BCHM 4611 Final Exam 2025
Prokaryotes - -2 domains: archaea and bacteria, exclusively single cell organisms, no
nucleus
Benefits of being prokaryotic - -More adaptable to changing environments, species have
evolved to colonize extreme environments due to their simplicity and rapid cell division
Eukaryotes - -Multicellular and unicellular organisms, more complex cellular
organization with membrane-enclosed organelles that have specialized functions, DNA
stored in nucleus
Classes of monomers - -Amino acids, monosaccharides, nucleotides, and lipids
Classes of polymers - -Polypeptides, polysaccharides, nucleic acids (no true polymers
for lipids - form non-covalent aggregates)
Polypeptide/protein - -Polymer of amino acids linked together by peptide bonds
Residue - -Monomer that has been incorporated into a polymer
Protein major roles - -Carry out metabolic reactions, support cellular structures
Protein minor role - -Store energy
Nucleic acid major role - -Encode information
Nucleic acid minor roles - -Carry out metabolic reactions, support cellular structures
Polysaccharides major roles - -Store energy, support cellular structures
Polysaccharides minor role - -Encode information
Open system - -Energy can be transferred between the system and its surroundings
Closed system - -Only exchanges energy with its surroundings, not matter
Isolated system - -Does not exchange energy or matter with its surroundings
Gibbs free energy (G) - -Thermodynamic quantity whose change indicates the
spontaneity of a process. For spontaneous/favorable processes, ΔG < 0, whereas for a
process at equilibrium, ΔG = 0
BCHM 4611
,BCHM 4611
Enthalpy (H) - -Heat content of a biochemical system
Entropy (S) - -Degree of randomness or disorder of a system
Free energy change equation - -ΔG = ΔH - TΔS
Coupled reaction - -Reactions that occur in concert with each other; product of the first
reaction is a reactant for the second reaction; ΔG values are added when reactions are
combined
Why is ΔG independent of path chosen? - -Depends only on the initial and final states of
the system, without regard to the specific chemical or mechanical work that occurred in
going from one state to the other
Oxidation - -Loss of electrons through the addition of oxygen or removal of hydrogen;
oxidation of carbon is thermodynamically favorable so it can be coupled with otherwise
unfavorable processes
Catabolism - -Breaking down molecules, yielding energy; some of this free energy may
be conserved in the formation of nucleotide triphosphates (NTPs) such as ATP or
reduced cofactors such as NADP+ or Q
Anabolism - -Building complex molecules at the expense of energy
H2O structure/geometry - -Central oxygen atom forms covalent bonds with two
hydrogen atoms, leaving two unshared pairs of electrons; tetrahedral geometry
How does water's structure affect its properties and interactions with other molecules? -
-It is polar (uneven distribution of charge) which allows it to form hydrogen bonds with
other water molecules, this makes water highly cohesive; has high dielectric constant
which means ionic compounds dissolve in it well; polar compounds also dissolve well
due to hydrogen bonding with water
Covalent bond - -Formed when two atoms share electrons
Ionic interaction - -Electrostatic interaction between two groups that is stronger than a
hydrogen bond but weaker than a covalent bond
Hydrogen bond - -Partly electrostatic, partly covalent interaction between a donor group
such as OH or NH and an electronegative acceptor atom such as O or N
Types of Van der Waals interactions - -Dipole-dipole, dipole-induced dipole, and London
dispersion forces
BCHM 4611
,BCHM 4611
Van der Waals interactions - -Weak non-covalent association between molecules that
arises from the attractive forces between polar groups (dipole-dipole interactions) or
between non-polar groups whose fluctuating electron distribution gives rise to temporary
dipoles (London dispersion forces)
Relative strengths of chemical bonds (weakest to strongest) - -Van der Waals, hydrogen
bond, ionic, covalent
Amphipathic/amphiphilic - -Having both polar and non-polar regions and therefore being
both hydrophilic and hydrophobic
How do amphiphilic molecules behave in aqueous solutions? - -Polar groups of
amphiphiles orient themselves toward the solvent molecules and are therefore
hydrated, while the nonpolar groups tend to aggregate due to the hydrophobic effect; as
a result, amphiphiles may form a spherical micelle, a particle with a solvated surface
and a hydrophobic core
Hydrophobic effect - -Exclusion of non-polar substances from an aqueous solution; non-
polar molecules are driven out of the aqueous phase by the unfavorable entropy cost of
individually hydrating them
Buffer - -Solution containing an acid and its conjugate base, resists changes in pH when
more acid or base is added
Buffer effective range - -Within one unit of the pKa (pKa +/- 1)
Bicarbonate buffer system - -CO2 in blood plasma reacts with water to form carbonic
acid, H2CO3, which ionizes to HCO3-
Why is bicarbonate buffer system effective? - -Excess hydrogen ions can not only be
buffered but can also be eliminated from the body because after the H+ combines with
HCO3− to re-form H2CO3 (which rapidly equilibrates with CO2 + H2O), some of the
CO2 can be given off as a gas in the lungs; breathing can be adjusted to help control
blood pH
What determines whether a reaction is spontaneous or not? - -The sign of the change in
free energy (ΔG) of the reaction
What determines the rate of the reaction? - -The magnitude of the activation energy
(ΔG‡)
The reaction coordinate for covalent catalysis has... - -Two peaks, with a trough in
between them where the stable intermediate is formed
BCHM 4611
, BCHM 4611
In the chymotrypsin reaction, how is the tetrahedral intermediate stabilized? - -Oxyanion
hole stabilization through hydrogen bonding with H's on Ser195 and Gly193
Competitive inhibitor - -Competes with the substrate for binding at the enzyme's active
site; frequently resemble the substrate or product of a reaction
The best competitive inhibitors... - -Mimic the transition state of the reaction
Triacylglycerols (triglycerides) - -A glycerol molecule esterified to three fatty acid
molecules; the most common form of fatty acid storage
Integral membrane proteins - -Have hydrophobic peptide regions embedded in the lipid
bilayer and these proteins require strong detergents to isolate
Peripheral membrane proteins - -Associate with the polar head groups of membrane
lipids or with the exposed regions of other membrane proteins; can be isolated with mild
salt solutions which will compete to bind with these regions
Lipid-linked proteins - -Insert a hydrophobic anchor into the membrane
Types of lipid-linked proteins - -Myristoylated, palmitoylated, prenylated, and GPI-linked
Myristoylated protein - -A myristoyl group (C14:0) attached to an N-term Gly via an
amide linkage
Palmitoylated protein - -A palmitoyl group (C16:0) reversibly attached to a Cys side
chain via a thioester linkage
Prenylated protein - -An isoprenoid group linked to a C-term Cys via a thiother linkage
GPI-linked proteins - -GPI group linked to the C-term of the protein
How do ion movements during an action potential affect membrane potential? - -Influx
of Na+ causes depolarization (more positive membrane potential) which triggers
opening of K+ channels to restore the resting potential (more negative)
Exocytosis - -Vesicles fuse with the plasma membrane, allowing substances to cross
the membrane without using transporters
Lipid hormones - -Move inside the cell to activate intracellular receptors
What alternatives to common NSAIDs such as aspirin exist and why? - -Traditional
NSAIDs target cyclooxygenases to prevent prostaglandin production and inhibit both
COX-1 and COX-2; COX-2 inhibition reduces pain and inflammation but COX-1
BCHM 4611