Biological Molecules Flashcards

(46 cards)

1
Q

what is the meaning of a monosaccharide, disaccharide, and polysaccharide?

A

monosaccharides - simplest carbohydrates consisting of only one sugar molecule
disaccharides - formed by joining two monosaccharides together in a condensation reaction
polysaccharides- are carbohydrate polymers made up of many monosaccharides

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2
Q

combining alpha glucose with alpha glucose gets you which sugar? and where is it found in?

A

maltose - found in germinating seeds as more complex carbohydrates are broken down for energy

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3
Q

combining alpha glucose with fructose gets you which sugar? and where is it found?

A

sucrose - mostly found in plants because sucrose is transported in the phloem to provide sugars to other parts of the plants

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4
Q

combining alpha glucose with galactose gets you which sugar? and where is it found?

A

lactose - found in mammalian milk to provide energy for infant mammals

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5
Q

how is a condensation reaction formed? and what bond is formed

A

condensation reaction forms water as one oxygen and two hydrogen atoms are removed from the monosaccharides. This bonds the monosaccharides together, forming a disaccharide.
this bond is known as glycosidic bond

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6
Q

what is a glycosidic bond?

A

glycosidic bond is a covalent bond formed between two monosaccharides by a condensation reaction

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7
Q

why is water a good solvent?

A

due to the unequal distribution of electrons, it’s a polar molecules, so many ions and covalently bonded polar substances will dissolve in it. Leads to chemical reaction to occur

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8
Q

properties of water and its functions

A
  • high specific heat capacity because many hydrogen bonds present in water - takes a lot of thermal energy to break and can maintain stable temp in environments
  • cohesion : attraction of water molecules to each other —> surface tension
  • adhesion : attraction of water molecules to other objects —> capillary action + transpiration
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9
Q

how is a disaccharide broken down?

A

disaccharides are broken down through a hydrolysis reaction to form two monosaccharides

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10
Q

structure of amylose

A

amylose is a long chain of a-glucose molecules joined together by 1,4 glycosidic bonds. It coils into a helix shape that makes it more compact so more energy can be stored

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11
Q

structure of amylopectin

A

a long chain of a-glucose joined together with 1,4 and 1,6 glycosidic bonds. 1,6 glycosidic bonds cause amylopectin to have side branches, this is good due to terminal glucose molecules that can be easily hydrolyzed for use during cell respiration

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12
Q

what are the two types of starch

A

amylose and amylopectin

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13
Q

what is glycogen and where is it normally found?

A

Glycogen is found in cells with a high metabolic rate (liver cells and muscle cells)

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14
Q

structure of glycogen?

A

many alpha glucose molecules joined together by 1,4 and 1,6 glycosidic bonds, resulting in a highly branched structure. Therefore has a very high number of accessible ends

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15
Q

difference between monosaccharides, disaccharides, and polysaccharides?

A

mono and di are both sugars that are sweet tasting and soluble while poly does not taste sweet and is not soluble, its not a sugar

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16
Q

what is the role of a-glucose?

A

alpha glucose is the main source of energy in respiration.
excess chemical energy is stored in cells by forming polysaccharides of alpha glucose

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17
Q

how is a-glucose well suited for energy storage?

A
  1. they are compact so a lot of energy can be stored in a small space
  2. they are insoluble in water so they do not impact the water potential of a cell, so does not affect the osmotic effect of the cells
  3. they are large so they do not diffuse out of the cell unlike monosaccharides that can leave by carrier protein
  4. can easily be hydrolyzed to
    a-glucose when energy is needed
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18
Q

where is starch normally found?

A
  • found in photosynthesizing cells in leaves and storage cells in seeds and storage organs.
  • compacted into dense, insoluble grains stored in special organelles called amyloplasts
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19
Q

differences between amylose and amylopectin

A

amylose = only 1,4 glycosidic bonds
amylopectin = 1,4 and 1,6 glycosidic bonds, and amylopectin has more accessible ends meaning that it releases energy quicker than amylose which is better suited for respiration

20
Q

where is amylose, amylopectin, and glycogen found?

A

amylose + amylopectin are both found in plants while glycogen is found in animals

21
Q

what is cellulose and its function?

A

cellulose is a polysaccharide that makes up the cell wall, it is very strong and stops plant cells from bursting when too much water enters by osmosis - it makes the cells turgid

22
Q

structure of cellulose

A

cellulose is composed of many thousands of B-glucose molecules joined together by 1,4 glycosidic bonds

23
Q

how are cellulose fibers formed?

A

hydrogen bonds that cross-link the cellulose chains allow the chains to form stronger fibers

24
Q

what are microfibrils?

A

strong threads made of long cellulose chains, parallel to one another, joined by hydrogen bonds forming strong cross linkages

25
where is chitin found, and what is it used for?
in fungi, chitin is used to strengthen the cell wall
26
the function of chitin in insects
give strength to insects' exoskeleton waterproof - helps insects prevent water loss from their body
27
structure of chitin?
B-glucose joined together with 1,4 glycosidic bonds, similar to cellulose
28
difference in structure of chitin and cellulose
chitin contains acetylamine groups bonded to carbon 2 of the B-glucose monosaccharides
29
difference between fats and oil and what causes the difference in state?
fats are solid at rtp oils are liquid at rtp difference in the state is due to the presence of double bonds between carbon atoms and fatty acids
30
what are saturated hydrocarbon chains
fatty acids with hydrocarbon chains that have no double bond between carbon atoms
31
what are unsaturated lipids
32
how is a triglyceride synthesized
the formation of ester bonds during condensation reactions between glycerol and three fatty acids
33
why are unsaturated hydrocarbon chains liquid at rtp
because the fatty acid tails bend due to the presence of the c=c bond, the bent tail pushes the molecules further apart. This then weakens the intermolecular forces between the unsaturated triglyceride molecules so they form liquid at rtp
34
how do triglycerides play a role in respiration
triglycerides can be broken down into glycerol and fatty acids, used in respiration
35
asides from glycerol and fatty acids, what molecule is released when triglycerides are broken down during respiration
water, it is a good source of metabolic reactions
36
why are triglycerides good energy storer
- provide the most energy per unit of mass, useful for animals as it reduces the mass that must be carried around
37
uses of fats by animals
- protect internal organs - thermal insulation - aquatic animals produce oil to waterproof their fur
38
how is the structure of a phospholipid different from triglyceride
the difference is that one of the fatty acids is replaced by a phosphate molecule, which occurs through condensation reactions
39
what happens to phospholipids when they are in water
hydrogen ions dissociate from the phosphoric acid, forming a phosphate group that has a negative charge
40
which part of the phospholipid is hydrophilic
heads
41
which part of the phospholipid is hydrophobic
tails
42
what is a monolayer of phospholipids called
micelles
43
structure of a phospholipids bilayer
the hydrophilic heads form two rows on the outside while the hydrophobic tails are sheltered in the middle where there is no water
44
unique structure of the phospholipid bilayer
will never expose the hydrophobic tails to the water keeping the membrane stable
45
importance of the phospholipid bilayer
- a barrier, that controls substance that goes in and out of the cell - electrical insulation - the area in the middle is a non-aqueous environment so this creates a barrier to charged molecules which are dissolved in water
46
what molecules can pass through the membrane?
oxygen: enter cells for respiration carbon dioxide: leaves the cell as a waste product both are small and non-polar