Biomolecules - Classification of Monosachharides
- Monosachharides are the simplest form of carbohydrates
- They cannot be hydrolyzed further to give simpler units
- Monosachharides are classified based on the number of carbon atoms
- They can be classified as trioses (3 carbons), tetroses (4 carbons), pentoses (5 carbons), and hexoses (6 carbons)
- Examples of trioses include glyceraldehyde and dihydroxyacetone
Biomolecules - Classification of Monosachharides
- Examples of tetrose include erythrose and erythrulose
- Examples of pentose include ribose, deoxyribose, and ribulose
- Ribose is present in RNA while deoxyribose is present in DNA
- Ribulose is an important molecule in photosynthesis
- Examples of hexose include glucose, fructose, and galactose
Biomolecules - Classification of Monosachharides
- Glucose is an important source of energy for cells
- Fructose is a sweet-tasting sugar found in fruits and honey
- Galactose is found in milk and is converted to glucose in the liver
- Monosachharides can exist in different forms, including linear and cyclic forms
- In the linear form, the carbon chain is straight
Biomolecules - Classification of Monosachharides
- In the cyclic form, the carbon chain forms a ring structure
- The cyclic form can be further classified as either pyranose or furanose
- Pyranose has a six-membered ring while furanose has a five-membered ring
- Glucose can exist in both the linear and cyclic forms
- In the cyclic form, it is commonly found as a pyranose
Biomolecules - Classification of Monosachharides
- Glucose can also exist in different anomeric forms, known as alpha and beta
- The alpha form has the hydroxyl group (-OH) on the first carbon atom pointing downwards
- The beta form has the hydroxyl group pointing upwards
- These anomeric forms have different properties and reactivities
- Fructose also exists in cyclic form as a furanose
Biomolecules - Classification of Monosachharides
- Fructose can also exist in different anomeric forms, similar to glucose
- Galactose mostly exists in cyclic form as a pyranose
- Monosachharides have multiple hydroxyl groups that can undergo various reactions
- They can undergo oxidation reactions to form aldehydes or ketones
- They can also undergo reduction reactions to form alcohols
Biomolecules - Classification of Monosachharides
- Monosachharides can participate in glycosidic bond formation to form disachharides
- For example, glucose and fructose can form sucrose, a common table sugar
- Glucose and galactose can form lactose, the sugar found in milk
- Glucose and glucose can form maltose, a sugar found in malted grains
- These disachharides have different properties and functions
Biomolecules - Classification of Monosachharides
- Monosachharides can also undergo intramolecular reactions to form cyclic hemiacetals
- These reactions involve the carbon atom containing the carbonyl group and an adjacent hydroxyl group
- The resulting cyclic structure is stabilized by the formation of a hemiacetal or hemiketal
- The formation of these cyclic structures is reversible and can form a dynamic equilibrium
- The equilibrium between the linear and cyclic forms is important in biological processes
Biomolecules - Classification of Monosachharides
- The classification of monosachharides is important in understanding their properties and functions
- Different monosachharides have different sweetening power, solubility, and roles in metabolism
- The cyclic and anomeric forms of monosachharides affect their reactivity and participation in reactions
- Monosachharides are building blocks for larger carbohydrates like polysachharides
- Understanding their classification is fundamental in the study of biochemistry
Biomolecules - Classification of Monosachharides
- Monosachharides are classified based on the number of carbon atoms
- Trioses, tetroses, pentoses, and hexoses are examples of monosachharides
- Examples of trioses: glyceraldehyde, dihydroxyacetone
- Examples of tetroses: erythrose, erythrulose
- Examples of pentoses: ribose, deoxyribose, ribulose
- Examples of hexoses: glucose, fructose, galactose
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Biomolecules - Classification of Monosachharides
- Glucose is an important source of energy for cells
- Fructose is a sweet-tasting sugar found in fruits and honey
- Galactose is found in milk and is converted to glucose in the liver
- Monosachharides can exist in different forms (linear and cyclic)
- Glucose can exist in both linear and cyclic forms (pyranose)
- Fructose exists in cyclic form as a furanose
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Biomolecules - Classification of Monosachharides
- Glucose and fructose can form sucrose (table sugar)
- Glucose and galactose can form lactose (milk sugar)
- Glucose and glucose can form maltose (malted grains)
- Monosachharides can undergo oxidation reactions to form aldehydes or ketones
- Monosachharides can undergo reduction reactions to form alcohols
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Biomolecules - Classification of Monosachharides
- Monosachharides can participate in glycosidic bond formation to form disachharides
- Example: Glucose + fructose = sucrose
- Example: Glucose + galactose = lactose
- Example: Glucose + glucose = maltose
- Disachharides have different properties and functions
- Formation of glycosidic bonds require the elimination of a water molecule
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Biomolecules - Classification of Monosachharides
- Monosachharides can undergo intramolecular reactions to form cyclic hemiacetals
- Formation of cyclic structures involves the carbonyl group and an adjacent hydroxyl group
- The cyclic structure is stabilized by the formation of a hemiacetal or hemiketal
- Formation of cyclic structures is reversible and forms a dynamic equilibrium
- The equilibrium between linear and cyclic forms is important in biological processes
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Biomolecules - Classification of Monosachharides
- Classification of monosachharides is important in understanding their properties and functions
- Different monosachharides have different sweetening power, solubility, and roles in metabolism
- Cyclic and anomeric forms of monosachharides affect their reactivity and participation in reactions
- Monosachharides are building blocks for larger carbohydrates like polysachharides
- Understanding their classification is fundamental in the study of biochemistry
- Monosachharides - Linear and Cyclic Forms
- Monosachharides can exist in linear and cyclic forms
- The linear form has a straight carbon chain
- The cyclic form involves the formation of a ring structure
- Glucose can exist in both linear and cyclic forms
- In the cyclic form, glucose is commonly found as a pyranose
- Monosachharides - Anomeric Forms
- Monosachharides can exist in different anomeric forms
- The alpha form has the hydroxyl group on the first carbon pointing downwards
- The beta form has the hydroxyl group pointing upwards
- Glucose can exist as both alpha and beta anomers
- Fructose also exists in cyclic form as a furanose with alpha and beta anomers
- Monosachharides - Galactose
- Galactose is a monosachharide found in milk
- It is converted to glucose in the liver
- Galactose primarily exists in cyclic form as a pyranose
- It can also form glycosidic bonds to form disachharides
- Example: Galactose + glucose = lactose (milk sugar)
- Monosachharides - Oxidation Reactions
- Monosachharides can undergo oxidation reactions
- These reactions involve the conversion of the aldehyde or ketone group to a carboxylic acid group
- Glucose can be oxidized to produce gluconic acid
- Oxidation reactions are important in cellular respiration and energy production
- Monosachharides - Reduction Reactions
- Monosachharides can undergo reduction reactions
- These reactions involve the conversion of a carbonyl group to a hydroxyl group
- Glucose can be reduced to form sorbitol
- Reduction reactions are important in the synthesis of certain pharmaceuticals and chemicals
- Monosachharides - Formation of Disachharides
- Monosachharides can form glycosidic bonds to form disachharides
- Example: Glucose + fructose = sucrose (table sugar)
- Example: Glucose + galactose = lactose (milk sugar)
- Example: Glucose + glucose = maltose (malted grains)
- Disachharides have different properties and functions
- Monosachharides - Cyclic Hemiacetals and Hemiketals
- Monosachharides can undergo intramolecular reactions to form cyclic structures
- These reactions involve the formation of a hemiacetal or hemiketal
- The cyclic structure is stabilized by the formation of a ring structure
- Glucose forms a cyclic hemiacetal in the formation of a pyranose ring
- Fructose forms a cyclic hemiketal in the formation of a furanose ring
- Monosachharides - Equilibrium Between Linear and Cyclic Forms
- The formation of cyclic structures is reversible
- Monosachharides can exist in a dynamic equilibrium between the linear and cyclic forms
- The equilibrium is influenced by factors such as temperature and pH
- The equilibrium between linear and cyclic forms is important in biological processes
- It affects the reactivity and participation of monosachharides in various reactions
- Monosachharides - Properties and Functions
- Different monosachharides have different properties and functions
- Glucose is an important source of energy for cells
- Fructose is a sweet-tasting sugar found in fruits and honey
- Galactose is found in milk and plays a role in lactose metabolism
- These monosachharides have different sweetening power, solubility, and roles in metabolism
- Summary - Monosachharides
- Monosachharides are the simplest form of carbohydrates
- They can exist in linear and cyclic forms
- Monosachharides can undergo oxidation and reduction reactions
- They can form glycosidic bonds to form disachharides
- Monosachharides participate in intramolecular reactions to form cyclic structures
- Understanding the properties and functions of monosachharides is important in biochemistry.