Lec 3: Carbohydrates Flashcards

(43 cards)

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

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

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
what is lactose formed by?
made up of: beta glucose and galatose molecules beta-1,4 glycosidic link
26
what is sucrose made up of? where does the glyocosidic link occur?
made up of: alpha glucose and fructose molecules alpha-1,2 glycosidic link
27
what enzyme digests sucrose?
sucrase
28
what is the difference between oligosaccharides and polysaccharides?
oligosaccharides: small polymers, 3-20 monosaccharides polysaccharides: long chains/branched
29
what is amylose?
long linear chains of alpha-1,4-linked-D-glucose residues that has a coiled structure
30
what is amylopectin
linear chains of α-1,4-linked D-glucose residues joined through α-1,6-linked branch points Has a brush-like structure
31
what enzymes digest starch? and which bonds do they break? where are these enzymes found?
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
what is glycogen made up of?
- complex branched polysaccharide - linear chains - of alpha 1,4-linked D-gluose residues joined through alpha-1,6-linked branch points
33
what is the difference between amylose, amylopectin and glycogen?
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
where is starch found vs glycogen?
starch: amyloplasts (non pigmented plant cell organelles) and chloroplasts (from roots, tubers, seeds and fruits) glycogen: in animals, liver and muscle cells
35
what are glycoproteins?
Proteins that contain oligosaccharide chains attached covalently to the protein structure
36
what are secreted glycoproteins made up of?
mucins and glucocalyx
37
what are mucins
prinicipal components of mucus by mucous membrsnes (lining of body cavitities open to the exterior) and as component of saliva
38
what are glycolipids and what are they associated with?
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
what are glycocalyx
Glycoprotein covering surrounding cell membranes of epithelial and other cell types as well as bacteria
40
what are sphingolipids?
they are subtype of lipids they include: - cermide (signalling molecule) - sphingomyeline (membranes)
41
what are glycosphingolipids
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
what is a carbohydrate?
Formula = Cm(H2O)n
43
what is the function of glycosylated membrane proteins?
immune recognition