Biochemistry of Metabolism Flashcards

1
Q

what is glycogen?

A

major storage molecule for carbohydrates (glucose) in liver and muscle cells

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2
Q

what is glycogenesis?

A

synthesis of glycogen from glucose

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3
Q

what is glycogenolysis?

A

breakdown of glycogen to form glucose by cleaving glucose off the ends of the chains
Occurs in liver and muscle cells

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4
Q

how if glycogen stored in the liver?

A

can be broken down between meals and released to maintain blood glucose levels for RBCs and brain without food

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5
Q

how is glycogen stored in the muscle cells?

A

not available for maintenance of blood glucose

provides energy for the muscle cells via glycolysis and TCA during bursts of physical activity

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6
Q

what is gluconeogenesis?

A

pathway which generates glucose from non-carbohydrate precursors

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7
Q

how does dietary glucose affect blood glucose?

A

increases it quickly after meals, but it falls again quickly

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8
Q

when is blood sugar lowest and why?

A

in the morning, before breakfast as long time between last meal and liver cant break down any more glycogen

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9
Q

what is the primary source of glucose overnight?

A

gluconeogenesis

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10
Q

what is the structure of glycogen? (what bonds)

A

branched chain made of many glucose molecules joined together in chains via alpha 1-4, glycosidic bonds.
Branches are introduced by alpha 1-6, glycosidic bonds

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11
Q

what is the function of glycogenin?

A

has catalytic activity, acts as a primer
can add up to 4 glucose molecules to itself which allows glycogen synthase to create glycogen as it can only add on glucose, it cant start it

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12
Q

how is glycogen synthesised?

A

glucose phosphorylated to glucose 6 phosphate > glycolysis if needed or converted to glucose 1 phosphate > activated to UDP glucose > glycogen synthase bonds together glucose parts of UDP glucose (UDP recycled to make more UDP glucose using 1 ATP)

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13
Q

what is UDP glucose?

A

uridine diphosphate + glucose molecule connected via phosphate ester bond
Activated form of glucose (glucose transfer molecule)

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14
Q

what is the importance of the phosphate ester bond of UDP glucose?

A

contains high energy which can be released to transfer the glucose to the glycogen molecule (hydrolysis)

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15
Q

what is the function of glycogen synthase?

A

Rate limiting enzyme of glycogenesis

Synthesises glycogen by adding glucose from UDP glucose to the ends of glycogen chains

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16
Q

what is the branching enzyme?

A

transglycosylase that introduces 1-6 glycosidic branches to glycogen chains

17
Q

what enzyme catalyses glycogenolysis?

A

glycogen phosphorylase

takes glucose off the end of glycogen and adds a phosphate > glucose 1 phosphate > glucose 6 phosphate

18
Q

what are the steps of glycogenolysis?

A

glucose cleaved off end of glycogen and converted to glucose 1 phosphate by adding a phosphate (via glycogen phosphorylase) > glucose 1 phosphate > glucose 6 phosphate > dephosphorylated in liver and resulting glucose released into blood stream (via GLUT 2 transporter) OR undergoes glycolysis in skeletal muscle

19
Q

what 2 enzymes regulate glycogenesis and glycogenolysis overall, and via which hormones?

A
glycogenesis = glycogen synthase 
glycogenolysis = glycogen phosphorylase
20
Q

what effect does insulin have on glycogen synthase and glycogen phosphorylase?

A

hormone of the fed state

activates synthase, inhibits phosphorylase

21
Q

what effect does glucagon have on glycogen synthase and glycogen phosphorylase?

A

hormone of starved state
inhibits synthase
activates phosphorylase (as does adrenaline and cortisol)

22
Q

what are glycogen storage diseases?

A

diseases due to problems with enzymes of glycogenesis/glycogenolysis

23
Q

what are the 3 precursors used in gluconeogenesis?

A

lactate (lactic acid)
amino acids (from muscle)
glycerol (from fat)

24
Q

where does gluconeogenesis get energy?

A

from oxidation of fatty acids or muscle protein

25
Q

where does gluconeogenesis occur?

A

liver

small amounts in the kidneys

26
Q

how does the liver keep blood sugar levels constant?

A

glycogen synthesis/breakdown

gluconeogenesis

27
Q

gluconeogenesis is like glycolysis in reverse, true or false?

A

true (almost)

BUT - special reactions required to bypass the 3 irreversible reactions in glycolysis using 4 liver enzymes

28
Q

what is oxaloacetate?

A

4 carbon compound synthesised from pyruvate
allows gluconeogenesis to proceed
accepts acetyl groups in citric acid cycle during glycolysis

29
Q

is gluconeogenesis energy dependant?

A

yes

requires 6 for every glucose made

30
Q

what is the cori cycle?

A

lactic acid made from anaerobic glycolysis, taken to liver and glyconeogenesis occurs producing glucose

31
Q

what are the 2 classes of amino acids?

A
glucogenic = can be used to make glucose
ketogenic = cant be used to make glucose
32
Q

do amino acids enter gluconeogenesis via the citric acids cycle or via converting to pyruvate?

A

both

33
Q

what is the first step of gluconeogenesis?

A

conversion of pyruvate to oxaloacetate, stopping the citric acid cycle

34
Q

how are glycolysis and glyconeogenesis regulated?

A

1) hormonally (glucagon - stimulates neogenesis, inhibits glycolysis, Insulin = opposite)
2) allosteric effectors in cells (ADP/AMP, ATP, fructose 2,6 biphosphate, citrate/alanine/acetyl CoA)