new carbohydrates Flashcards

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1
Q

Why are carbohydrates a major energy source?

A

They are highly oxidisable - high energy H atom-associated electrons

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2
Q

Name 3 important monosaccharides.

A

Glucose, galactose and fructose.

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3
Q

Name 3 important disaccharides.

A

Sucrose, lactose and maltose.

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4
Q

Which disaccharides are reducing and which are non-reducing?

A

Maltose and lactose are reducing sugars. Sucrose is a non-reducing sugar.

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5
Q

Which glucose polymers are found in starch (plants)?

A

25% amylose and 75% amylopectin. Amylose is unbranched (alpha 1,4), amylopectin is branched and unbranched (alpha 1,4 and 1,6)

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6
Q

Where is glycogen in the body?

A

90% in the liver and skeletal muscle. Liver: blood glucose falls? G6P –> glucose released into the blood. Skeletal muscle: no G6P –> glycogen –> G6P by glycolysis –> lactate.

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7
Q

What are GAG’s (mucopolysaccharides) and where are they found?

A

Un-branched polymers made from repeating units of hexuronic acid and an AA sugar. Found in mucus and in synovial fluid around joints.

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8
Q

Give an example of a mucopolysaccaridoses.

A

Hurler syndrome.

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9
Q

Define the 9 major carbohydrates in the diet.

A

Glucose, fructose, sucrose, maltose, lactose, starch, glycogen and undigested hemi-cellulose and cellulose.

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10
Q

Describe the digestion of carbohydrates.

A

Mouth: salivary amylase hydrolyses alpha 1,4 bonds of starch. Stomach: no digestion. Duodenum: pancreatic amylase hydrolyses alpha 1,4 bonds. Jejunum: final digestion by mucosal cell-surface enzymes isomaltase, glucoamylase, sucrase and lactase.

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11
Q

How are glucose and galactose absorbed?

A

Glucose via an ATP-driven Na pump that moves Na out and brings glucose in, even against its concentration gradient. Galactose also uses concentration gradients.

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12
Q

How is fructose absorbed?

A

Binds to GLU5 and moves down its concentration gradient (high in gut lumen, low in blood).

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13
Q

How are hemicellulose and cellulose absorbed?

A

They cannot be digested. They increase faecal bulk. Gut bacteria can break them down a bit and yield methane and H2.

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14
Q

What is the most common disaccharidase deficiency?

A

Lactose intolerance. Lactase in lacking and so digestion of milk causes abdominal distension, cramps etc. Lactose in osmotically active - diarrhoea.

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15
Q

What do glucokinase and hexokinase do?

A

Digested glucose diffuses through intestinal epithelial cells into the portal blood then onto the liver. Glucose is immediately phosphorylated into G6P in cells so it is trapped. Glucokinase does this in the liver and hexokinase in other tissues.

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16
Q

Describe the Km and Vmax for glucokinase and hexokinase.

A

Glucokinase: high Km and high Vmax. Good enzyme but low affinity for glucose - most absorbed glucose trapped in liver. Hexokinase: low Km low Vmax. High affinity for glucose so when concentrations are low in the blood it can still find some. Not a good enzyme.

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17
Q

How is glycogen synthesised?

A

Glycogenin binds to glucose via UDP. Glycogen synthase takes over and extends the chains. Chains are broken and reformed (alpha 1,6) by glycogen branching enzyme.

18
Q

How is glycogen degraded?

A

Glucose monomers removed 1 at a time from the non-reducing end as G1P (glycogen phosphorylase). G1P converted to G6P. Liver? G6-phosphatase –> glucose –> blood. Skeletal muscle? Substrate-level phosphorylation for muscle contraction to produce lactate.

19
Q

What is Von Gierke’s disease?

A

Liver, kidney and intestine G6-phosphatase deficiency. G6P cannot be broken down to glucose so all glucose must come from the diet. High lactate in blood and hypoglycaemia

20
Q

What is McArdle’s disease?

A

Skeletal muscle phosphorylase deficiency. High blood glycogen, weakness and cramps after exercise.

21
Q

How is energy made when cells lack energy or don’t have mitochondria?

A

Glycolysis - substrate-level phosphorylation.

22
Q

Where does glycolysis occur?

A

The cytosol.

23
Q

What are the 2 phases of glycolysis?

A

Preparatory and payoff

24
Q

What is the net gain of ATP and NADH per glucose molecule in glycolysis?

A

2 ATP and 2 NADH.

25
Q

What are the first 3 steps of glycolysis?

A

1) Glucose –> G6P by hexokinase, 2) G6P –> F6P by phosphokinase isomerase, 3) F6P –> F-1,6-bisP by PFK1 - first committed step of glycolysis

26
Q

What are the 2 splitting reactions of glycolysis (steps 4 and 5)?

A

4) Cleavage of F-1,6-bisP into 2 x 3C sugars, 5) interconversion so both sugars are G3P

27
Q

Which reactions produce NADH and ATP in glycolysis?

A

6) oxidation of G3P (G3P dehydrogenase) to 1,3-bisPG, 7) P transfer from 1,3-bisPG to ADP (PG kinase). These reactions are energy-coupled.

28
Q

What is the difference between substrate-level and respiration-linked phosphorylation?

A

Substrate level: soluble enzymes and chemical intermediates. Respiration-linked: membrane bound enzymes and gradients of protons.

29
Q

What are the final 3 steps of glycolysis?

A

8) conversion of 3PG –> 2PG by PGmutase, 9) dehydration by endolase of 2PG –> PEP, 10) transfer of P from PEP to ADP by pyruvate kinase. Pyruvate and 2 ATP are produced.

30
Q

How can NAD+ be regenerated?

A

Niacin (vitamin) and lactate (made from pyruvate). NAD+ is essential for glycolysis.

31
Q

What happens to excess pyruvate in humans?

A

Can be reduced by lactate dehydrogenase into lactate.

32
Q

What is the cori cycle?

A

During strenuous exercise, ATP is made via substrate-level phosphorylation. Lactate made then converted to glucose in the liver by gluconeogenesis.

33
Q

What happens to pyruvate in cells with excess O2?

A

Pyruvate is oxidised to acetyl CoA in the mitochondria.

34
Q

Which tissues rely completely on glucose as their source of energy?

A

Brain, NS, RBC’s, testes and embryonic tissues.

35
Q

Which steps in glycolysis are irreversible?

A

1, 3 and 10.

36
Q

What is the final step of gluconeogenesis that makes free glucose?

A

G6Phosphatase converts G6P to glucose in the ER.

37
Q

How many bypass reactions are there in gluconeogenesis and what is their function?

A

There are 4 bypass reactions. They sidestep the 3 irreversible reactions of glycolysis. They utilise the cytosol and mitochondria.

38
Q

How are fructose and galactose metabolised?

A

The body doesn’t have distinct pathways for them. Fructose is mostly metabolised by the liver. Fructose is broken down via the F1P pathway to F1P then G3P. Galactose is converted to G1P.

39
Q

What is the function of the pentose-phosphate pathway?

A

Produces NADPH and pentoses - 5C sugars which are precursors for ATP, DNA and RNA.

40
Q

What are the 2 phases of the pentose-phosphate pathway?

A

1) oxidative/irreversible: generates NADPH (lots of NADPH required), 2) reversible/non-oxidative: interconverts G6P and PP to makes lots of different sugars (lots of nucleotides required)

41
Q

What happens when alcohol is ingested?

A

NAD+ is reduced to NADH in the liver. Gluconeogenesis is inhibited –> lacticacidaemia and hypoglycaemia.

42
Q

What is black water fever?

A

G6P dehydrogenase deficiency. Causes haemolytic anaemia.