TOPIC 7 CARBOHYDRATES OBJs Flashcards

1
Q
  1. Identify the major sites of digestion and absorption in humans
A

a. Mouth (limited)
b. Stomach (some)
c. Small intestine (bulk)

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2
Q

Wheres does the bulk of carbohydrate digestion and absorption occur

A

Small intestine

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3
Q

Ceullose source, subunit and bonds

A

plant
B-glucose
1-4

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4
Q

Starch source, subunit, bonds

A

Amylose
Plant
a-glucose
1-4

Amylopectin
a-glucose
1.4 , 1,6

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5
Q

Glycogen source, subunit, bonds

A

Animal
a-glucose
1,4 and 1,6

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6
Q

Carbohydrate digestion occurs by break of the ____ by enzymes called _________

A

glycosidic bonds

endoglycosidases

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7
Q

Digestion of glycogen, starch and cellulose in humans

A

The mouth
- α-amylase, secreted from the parotid salivary glands, acts on starch and glycogen
- Breaks α -1-4 glycosidic bonds
- Digestion is limited – amount of time spent there

The stomach
o Salivary amylase is inactivated due to low pH
o No digestion here!
o Oligosaccharides pass into small intestine

The small intestine
o Pancreas releases pancreatic α-amylase
o Digests the oligosaccharides into disaccharides

Cellulose?
o Cellulose (β1-4) cannot be broken down in most animal guts
o In humans, cellulose passed out via the faeces undigested, as we lack the enzyme capable of breaking the bond

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8
Q

What are sucrose, lactose, maltose and isomaltose

A

disaccharides

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9
Q

Carbohydrates from starch and glycogen breakdown digests into

A

disaccharides

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10
Q

what can be absobed by small intestine

A

monosaccharide

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11
Q

Mastose goes to ________ by what enzyme

A

2 glucose by maltase

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12
Q

isomaltose goes to _____ by what enzyme

A

2 glucose by isomaltase

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13
Q

Sucrose goes to _____ by what enzyme

A

glucose and fructose by sucrase

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14
Q

lactose goes to _____ by what enzyme

A

galactose and glucose by lactase

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15
Q

disacchardies are associated with

A

brush border epithelial cells of small intestine

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16
Q
  1. Explain how glucose, fructose and galactose are absorbed in the small intestine
A
  • SGLT-1 – absorbs glucose and galactose
  • GLUT-5 – facilitated transporter, uptake of fructose
  • All three are transported into circulation through GLUT-2
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17
Q
  1. Distinguish between the roles of glycogen in animal skeletal muscle and liver cells
A
  • In skeletal muscle cells, glycogen acts as an energy store for strenuous exercise or ‘fight or flight’ response
  • In liver cells, glycogen is primarily a store of glucose to provide to body cells when blood glucose is low
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18
Q
  1. Identify the reducing and non-reducing ends of a glycogen molecule and relate the non-reducing end to the sites of glycogen synthesis and degradation
A
  • Enzymes act on non-reducing ends for synthesis and degradation
  • Having many means can be rapid
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19
Q
  1. Define the roles of the branching and debranching enzymes and glycogenin
A
  • Branching enzymes: forms the α-1,6 bonds
  • Debranching enzymes: breaks or makes the α-1,6 bonds
  • Glycogenin: can initiate glycogenesis when no glycogen molecules are available
20
Q
  1. Explain the importance of branching in glycogen
A
  • Two main roles:
    1. Increases solubility of glycogen
    2. Creates more non-reducing ends, which are the reactive sites upon which phosphorylase and glycogen synthase act.
  • Therefore, increases the rate synthesis and degradation
21
Q

What is glycogen

A
  • Glycogen is a polymer of glucoses bonded by glycosidic bonds (have branches too which make it easier to add and take)
  • Glycogenesis high in fed state
  • Liver and skeletal muscles
22
Q

Glycogenesis

A

glycogen synthesis

23
Q

4 steps of glycogenesis

A

1) Attaching uridine diphosphate (UDP) to glucose
- Phosphoglucomutase
- UDP-glucose phosphorylase
2) Creating glycogen,
- Glycogen synthase catalyzes the bonding of the glucose of one UDP-glucose to another, forming an alpha 1,4 glycosidic bond
- Glycogenin
3) Adding branches to glycogen molecule or polymer
- Branching enzyme
- Glycogen synthase

24
Q

Glycogenolysis

A

Glycogen degradation

25
Q

Glycogenolysis steps

A

1) Starts with the branches
- Glycogen phosphorylase cleaves alpha 1,4 glycosidic bonds, and catalyzes transfer of a phosphate to the free glucose – releasing 1 glucose-1-phosphate molecule at a time, does this until 4 glucose made
- Debranching enzyme cleaves 1,6 bonds and they are added back to 1,4 linear one, extending it & can also cleave the 1,6 releasing a free glucose
-
2) Conversion to **glucose-6-phosphate **by **phosphoglucomutase **
Liver:
o Has glucose-6-phosphatase, which removes the phosphate and released into the blood
Skeletal muscle:
o DOES NOT have glucose-6-phosphatase, so it sends glucose-6-phosphate into glycolysis to release energy

26
Q
  1. Explain the cAMP-dependent pathway by which adrenaline and glucagon trigger the breakdown of glycogen
A
  • They bind to G-coupled protein receptor which activates adenylyl cyclase which converts ATP to cAMP
  • cAMP activates protein kinase A, which adds a phosphate to glycogen phosphorylase kinase , activating phosphorylase, increasing glycogen breakdown and decreasing glycogen synthesis by glycogen synthase
27
Q

Glycogen synthase

A

Makes glycogen
Insulin increases this because its increasing the stores

28
Q

Glycogen phosphorylase

A

Removes phosphates
Glucagon increases this to release glucose

29
Q

To access stored energy from macromolecules they need to be

A

digested and absorbed

30
Q

plant carbohydrates

A

starch and cellulose

31
Q

animal carbohydrates

A

glycogen, disac lactose and succrose

32
Q

glycogen is a

A

major glucose storage in liver

33
Q

Digestion of carbohydrate in mouth

A

a-amylase secreted from parotid salivary glands acts on starch and glycogen, breaking the a 1-4 glycosidic bonds, results in oligosaccharide

  • amylose, amylopectin or glycogen
34
Q

what is oligosacharide

A

small chain of glucose joined together

35
Q

Carbohydrate digestion in stomach

A

none

36
Q

Carbohydrate digestion in small intestine

A

Pancreas releases pancreatic a-amylase
oligosaccharides are digested to disaccharides
also by cleaving a-1-4 glycosidic bonds

  • maltose and isomaltose result
37
Q

What about cellulose

A

cellulose (b1-4) cannot be broken down by body enzymes

38
Q

disaccharidases act where

A

small intestine

39
Q

disaccharidases are associated with the

A

brush border epithelial cells

40
Q

how do monosaccharides occur

A

disaccharidases cleave disaccharides into monosaccharides and now they can be absorbed

41
Q

monosaccharides

A

glucose
fructose
galactose

42
Q

how is glucose absorbed

A

Na+/glucose symporter

43
Q

Na+/glucose symporter is an example of

A

secondary active transport

44
Q

glucose transport in humans is by _____ systems

A

GLUT

45
Q

what does the body do with excess glucose

A

stored as glycogen or fat

46
Q

Glycogen storage occurs in what state and where

A

fed state
liver and skeletal muscle

47
Q

what triggers glycogen breakdown

A

adrenaline (fight or flight) or low blood glucose (glucagon)