carbohydrates Flashcards

1
Q

what bonds do carbohydrates contain? why are they important?

A
  • rich in C-H bonds
  • important in yielding energy
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2
Q

what is breakdown of glucose associated with?

A
  • negative change in Gibbs free energy
  • negative enthalpy- huge drop in Gibbs free energy
    -707kcal.mol-1
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3
Q

what are the subunits linked together by in disaccharides, oligosaccharides and polysaccharides?

A
  • linked by a (1-4) glycosidic bond
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4
Q

what happens as glucose is broken down? what are they passed down to?

A
  • as glucose is broken down electrons in the chemical bonds are passed down to electron carriers which yield energy
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5
Q

what are carbs and glycogen in human cells branched with?

A
  • a (1-6) glycosidic bonds
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6
Q

how many times do a(1-6) repeat?

A
  • repeat every 20-30 residues for starch
  • every 8-12 for glycogen
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7
Q

what are the specialised features of carbs and what does this allow

A
  • compact
  • hydrophilic
  • high surface area
  • optimise digestion and energy provision
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8
Q

where does digestion of carbohydrates start?

A
  • in the mouth (saliva)
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9
Q

what happens in the small intestine?

A
  • pancreatic juices
  • enzyme a- amylase hydrolyses hydrolyses a(1-4) glycosidic bonds
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10
Q

what does the enzyme a- amylase hydrolyse?

A
  • glycosidic bonds in starch to short chain carbohydrates (oligosaccharides)
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11
Q

where are oligosaccharides broken down and what into?

A
  • broken down in villi of small intestine
  • into disaccharides
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12
Q

what are the specific enzymes that break disaccharides into monosaccharides?

A
  • lactase, maltase and sucrase
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13
Q

what does lactase breakdown?

A
  • lactose
  • galactose and glucose
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14
Q

what does maltase breakdown?

A
  • maltose
  • glucose and glucose
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15
Q

what does sucrase breakdown?

A
  • sucrose
  • fructose and glucose
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16
Q

how are monosaccharides absorbed?

A
  • absorbed into cytosol of enterocytes and transported into capillaries that empty into venous blood and portal vein that supplies liver
17
Q

where is glycogen stored?

A

-liver (3-7%)
-muscle (1-1.5%)

18
Q

where is glycogen optimally located?

A
  • located between thick and thin filaments near the mitochondria
19
Q

how is glycogen stored?

A
  • stored in granules containing enzymes needed for its breakdown and storage
20
Q

how is ATP provision in muscle enhanced?

A
  • enhanced by breakdown of liver glycogen during exercise
  • communication between these two tissues
21
Q

describe the synthesis of glycogen

A
  • anabolic condensation reaction> requires energy to build up molecules
22
Q

what does glucose react with to provide energy to build the glycogen chain? how many glucose residues?

A
  • reacts with uridine triphosphate
  • 30- 60,000 glucose residues
23
Q

what is the process of glucose synthesis?

A
  1. Glycogenin adds 4 glucose residue cells to it cell
  2. Glycogenisnthase uses UT to build the molecule
  3. Branching occurs through branching enzyme
24
Q

what reaction is the breakdown of glycogen? what does it involve?

A
  • catabolic hydrolysis reaction
  • phosphate group added to glucose to release it from the glycogen chain
25
Q

how does exercise regulate the breakdown of glucose?

A
  • breakdown increases during muscle contraction due to ATP demand
26
Q

what happens when muscle stores decrease? what activity increases?

A
  • signal sent to liver to ^ breakdown
  • glycogen phosphorylase activity in muscle ^ due to ^ in Pi, ^ in AMP, ^ in adrenaline, ^Ca2+
27
Q

what happens to synthesis in hard exercise?

A
  • synthesis is inhibited although prolonged periods may activate it to maintain balance
28
Q

what happens to synthesis post exercise?

A
  • rapidly activated
29
Q

describe phosphorylation as a method

A
  • quick and energetically favourable control mechanism
  • regulates enzyme function w/ out need to deconstruct a protein