Carbohydrates Flashcards

(38 cards)

1
Q

Give some properties of carbohydrates

A

Highly oxidisable
Storage form of energy
Structure and protection
Cell to cell communication (ABO blood group antigens)

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2
Q

What are monosaccharides?

A

Sugars that can’t be hydrolysed to form a simple sugar.

Most commonly hexoses (6carbons)

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3
Q

What are the 3 main hexoses in human biochemistry?

A

Glucose
Galactose
Fructose

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4
Q

What are disaccharides?

A

2 monosaccharides linked together by glycosidic bonds

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5
Q

What is a glycosidic bond?

A

Covalent bond from when hydroxyl group of one monosaccharide reacts with an anomeric carbon of another monosaccharide.

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6
Q

What are the 3 main disaccharides of human biochemistry?

A

Maltose
Sucrose
Lactose

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7
Q

What is an anomeric carbon?

A

Mirror images of each other

It is carbon 1 on the glucose residue. Stabilises glucose and is the only residue that can be oxidised

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8
Q

What is the difference between homo- and heteropolysaccharides?

A

Homo- single monomeric species

Hetero- have 2 or more monomer species

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9
Q

What makes glycogen more extensively branched than starch?

A

It has alpha 1-6 bonds every 8-12 residues instead of every 24-30

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10
Q

What are glycoproteins?

A

Proteins that have carbohydrates covalently attached

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11
Q

What are the functions of carbohydrates attached to proteins?

A

Increase protein solubility
Influence folding and conformation
Protect it from degradation
Act as communication between cells

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12
Q

What are GAGs?

A

Glycosaminoglycans

Unbranched polymers made from repeating units of hexuronic acid and an amino sugar which alternate through the chains

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13
Q

What are Proteoglycans?

A

GAGs that have a protein covalently attached.

They form part of many connective tissues in the body.

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14
Q

What are Glycoproteins?

A

Very similar to proteoglycans but there is more protein present than carbohydrate.

Found in ECM, cell membrane, blood and within cells

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15
Q

What catalyses the final digestion of carbohydrates in the jejunum?

A

Mucosal cell surface enzymes

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16
Q

What are the main products of carbohydrate digestion?

A

Glucose
Galactose
Fructose

17
Q

What type of carbohydrates cannot be digested by the gut?

A

Oligosaccharides

E.g cellulose and hemicellulose

18
Q

What are the benefits of oligosaccharides not being digested?

A

Increase faecal bulk and decrease transit time

19
Q

What are some causes of disaccharide deficiencies?

A

Severe intestinal infection
Inflammation of gut lining
Drugs injuring gut wall
Surgical removal of intestine

20
Q

What characterises disaccharide deficiencies?

A

Abdominal distension and cramps

21
Q

What is the most common disaccharide deficiency?

A

Lactose intolerance

22
Q

Why does the lack of lactase give disaccharide deficiency symptoms?

A

Undigested lactose is broken down by gut bacteria causing a build up of gas and irritant acids

Lactose is osmotically active so draws water from gut into lumen causing diarrhoea

23
Q

Why is glucose immediately phosphorylated when it reaches the liver or certain cells?

A

Glucose-6-phosphate can’t diffuse out of cells as GLUT transporters can’t recognise it

24
Q

What enzymes catalyse the phosphorylation of glucose into glucose-6-phosphate?

A

Glucokinase (liver)

Hexokinase (other tissues)

25
What does the low Km and Vmax of hexokinase mean for tissue cells?
Low Km- even at low glucose levels tissues can grab glucose effectively. Low Vmax- tissues are easily satisfied so don’t keep grabbing glucose
26
Give some fates of glucose-6-phosphate?
Pentode phosphate pathway Glycolysis Glycogen storage
27
What is the role of glucose-6-phosphatase?
Catalyses the release of glucose into the blood by converting glycogen into glucose-6-phosphate and then glucose.
28
What is von Gierke’s disease?
Liver, kidney and intestine glucose-6-phosphate deficiency
29
What is McArdle’s disease?
Skeletal muscle phosphorylase deficiency
30
Describe the process of glycolysis?
A catabolic pathway that saves potential energy from glucose by forming ATP through substrate level phosphorylation
31
What is the first committing step of glycolysis?
Phosphorylation of F-6-P to F-1,6 bisP. F-1,6bisP is solely destined for glycolysis. Irreversible step
32
Where does glycolysis occur?
In the cytosol
33
What does substrate level phosphorylation require?
Soluble enzymes and chemical intermediates
34
Why does NAD+ need to be replenished?
NAD+ needs to be regenerated as it is limited within the cell. It’s comes from niacin an essential vitamin. Pyruvate replenishes this supply by oxidising NADH. NAD+ required for metabolising various intermediates within glycolysis
35
What is the Cori cycle?
When the liver repays the oxygen debt muscles run up by converting lactate into glucose during gluconeogenesis
36
What are the 4 bypass reactions of gluconeogenesis?
1 - pyruvate to oxaloacetate 2- oxaloacetate to PEP 3- F-1,6bisP to F-6-P 4- Dephosphorylation of G-6-P to Glucose
37
Where does the last step in gluconeogenesis take place?
In the lumen of the ER. | Requires G-6-P to be shuttled in and glucose is then shuttled out
38
What is the name of the pathway that produces NADPH for all organisms?
Pentode phosphate pathway