NPLEX Biochem Carbs

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Biochemistry ~ Carbohydrates

OVERVIEW - compounds that contain at least 3 carbon atoms + hydroxyl groups and usually an aldehyde
or ketone group
glucose
= major product of digestion (some galactose and fructose also produced)
= major fuel source oxidized by cells for energy
= stored as glycogen or triacylglycerols after a meal
= converted to glucose 6-phosphate when enters cell, then G6P enters glycolysis ( NADH
& ATP) or pentose phosphate pathway ( NADPH)
Glycogen:
- major storage form of carbs in animals
- largest stores in mm and LV
- mm glycogen used to generate ATP for mm contraction
- LV glycogen used to maintain blood glucose during fasting or exercise
- LV produces glucose from glycogenolysis & gluconeogenesis
A.) Types: MONO- - cannot be reduced or hydrolyzed into smaller or simpler sugars
SACCHARIDES - produced by the breakdown of dietary carbohydrates
- major energy source for the body
- usually found as D-series vs its enantiomer (mirror image) L-series

Structure: (formula = CH2O)n


- all of the above are hexose (6carbon) monosaccharides)
- mainly ring structures where aldehyde or ketone group reacts with hydroxyl group
- structural formula is C6H12O6 (differ in the position of the =O)
- epimers: stereoisomers that differ in the position of the hydroxyl group at only 1 assymetric carbon
- aldose or ketose depending on aldehyde or ketone as most oxidized functional group

Fructose glucose Glucose: - most important & abundant


- body uses glucose to synthesize other carbs
- glucose, - major source of fuel in the body
- fructose,
- galactose, Fructose: can be converted to glucose
- mannose - a ketose (all others = aldoses)
(all isomers of - forms furanose rings vs. pyranose rings
eachother) - metabolized mainly in the liver  glyceraldehydes 3-P (intermediate of glycolysis)
- can be produced from sorbitol (generated from glucose)

Galactose:
- converted to glucose when taken into the body

Mannose:
- constituent found in the glycoproteins of plant gums

DI-SACCHARIDE: - 2 monosaccharides covalently bonded via glycosidic attachment


- glycosidic attachment can also bond carbs to purines, pyrimidines, aromatic rings, lipids etc…
- sucrose, - bond is between anomeric carbon of one molecule & different C of 2nd molecule
lactose, maltose,
isomaltose Sucrose: (glucose + fructose)  table sugar
- both use anomeric carbon  ring can’t open  NO alpha or beta ring structure

Lactose: (glucose β-1,4 linked to galactose) - milk sugar


- galactose uses anomeric carbon
- glucose does not use anomeric C, so can open and form alpha or beta ring structure

Maltose: (glucose + glucose)


- one glucose uses anomeric carbon
- other glucose does not use anomeric C, so can open and form alpha or beta ring structure

Isomaltose: (glucose + glucose) – like maltose


- bound by alpha-1,6 glycosidic linkage (vs. alpha-1,4 in maltose)
POLY- >6 monosaccharides
SACCHARIDE: - can be linear or branched
- major role = storage of monosaccharides (starch, amylase, amylopectin)
Amylase, - major role = structural support (cellulose, chitin)
amylopectin,
glycogen, inulin
Amylose: ( lots of glucose molecules)
- non branching (unbranched) starch of alpha-1,4 glycosidic linkages
- spiraling helical shape or coil
- abundant in many plants
Amylopectin: 1
- branching starch of alpha-1,4 glycosidic linkages
- branch points = alpha- 1.6 linkages
- branch points at about every 24- 30 glucose residues (not how described in H.M. pg 125)
Glycogen:

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