Exam 4 Flashcards
what are the most abundant micronutrients on earth
carbs
what are carb polymers called
glycans
what important function do they play in joints
lubrication
what is their primary function in the body
energy
what are they used for within cells
signaling molecules
what two functional groups describe all carbs
aldehydes
ketones
which functional group is most common
(CH2O)n
what suffix do carbs end in
-ose
what is a 1 sugar carb called
monosaccharide
what flavor is a monosaccharide
sweet
what is the most abundant monosaccharide
D-glucose (AKA dextrose)
what is a 2 sugar carb called
disaccharide
what type of bond holds disaccharides together
glycosidic bond
what flavor are disaccharides
sweet
what are some examples of disaccharides
sucrose and lactose
what language and word is saccharide derived from
greek; sakcharon
what is the sweetest sugar
fructose
a 3-10 sugar carb is called what
an oligosaccharide
are oligosaccharides free in a cell
no - they are bound to lipids or proteins in glycoconjugates
can we digest oligosaccharides
no - they are highly fermentable and cause gas
a carb with 10 or more sugars is called what
a polysaccharide
what are polysaccharides primarily used for
storage and signaling
what are some examples of polysaccharides
cellulose, glycogen, starch
how many carbons could a monsaccharide have
3-7
what is the most common number of carbons in a monosaccharide
6
what is a 3 carbon sugar called
triose
what is a 4 carbon sugar called
tetrose
what is a 5 carbon sugar called
pentose
what is a 6 carbon sugar called
hexose
what is the most important functional carbon called
anomeric carbon
where is the anomeric carbon located in an aldose
carbon 1
where is the anomeric carbon located in a ketose
carbon 2
what is the chemical formula for an aldehyde
CHO
what is the chemical formula for a ketone
C=O
what is the scientific name of a 5 carbon aldehyde and what is an example
aldopentose
ribose
what is the scientific name of a 6 carbon aldehyde and what is an example
aldohexose
glucose and galactose
what is the scientific name of a 5 carbon ketone
ketopentose
what is the scientific name of a 6 carbon ketone and what is an example
ketohexose
fructose
what geometric change creates isomerization in carbs
whether a hydroxyl group is facing left or right
why is isomerization so important
it determines function
what factor makes one sugar different than all the others
location of hydroxyl groups
what is crucial for enzyme interaction
specific hydroxyl patterns
What determines if a carb is D or L
position of the OH group on the HIGHEST NUMBER CHIRAL CARBON
is D right or left
right
is L right or left
L
Does D or L reference rotation of polarized light
no
are most sugars L or D
D
where is the highest numbered chiral carbon usually located
next to the last carbon (above the last CH2OH)
what is an epimer
an isomer in which the only difference is the rotation around 1 carbon (type of diastereomer)
what does a single line represent in a Fisher Projection
an OH group
what form are carbs usually found in
cyclic structures
what is a cyclized aldose called
hemiacetal
what is a cyclized ketose called
hemiketal
what component of the anomeric carbon group makes it vital in becoming a cyclic structure
the double bonded Oxygen
what components make up a Pyranose ring (P-ring)
5 Carbon, 1 oxygen
what components make up a Furanose ring (F-ring)
4 Carbon, 1 Oxygen
why are aldohexoses found in pyranose rings
aldo- implies one CH2OH group.
hexose implies a GRAND TOTAL of 6 carbons.
So there is a total of 6 carbons.
why are ketohexoses found in a furanose ring
keto- implies 2 CH2OH groups (5+1)
hexose implies a GRAND TOTAL of 6 carbons.
So there is a total of 6 carbons (4+2)
Why are aldopentoses found in a furanose ring
aldo-implies one CH2OH group.
pentose implies a GRAND TOTAL of 5 carbons
So there is a total of 5 carbons (4+1)
In a cyclic projection of a carb, what determines if the sugar is D or L
If it is D, the last carbon points up (Dicks go up)
If it is L, the last carbon point down (Lesbians go down)
what tells us whether a cyclic carb structure is alpha or beta
the direction of the new OH group on the anomeric carbon once the cyclic structure is formed
what direction does the OH group point on an alpha carb
down (fish swim)
the alpha symbol looks like a fish
what direction does the OH group point on a beta carb
UP (Birds fly)
Beta=Bird
if the OH on the anomeric carbon is not bounds to another sugar what can it do
it can open and flip back and forth between alpha and beta
what is this flipping phenomenon called
mutarotation
what sugar acid found on gangliocides is common in the body
N-acetylneuraminic acid
what determines if a sugar is a reducing sugar
if it has a free aldehyde or a free ketone, it is a reducing sugar
which two classifications of sugars are always reducing sugars
monosaccharides and discaccharides
what do oligosaccharides and polysaccharides have
at least 1 reducing end
what is used to test for reducing sugars
FEHLING’S REAGENT
what type of reaction creates disaccharides
dehydration/condensation
what two elements can be at the center of a glycosidic linkage
Nitrogen or Oxygen
O-glycosidic or N-glycosidic bond
what forms glycosidic bonds
glycosyltransferases
what must be stated in the naming of a glycosidic bond
the carbons participating
can disaccharides be reducing sugars
YES - as long as there is one free anomeric carbon
what other factor is necessary in naming a glycosidic bond
the direction of the OH group on the anomeric carbons involved
(alpha or beta)
what is the disaccharide formula for maltose
GLUCOSE-alpha(1–>4)-GLUCOSE
what are easier to digest, disaccharides with alpha or beta bonds
alpha is easier
how many sugars in a polysaccharide
10 or more
what is the most abundant type of carb in nature
polysaccharides
what are they also known as
glycans
what two factors create different polysaccharides
type of sugar and branching locations
what are two major functions of polysaccharides
storage and structure
where are polysaccharides typically found
extracellularly
if all the constituent sugars of a glycan are the same what is the glycan called
a homoglycan
if there are multiple types of sugars in a glycan what is the glycan called
heteroglycan
what are the four types of complex carbs (polysaccharides)
starch
glycogen
soluble fiber
insoluble fiber
is starch a hetero- or homo- glycan
homoglycan
is glycogen a hetero- or homo- glycan
homoglycan
is soluble fiber a hetero- or homo- glycan
trick question
it can be both
is insoluble fiber a hetero- or homo-glycan
it can also be both
what is the storage form of carbs in plants
starch
what simple sugar is repeated over and over in starch
D-glucose
where in the plant is the starch stored
the endosperm
what is the storage form of carbs in mammals
glycogen
which simple sugar is repeated over and over in glycogen
D-glucose
where in mammals is glycogen formed
cytosol of liver and muscle
what do both starch and glycogen have a lot of that makes them attract water molecules
hydroxyl groups
why are starch and glycogen considered HEAVILY HYDRATED
because of the high number of hydroxyl groups
what two compounds is starch made of
amylose and amylopectin
what is the only bond found in amylose
glycose-alpha(1–>4)glucose
what makes amylopectin different from amylose
it is highly branched
what bonds constitutes most of amylopectins bonds
glucose-alpha(1–>4)glucose
what bond makes amylopectin unique and how often does it occur in starch
alpha(1–>6) bonds found every 24-30 glucose residues
what is starch easily digested into
glucose
is starch rapidly absorbed
yes
what physiological effect does starch have
causes a significant and rapid rise in blood sugar
does the body know the difference between High Fructose corn syrup and naturally occurring fructose
no
where are most bonds found in glycogen
alpha(1–>4)