carbohydrates Flashcards
carbohydrates are
biological macromolecule containing C=O and OH group.
major type of carbohydrates
sugar (saccharides)
functions of carbohydrates
significant fraction of the dietary calories
storage form of energy
cell membrane components
structural component of organisms
glyceraldehyde is a
a) aldose , triose sugar
b)ketose , triose sugar
c) aldose ,pentose sugar
d)ketose ,hexose sugar
aldose, triose sugar
dihydroxyacetone is a
a) aldose , triose sugar
b)ketose , triose sugar
c) aldose ,pentose sugar
d)ketose ,hexose sugar
ketose, triose sugar
sugar building block of DNA
D-Ribose sugar
most common and important aldohexose sugar
glucose (building unit of starch, cellulose, and sucrose)
most common naturally occurring ketose sugar found in plants , bonded to glucose to form sucrose
D-Fructose
measurement of Hba1c levels can determine
glycemic control
compounds that have the same chemical formula but have different structure are called
isomers
examples of isomers
fructose, glucose, mannose, galactose isomers having chemical formula C6H12O6
epimers are
carbohydrate isomers that differ in configuration around only one specific carbon atom
example of epimer
glucose and galactose {C4 epimer}
glucose and mannose {c-2 epimer}
why glucose and mannose are isomers but not epimer
differ in position of -oh grp in c-4 and c-2
special type of isomerism in the pair of structures that are mirror images of each other
enantiomers
the two members of the pair are designated as
D- nd L- sugar
vast majority of the sugar in humans are
D- sugar
difference between D- and L- isomers
-OH group on the asymmetric carbon that is farthest atom from the carbonyl carbon is on the
D- isomer: right
L-isomer: left
name the enzyme that can interconvert D- and L- isomers
Racemases
(enzymes are specific in binding either the D or L form)
less than 1% of each of the monosaccharides 5 or more carbon exist in which form in solution
open chain or acyclic
99% of monosaccharide found in solution are
ring or cyclic form
creation of anomeric carbon generate a new pair of isomer
α and β configurations (α-D-glucopyranose and β-D-glucopyranose)
alpha and beta are referred as
diastereomers (not mirror images)
enzymes can distinguish between these two structures and use one or the other preferentially
glycogen and cellulose are synthesized from
glycogen: α-D-glucopyranose
cellulose: β-D-glucopyranose.
the cyclic alpha and beta anomers of a sugar in a solution spontaneously form a equilibrium mixture the process is called
mutarotation
if hydroxyl group on the anomeric carbon of a cyclized sugar is not linked to another compound by glycosidic bond
sugar act as a reducing agent (reducing sugar)
sugar that react with chromogenic agents causing reagent to be reduced and colored
reducing sugar (aldehyde group of acyclic sugar become oxidized
reducing sugar groups
all monosaccharides but not all disaccharides
test that can detect a reducing sugar in urine
colorimetric test
positive colorimetric test indicates
underlying pathology (sugars are normally present in urine)
monosaccharides can joint to form
disaccharides, oligosaccharides, polysaccharides
lactose is made of
galactose + glucose