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hydrolysis
chemical reaction
water molecule added
break chemical bonds of a larger compound
polymers broken down → monomers
dehydration synthesis
chemical reaction
builds large polymers from smaller monomers
removing a water molecule
saturated fatty acid / unsaturated fatty acid
the presence / absence of carbon-carbon double bonds in their hydrocarbon chains
fatty acids make up the hydrophobic tails of phospholipids in cell membranes
saturated: only single bonds btwn C and hydrocarbon chain (carbon skeleton), straight line→fatty acids can stack on top of each other
unsaturated: >= 1 double bonds, kinked/bend, packed loosely
peptide bond
covalent chem bond
links two amino acids tgt during protein synthesis
form polypeptides/proteins
formed through dehydration synthesis
covalent bond formed btwn C atom of the carboxyl group (COOH) of one amino acid & N atom of the amino group (NH2) of an adjacent amino acid
cohesion
adhesion
hydrogen bond
phospholipid
amphipathic lipid molecule made of
glycerol backbone
polar phosphate head group
two nonpolar fatty acid tails
form the primary structural basis of cell membranes
polar head: phosphate group (PO4) and glycerol→hydrophilic (water-loving) & charged→interacts with water
non-polar tails: two long hydrocarbon chains (fatty acids) that are hydrophobic (water-fearing) & repel water
spontaneous bilayer formation: in aqueous (watery) environments, self-organize into a phospholipid bilayer, hydrophilic heads facing outward toward the cytoplasm and extracellular fluid, and hydrophobic tails tucked safely inside the core
selective permeability: The hydrophobic interior acts as a barrier that stops large, polar, or charged molecules from crossing freely, while allowing small, nonpolar molecules to slip through
membrane fluidity: saturated & unsaturated fatty acid tails adjust membrane flexibility; kinks in unsaturated tails prevent tight packing in cold environments to keep the membrane fluid
polypeptide
cholesterol
amino acid
monosaccharide
hydrophobic / hydrophilic
deoxyribonucleic acid
disulfide bridges