biomed week 6 Flashcards
what is mutarotation
when linear monosaccharides take on a cyclic form they have additional “alpha” or “beta” designation
monosacharides form cyclic structures when ….
one of their alcohol groups reacts with the aldehyde or ketone group
linear monosaccharides are only found when ….
interconverting between various cyclic forms
these conversions = mutarotation
what is the favoured D glucose mutarotation alpha or beta?
beta
what is a nucleophile
attracted to the nucleus
- usually a negative charge
ex. water
what is a electrophile
usually have a positive charge
ex . H+
where can oxidation happen in redox reactions of glycoside formation
terminal CH2OH abd or the aldehyde end of straight chain forms
where does reduction happen in redox reactions of glycoside formation
can happen at the aldehyde end of straight chain forms
is D glucuronic acid hydrophobic or hydrophilic why?
hydrophillic because its very electronegative creating a polar structure
stereoisomers are
same atoms in the same order but different spatial arrangement (must have chiral carbon
enantiomers are
mirror images of each other
given D or L designations based on position of OH group attached to the chiral carbon C atom furthest from the aldehyde or ketone group
structural isomers are
same atoms but not the same order
ex
C1 C2 glucose vs fructose
diastereomers are
not mirror images
may or may not be epimers
(epimers differ at only 1 chiral carbon)
what carbon is the ketone group on
C2
stereoisomers can be ……. or …..
diastereosomers or enantiomers
any stereoisomer that is not an enantiomer is a ….
diastereomer
diastereomers may or may not be
epimers
what is an epimer?
vary in one position for the placement of OH group
what is galactose
an epimer of glucose, often attached to lipids to make glucolipids or to protiens to make proteoglycans and glycoprotiens
lactose is composed of …….. and …… in a …… linkage
galactose and glucose in a beta 1-4 linkage
how do you identify a reducing sugar?
if it has a OH group on its anomeric carbon
has free aldehyde and ketone groups
- nothing attached to the OH
describe the non reducing end
C1 carbon is attached to the next monosaccharide
what do more branch points create
more non reducing ends
which way is an alpha sugar facing
downwards