Lec 3: Carbohydrates Flashcards

1
Q

what are the fucntions of carbohydrates?

A
  • provide a rapid and readily available supply og energyfor celular reactions e.g muscle l & liver glycogen
  • Form part of important molecules in the cell e.g Sugar-phosphate backbones in DNA double helix
  • Form markers on the cell surface which aid cell recognition e.g Blood group markers
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2
Q

what is monosacchride and disaccharide? what is the general formula

A

monosaccharides: any of the class of sugars (e.g. glucose) that cannot be hydrolysed to give a simpler sugar.

general formula: (CH2O)n

disaccharide: dimer= 2 monoscaccharides

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3
Q

what is a oligosaccharide

what is a polysaccharide

A

Oligosaccharide: is a saccharide polymer containing a small number (typically three to ten) of monosaccharides (simple sugars)

Polysaccharide: polymer of monosaccharide units linked together

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4
Q

which is the Fischer Projection and Haworth Projection of this glucose molecule

A
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5
Q

*Note*: Naming monosaccharides

A

*Monosaccharides contain an aldehyde or ketone functional group and hydroxyl groups

3 C- triose

4 C- tetrose

5 C- pentose

6 C- hexose

7 C- heptsoe

8 C- octose

9 C- nonose

10- decose

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6
Q

what is the name of the molecule?

A
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7
Q

*Note*: isomers of aldohexose

what is the chemical formula?

A

C6H12O6

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8
Q

what are n-deoxymonosaccharides?

A

these are monosaccharides where the hydroxyl group [OH] is replaced with [H]

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9
Q

what is a stereoisomers?

A

each of two or more compounds differing only in the spatial arrangement of their atoms

They have:

  • they have the same chemical formula
  • the same orders and types of bonds

but are non -overlapping mirror images of each other and thus have

  • Different spatial arrangements
  • Different biological functions

D-isomers and L-isomers

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10
Q

what is a chiral carbon centre

A

carbon with 4 different groups coming of it

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11
Q

what is meant by the oxidation/reduction of a carbon

A

oxidation is a process by which a carbon atom gains bonds to more electronegative elements, most commonly oxygen. Reduction is a process by which a carbon atom gains bonds to less electronegative elements, most commonly hydrogen.

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12
Q

*Note*: How to assign sugars as L or D

A
  • If the OH on the bottom chiral centre points to the right = D
    • If the OH on the bottom chiral centre points to the left = L
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13
Q

what is cyclization

in what conditions to monosaccharides cyclize?

A

this is where the hydroyl [OH] group on the second to last carbon reacts with carbonyl group [C=O]

Resulting product for an aldose = a hemiacetal

Resulting product for a ketose = a hemiketal

monosaccharides cyclize spontaneously under normal conditions

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14
Q

what is an anomeric carbon?

A
  • an anomeric carbon is a stereocenter
  • It depends on which direction the hydroxyl [OH] group attaches to the carbon
  • so the anomeric carbon is either alpha or beta

(alpha= H above, beta= H below)

can happen for both hemiacetal and hemiketals

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15
Q

what 2 possible products arise from the cyclization of D-glucose?

A

the OH group can attack planar C=O gorup from either side

so you get:

α and β anomers of D-glucopyranose

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16
Q

how can you tell the difference between alpha and beta glucose?

A

in alpha glucose the OH is below the plane

in beta glucose the OH is above the plane

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17
Q

how is glucose generated?

A

from the production of starch

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18
Q

*Note* Generation of ATP from glucose

A
19
Q

what is a furan-based ring structure?

A

Furan is a heterocyclic organic compound, consisting of a five-membered aromatic ring

e.g furanose= 5 membered cyclization product despite being a hexose (=6C)

20
Q

*Note* Fructose structure

A
21
Q

what is the primary function of disaccharides?

A

nutritional source of monosaccharides

22
Q

what is maltose made up of? where does the glycosidic link form?

where is it usually present

A

made up of: a-1,4 alpha glucose and a-1,4 beta glucose

alpha - 1,4 glycosidic link

present in;

  • germinating seeds/grains
    • metabolism of maltose by yeast yields ethanol and CO2
23
Q

what is maltose digested into and by what?

A

It is digested by maltase

into alpha-1,4 glucose and beta- 1,4 glucose

24
Q

what does the metabolism of maltose yield?

A

it yields ethanol and CO2

25
Q

what is lactose formed by?

A

made up of: beta glucose and galatose molecules

beta-1,4 glycosidic link

26
Q

what is sucrose made up of? where does the glyocosidic link occur?

A

made up of: alpha glucose and fructose molecules

alpha-1,2 glycosidic link

27
Q

what enzyme digests sucrose?

A

sucrase

28
Q

what is the difference between oligosaccharides and polysaccharides?

A

oligosaccharides: small polymers, 3-20 monosaccharides
polysaccharides: long chains/branched

29
Q

what is amylose?

A

long linear chains

of alpha-1,4-linked-D-glucose

residues that has a coiled structure

30
Q

what is amylopectin

A

linear chains of α-1,4-linked D-glucose residues

joined through α-1,6-linked branch points

Has a brush-like structure

31
Q

what enzymes digest starch? and which bonds do they break?

where are these enzymes found?

A

amylase and maltase: alpha-1,4 glycosidic lin

Isomaltase: alpha-1,6 glycosidic link

broken down to dextrins = oligosaccharides, maltotriose, maltose, isomaltose and glucose

amylase - saliva and gut

maltase and isomaltase - gut only

32
Q

what is glycogen made up of?

A
  • complex branched polysaccharide
  • linear chains
  • of alpha 1,4-linked D-gluose residues

joined through alpha-1,6-linked branch points

33
Q

what is the difference between amylose, amylopectin and glycogen?

A

they are all made up of alpha 1,4-linked D-glucose residues

However:

amylose has a coiled structure

amylopectin has a brush-like structure due to the alpha 1,4-linked D-glucose residues joined through alpha-1,6-linked branch points

glycogen is similar to amylopectin but the branch points occur more frequently (every 8-12 residues vs 24-30 in amylopectin)

AND amylose and amylopectin make up starch which is only found in plants, glycogen is found in animals

34
Q

where is starch found vs glycogen?

A

starch: amyloplasts (non pigmented plant cell organelles) and chloroplasts (from roots, tubers, seeds and fruits)
glycogen: in animals, liver and muscle cells

35
Q

what are glycoproteins?

A

Proteins that contain oligosaccharide chains attached covalently to the protein structure

36
Q

what are secreted glycoproteins made up of?

A

mucins and glucocalyx

37
Q

what are mucins

A

prinicipal components of mucus by mucous membrsnes (lining of body cavitities open to the exterior) and as component of saliva

38
Q

what are glycolipids and what are they associated with?

A

Lipids that contain oligosaccharide chains attached covalently to their lipid structure

Often associated with phospholipids on outer surface of the cell membrane

Function:

Recognition signals

Attachment factors

Membrane stabilisers

39
Q

what are glycocalyx

A

Glycoprotein covering surrounding cell membranes of epithelial and other cell types as well as bacteria

40
Q

what are sphingolipids?

A

they are subtype of lipids

they include:

  • cermide (signalling molecule)
  • sphingomyeline (membranes)
41
Q

what are glycosphingolipids

A

Glycosphingolipids are a subtype of glycolipids containing the amino alcohol sphingosine

this includes:

Cerebrosides: found in muscles and nerves

Gangliosides: found in plasma membranes

42
Q

what is a carbohydrate?

A

Formula = Cm(H2O)n

43
Q

what is the function of glycosylated membrane proteins?

A

immune recognition