Lecture 2 - Carbohydrates Flashcards

(23 cards)

1
Q

What are macromolecules

A
  • large highly organized molecules that form cellular structures and carry out the activities of cells
  • most are short lived, except DNA, and are continually broken down and replaced
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2
Q

what are the 4 major categories of macromolecules

A
  1. proteins
  2. nucleic acids
  3. polysaccharides
  4. lipids
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3
Q

Which 3 macromolecules are made up of repeating units of monomers making them polymers?

A
  1. proteins
  2. nucleic acids
  3. polysaccharides
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4
Q

What roles do carbohydrates have

A
  • energy (storage and immediate)
  • metabolic intermediates (can be precursors for other molecules)
  • structural components of RNA and DNA
  • structural components of cell walls of bacteria and plants
  • glycoproteins and glycolipids
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5
Q

what type of sugar is it if the carbonyl group is located at an internal position

A

ketose

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6
Q

what molecule is it if the carbonyl is located at one end

A

aldose

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7
Q

what affect do hydroxyl groups have on sugars

A

highly water soluble

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8
Q

formula for stereoisomers

A

2^n
n=chiral centers
- half are D form and other half are L form

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9
Q

which form are most naturally occurring sugars in

A

d-form

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10
Q

what is the anomeric carbon

A

carbon derived from the carbonyl carbon of the open chain form of the carbohydrate molecule

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11
Q

different types of pyranose (alpha and beta)

A

alpha - OH projection below the plane of ring
- less steric hindrance
- 64%
beta - OH projection upward
- 36%

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12
Q

What happens when A1C is high

A
  • excess glucose binds non-enzymatically to proteins, lipids, and nucleic acid
  • this creates AGEs which damage blood vessels, nerves, and organs by
  • promoting inflammation
  • increasing oxidative stress
  • causing loss of protein function
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13
Q

how are monosaccharides connected

A
  • glycosidic bonds
  • glycosidic bonds connect anomeric carbon to hydroxyl group
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14
Q

what is the structural difference between maltose and cellubiose

A
  • nature of glycosidic bond
  • alpha 1-4
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15
Q

why do sucrose and lactose differ in glycosidic bonds

A
  • due to bond orientation on anomeric carbon
  • sucrose alpha 1-4
  • lactose beta 1-4
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16
Q

what are storage polysaccharides and their role

A

glucose
- starch in plants - two forms amylose and amylopectin
- glycogen in animals

17
Q

what distinguishes amylose from amylopectin

A

amylose - unbranched
amylopectin - branched

18
Q

what are the two major sites of storage for glycogen

A

liver and skeletal muscle

19
Q

explain structural polysaccharides

A
  • most abundant organic material on earth
  • cant be digested by humans but provides dietary fiber
    -cellulose - plant product made of unbranched polymers
  • chitin
20
Q

what is chitin

A
  • component of invertebrate exoskeleton
  • found in fungi cell walls, mollusk, shells and fish scales
21
Q

what affect can different bonds types have on the structure of the polysaccharide

A
  • alpha glycosidic bonds allow for the spontaneous formation of helical shapes
  • both starch and glycogen can form these loose coils
  • branching disrupts this structure
  • beta glycosidic bonds form rigid linear rods
  • these rods aggregate into microfibrils
22
Q

what is the difference between starch and glycogen

A

starch
- Found in plants
- Used for long-term energy storage
- Made of amylose (unbranched) and amylopectin (branched)
- Has α(1→4) and some α(1→6) glycosidic bonds
- Moderately branched
- Less soluble in water
- Digested more slowly

glycogen
- Found in animals (especially liver and muscle cells)
- Used for quick energy release
- Made of glucose units only
- Has α(1→4) and many α(1→6) glycosidic bonds
- Highly branched (more than amylopectin)
- More soluble in water
- Digested quickly due to high branching

23
Q

what are glycomics

A
  • systematic characterization of all of the carbohydrate components of a cell or tissue