Carboydrates Flashcards

1
Q

What are the functions of carbs?

A
  • Energy source
  • Immune functions
  • Intracellular communication
  • Energy storage
  • Structural functions e.g. cell walls of bacteria, or exoskeletons of insects, cellulose of cell wall of plants.
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2
Q

Classification and general structure of carbohydrates?

A
  • Consist of carbon, oxygen and hydrogen
  • Ratio of H to O = ~ 2:1
  • General formula = (CH2O)n

Monosaccharides - 1 sugar unit
Disaccharides- 2 sugar units
Oligosaccharides 3-10 sugar units
Polysaccharides- 11 to >100 sugars units

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3
Q

How does the body obtain monosaccharides?

A

Present in the diet or obtained via digestion of more complex carbohydrates.

Can be synthesised in the body from non-carbohydrate sources (glucogenesis) - their external supply is therefore not required for survival.

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4
Q

How are monosaccharides classified?

A
  • Their number of carbon atoms
  • Any functional groups

No of C atoms:
- 3= triose e.g. glyceraldehyde
- 5= pentose e.g. ribose & deoxyribose
- 6-= hexose e.g. glucose

Functional group:
- contains an aldehyde group- aldoses (-ose ending)
- contains a ketone group- ketoses (-ulose ending)

  • The first carbon is the carbon attached to the carbonyl group e.g. ketone
  • Black wedges = above plane
  • Dotted wedge = below plane
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5
Q

What are the 3 important monosaccharides & their source?

A
  1. Glucose
    - Source= diet, degradation of glycogen, gluconeogenesis
    - Preferred energy source of brain. Required energy source of cells with few or no mitochondria. Essential in exercising muscle
  2. Fructose
    - Source= fruits, vegetables, honey
    - Sweeter than glucose
  3. Galactose
    - Source= dairy products
    - Less sweet than glucose
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6
Q

Define isomers

A

Compounds that have the same chemical formula but different structures

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7
Q

Define epimers. Give 2 examples?

A

Carbohydrate isomers that differ in configuration around only 1 specific carbon atom.

e.g. glucose & galactose are C4 epimers

e.g. Glucose & mannose are C2 epimers

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8
Q

Define enantiomers

A

Pairs of structures that are mirror image of each other & non-superimposable

They are a type of stereoisomer & have this property due to chiral carbons (have 4 different groups attached to C atom)

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9
Q

How does cyclisation of a monosaccharide occur? What are the common ring structures? Define anomeric carbon.

A

99% of monosaccharides w/ 5 or more carbon atoms form a ring structure.

The carbonyl functional group reacts w/ hydroxyl group.
- 5C + 1O = pyranose ring
- 4C + 1O = furanose ring

Cyclisation creates an anomeric carbon atom because the -OH group can end up above the plane of the C atoms or below.
- So a molecule of D-glucose can form an α-anomer or a β-anomer.

NOTE- view diagram on notes!

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10
Q

Give 3 examples of dietary disaccharides - include their monomers, bonds & sources.

A

Formed from 2 identical or different monosaccharide units linked together by aglycosidic bond.

  1. Sucrose
    - Monomers= glucose + fructose
    - Bonds= α-1,2-β-glycosidic bond
    - Source= prevalent in sugar cane & table sugar
  2. Maltose
    - Monomers= glucose + glucose
    - Bonds= α-1,4-glycosidic bond
    - Source= starch. malt sugar
  3. Lactase
    - Monomers= Glucose + galactose
    - Bonds= β-1,4-glycosidic bond
    - Source= mammalian milk. milk sugar
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11
Q

Explain the bonding in disaccharides?

A
  • Numbered according to the number of the carbon atom the bond is attached to.
  • Also according to the position of the anomeric carbon atoms in the ring.
  • If the hydroxyl group is in the alpha configuration, the bond is an α-glycosidic bond.
  • e.g. In sucrose, the bond is an α-1,2-β-glycosidic bond because
    -OH of glucose in alpha configuration on carbon 1 has reacted w/ OH group of fructose in beta configuration on carbon 2.
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12
Q

What are the 3 important polysaccharides?

A
  1. Starch
    - Amylose
    - Amylopectin
  2. Cellulose
  3. Glycogen
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13
Q

Explain the source, function, structure, monomers, bonds & digestion of Starch.

A
  1. Amylose
  • Source= plants, seeds & tubers.
  • Function= stores carbs in plants
  • Structure= unbranched, spiral
  • Monomers= α-glucose
  • Bonds= α-1,4-glycosidic bonds
  • Digestion= Amylases secreted by salivary glands & pancreas digest amylopectin, releasing glucose, maltose & isomaltose.
  1. Amylopectin
  • Source= plants, seeds & tubers.
  • Function= stores carbs in plants
  • Structure= Branched (every 20-30 residues), spiral
  • Monomers= α-glucose
  • Bonding= α-1,4- & α-1,6-glycosidic bonds
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14
Q

Explain the source, function, structure, monomers, bonds & digestion of Cellulose.

A

Source= plant cell walls

Function= structural polysaccharides for plants

Structure= Unbranched

Monomers= β-glucose

Bonds= β-1,4-glycosidic bonds

Digestion= Important as dietary fibre as humans don’t have the enzyme to digest cellulose.

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15
Q

Explain the source, function, structure, monomers, bonds & digestion of Glycogen.

A

Source= Liver & skeletal muscle

Function= Carbohydrate storage molecule in humans.

Structure= Branched (every 8-10 residues)

Monomers= α-glucose

Bonds= α-1,4- & α-1,6-glycosidic bonds

Digestion= The high level of glycogen branching means that the molecule has a large number of free ends - allows for rapid degeneration to glucose.

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16
Q

Explain the digestion of polysaccharides

A
  1. Mouth - salivary α-amylase hydrolyses the α-1,4-glycosidic bonds in starch. This yields maltose & dextrin. Dextrin is a polymer of glucose linked by α-1,4 & α-1,6 glycosidic bonds.
  2. Small intestine - pancreatic α-amylase breaks the starch further, creating more maltose & dextrin.
  3. Mucosal lining of the upper jejunum - brush border associated oligosaccharidases & disaccharidases of intestinal mucosal cells hydrolyse bonds:
    - Dextrinase hydrolyses α-1,6-bonds in dextrin = debranching enzyme.
    - Amylase hydrolyses α-1,4- & α-1,6-glucosidic bonds in dextrin to yield glucose.