Unit 5 - Intro to Carbohydrates Flashcards
how are monosaccharides classified?
- number of carbons (5 = pentose, 6 = hexose, 3 = triose)
- chemical nature of carbonyl group (aldose = aldehyde, ketose = ketone)
how are monosaccharides numbered?
carbons are numbered beginning with the carbon closest to the carbonyl group (carbonyl = anisomeric carbon = 1 if aldose, 2 if ketose)
what are the most common aldoses?
glyceraldehyde (triose)
ribose (pentose)
glucose, mannose, galactose (hexose)
what are the most common ketoses?
dihydroxyacetone (triose)
ribulose (pentose)
fructose (hexose)
what are enantiomers? which form is more abundant in body?
the D and L forms of monosaccharides; mirror images (D is more common)
- designation based on configuration of asymmetric carbon farthest from carbonyl group
- -if on right/up, is D
- -if on left/down, is L
what is the anisomeric carbon?
the former carbonyl carbon (1 in aldose, 2 in ketose) that occurs in cyclic form
how to tell if alpha or beta anomer
alpha will have the anomeric carbon’s OH group trans from the CH2OH (OH points down, CH2OH points up)
beta will have the anomeric carbon’s OH cis from the CH2OH (both going up)
what makes something a reducing sugar
if the O (of the OH) of the anomeric carbon is not bound to any other molecule (anomeric C is reducing end)
how are glycosidic linkages named?
- alpha/beta configuration of anomeric carbon
- numbers of connecting carbons
how much of the typical diet consists of CHO?
40% (in the form of starch, lactose, and sucrose)
what is amylose structure?
linear; glucose residues in alpha-1,4 linkage
what is amylopectin structure?
linear and branched; glucose in alpha-1,4 and alpha-1,6
what is lactose structure?
galactose and glucose in beta-1,4 linkage
how to tell glucose from galactose?
glucose has alternating OH groups going up and down; galactose has C2 down and all the rest up
what is sucrose structure?
glucose and fructose in alpha-1,2 linkage, and non-reducing sugar b/c OH’s aren’t free
what is glycogen structure and what is it similar to?
same overall structure as amylopectin, but more highly branched
-linear and branched; glucose in alpha-1,4 and alpha-1,6
what is glycogen used for and where is it mostly?
major storage form for glucose, and found mostly in liver and skeletal muscle
what is cellulose structure?
linear glucose residues in beta-1,4 linkage
what are the 3 classes of glycosidases?
endoglycosidase - cleave internal glycosidic bonds
exoglycosidase - cleave terminal glycosidic bonds
disaccharidases - cleave glycosidic bonds in disaccharides only
what is the specificity of each glycosidase based on?
- structure of glycosidic linkage (alpha-1,4, etc.)
- specific sugars on either side of glycosidic linkage (glucose - glucose VS glucose - galactose)
- position of glycosidic linkage w/in polymer (internal VS terminal)
what is alpha-amylase? what does it break down? what are the 2 types?
endoglucosidase; hydrolyzes random internal alpha-1,4 bonds between glucose residues in starch (ex: amylopectin, amylose)
-there is salivary and pancreatic alpha-amylase
salivary VS pancreatic alpha amylase and what they produce
S: made by salivary glands in mouth; inactivated by acid in stomach
P: made in pancreas, secreted into duodenum; continues where SAA left off, producing maltose, maltotriose, alpha-dextrins, isomaltose, etc.
HOWEVER, WILL NOT PRODUCE GLUCOSE
what are alpha-dextrins?
oligosaccharides that have at least 1 alpha-1,6 branch
what must happen to carbohydrates before they are transported into epithelial cells?
must be cleaved into monosaccharides enzymatically