SfM- Carbohydrates Flashcards

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1
Q

name the two types of starch polymers

A
  • amylose (glucose joined via a1-4 glycosidic bonds)

- amylopectin (mainly a1-4 glycosidic bonds but a1-6 every 20-30 residues = branching)

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2
Q

what is glycogen?

A
  • glycogen is a strategy to store glucose in body
  • polymer of glucose of a1-4 bonds but a1-6 more frequent
  • makes glycogen more extensively branched than starch (more glucose can be stored in a small space)
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3
Q

why store glucose as glycogen?

A
  • more compact
  • has many non-reducing end, means it can be synthesised and degraded easily
  • polymers form gels - making it osmotically active but doesn’t disrupt cell balance
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4
Q

what are glycoproteins?

A
  • proteins that have carbohydrates covalently attached

- can vary from 1-80& carbohydrate mass

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5
Q

how can carbohydrates affect protein?

A
  • increase proteins solubility
  • influence protein confirmation
  • increases stability
  • act as communication between cells
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6
Q

what are glycosaminoglycans (GAGs)?

A
  • unbranched polymers of hexuronic acid and an amino-sugar
  • very slippery and sticky - also called mucopolysaccharides
  • there are groups of genetic disorders meaning the enzymes that breakdown GAGs - can build up in tissues throughout the body (Hurler Syndrome)
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7
Q

what are proteoglycans?

A
  • more carbohydrate than protein

- formed from GAGs attaching to proteins - when next to each other - can interlink = stronger

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8
Q

what are glycoproteins?

A
  • more protein than carbohydrates
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9
Q

different types of carbohydrates

A
  • starch (cereals, potatoes, rice)
  • glycogen (meat)
  • hemi/cellulose (plant cell walls - don’t digest it)
  • oligosaccharides (peas, beans, lentils - a1-6 bonds don’t digest
  • lactose/sucrose/maltose - (milk, sugar, beer)
  • glucose/fructose (fruit, honey)
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10
Q

how are carbohydrates digested?

A
  1. mouth - amylase breaks starch into glucose
  2. duodenum - pancreatic amylase (same function as mouth)
  3. jejunum - digestion by mucosal cell-surface enzymes (isomaltases, glucoamylase, sucrase, lactase)
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11
Q

how is glucose absorbed?

A
  • Na+-glucose symporter transports both Na and glucose into the cell (relies on high extracellular Na)
  • glucose uniporter moves glucose out of cell into blood
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12
Q

how are monosaccharides absorbed?

A
  • ATP-driven Na+ pump maintains low cellular Na+ to allow glucose to be continually pumped into cell
  • galactose also uses gradients to transport
  • fructose binds to the channel GLUT5 - moves down conc gradient
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13
Q

how is hemi/cellulose absorbed?

A
  • these cannot be digested by the gut but increase faecal bulk, increases speed of digestion
  • polymers are broken down by gut bacteria - yields CH4 and H2 = FARTS
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14
Q

what are the characteristics of a disaccharide deficiency?

A
  • abdominal distension (bloat)
  • cramps
  • diarrhoea
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15
Q

what is lactose intolerance?

A
  • lactase deficient so lactase can’t be digested
  • undigested lactose is broken down by gut bacteria - causes gas build up and irritant acids
  • lactose is osmotically active, thus drawing water from the gut into the lumen causing diarrhoea
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16
Q

what is the fate of glucose?

A
  • Glc diffuses through intestine epithelium, into blood and into liver
  • Glc is immediately phosphorylated to Glc-6-phosphate - effectively trapping it in cell
  • GLUT transporters don’t recognise phosphorylated form
  • catalysed by glucokinase (liver), hexokinase (any tissue)
17
Q

what is the role of glycogenin?

A
  • glycogenin begins binding glucose molecules to itself - forms chains of 8 glucose residues
18
Q

what does glycogen synthase do?

A
  • glycogen synthase takes over from glycogenin, extends the glucose chains
  • chains formed by glycogen synthase are then broken down by glycogen-branching enzymes and re-attached via a1-6 bonds = branching
19
Q

how is glycogen degraded?

A
  • glycogen phosphorylase removes glucose monomers
  • glucose-1-phosphate is left but not a free molecule
  • transferase activity of debranching enzyme removes 3 Glc residues and attaches them via a1-4
  • Glucosidase activity then removes final Glc by breaking an a1-6 linkage to release free Glc