Carbohydrates Flashcards
1
Q
What are carbohydrates?
A
- Consist of only Carbon, Hydrogen and Oxygen.
- General formula: Cx(H2O)y
- Single sugar unit is knows as Monosaccharide e.g glucose, fructose and ribose.
- When two monosaccharides link they form polymer called polysaccharide e.g glycogen, cellulose and starch.
2
Q
Glucose
A
- Has six carbon atoms so called Hexose monosaccharide.
- The basic building blocks of some biological important large carbohydrates. C6H12O6.
- Alpha glucose has OH at the bottom.
- Beta has OH at the top.
- Glucose molecules are polar and soluble in water because of the hydrogen bonds that form between the hydroxyl groups and water molecules.
- This allows it to be dissolved in the cytosol of cells.
3
Q
Condensation reaction
A
- When 2 Alpha glucose molecules are side by side, 2 hydroxyl group interact.
- This produces MALTOSE + WATER.
- A covalent bond called a glycosidic bond forms between carbons 1 and 4. This is called 1,4 glycosidic bond.
- The ‘O’ that is left from the two OH on Alpha molecules is the one that joins the two.
4
Q
Other sugars
A
- Fructose and galactose are also hexose monosaccharides.
- Fructose naturally occurs in fruit; combines with glucose to form Sucrose.
- Galactose + glucose form Lactose.
- Fructose is sweeter than glucose and glucose is sweeter than galactose.
- Pentose monosaccharides contain 5 carbon atoms.
- Ribose is a pentose sugar and it’s in RNA and Deoxyribose is in DNA.
5
Q
Starch
A
- Glucose in plant cells is stored as starch, making its the main energy storage material in plants.
- Starch is INSOLUBLE so it doesn’t cause water to enter cells by osmosis (which would make them swell).
- Starch is a mixture of 2 polysaccharides of alpha-glucose: amylose and amylopectin.
6
Q
Amylose
A
- Long, unbranched chain of alpha-glucose.
- Formed by condensation reactions making glycosidic bonds at carbon 1 and 4.
- Angles of glycosylic bonds give it a coiled structure.
- Making it compact which is good for storage as it can fit in small spaces.
7
Q
Amylopectin
A
- Long, branched chain of alpha-glucose.
- Also made by 1,4 glycosidic bonds but also some glycol bonds are formed by condensation reactions between carbon 1 and 6, giving branched structure.
- 1-6 branching points occur approx. once ever 25 glucose subunits.
- Side branches allow enzymes that break down the molecule to get at the glycosidic bonds easily.
- This allows glucose to be released quickly.
8
Q
Glycogen
A
- Main energy storage material in animals.
- Animal cells store excess glucose as glycogen.
- Has more side branches that amylopectin.
- Many branches = glucose can be released quickly.
- Also very compact and insoluble so it’s good for storage.
9
Q
Hydrolysis reactions
A
- Glucose is stored until its needed for respiration - the process in which biochemical energy in these stored nutrients is converted into useable energy source for the cell.
- To release glucose, starch or glycogen undergo hydrolysis reactions which requires adding water molecules.
- Reactions are catalysed by enzymes.
- These are the reverse of condensation reactions.
10
Q
Cellulose
A
- Beta-glucose are unable to join in the same way as alpha because the hydroxyl groups on carbon 1 and 4 of the 2 glucose molecules are too far away.
- Only way they can join is if alternate beta-glucose molecules are turned upside down.
- This prevents it from coiling or branching and creates cellulose.
- Cellulose is the major component of cell walls in plants.
- The cellulose chains are linked together by H-bonds to form strong fibres called microfibrils. Microfibrils join together to form macrofibrils, which combine to produce fibres.
- This makes cellulose able to provide structural support for cells.