Carbohydrates Flashcards

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
Q

What does the low Km and Vmax of hexokinase mean for tissue cells?

A

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
Q

Give some fates of glucose-6-phosphate?

A

Pentode phosphate pathway
Glycolysis
Glycogen storage

27
Q

What is the role of glucose-6-phosphatase?

A

Catalyses the release of glucose into the blood by converting glycogen into glucose-6-phosphate and then glucose.

28
Q

What is von Gierke’s disease?

A

Liver, kidney and intestine glucose-6-phosphate deficiency

29
Q

What is McArdle’s disease?

A

Skeletal muscle phosphorylase deficiency

30
Q

Describe the process of glycolysis?

A

A catabolic pathway that saves potential energy from glucose by forming ATP through substrate level phosphorylation

31
Q

What is the first committing step of glycolysis?

A

Phosphorylation of F-6-P to F-1,6 bisP. F-1,6bisP is solely destined for glycolysis. Irreversible step

32
Q

Where does glycolysis occur?

A

In the cytosol

33
Q

What does substrate level phosphorylation require?

A

Soluble enzymes and chemical intermediates

34
Q

Why does NAD+ need to be replenished?

A

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
Q

What is the Cori cycle?

A

When the liver repays the oxygen debt muscles run up by converting lactate into glucose during gluconeogenesis

36
Q

What are the 4 bypass reactions of gluconeogenesis?

A

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
Q

Where does the last step in gluconeogenesis take place?

A

In the lumen of the ER.

Requires G-6-P to be shuttled in and glucose is then shuttled out

38
Q

What is the name of the pathway that produces NADPH for all organisms?

A

Pentode phosphate pathway