, as shown in Figure 1.
properties of glucose molecules
are polar and soluble in water.
This is due to the hydrogen bonds that form between the hydroxyl groups and water molecules.
This solubility in water is important, because it means glucose is dissolved in the cytosol of the cell.
Condensation reactions:
p1
- When two alpha glucose molecules are side by side, two hydroxyl groups interact (react).
- When this happens bonds are broken and new bonds reformed in different places producing new molecules.
- As you can see in Figure 2, two hydrogen atoms and an oxygen atom are removed from the glucose monomers and join to form a water molecule.
- A bond forms between carbons 1 and 4 on the glucose molecules and the molecules are now joined.
- A covalent bond called a glycosidic bond is formed between two glucose molecules.
- The reaction is called a condensation reaction because a water molecule is formed as one of the products of the reaction.
- Because in this reaction carbon 1 of one glucose molecule is joined to carbon 4 of the other glucose molecule, the bond is known as a 1,4 glycosidic bond.
- In this reaction the new molecule is called maltose.
- This is an example of a disaccharide (a molecule made up of two monosaccharides).
Other sugars:
- Fructose and galactose are also hexose monosaccharides.
- Fructose naturally occurs in fruit, often in combination with glucose forming the disaccharide sucrose, commonly known as cane sugar or just sugar.
- Galactose and glucose form the disaccharide lactose.
- Lactose is commonly found in milk and milk products.
- Fructose is sweeter than glucose and glucose is sweeter than galactose.
- Pentose monosaccharides are sugars that contain five carbon atoms.
- Two pentose sugars are important components of biological molecules - ribose is the sugar present in RNA nucleotides and deoxyribose is the sugar present in DNA nucleotides.
starch.
Many alpha glucose molecules can be joined by glycosidic bonds to form two slightly different polysaccharides known collectively as starch.
Glucose made by photosynthesis in plant cells is stored as starch. It is a chemical energy store.
- the polysaccharides in starch is amylose amylopectin.
Glycogen
Amylose
formed by alpha glucose molecules joined together only by 1-4 glycosidic bonds.
The angle of the bond means that this long chain of glucose twists to form a helix which is further stabilised by hydrogen bonding within the molecule.
This makes the polysaccharide more compact, and much less soluble, than the glucose molecules used to make it.
amylopectin.
Another type of starch is formed when glycosidic bonds form in condensation reactions between carbon 1 and carbon 6 on two glucose molecules.
also made by 1-4 glycosidic bonds between alpha glucose molecules, but (unlike amylose) in amylopectin there are also some glycosidic bonds formed by condensation reactions between carbon 1 and carbon 6 on two glucose molecules.
this means that amylopectin has a branched structure, with the 1-6 branching points occurring approximately once in every 25 glucose subunits.
glycogen
The functionally equivalent energy storage molecule to starch in animals and fungi
Glycogen forms more branches than amylopectin, which means it is more compact and less space is needed for it to be stored.
This is important as animals are mobile, unlike plants.
The coiling or branching of these polysaccharides makes them very compact, which is ideal for storage.
The branching also means there are many free ends where glucose molecules can be added or removed
This speeds up the process of storing or releasing glucose molecules required by the cell.
key properties of amylopectin and glycogen
insoluble, branched, and compact.
These properties mean they are ideally suited to the storage roles that they carry out.
Hydrolysis reactions:
Glucose is stored as starch by plants or glycogen by animals and fungi.
until it is needed for respiration - the process in which biochemical energy in these stored nutrients is converted into a useable energy source for the cell.
To release glucose for respiration, starch or glycogen undergo hydrolysis reactions, requiring the addition of water molecules.
The reactions are catalysed by enzymes.
these are the reverse of the condensation reactions that form the glycosidic bonds.
Cellulose: p1
Beta glucose molecules are unable to join together in the same way that alpha glucose molecules can.
As you can see in Figure 5, the hydroxyl groups on carbon 1 and carbon 4 of the two glucose molecules are too far from each other to react.
The only way that beta glucoses molecules can join together and form a polymer is if alternate beta glucose molecules are turned upside down as in Figure 6.
When a polysaccharide is formed from glucose in this way it is unable to coil or form branches.
A straight chain molecule is formed called cellulose
Cellulose: p2
Cellulose molecules make hydrogen bonds with each other forming microfibrils.
These microfibrils join together forming macrofibrils, which combine to produce fibres (Figure 8).
These fibres are strong and insoluble and are used to make cell walls.
Cellulose is an important part of our diet, it is very hard to break down into its monomers and forms the ‘fibre’ or ‘roughage’ necessary for a healthy digestive system.