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CARBOHYDRATES
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Properties CCarbohydrates – Carbon/Hydrogen/Oxygen FFormula – (CH 2 O) n RRatio: Carbon 1: Hydrogen 2: Oxygen 1 UUSES: energy source, structural components, combination with other compounds such as GLYCOPROTEINS IISOMERS are different structural arrangements of the same number and types of atoms Eg. C 6 H 12 O 6 – glucose, fructose and galactose OOPTICAL ISOMERS are identical in every way but are mirror images of each other Eg. α Glucose and β Glucose rings
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Monosaccharides Simple sugars containing 3 to 7 carbon atoms Primary energy source for fuelling cell metabolism Reducing sugars and soluble in water Can bond together to form disaccharides and polysaccharides Egs. TRIOSE (3 carbon) glyceraldehyde *intermediate in carbohydrate metabolism PENTOSE (5 carbon) ribose *sugar unit of RNA HEXOSE (6 carbon) glucose fructose galactose *energy Most pentose & hexose sugars can exist in the form of rings and straight lines - rings provide the sub-units needed for building complex carbohydrates α- glucose & β- glucose differ in the position of the –OH and –H attached to the 1 st carbon atom (see above). This is an example of an OPTICAL ISOMER
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Condensation of Glucose/Fructose When simple carbohydrates are joined to make complex carbohydrates the process is called CONDENSATION Macromolecules (such as sucrose) are often formed by removing ‘H’ from one atom and ‘OH’ from the other The ‘H’ and ‘OH’ combine to form water Monomers are joined to build macromolecules by the removal of water The reverse reaction when a polysaccharide has water added and is broken down into mono and disaccharides is known as HYDROLYSIS Eg. Sucrose (carbohydrate) is formed when glucose and fructose are joined via a condensation reaction Energy is required to form the bond (anabolic) The bond is known as an a alpha (1-2) glycosidic bond
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Disaccharides C omposed of 2 monosaccharides joined together by a condensation reaction Joined by a GLYCOSIDIC BOND Soluble in water Eg. SUCROSE (glucose + fructose) table sugar LACTOSE (glucose + galactose) milk MALTOSE (glucose + glucose) grains
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Polysaccharides Polymers with monosaccharide sub-units, joined via condensation reactions and glycosidic bonds The polysaccharide can be made of several thousand monosaccharides (forming a macromoleclule) Poly saccharides are not sugars and are generally insoluble Glucose accumulation will affect cell osmotic properties as well as reacting with various chemicals - therefore stored as a polysaccharide Glucose can be made available again quickly by an enzyme controlled reaction
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Examples of Polysaccharides STARCH (PLANT CARBOHYDRATE) EEnergy storage molecule in plants LLong chains of α- glucose molecules CContains 25 – 30% AMYLOSE & 70 – 75% AMYLOPECTIN EEasily hydrolysed into soluble sugars when required CChains can be branched or helixed (amylopectin) or straight (amylose) GLYCOGEN (ANIMAL CARBOHYDRATE) EEnergy storage in liver and muscles of animals BBranched polysaccharide composed of α- glucose molecules with different links to starch MMore water soluble than starch EEasily hydrolysed by enzymes into glucose
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CHITIN (ARTHROPOD EXOSKELETONS/FUNGI CELL WALLS) TTough modified polysaccharide made up of β-glucose molecules SSimilar to cellulose but each glucose has an amine (NH 2 ) group attached 22 nd most abundant carbohydrate CELLULOSE (STRUCTURAL MATERIAL IN PLANT CELL WALLS) LLinear polysaccharide made of β- Glucose joined by glycosidic links MMost abundant organic material PParallel chains become cross-linked with hydrogen bonds and form microfibrils MMicrofibrils are very strong (major structural component of plants) DDifficult to digest, humans cannot as they lack relevant enzymes AAnimals such as herbivores have modified digestive systems that harbour bacteria that can breakdown cellulose
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Cellulose cont......... The nature of the glycosidic bond means that each glucose molecule is 180° rotated compared to those next to it (SEE ABOVE) This gives cellulose its linear shape and strength Allows many hydrogen bonds between parrallel cellulose chains
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Hydrogen bonds between cellulose chains
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Free to share, print, make copies and changes. Get yours at www.boundless.com Biological Macromolecules Which of the following describe disaccharides? A) Glucose, galactose, and fructose are isomers with more than one asymmetric carbon. B) They are a long chain of monosaccharides linked by glycosidic bonds. C) Cellulose is the result of two monosaccharides that have undergone a condensation reaction. D) Lactose, maltose, and sucrose are the result of bonded monosaccharides after a dehydration reaction.
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Free to share, print, make copies and changes. Get yours at www.boundless.comwww.boundless.com Boundless - LO. "Boundless." CC BY-SA 3.0 http://www.boundless.com/CC BY-SA 3.0http://www.boundless.com/ Biological Macromolecules Which of the following describe disaccharides? A) Glucose, galactose, and fructose are isomers with more than one asymmetric carbon. B) They are a long chain of monosaccharides linked by glycosidic bonds. C) Cellulose is the result of two monosaccharides that have undergone a condensation reaction. D) Lactose, maltose, and sucrose are the result of bonded monosaccharides after a dehydration reaction.
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Free to share, print, make copies and changes. Get yours at www.boundless.com Biological Macromolecules Why are carbohydrates an essential part of our diets? A) All of these answers. B) Carbohydrates provide more energy than lipids. C) Carbohydrates contain only soluble elements that are vital to the health of our bodies. D) Carbohydrates provide energy from our diets.
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Free to share, print, make copies and changes. Get yours at www.boundless.comwww.boundless.com Boundless - LO. "Boundless." CC BY-SA 3.0 http://www.boundless.com/CC BY-SA 3.0http://www.boundless.com/ Biological Macromolecules Why are carbohydrates an essential part of our diets? A) All of these answers. B) Carbohydrates provide more energy than lipids. C) Carbohydrates contain only soluble elements that are vital to the health of our bodies. D) Carbohydrates provide energy from our diets.
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