Carbohydrates Flashcards

Describe properties of alpha and beta glucose Describe formation and breakage of glycosidic bond Describe structure and properties of starch (amylose+amylopectin), cellulose and glycogen

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1
Q

Monosaccharide

A

a) Carbohydrate which cannot be hydrolysed to simpler carbohydrates
b) Carbonyl group (C=O)
c) Multiple hydroxyl groups (OH)

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2
Q

Aldose (aldehyde sugar)

A

Carbonyl group at the beginning of the carbon skeleton

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3
Q

Ketone (ketone sugar)

A

Carbonyl group nested within the carbon skeleton

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4
Q

Difference between alpha and beta glucose

A

OH group attached to C1:
Below plane of the ring in alpha
Above plane of the ring in beta

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5
Q

Significance of molecular structure of monosaccharides

A
  1. Small in size and many hydroxyl groups that can form hydrogen bonds with water -> readily soluble in water -> can be transported easily
  2. Linear form has free carbonyl group -> reducing ability -> reducing sugars
  3. Pentose and hexoses can exist as rings-> stable building blocks for larger molecules
  4. alpha and beta isomerism -> same chemical formula different structural molecules -> diversity
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6
Q

Disaccharide

A

2 monosaccharides joined by glycosidic bond/linkage via condensation -> loss of 1 water molecule
Hydrolyse -> add one molecule of water

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7
Q

Maltose

A

alpha-glucose + alpha-glucose -> alpha(1-4) glycosidic bond

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8
Q

Sucrose

A

alpha-glucose + beta-fructose -> alpha(1-2) glycosidic bond

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9
Q

Reducing sugars

A

All monosaccharides

Some disaccharides except sucrose

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10
Q

Test for reducing sugars

A

Benedict’s Test
2cm3 test solution + equal volume of Benedict’s reagent -> shake -> immerse in boiling water bath
Green -> yellow -> orange -> brick red

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11
Q

Test for non-reducing sugars

A

Acid hydrolysis first -> boil with dilute HCL (1min) -> cool + neutralise with sodium bicarbonate solution
Then Benedict’s Test

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12
Q

Amylose

A

alpha-glucose monomers forming unbranched polymers
alpha(1-4) glycosidic bonds
Coiled into a helix

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13
Q

Amylopectin

A

alpha-glucose monomers forming branched polymers
alpha(1-4) glycosidic bonds within a branch and alpha(1-6) glycosidic bonds at branch points (every 20-30)
Helix + helical side chains

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14
Q

Test for starch

A

Iodine test

Triiodide ion complex fits into centre of amylose helix -> starch-iodine complex -> blue-black colouration

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15
Q

Glycogen

A

Similar to amylopectin but more extensively branched

Branch points every 12 monomers

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16
Q

How do the structures of amylose, amylopectin and glycogen determine their function as storage molecules?

A
  1. Many glucose residues
    Large energy store -> hydrolysed to many monosaccharides
  2. Insoluble in water -> will not affect water potential of cells
    Large molecule
    Intramolecular hydrogen bonding and projection of hydroxyl groups into core of helix formation -> relatively fewer hydroxyl groups available for hydrogen bonding with water
  3. Comprise of helices
    Pack many subunits per unit volume
  4. Branched
    Multiple hydrolytic enzymes can work at the same time -> increase energy generation per unit time
17
Q

Cellulose

A

beta glucose monomers
beta(1-4) glycosidic bonds
alternate monomers rotated 180 degrees wrt each other
Linear unbranched molecule with OH groups projecting out in both directions
Parallel chains held together by intermolecular hydrogen bonds -> cross-linking -> microfibril -> criss
crossing -> cell wall

18
Q

How do the structures of cellulose determine their function as structural molecules?

A
  1. High tensile strength
    Adjacent beta glucose monomers rotated 180 degrees wrt each other -> linear -> OH groups bond extensively with adjacent chains lying parallel -> microfibrils
  2. Insoluble in water
    Few OH groups available for H-bonding with water
  3. Meshwork of microfibrils
    Porous structure -> freely permeable to water
    Strong and rigid and distributes stress in all directions to prevent plant cells from bursting due to osmotic stress
  4. Cellulases not commonly available -> not readily hydrolysed