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Carbohydrate Characters

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Carbohydrate Characters

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shubhammallik463
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Carbohydrate

Lalita Barjatiya
Assistant Professor , Biochemistry

Lalita Barjatiya
Asisstant Professor , Biochemistry
CARBOHYDRATE ?


What are

Carbohydrates?
The term “Carbohydrate” was coined by “Karl
Schmidt”.
 They are organic biomolecules abundantly
present in the nature.
 Found in the cells of plants and animals.

 The most abundant organic molecules in nature.

 Main source of energy.


• They contain group of carbonyl
compounds.
• Compounds contain C, H, O with
general formula of Cn(H2O)n.
• All have C=O and -OH functional
groups
• Classified based on the degree of
polymerization.
Why do we need
carbohydrate?
FUNCTION
 Carbohydrates serve as primary source of
energy/Fuel of body.
 Sparing protein.
 It is oxidized in living cells of human body to
produce CO2, H2O, and energy(ATP).
 Build macromolecule.
 Provide skeletal framework to cells ,tissues,
and organs of body.(Structural role)
Types of Carbohydrates

Monosaccharides Polysaccharides
Oligosaccharides

Disaccharides
MONOSACHARIDES
 Monosaccharides (Simple Sugars)
 Simplest class of Carbohydrates.
 They are composed of one saccharide
unit.
 They cannot be further hydrolyzed.
 They are building blocks/monomeric units
of higher forms of Carbohydrates.
CLASSIFICATION

Aldose sugar Ketone sugar


ALDOSE SUGAR
 When the functional group is
aldehyde.
 Eg:-aldotriose – glyceraldehyde
 Aldotetrose
 Aldopentose
 aldohexose
KETOSE SUGAR
 When the functional group is keto group .
 Eg fructose , dihydroxyacetone
OLIGOSACCHARIDES
 Carbohydrates formed by the
condensation of 2-9 monomers are called
oligosaccharides.
 They are normally present as glycans.
Trisaccharides Tetrasaccharides pentasac
charides etc.
 Maltotriose, melezitose, maltotriulose,
raffinose.
DISACCHARIDES
 Disaccharides has 2
Monosaccharide units linked
by glycosidic bond.
 Disaccharides may be
reducing or non reducing.
Examples Of Reducing
Sugars

 All Monosaccharides are reducing sugars.


 Monosaccharides are strong reducing
agents.
 Monosaccharides–
 Ribose, Glucose, Galactose, Fructose.
 Disaccharides are weak reducing agents.
 Reducing Disaccharides-
 Lactose, Maltose.
Non Reducing Sugars

 They do not possess free or potential


aldehyde or ketone group in its structure
is termed as non reducing sugar.
 Non reducing sugar does not show
reducing property and do not reduce
metallicions.
 Eg - sucrose
MALTOSE SUGAR
 A substance obtained when the grain is softened in
water and germinates.
 It is a disaccharide formed from two units
of glucose joined with an α(1→4) glycosidic bond.
 When beta-amylase breaks down starch, it removes
two glucose units at a time, producing maltose.
 It can be broken down to glucose by
the maltase enzyme, which catalyses the hydrolysis
of the glycosidic bond.
 Eg - Corn syrup and acid-thinned starch
LACTOSE SUGAR
 Milk sugar which is white, water-soluble, non-hygroscopic
solid with a mildly sweet taste.
 It is a disaccharide sugar synthesized
by galactose and glucose subunits and has the molecular
formula C12H22O11.
 Derived from the condensation of galactose and glucose,
which form a β-1→4 glycosidic linkage.
 Lactose also helps your body absorb a number of other
minerals, such as magnesium and zinc.
 It is used in the food industry.
LACTOSE INTOLERANCE
 Too little of an enzyme produced in your
small intestine (lactase) is usually
responsible for lactose intolerance.
 If lactase levels are too low you become
lactose intolerant.
 Symptoms- Diarrhea, Nausea, and
sometimes, vomiting, Stomach cramps,
Bloating, Gas
SUCROSE SUGAR
 Non reducing sugar.
 It is a sugar composed
of glucose and fructose subunits. It is produced
naturally in plants and is the main constituent
of white sugar. It has the molecular
formula C12H22O11.
 The monomers glucose and fructose are linked via
an ether bond between C1 of α and C2 of β unit.
The bond is called a glycosidic linkage.
 Cannot form osazone.
 For human consumption, sucrose is extracted and
refined from either sugarcane or sugar beet.
Number of Type Of Oligosaccharides
(3-10 Monosaccharide Units )
Monosaccharid
e Units
1 Trisaccharides
Maltotriose ,Raffinose

2 Tetrasaccharides
Stachyose
3 Pentasaccharides
Verbascose
POLYSACCHARIDES
 Polysaccharides are complex carbohydrates
formed by the polymerization of a large number
of monomers. Eg:- starch, glycogen, cellulose,
etc.
 They have two or more sugar molecules, hence
they are referred to as starchy foods.
 In complex carbohydrates, molecules are
digested and converted slowly compared to
simple carbohydrates.
 Found in lentils, beans, peanuts,, peas, corn,
whole-grain bread, cereals, etc.
Polysaccharides

Homopolysaccharides Heteropolysaccharides
Homopolysaccharides

 Starch
 Glycogen
 Cellulose
 Inulin
 dextrin etc.
STARCH

 Starch polymeric carbohydrate


 Homopolymer of d glucose units held by glycosidic linkage –
glucan/ glucaosan.
 Present in wheat, potatoes, maize, rice, and
 It is a white, tasteless and odorless powder that is insoluble in
cold water or alcohol.
 It consists of helical amylose and the branched amylopectin .
 Amylose – unbranched chain with α(1-4) glycosidic linkage.
 Amylopectin - Branched chain with α(1-6) glycosidic linkage.
Glycogen
 It is a multibranched polysaccharide of glucose
 It is a storage form of animals.
 Present in high concentration in liver skeletal
muscle and brain.
 Also found in plants with no chlorophyll eg
yeast, fungus.
 Glucose as a repeating unit withα(1-4) glycosidic
linkage and α (1-6) glycosidic linkage.
 In humans, glycogen is made and stored
primarily in the cells of the liver and skeletal
muscle.
CELLULOSE

 Observed in plants cell wall .


 Cellulose is mainly used to produce paperboard
and paper
 β-1→4 glycosidic linkage.
 Not digested in mammals .
 Not digestable fiber.
 Hydrolysis yields disaccharide cellobiose and β D
glucose.
Heteropolysaccharides

 Hyaluronic acid
 Heparin
 Chondroitin sulfate
 Dermatan sufate
 Keratan sulfate

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