Biochemistry - Carbohydrates & Lipids Flashcards
Aldose examples
Glucose, Galactose, Ribose, & Mannose
Ketose examples
Fructose & Sedoheptulose
Stereoisomers
Same chemical formula but different position of one or more hydroxyl group
Epimers
Stereoisomers with difference in rotation of hydroxyl group at one carbon
Enantiomers
Mirror images, possesses possible identical chemical characteristics, occurs are either D or L. Naturally occurring sugars occur in the D conformation.
Glycation
Non-enzymatic covalent linear monosaccharide addition to protein. Forms Schiff bases (linear monosaccharide attached to a protein.) Schiff bases can oxidize to form Advance Glycation End (AGE) products.
Glycosylation
Enzymatic covalent oligio/polysaccharide addition to proteins/lipids (Purposeful). Occurs in the ER and Golgi through Post-Translational Modification, results in glycollipids or glycoproteins.
Glycosaminoglycans
Linear polymers of repeating disaccharides that form the ground substance of the EM, Negatively charged at physiological pH allowing water absorptive qualities.
Glycosides
Sugar bonded to oxygen or nitrogen based functional groups
O-linked glycosidic bonds
Found in Sugar-Sugar or Sugar-Protein attachment
N-linked glycosidic bonds
Found in nucleosides & nucleotides
Reduced sugars (Sugar Alcohols)
Sugars reduced at the aldehyde carbon.
Sorbitol
Reduced glucose
Galactitol
Reduced galactose
Iduronic acid
Oxidized glucose