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Name the 5 characteristics of life
Made of cells (multicellular/unicellular)
Metabolism, takes in energy and nutrients to maintain homeostasis
Replicates/reproduces
Has genetic info
Product of evolution, populations continue to evolve
Name NASA’s definition of life
Self-sustaining
Darwinian evolution (natural selection)
Includes viruses, cells, genes
Correlate the # of covalent bonds an atom can make based on its valence number (1, 4, 5, 6, 7)
1 valence - 1 bond
4 valence - 4 bonds
5 valence - 3 bonds
6 valence - 2 bonds
7 valence - 1 bond
Correlate hydrogen, oxygen, nitrogen, and carbon to the number of bonds they make
H - 1
O - 2
N - 3
C - 4
Why is water polar?
Oxygen is more electronegative, causing electrons to share unequally; oxygen is partially negative while hydrogen is partially positive
It is a bent molecule, so its dipoles do not cancel
Water can form hydrogen bonds because
Oxygen has lone pairs and a partial negative charge, while hydrogens are partially positive
Hydrophilic molecules are
polar and charged
Hydrophobic molecules are
nonpolar
What feature allows water to form hydrogen bonds with polar/hydrophilic molecules?
Partial charges
What feature allows water to dissolve charged molecules and ions (ionic compounds)?
Water’s full dipole/partial charges
What feature allows water to exclude nonpolar/hydrophobic molecules?
High cohesive hydrogen bonding network between water molecules
Explain London dispersion forces
In nonpolar molecules, the constant movement of electrons creates small dipoles, resulting in weak electrostatic attractions between adjacent nonpolar molecules
Stronger London dispersion forces have
Longer carbon chains, more electrons/surface area
How does shape affect the strength of London dispersion forces?
Straight hydrocarbon chains have more surface area compared to kinked chains
What does boiling do to molecules joined together?
The thermal energy overcomes the noncovalent attractions between separate molecules only
Stronger London dispersion forces mean
more energy, higher boiling point
Weaker London dispersion forces mean
less energy, lower boiling point
Name the monomer and bonds for each macromolecule
Proteins - amino acids/peptide bonds
Carbs - monosaccharides/glycosidic linkages
Nucleic acids - nucleotides/phosphodiester bonds
Lipids - fatty acids/ester linkages
Hydrolysis _______ water
Consumes/splits
Condensation/dehydration synthesis _______ water
produces
Tertiary structure
Overall 3D structure of a single polypeptide chain, stabilized by side chain interactions
Quaternary structure
Overall 3D structure and assembly of multiple separate polypeptide chains, held together by the same interactions as tertiary structure but instead between the contact surface of subunits
How can a mutant subunit of a dimer fold normally but fail to form a dimer?
A mutation that alters charge, polarity or size destroys the noncovalent attractions between subunits; still folds normally because the mutation is on the exterior and the protein retains its tertiary fold
Conservative amino acid disruptions
Replaced with amino acid that has similar charge, polarity, size, or shape; can do same noncovalent interaction
Non-conservative amino acid disruption
Replacing amino acid with one from a completely different chemical class
Electrically charged, acidic (negative at physiological pH) amino acids contain
Carboxyl (-COO-); forms ionic bonds with positively charged groups
aspartate, glutamate
Electrically charged, basic (positive at physiological pH) amino acids contain
Amino/amine (-NH3+); forms ionic bonds with negatively charged groups
lysine, arginine, hystidine
Polar uncharged (hydrophilic, neutral) amino acids contain
Hydroxyl (-OH) or Amide (C=0 + amine); possess partial charges and form hydrogen bonds
Nonpolar (hydrophobic) amino acids contain
Hydrocarbons (C-H) and sulfur (thiol/sulfhydryl); interact through vdWs (London dispersion forces) and cluster away from water
-COO-
Carboxyl
-NH3+
Amine/amino
-OH
Hydroxyl
(C=O + -NH3+)
Amide
C-H
Hydrocarbon
-SH
Sulfhydryl
Shifting pH alters ionizable acidic and basic functional groups
Altering charges in ionic bonds (salt bridges) disassociates subunits into monomers
Heating/boiling/detergents will
denature and unfold both tertiary and quaternary proteins
Reducing agents…
break through covalent disulfide bonds
Acidic (-1)
Carboxyl (-COOH) → (-COO-)
Phosphate groups
Donate protons
Basic (+1)
Amino/amine (-NH2) → NH3+
Accepts H+ from solution at physiological pHnchU
Uncharged (0)
Amides (C=O + amine) do not accept protons
Hydroxyl (-OH), carbonyl (C=O), sulfhydryl (-SH), methyl and hydrocarbons do not form full charges
N-terminus
Beginning, -NH3+ or -NH2
C-terminus
End, -COO- or -COOH
Peptide bonds are
Covalent amide linkages (C-N) between carbonyl carbon and amino nitrogen
Tetrapeptide is
4 amino acid residues, 3 peptide bonds
SDS-PAGE separates polypeptides by
Size/weight, smaller proteins are faster
What does SDS-PAGE do to proteins?
Denatures proteins and coats them with negative charge
What does boiling do to proteins?
Disrupts all noncovalent interactions
What do reducing agents (BME or DTT) do to proteins?
Cleave disulfide bonds between cysteine side chains
If there is a disulfide (covalent) bond, without the reducing agent the protein
remains a single band
If there is a disulfide (covalent) bond, with the reducing agent the protein
will have two bands
If there are noncovalent bonds, and boiling and SDS disrupt all noncovalent interactions of the protein
there will be 2 bands
A sample taken halfway through activation reaction will have a mixture of starting materials and products, including
Unprocessed pro-H protein, mature H complex/fragments (N and C terminus), and a released middle segment
If a sample taken halfway through activation reaction has been reduced, the mature H will
be split into two bands, the overall mixture will have 4 pieces
If a sample taken halfway through activation reaction has NOT been reduced, the mature H will
be linked, the overall mixture will have 3 pieces
Difference between DNA and RNA base pairs
DNA has thymine, RNA has uracil
Double stranded DNA and RNA have
complementary strands, A=T/U, C=G
Single-stranded DNA and RNA have
non-equal base pairs
Describe the two ends of DNA
5’ unbound phosphate → 3’ free hydroxyl group; complementary strands run antiparallel
How do you classify sugars by counting carbons?
triose, tetrose, pentose, hexose
In linear form monosaccharides contain
One carbonyl (C=O) and all other carbons bear a hydroxyl group
A carbonyl at the end means
aldose
A carbonyl in the middle means
ketose
What is the first step to determining aldose or ketose?
Locate the intra-ring oxygen and examine the 2 carbons bonded to it, then identify which is attached to -OH.
If the carbon is attached to -H and -OH
it is at the end of the chain (C1) and is aldose
If the carbon is attached to -CH2OH
it is in the middle of the chain (C2) and is ketose
How do carbohydrates function as energy storage polysaccharides?
Starch (plants) and glycogen (animals) store monosaccharides that have been broken down for later ATP energy
They feature alpha glycosidic linkages that produce flexible, helical structures
They allow for a high degree of branching, with many free ends for enzymes to hydrolyze and release glucose for energy
How do carbohydrates function as structural support polysaccharides?
Cellulose in plant walls, chitin in fungal cell walls, and peptidoglycan in bacterial cell walls
Parallel linear strands via hydrogen bonds form tough, insoluble structural sheets
Few organisms produce enzymes that can hydrolyze these, instead they break down in digestive tracts
How do carbohydrates function in cell identification and surface signaling?
Oligosaccharides attach covalently to glycoproteins or glycolipids on the exterior interface of the cell membrane
These aid in cell identification communication, as well as protection
Describe steroid structure and diffusion
Lipid made up of nonpolar hydrocarbon rings and tails; small, nonpolar, hydrophobic nature allows for simple diffusion
What molecules pass through a membrane easily?
Small, nonpolar molecules
What molecules pass through a membrane slowly?
Small, uncharged polar molecules
What molecules cannot pass through a membrane without assistance?
Large uncharged polar or charged molecules/ions
Attaching what to a steroid would make it unable to cross a membrane on its own?
A polar, charged, or large hydrophilic group would alter the steroid to become polar/charged/hydrophilic
What would attaching a large hydrophilic, charged/polar group to a steroid do to its biological function?
It cannot cross the membrane on its own anymore, therefore it cannot enter the cell to bind to its target receptor and its intended biological response is blocked
When salt washes into soil
the Na+ and Cl- make the water a high solute concentration solution
High solute concentration on the outside is
hypertonic
Low solute concentration on the outside is
hypotonic
High solute concentrated soil water would be _____ relative to the cytoplasm of roadside plant cells
hypertonic
Osmosis is
net diffusion of water across a selectively permeable membrane, water moves to a high concentration
When salt washes into soil, water would move ______ plant cells
Water would move out of plant cells into the higher solute concentration; the loss of turgor pressure would cause the cells to shrink and even lead to plant damage or death
How do the double bonds/kinks in unsaturated fatty acids affect vdWs, membrane fluidity, and melting point?
The kinks prevent packing and surface contact, resulting in weaker vdWs. The membrane will be more fluid at lower temps due to lower melting point
How do the single carbon-carbon bonds and straight hydrocarbon chains in saturated fatty acids affect vdWs, membrane fluidity, and melting point?
The straight chains are able to pack together more easily, resulting in stronger vdWs. The membrane is less fluid and more rigid, as well as less permeable due to its higher melting point
Short tails in fatty acids mean
less surface contact, weaker vdWs and more fluidity
Long tails in fatty acids mean
more surface contact, stronger vdWs, more rigidity
How do organisms adapt in cold temperatures to prevent lipid slowness, packing, rigidity, and freezing?
They synthesize phospholipids with a higher percentage of unsaturated fatty acids/shorter hydrocarbon tails
How do organisms adapt in warm temperatures to prevent fluid/leaky lipid membranes?
They synthesize phospholipids with higher percentage of saturated fatty acids/longer hydrocarbon tails
A species with more unsaturated fatty acids and shorter chains will be in a
cold environment
A species with more saturated fatty acids and longer chains will be in a
warm environment
Entropy is
the amount of disorder/even spread
An increase in disorder is
positive delta S, drives a process to be spontaneous
A decrease in disorder is
negative delta S
Dissipating a concentration/ion gradient decreases or increases entropy?
Increases; diffusing increases spread
Osmosis when a cell is placed in a hypotonic solution increases/decreases entropy?
Increases; water will move into the cell, evening out solute distribution
Macromolecule hydrolysis increases or decreases entropy?
Increases; cleaving the polymer into monomers increases free movement
The phase change of ice melting increases or decreases entropy?
Increases; ice melting from solid to liquid state increases molecular movement
Establishing a concentration gradient increases or decreases entropy?
Decreases; ions/solutes are all pumped to one side
Dehydration synthesis/condensation (polymerization) increases or decreases entropy?
Decreases; joining the monomers restricts the free units
Protein assembly/folding increases or decreases entropy?
Decreases; this constrains polypeptide chains into structured complexes
For delta G to be negative (reaction is spontaneous/favorable), delta S must be
greater than 0 (positive)