Chapter 3 - Biological Molecules Flashcards
Carbohydrates (polymers)
Carbon, Oxygen, Hydrogen
➜ provides energy and build body structures
➜ Formula: Cx(H2O)y
Lipids
Carbon, Hydrogen, Oxygen
➜ insoluble in water
➜ soluble in alcohol
Proteins
Carbon, Hydrogen, Oxygen, Nitrogen, Sulfur (usually but not all)
Nucleic acid
Carbon, Hydrogen, Oxygen, Nitrogen, Phosphorus
- made of nucleotide monomers and phosphodiester bonds between monomers
- consist of phosphate group between pentose molecules forming BACKBONE
- in DNA hydrogen bonding between 2 antiparallel strands causing double helix shape
Water
➜ Polar - acts as solvent for ions
➜ Cohesion (between H20 mol) - water drawn up xylem
& Adhesion (H bond to other molecules) - capillary action
➜ Doesn’t change state (high specific heat capacity) - constant temp
➜ Surface tension - allows insects to live on water
➜ Ice less dense - habitat due to H bonding so ice floats and provides a habitat
➜ High latent heat of vaporisation - acts as a coolant- due to H bonds
➜ ice insulates water below
➜ transparent so plants under surface can photosynthesis as light penetrates
➜ Incompressible - can prevent plants from wilting & act as a hydrostatic skeleton for invertebrates
Ribose
Carbon, Oxygen, Hydrogen
➜ carbohydrate - pentose monosaccharide
Glucose
➜ carbohydrate - hexose (6C) monosaccharide
Alpha - down OH
Beta - Up OH
➜ soluble - easily transported
➜ chem bonds = lots of energy
Condensation
➜ Bond formed between H atom on one monosaccharide (glucose) and OH hydroxyl group on other mono (glucose) releasing WATER
- molecule of water released during the reaction
➜ Covalent bond = Glycosidic bond
➜ Allows monosaccharides to make polysaccharides
Amylose
➜ alpha glucose in 1, 4 glycosidic bonds - long and unbranched
➜ coiled shape formed with hydrogen bonds - causes it to be compact -> good for storage - more fits in less space
➜ less soluble than the glucose used to make it
Amylopectin
➜ alpha glucose in between 1,4 glycosidic bond - long branched
➜ some glycosidc bond between 1,6 carbon
➜ side branches allow enzymes to break down molecule to get to glycosidic bond quickly = glucose released quickly
➜ insoluble
Hydrolysis
➜ glucose is released for respiration from starch or glycogen
➜ allows polysaccharides break apart
➜ molecule of water added
Monosaccharides
➜ Formula: (CH2O)n
➜ n = 3 triose
n = 5 pentose
n = 6 hexose
Disaccharide
➜ 2 mono..
• glucose + glucose ➜ maltose
• glucose + galactose ➜ lactose
• glucose + fructose ➜ sucrose
➜ formed via glycosidic bonds
Cellulose
➜ 1,4 bonds - Beta glucose joined together
➜ Alternate beta glucose molecule is flipped upside down
➜ straight chain
➜ Cellulose make H bonds with each other forming microfibrils
Reducing Sugar Test
• Add Benedict’s
• becomes brick red from blue
Non reducing sugar test
➜ Benedict’s Solution:
• Boil with HCL
• Neutralise with sodium hydrogen carbonate
• Add benedicts
• becomes brick red
➜ Reducing sugar has become hydrolysed
Starch test
➜ Iodine is added to solution
➜ Positive test = yellow/brown to purple/black
Lipid test
➜ Sample mixed with alcohol
➜ Mixed with water and shaken
➜ Positive test = white emulsion layer formed on top of solution
Triglycerides
➜ type of lipid
➜ One glycerol molecule and 3 fatty acids
➜ Synthesis of triglyceride from glycerol and 3 fatty acids by the formation of ester bonds, producing 3 water molecules - condensation reaction
➜ insoluble - prevent water entering cell via osmosis
Saturated fatty acids
No double bonds
eg butter
Unsaturated fatty acids
➜ One double bond = monosaturated
➜ More than one double bond = polyunsaturated
➜ Presence of double bond causes molecule to bend
➜ Therefore, liquid at room temp
Phospholipid
➜ Contain phosphorus
• modified triglyceride
➜ One fatty acid replaced with phosphate group
➜ Phosphate group = hydrophilic head = polar
➜ Fatty acid chain = hydrophobic tail = non polar