Definition: Disaccharides consist of two monosaccharides linked together through a dehydration reaction.
Example: Lactose forms from beta d-galactose and alpha d-glucose.
Glycosidic Bond: The bond that links monosaccharides in a disaccharide.
Formed when the hydroxyl group at the anomeric carbon (carbon 1 of galactose) reacts with a hydroxyl group (position 4 of glucose).
A water molecule is released during this reaction.
Lactose: Formed from beta d-galactose and alpha d-glucose.
Notation: beta d-gal 1 -> 4 d-glucose indicates the bond formation between the specific carbons.
Anomeric configurations:
The configuration of galactose retains beta while glucose can exist as either alpha or beta due to free anomeric OH.
Sucrose: Formed from alpha d-glucose and beta d-fructose.
Notation: alpha d-glucose 1 -> 2 beta d-fructose, illustrating the linkage between anomeric sugars.
Both anomeric positions are involved in glycosidic bonds, locking their configurations.
Definition: Long chains of monosaccharides.
Glycogen: The storage form of glucose in animals.
Structure: Composed of glucose units linked by alpha 1 -> 4 linkages with branches every 10 units defined by alpha 1 -> 6 linkages.
Starch: Major plant energy storage, consisting of two types:
Amylose: Unbranched polyglucose chain linked by alpha 1 -> 4 linkages.
Amylopectin: Branched polymer also linked by alpha 1 -> 4 with branches every 30 residues.
Cellulose: Structural polysaccharide found in plant cell walls, composed of beta 1 -> 4 linked glucose monomers, creating a rigid structure due to hydrogen-bonding between chains.
A polysaccharide similar to cellulose, found in insect exoskeletons.
Contains N-acetylglucosamine units linked by beta 1 -> 4 linkages.
Glycoproteins: Proteins with carbohydrate attachments (polysaccharides), important for cell recognition and signaling.
Types:
O-linked: Attachment via serine or threonine residues.
N-linked: Attachment via asparagine residues.
Glycosaminoglycans: Polysaccharides composed of repeating disaccharide units of amino sugars, serving as shock absorbers in joints due to their ability to retain water and form gel-like substances.
Examples: Hyaluronic acid, important in skin care, is a glycosaminoglycan.
Cellulose: Arranged in linear chains with hydrogen bonds between chains resulting in rigidity.
Opposite directional orientations (flipping each unit) enhance stabilization through additional hydrogen bonding.
Distinct structures and linkages (alpha vs beta) affect functionality in biological systems.
Understanding glycosidic bonds and structural arrangements helps in identifying different carbohydrate types and their roles in biological systems.