Carbohydrates Flashcards

1
Q

Carbohydrates are highly oxidisable or not l

A

Yes they are

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2
Q

Carbohydrate functions

A

Structure in cell walls and ECM of animal cells. Store energy as starch in plants and glycogen in animals. Cell to cell communication eg ABO blood groups

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3
Q

Types of monosaccharides

A

Glucose fructose galactose

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4
Q

Disaccharide

A

Formed from monomers that are linked by glycosidic bonds

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5
Q

Glycosidic bonds

A

Covalent bond formed between hydroxyl group and anomeric carbon of different monosaccharide

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6
Q

Anomeric carbon

A

Anomers are mirror images of each other( left and right handed forms ). Stabilises the structure of glucose. Only residue that can be oxidised

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7
Q

Types of disaccharide

A

Maltose lactose sucrose

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8
Q

Sucrose is a reducing sugar true or false and why

A

False because no free anomeric carbon

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9
Q

Polysaccharides

A

Polymers of medium to high molecular weight

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10
Q

Types of polysaccharides

A

Homopolysaccharides - single monomer species

Heteropolysaccharides- have two or more monomer species

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11
Q

Starch contains

A

Amylose mainly straight and amylopectin (75% of it) (got alpha 1-4 chains and 1-6 chains). Non reducing ends

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12
Q

What is more extensively branched glycogen or starch

A

Glycogen

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13
Q

Glycogen is in what part of the body

A

Liver (replenish blood) and skeletal muscle (produces atp for contraction)

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14
Q

Why store glucose in polymers

A

Compactness, have lots of non reducing ends so can be readily synthesised and degraded, form hydrated gels and not rlly in solution - omsotically inactive

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15
Q

What do carbohydrates attached to proteins do

A

Communication between cells, protect it from degradation, influence folding, increase solubility

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16
Q

Glycosaminoglycans

A

Found in mucus, un branched polymers made from units of hexuronic acid and amino sugar which alternates through the chains

17
Q

Proteoglycans

A

Carbohydrate part muchhh more than protein. Formed from GAGs. They are macromolecules found on surface of cells or in between cells in the ECM. Form part of connective tissue

18
Q

Glycoproteins

A

V similar to proteoglycans but protein part more than glucose. Found in blood and in cells in secretory system

19
Q

Carbohydrate digestion order

A

Mouth- salivary amylase
Duodenum- pancreatic amylase
Jejunum (small intestine)- mucosal cell surface enzymes

20
Q

Glucose is absorbed how

A

Using glucose symport and sodium potassium pump in epithelial cells of the small intestine

21
Q

Fructose is absorbed how

A

Uses GLUT5 transporter. Then goes down the conc gradient high in gut lumen low in blood

22
Q

Cellulose and hemicellulose break down

A

Don’t get digested but they get broken down. Increase faecal bulk and decrease transit time. Break down yields CH4 and H2 (farts)

23
Q

Disaccharide deficiencies

A

Genetic, cramps because struggle to break down. Enzyme tests to see if they are working. Lactose intolerance

24
Q

Fate of absorbed glucose

A

Goes from epithelial cells into blood then to liver. Converted into glucose-6-phosphate which cannot diffuse out of cell because GLUT transporters won’t take it so it is trapped. Enzymes work on it. Then go through blood as glucose to other tissues

25
Q

What enzyme is better for glucose- glucokinase or hexokinase

A

Hexokinase (low Km but low Vmax)

26
Q

In skeletal muscle what does glycogen get broken down into

A

Lactate because of glycolysis

27
Q

Synthesis of glycogen

A

1- glycogenin binds glucose to form short chains then glycogen synthase extends the chains
2- chains broken by glycogen branching enzyme and react hard via alpha1-6 bonds to give branch points

28
Q

Degradation of glycogen

A

Glucose monomers are removed by glycogen phosphoylase one at a time from non reducing ends as G1P. Then glucose is removed then reattached at the nearest non reducing end. Glucosidase then removes the final glucose by breaking a alpha1-6 link to release free glucose

29
Q

What happens to pyruvate at the end of glycolysis

A

Converted into ethanol and carbon dioxide, lactate or carbon dioxide and water

30
Q

What coenzyme is needed in glycolysis

A

NAD and NADH

31
Q

What is glycolysis

A

Catabolic pathway that saves some potential energy from glucose by forming ATP through substrate level phosphorylation.only way energy can be made when oxygen is in short supply

32
Q

Process of glycolysis

A

Glucose to F-1,6-BP (Used 2ATP) then to G3P to PEP to pyruvate or to DHAP. Produces 4 ATP

33
Q

When is cori cycle used

A

When the muscles don’t receive oxygen fast enough to make ATP so ATP is made via substrate level phosphorylation which produces lactate. Lactate converted and then the liver repaid oxygen debt to molecules

34
Q

Gluconeogenesis is

A

Process that transforms non carbohydrate substances such as glycerol, amino acids, lactate into glucose

35
Q

What is cori cycle

A

Interaction between muscle and liver with glucose

36
Q

How can glycolysis and gluconogenesis be independently controlled

A

Bypass reactions that sidestep the irreversible ones of glycolysis. Prevents them cancelling each other out

37
Q

What other sugars can be added to glycolysis

A

Galactose at beginning (converted into glucose 6P) and then fructose at second stages (converted into fructose 6P) or from liver converted into GAP or DHAP