ch 2: biological molecules Flashcards
monosacch
formula: (CH2O)n
-trioses intermediate to respiration and photosynthesis
-pentoses
°ribose for DNA and ATP
°deoxyribose for DNA
-hexoses as glucose, fructose they are used in respiration and energy release and in the formation of di/poly-sachh
properties of monosacch
all are reducing sugars
they have a reactive group to reduce benedict.
all are water soluble
polar, so water molecules can cluster around them and hydrogen bond with them
-sweet
-crystalline
-formed of one carbon ring
polysacch
-starch
-glycogen
-cellulose
-chitin
-starch and glycogen has metabolic functions.
they can be stored as they are not reactive and soluble
-cellulose has a structural function.it enters in the formation of cell wall as it has a high tensile strength
properties of disacch
maltose and lactose are reducing sugars while sucrose is non reducing sugar (why?)
-all are water soluble but less soluble than monosachh
-sweet
-crystalline
-formed of 2 carbon rings
disachh
formula C12 H22 O11
-sucrose
-lactose
-maltose
-sucrose is translocated in the phloem as it is less reactive than glucose and more soluble than starch
properties of polysacch
all non reducing sugars
water insoluble
-not sweet
-not crystalline
-formed of more than 2 carbon rings
how a-glucose differs from B-glucose (2marks)
a-glucose has its -OH group of carbon atom number one pointing downwards while that of B-glucose has the OH group pointing upwards
breakage of glycosidic bond
it occurs as a result of hydrolysis reaction which involves
-the addition of water
- the transformation of large mol into smaller
-it is controlled by specific enzymes
formation of glycosidic bond
it occurs as a result of condensation reaction while involves:
-the removal of water
-the transformation of monomers into larger mol
it i controlled by specific enzymes
why sucrose is non reducing sugar?
-doesn’t react with benedict to give brick-red colour
-it doesn’t have a reactive group to reduce benedict
-needs to be boiled with dilute HCL to breakdown glycosidic bond
starch has 2 forms
amylose and amylopectin
describe the structure of amylose and how it relate to it function
it is a polymer of a-glucose
linked by 1,4 glycosidic bond
it is non branching and takes a helical shape
-most of their OH group pointing inward
structure of amylopectin and how it relate to its function
polymer of a-glucose
linked by 1,4 glycosidic and 1,6 glycosidic bonds
not helical
-branching
this structure makes the amylopectin and glycogen insoluble, compact & easily hydrolyzed. by this amylopectin and glycogen have a metabolic function as they are convenient energy storage molecules.
what makes amylose convenient storage molecule
-insoluble: so will not lower the water potential and will not change the osmotic pressure inside the cell. it will affect on the chemical reaction inside the cell
-compact: so will take small room inside the cell
easily hydrolyzed by specific enzymes, to give glucose for respiration and energy release
why is it an adv for animal cell to store glycogen not amylopectin
glycogen is more branching so has more free ends for enzymes to work, so more glucose produced by unit time for more respiration also more glucose added
describe glycogen and how it relate to it function
glycogen is similar to amylopectin but more branching
what makes cellulose mol flat ribbon?
the OH group on carbon atom one is pointing upwards and the OH group of carbon number 4 is pointing downwards- to form 1,4 glycosidic bond, one glucose mol has to turn up side down relative to the other, that is rotated 180°
describe cellulose structure and how it relate to it function
-cellulose is a polysacch
-it is a polymer of B-glucose
-linked by B-1,4 glycosidic bond
-straight chains and not branching
-cellulose molecule are arranged parallel to each other.
-so OH group pointing in all directions so many hydrogen bonds form between cellulose molecules to form bundles of microfibrils, that cross link together with many hydrogen bonds to form cellulose fibers.
-this gives an extremely strong,insoluble,and slightly elastic structure that enters in the formation of cell wall as it has high tensile strength to withstand high turgor pressure inside the cell.
lipids forms
-triglycerides
-phospholipids
-cholesterol
elements: C H O
-proportion of the oxygen is much reduced in lipids that carbohydrates
triglycerides structure
glycerol & 3 fatty acid tails
triglycerides differ from each other according to no of CH2 in hydrocarbon chain that make tail vary in length
what makes cellulose have a high tensile strength that makes the it enter formation of the cell wall
many hydrogen bonds between cellulose mol to formation microfibrils
many hydrogen bonds between the bundles of microfibrils to form fibers
difference between saturated fatty acids and unsaturated fatty acids
-unsaturated fatty acid does not contain the max no of hydrogen atoms
-unsaturated fatty acids contains one or more double bonds between carbon atoms in hydrocarbon chain
-unsaturated fatty acid forms a kink
properties of triglycerides
-nolar as they have hydrophobic head and three hydrophobic tails
-head is made of glycerol and tail is made of three fatty acid tails
-some triglycerides are solid at room temp as they are formed of saturated fatty acids, others are liquid at room temp. formed of unsaturated fatty acids.
-less dense than water so can float