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Cheat Sheet

Fall Biology


Table of contents
  1. Terms and Concepts
    1. DNA Replication
    2. Transcription and Translation
    3. Cellular Respiration
    4. Meiosis
  2. Core Ideas
    1. Chemistry, Origin of Life, Nucleic Acids
    2. Chemical Foundation of Life Terms and Concepts
    3. Two Theories
    4. RNA vs DNA Levels of Structure
    5. 3 DNA Replication Hypotheses
    6. Proteins
    7. Protein Levels of Structure
    8. Protein Functions and Types
    9. Proteins Required for Synthesis in Bacteria
    10. Translation, Transcription, and the Genetic Code
    11. Complete Genetic Code Table
    12. Properties of the Genetic Code
    13. Types of Point Mutations
    14. The 3 Categories of Mutations
    15. Process of Initiating Transcription in Bacteria
    16. Process of Ending Transcription in Bacteria
    17. Processed mRNA Strand Diagram
    18. Process of Protein Synthesis in Ribosomes
    19. Process of Initiating Translation in Bacteria
    20. Process of Elongation Phase of Translation
    21. Process of Terminating Translation
    22. Complete Process of the Central Dogma
    23. Central Dogma in Bacteria vs Eukaryotes
    24. Cellular Respiration
    25. Process Input Output Table and Chemical Equation
    26. Cellular Respiration Diagram
  3. Meiosis and Mitosis
    1. Meiosis vs Mitosis Table
    2. Meiosis vs Mitosis Diagram
  4. Important Experiments
    1. Miller-Urey Experiment
    2. Griffith Experiment
    3. Avery-MacLeod-McCarty Experiment
    4. Herschey-Chase Experiment
    5. Meselson-Stahl Experiment
    6. Srb-Horowitz Experiment
    7. Zamecnik et al Experiment

Terms and Concepts

DNA Replication

TermDefinition
Chromosome theory of inheritanceProposed that chromosomes contain genes.
Nitrogen 14Normal nitrogen; used in the Meselson-Stahl experiment to distinguish parent strands from daughter strands.
Nitrogen 15Heavy nitrogen with one more neutron; used in the Meselson-Stahl experiment to distinguish parent strands from daughter strands.
5’ to 3’ DirectionThe direction in which DNA is synthesized.
Antiparallel strandsStrands of DNA that lie opposite each other.
Complementary base pairingBase A matched with base T, base G matches with base C.
Density gradient centrifugationSeparates molecules based on their density. Lower-density molecules cluster in bands high in the centrifuge tube, higher-density molecules cluster in bands lower in the tube.
dNTPDNA synthesis requires an input of energy, but potential energy of deoxyribonucleotide monomers is raiased by reactions tha add two phosphate groups, forming deoxyribonucleotide triphosphates (dNTPs). dNTP has high potential energy; forms phosphodiester bonds in DNA strand.
Discontinuous ReplicationProposed to explain how lagging strand was synthesized. Primase synthesizes new RNA primers for lagging strands as the moving replication fork opens single-stranded regions of DNA; DNA polymerase syntheses short DNA fragments from these primers. Fragments linked to form a continuous strand.
Lagging strandThe strand that runs opposite to the direction in which the replication fork is moving. This causes a lag.
Continuous strandThe strand that moves in the same direction as the replication fork.
Okazaki fragmentsShort DNA fragments attached to RNA primers produced by the lag of the lagging strnad.
Origin of ReplicationA sequence of bases that indicates the start of a replication bubble, in which two replication forks move in opposite directions to separate the DNA strand.
ReplisomeProteins and enzymes work in a macromolecular machine called the replisome. Replisome may contain up to three copies of DNA polymerase III.
RNA polymeraseA polymerase that can start synthesis from scratch. Primase is a RNA polymerase (enzymes that catalyze polymerization of ribonucleotides into RNA).
RNA primersBecause DNA polymerase cannot synthesize new nucleotides on its onw, but RNA polymerase (for example, primase) can. This is used to initiate building, and is later removed by DNA polymerase I.

Transcription and Translation

TermDefinition
mutationThe altering of genes of chromosomes in some sort of way.
codonA group of three nucleotide bases that specifies an amino acid.
fitnessIn the context of transcription and translation, the ability for a gene expression to positively impact the phenotype such that the genotype gets passed down to another generation.
frameshiftMutations that shift the reading frame. These are usually point addition or deletions that affect the position of every base after it.
gene expressionThe process by which gene information is used to produce a gene product.
genetic codeThe mapping of each codon to an amino acid.
messenger RNA (mRNA)The form of RNA used to carry information from the DNA in the nucleus to the ribosome in the cytoplasm to produce proteins.
mutantsGenes whose sequence or chromosomes that have been altered in some sort of way.
reading frameThe sequence of codons, the sequence broken down into groups of three beginning at the start codon and ending at the end codon.
RNA polymeraseA polymerase that can synthesize RNA without a primer, unlike DNA polymerase.
start codonA codon that indicates when protein synthesis should begin. This is AUG.
stop codonIndicate when protein synthesis should stop. There are three: UAA, UAG, and UGA.
transcriptionThe transferring of genetic information from DNA to forms of RNA.
translationThe transferring of information from RNA to proteins.
translocationA chromosomal error in which a broken piece of a chromosome is attached to a different chromosomes.
triplet codeA three-base code (forming codons).
3’ poly(A) tailEnzyme cuts the 3’ end of the pre-MRNA after the poly(A) signal, and specialized RNA polymerase adds 100 to 250 adenine nucleotides, forming this. It is not encoded by the DNA template strand, yet required for ribosomes to start translation and to protect the end of mRNA from attack by enzymes.
5’ capAn added cap consisting of odified guanine nucleotide linked to transcript in an unusual way when the 5’ end of pre-mRNA emerges. Enables ribosomes to bind to the mRNA and protects the 5’ end of the mRNA from enzymes that degrade RNA (ribonucleases).
aminoacyl tRNATHe amino acid attached to the transfer RNA.
aminoacyl/A siteThe first site an aminoacyl tRNA diffuses to in ribosomal protein synthesis. If its anticodon matches the codon in mRNA, it stays in the ribosome.
anticodonThe codon attached to tRNA that is the base-pair complement of a codon in the mRNA. For example, the anticodon of AAA is UUU.
AUG codonThe one start codon.
coding strandThe strand opposite to the one used during transcription to build the complementary pre-mRNA strand (template strand). The transcripted pre-mRNA is synthesized in the same direction as the coding strand.
downstreamThe RNA polymerase moves in this direction when moving along the DNA.
elongationOccurs after RNA polymerase leaves the promoter region as it synthesizes RNA, during which the enzyme reads the DNA template on the 3’ end at a rate of 50 nucleotides per second.
exit/E siteThe last of three sites through which tRNA passes through, in which the uncharged tRNA is ejected from the ribosome after dropping off its amino acid.
exonsRegions that are transcribed and represented in final RNA (expressed in mature DNA).
intronsRegions of a gene that are transcribed but not represented in the final RNA.
peptidyl/P siteThe second of three sites through which tRNA passes through, in which the amino acid attached to a tRNA forms a peptide bond with the existing polypeptide.
phosphorylationThe introduction of phosphate groups after a protein has been synthesized, which drastically increases the activity of the protein.
polyribosomesFormed in bacteria when ribosomes attach to mRNA and begin synthesizing proteins before transcription was complete. Polyribosomes increase the number of copies of a protein that can be made from single mRNA.
pre-mRNAEukaryotic genes initially copied from nonfunctional RNAs. Same as ‘primary RNA transcript’.
primary RNA transcriptEukaryotic genes initially copied from nonfunctional RNAs. Same as ‘pre-mRNA’.
promotersSites where transcription should begin.
protein foldingImpacts how the protein functions. Folding is often facilitated by molecular chaperones.
ribosomal RNACombined with proteins, these make up ribosomes. rRNA is found in ribosomes and constitutes most of the active site of ribosomes, which are considered ribozymes.
ribosomeA component of the cell outside of the nucleus that is responsible for reading mRNA and synthesizing an appropriate protein.
RNA processingIs used to convert primary transcripts (pre-mRNA) into mature and functional RNA.
RNA splicingIs the removal and rejoining of introns from a transcription. Done with snRNPs (small nuclear ribonucleoproteins).
spliceosomesAn aggregate macromolecular machine consisting of snRNPs (small nuclear ribonucleoproteins).
template strandThe strand used during transcription to build the complementary pre-mRNA strand.
terminationThe termination of a process is when it ends.
transfer RNA (tRNA)tRNA is the ‘intermediate’ step between mRNA and amino acids. Each tRNA has an amino acid has on the 3’ end of the molecule a site for amino acid attachment and on the opposite side an anticodon to attach to the mRNA.
upstreamDNA is upstream of the point of reference. The RNA polymerase moves in the opposite direction of this when moving along the DNA.
wobble hypothesisMost amino acids are specified by more than one codon. Codons for the same amino acid often have the same nucleotides for the first and second positions but different nucleotides in the third position. Certain bases bind to bases that do not match Watson-Crick base pairing, producing flexibility (‘wobble’) in base pairing. This allows tRNA to read more than one codon. Wobble pairing does not account fo redundancy.

Cellular Respiration

TermDefinition
GlycolysisMeans “breaking up glycose” (glycol = glycose, ysis = break up). Breaks up the glucose from a 6-carbon molecule (e.g. C-C-C-C-C-C) into two (C-C-C and C-C-C). Is the first process in cellular respiration. Releases 4 ATP and requires 2 ATP (net releases 2 ATP). Is an anaerobic process (does not need oxygen).
GlucoseA sugar (glucose = gluc (sweet) + ose (sugar)) in which carbohydrates are decomposed into. This is converted via cellular respiration into ATP.
ATPAbbreviated for adenosine triphosphate, ATP is a fundamental unit of energy in cells. Its energy is stored in chemical bonds between a phosphate group; this is released when one phosphate detaches and ATP becomes ADP (adenosine diphosphate).
PyruvateThe two 3-carbon molecules that result when glycolysis breaks down the 6-carbon glucose. Pyruvate is later converted into acetyl-CoA in acetyl-coenzyme A synthesis.
Citric AcidAnother name for the Krebs cycle.
Krebs CycleEach molecule of acetyl-CoA is metabolized; energy is released via electrons, which are used in the electron transport chain. Produces an additional 2 ATP and is an aerobic process (needs oxygen).
Acetyl CoAThe molecule pyruvate is converted to in acetyl-coenzyme A synthesis. This is later used in the Krebs cycle.
Electron transport chainA series of proteins that electrons are moved through; hydrogens and electrons are removed from NADH and FADH2 electron carriers for ATP synthesis.
NAD+/NADHAn electron carrier; oxidized form is NAD+ (is not carrying electrons) and reduced form is NADH (is carrying electrons). Will transition between these two states throughout cellular respiration.
FAD/FADH2An electron carrier; oxidized form is FAD (is not carrying electrons) and reduced form is FADH2 (is carrying electrons). Will transition between these two states throughout cellular respiration.
RespirometerA respirometer is composed of a vial and a volume of air. It measures the rate of consumption of oxyugen of a living organism.

Meiosis

TermDefinition
asexual reproductionReproduction in which the offspring’s genetic data is the exact same as their parent’s genetic information.
autosomesChromosomes that are not sex chromosomes (like X and Y 23rd chromosomes in humans).
centromereThe region of a chromosome to which the microtubules of the spindle attach, via the kinetochore, during cell division.
crossing overDuring prophase I, non-sister chromatids of homologous chromosomes exchange parts of their DNA at the same spots. This promotes genetic variation.
daughter cellThe cell produced by a parent cell.
diploid cellA cell with two versions of each chromosome. These are our somatic (body) cells.
haploid cellA cell with only one version of each chromosome. These are our sex cells (sperm and egg).
ploidyThe number of chromosome sets. Diploid cells have a ploidy of 2, haploid cells have a ploidy of 1. This is the coefficient of n when describing chromosome count.
genetic recombinationThe creation of new combinations of alleles.
homologous chromosomesChromosomes that are the same size and shape, and contain the same genes at the same location.
independent assortmentA phenomenon in which homologous chromosomes line up in meiosis I irrespective of what other chromosomes are. This allows for different combinations of alleles.
unreplicated chromosomeA chromosome that has not yet been replicated.
replicated chromosomeA chromosome that has been replicated, meaning that it consists of two chromatids, each the size of an unreplicated chromosome.
homologous pairA pair of chromosomes that are homologous. (see homologous chromosomes)
maternal and paternal chromosomesChromosomes that come from the mother and the father, respectively.
meiosisThe process by which four haploid daughter cells are generated from one diploid parent cell.
non-sister chromatidsChromatids in a chromosome from different homologs.
reduction divisionMeiosis I is a reduction division operation in that the number of chromoomes goes from 2n to n. Meiosis II is not so because the number of chromosomes goes from n to n, although the absolute quantity of DNA decreases.
sex chromosomesThe chromosomes that determine the offspring’s ex.
spermThe male sex cell.
zygoteThe cell fromed by the union of the sperm and egg.
eggThe female sex cell.
gameteA haploid sex cell.
sexual reproductionReproduction that requires the union of two gametes.




Core Ideas

Chemistry, Origin of Life, Nucleic Acids

Chemical Foundation of Life Terms and Concepts

TermDefinition
Atomthe smallest identifiable unit of matter.
Elementa substance that consists entirely of a single type of atom.
Isotopeforms of an element with different numbers of neutrons.
Atomic Numbercharacteristic number of protons in an atom.
Mass Numbersum of protons and neutrons in an atom.
Covalent Bondwhen two atoms share electrons, and the connected atoms form a molecule. Make the atoms more stable, often complete shells.
Compoundatoms of different elements are bonded together.
Electronegativitywhen atoms of different elements bond, they may pull electrons towards their nuclei with different strengths.
Nonpolar Covalent Bonda bond that involves equally shared electrons.
Polar Covalent Bonda bond that involves assymetrically shared electrons.
Ionic Bondelectrons in ionic bonds are completely transferred from one atom to another.
Solventan agent for dissolving, or getting substances into solution.

Two Theories

TheoryProcess
Prebiotic Soup ModelSimple molecules like N2, NH3, and CO were present in the atmosphere of ancient earth. Energy in sunlight drove reactions among simple molecules to produce molecules like formaldehyde and hydrogen cyanide. Stimulated by heat, the products formed more complex molecules like ribose, glycine, and acetaldehyde.
Surface Metabolism ModelSimple molecules like N2, NH3, and CO were present in early oceans and hydrothermal events. Vent minerals catalyzed spontaneous reactions among high-energy molecules to produce, for instance, acetic acid. Concentration and heat formed more complex molecules like ribose.

RNA vs DNA Levels of Structure

Level of StructureDNARNA
PrimarySequence of deoxyribonucleotides: bases are A, T, G, CSequence of ribonucleotides: bases are A, U, G, C
SecondaryTwo antiparallel strands twist into a double helix, stabilized by hydrogen bonding, hydrophobic bonding, hydrophobic interactions, and van der Waals interactionsSingle strand folds back on itself to form a double-helical ‘stem’ and an unpaired ‘loop’.
TertiaryDouble helical DNA forms compact structures by wrapping around histone proteins or twisting into supercoils.Secondary structures fold to form a wide variety of distinctive three-dimensional shape.

3 DNA Replication Hypotheses

HypothesisDescription
Semiconservative replicationIf parental strands of DNA separate, each could be used as a synthesis of a new daughter strand. Each daughter DNA molecule consists of one old strand and one new strand. Conserves only one of the strands.
Conservative replicationIf bases of strands turned out from the helix, they could serve as a template for an entirely new double helix all at once.
Dispersive replicationParental double helix was fragmented into small pieces before replication, and each piece was replicated either with conservative or semiconservative mechanisms. Fragments would be joined into two molecules that contained a mixture of parental and daughter strands.

Proteins

Protein Levels of Structure

Level of StructureDescriptionStabilized by
PrimaryEach protein has a unique primary structure, determined by the number and sequence of amino acids, making up the polypeptide chain. 20 amino acids are used to build proteins. Various amino acids could be linked in almost any sequence.Peptide bonds
SecondaryParts of the polypeptide chain are folded or coiled. For example, forms alpha helix - chain twists forms a helix or beta pleated sheats - chain folds back on itself, or two regions lie parallel. Results from hydrogen bonding between atoms of the polypeptide backbone.Hydrogen bonding between groups along the peptide-bonded backbone
TertiarySuperimposed on primary and secondary structure: irregular loops and folds that give the protein its 3d shape. Results from interactions along R groups - hydrophilic or polar R-groups may hydrogen bond with each other or turn outwards and bond with surrounding water and hydrophobic or nonpolar R groups cluster on the inside of the protein, away from water.Bonds and other interactions between R-groups or between R-groups and a peptide-bonded backbone; sulfur-containing strong covalent bonds
QuaternarySome proteins are made up multiple polypeptide chains. Results from combination of two or more polypeptideSame interactions that stabilize tertiary structure.

Protein Functions and Types

TypeFunctions
Structural ProteinsAnchors cell parts; serves as tracks along which cell parts can move. Binds cells together to form muscles, ligaments, etc.
Signal ProteinsHormonal proteins that coordinate an organism’s activity by acting as a signal between cells.
Transport ProteinsCarry molecules from place to place.
Sensory ProteinsDetect environmental signals like light.
Enzyme ProteinsA protein that changes the rate of a chemical reaction without itself being changed into a different molecule in the process.
Storage ProteinsStockpile materials used to make other proteins. Store nutrient and energy-rich molecules for later use.
Contractile (Motor) ProteinsMove parts of a cell.
Gene Regulatory ProteinsBind to DNA in particular locations and control whether certain genes will be read.
Defensive ProteinsDefensive proteins help organisms fight infection, heal damaged tissue, and evade predators.

Proteins Required for Synthesis in Bacteria

PurposeNameFunction
Opening the helixHelicaseCatalyzes the separation of DNA strands to open the double helix. Breaks hydrogen bonds.
Opening the helixSingle-strand DNA-binding Proteins (SSBPs)Stabilizes single-stranded DNA.
Opening the helixTopoisomeraseBreaks and rejoins the DNA double helix by breaking phosphodiester bonds to relieve twisting forces caused by the opening of the helix.
Leading-strand synthesisPrimaseCatalyzes the synthesis of the RNA primer.
Leading-strand synthesisDNA Polymerase IIIExtends the leading strand.
Leading-strand synthesisSliding clampHolds DNA in place during strand extention.
Lagging-strand synthesisPrimaseCatalyzes the synthesis of the RNA primer on the Okazaki fragment.
Lagging-strand synthesisDNA Polymerase IIIExtends an Okazaki fragment.
Lagging-strand synthesisSliding clampHolds DNA polymerase in place during strand extention.
Lagging-strand synthesisDNA Polymerase IRemoves the RNA primer and replaces it with DNA.
Lagging-strand synthesisDNA ligaseCatalyzes the jooining of Okazaki fragments into a continuous strand.

Translation, Transcription, and the Genetic Code

Complete Genetic Code Table

Complete Genetic Code

Properties of the Genetic Code

PropertyDescription
RedundantAll amino acids (except for 2) are coded for by more than one codon. Codons specifying the same amino acid are synonymous codons.
UnambiguousA given codon never codes for more than one amino acid.
Non-overlappingOnce the ribosome locks onto the first codon, the reading frame is established and the ribosome adds one codon one after another.
UniversalWith a few exceptions, codons specify the same amino acids in all organisms.
ConservativeSeveral codons specify the same amino acid, but the first two bases are usually identical.
  • If a change in DNA sequence leads to a change in the third position, it is less likely to alter the amino acid in the protein.
  • Genetic code minimizes the phenotypic affects of small alterations.
    • Genetic code not assembled randomly; honed by natural selection and is remarkably efficient.

Types of Point Mutations

Types of point mutations

The 3 Categories of Mutations

  1. Beneficial. Some mutations increase the fitness of an organism.
  2. Neutral. If the mutation has not effect on fitness, it is neutral. e.g. silent mutations.
  3. Deleterious. Most individuals are well-adapted to their current habitat and mutations are random changes in genotype; most mutations lower fitness.

Process of Initiating Transcription in Bacteria

  1. Initiation begins. Sigma binds to the promoter region of the DNA, characterized by the -35 box and the -10 box.
  2. Initiation continues. RNA polymerase opens up the DNA helix and transcription begins. NTPs are used to create the complement of the template strand.
  3. Initiation completes. Sigma is released from the core enzyme and RNA synthesis continues. The RNA polymerase moves downstream along the DNA.

Process of Ending Transcription in Bacteria

  1. Hairpin forms. RNA polymerase transcribes a transcription-termination signal, which codes for RNA that forms a hairpin.
  2. Termination. The RNA hairpin leads to the RNA separating from RNA polymerase, terminating transcription.

Processed mRNA Strand Diagram

Process of Protein Synthesis in Ribosomes

  1. Aminoacyl tRNA diffuses into the A site. If its anticodon matches a codon in mRNA, it stays in the ribosome.
  2. A peptide bond forms between the amino acid held by the aminoacyl tRNA in the A site and the growing polypeptide in the P site.
  3. The ribosome moves relative to the mRNA by one codon. All three tRNAs are shifted one position within the ribosome.
    • tRNA in E site exits.
    • tRNA in P site moves to the E site.
    • tRNA in A site switches to P site.
    • A site is empty and ready to accept another aminoacyl tRNA.

Process of Initiating Translation in Bacteria

  1. mRNA binds to a small subunit. A sequence in mRNA called the ribosome binding site binds to a complementary seuqnece in an RNA molecule, which is part of the small subunit of the ribosome. This is helped by initiation factors.
  2. Initiator aminoacyl tRNA binds to the start codon. This usually carries f-Met.
  3. The large subuit of the ribosome binds, completing the ribosome assembly; translation can begin.

Process of Elongation Phase of Translation

  1. Incoming aminoacyl tRNA moves into the A site. Its anticodon base pairs with the mRNA codon.
  2. Peptide bond formation. The amino acid attached to the tRNA in the P site is transferred by formation of a peptide bond to the amino acid of the tRNA in the A site.
  3. Translocation. The ribosome moves one codon down the mRNA with the help of elongation factors. THe tRNA attached to the polypeptide moves into the P site. The A site is empty.
  4. Incoming aminoacyl tRNA. A new charged tRNA moves into the A site, where its anticodon base-pairs with an mRNA codon.
  5. Peptide-bond formation. The polypeptide chain attached to the tRNA in the P site is transferred by peptide bond formation to the aminoacyl tRNA in the A site.
  6. Translocation. THe ribosome moves one codon down the mRNA. The tRNA attached to the polypeptide chain moves into the P site. Uncharged tRNA from P site moves to the E site, where tRNA is ejected. The A site becomes empty again.

Process of Terminating Translation

  1. Release factor binds to stop codon. When the translocating ribosome reaches a stop codon, a protein release factor fills up the A site and breaks the bond linking tRNA to the polypeptide chain.
  2. Polypeptide and uncharged tRNA are released.
  3. Ribosome subunits separate. They are ready to attach tot he start codon of another message.

Complete Process of the Central Dogma

  1. Through transcription, DNA stored in the nucleus of the cell is used via RNA polymerase to create pre-mRNA.
  2. Through RNA processing, the primary transcript (pre-mRNA), through which introns are removed and caps & tails are added to produce mature mRNA.
  3. Outside of the nucleus in the cytoplasm, the mature mRNA is translated to produce a polypeptide.
  4. Post-translational modifications, including folding, glycosylation, and phosphorylation are made to make the polypeptides formed by translation functional.

Central Dogma in Bacteria vs Eukaryotes

ProcessAspectBacteriaEukaryotes
TranscriptionRNA polymeraseOneThree, each produces a different class of RNA.
TranscriptionPromoter structureContains a -35 box and a -10 boxVariable and larger, often includes a TATA box about -30 from the transcription start site.
TranscriptionProteins that associate with promoterSigma and variantsGeneral transcription factors
RNA processing RareExtensive, several steps occur before RNA is exported to the cytoplasm.
TranslationInitiation and terminationLess complexMore complex
TranslationElongationSimilar to eukaryotesSimilar to bacteria

Cellular Respiration

Process Input Output Table and Chemical Equation

ProcessStarting MaterialNet Energy Output
Glycolysis1 Glucose2 NADH, 2 ATP
Acetyl-CoA Synthesis and the Krebs Cycle2 Pyruvate8 NADH, 2 FADH2, 2 ATP
Electron-Transport Chain10 NADH, 2 FADH232 ATP

Chemical Equation:

C6 H12 O6 + 6O2 ➡️ 6CO2 + 6H2O + Energy (36-38 ATP)

Cellular Respiration Diagram

Meiosis and Mitosis

Meiosis vs Mitosis Table

Meiosis vs Mitosis Diagram




Important Experiments

Miller-Urey Experiment

AspectDescription
QuestionCan simple molecules and kinetic energy lead to chemical evolution?
HypothesisChemical evolution of organic molecules will occur in environments simulating early Earth conditions.
Null HypothesisChemical evolution will not occur in early Earth simulations.
Prediction of HypothesisIf kinetic energy is added to a mix of simple molecules, complex organic compounds will be produced.
Prediction of Null HypothesisNo complex organic compounds will be produced.
ResultsSamples from solution contained formaldehyde, hydrogen cyanide, and several complex compounds with C=C bonds, like amino acids (e.g. glycine).
ConclusionChemical evolution occurs readily if simple molecules with high free energy are exposed to a source of kinetic energy.
SignificancePaved the idea for foundation for ideas of chemical evolution and sparked further experiments.

Griffith Experiment

AspectDescription
QuestionCan bacteria transfer genetic information through transformation?
HypothesisBacteria can transfer genetic information through tranformation.
Null HypothesisBacteria do not transfer genetic information through tranformation.
Experimental SetupTake four types of strains: rough strain (virulent), smooth strain (virulent), heat-killed smooth strain, and mix of rough strain and heat-killed smooth strain. Inject strains into mice and see if they live or die.
Prediction of HypothesisIf bacteria can transfer genetic information through transformation, the mix of rough strain and heat-killed smooth strain will kill the mouse.
Prediction of Null HypothesisIf bacteria do not transfer genetic information through tranformation, the mix of rough strain and heat-killed smooth strain will kill the mouse.
ResultsMice did not die from the rough strain, did die from the smooth strain, did not die from the heat-killed smooth strain, and did die from the mix of rough strain and heat-killed smooth strain.
ConclusionThere is a ‘transformation principle’ that is allowing the smooth strain, even if it has been killed, to transfer its genetic information to the rough strain to make it become a smooth strain, thus killing the mouse.
SignificanceProvided basis for the Avery-MacLeod-McCarty experiment.

Avery-MacLeod-McCarty Experiment

AspectDescription
QuestionWhat is causing the mix of rough strain and heat-killed smooth strain to kill the mouse in the Griffith Experiment?
HypothesisThe DNA in the heat-killed smooth strain is transfering genetic information and ‘corrupting’ the rough strain to kill the mouse.
Null HypothesisSome other aspect of the heat-killed smooth strain (i.e. proteins) is killing the mouse.
Experimental SetupPerform chemical actions to isolate parts of the mix of rough strain and heat-killed smooth strain. Mix each part with the rough strain, inject it into the mouse, and see if it lives or dies. Analyze the part that causes the mouse to die.
Prediction of HypothesisIf DNA in the heat-killed smooth strain is transfering genetic information, the part that kills the mouse will be DNA.
Prediction of Null HypothesisSome other aspect of the heat-killed smooth strain is killing the mouse, the part that kills the mouse will not be DNA.
ResultsWhen analyzing the ratios of nitrogen in the part that killed the mouse, it was confirmed that the part was DNA, not proteins.
ConclusionDNA is responsible for the transfer of genetic information.
SignificanceWas part of a growing field of research that proposed DNA, not proteins, held genetic information.

Herschey-Chase Experiment

AspectDescription
QuestionDo viral genes consist of DNA or protein?
DNA HypothesisT2 virus genes consist of DNA.
Protein HypothesisT2 virus genes consist of protein.
Experimental SetupLabel viruses (grow one set of TS w/ radioactive DNA and radioactive protein). Infect bacteria. Agitate cultures. Centrifuge solutions and force cells into pellet. Record location of radioactive labels.
Prediction of DNA HypothesisRadioactive DNA will be located within the pellet of the centrifuge.
Prediction of Protein HypothesisRadioactive protein will be located within the pellet of the centrifuge.
ResultsRadioactive DNA is in pellet. Radioactive protein is in solution.
ConclusionT2 virus genes consist of DNA.
SignificanceProved that heritable information takes the form of DNA, not proteins.

Meselson-Stahl Experiment

AspectDescription
QuestionIs replication semiconservative, conservative, or dispersive?
Hypothesis 1Replication is conservative.
Hypothesis 2Replication is semiconservative.
Hypothesis 3Replication is dispersive.
Experimental SetupGrow E. coli cells in medium with 15_N (heavy nitrogen, see DNA Replication Terms and Concepts). Transfer cells to medium with 14_N (regular nitrogen). Let the cells divide twice (total 3 generations). Centrifuge the three samples separately. Compare locations of DNA bands.
Prediction 1After two generations: 1/2 low-density DNA, 1/2 intermediate-density DNA.
Prediction 21/4 high-density DNA, 3/4 low-density DNA.
Prediction 3All intermediate-density DNA.
ResultsAfter 2 generations, 1/2 low-density DNA and 1/2 intermediate-density DNA.
ConclusionReplication is semiconservative.
SignificanceProved that, in accordance with Watson and Crick’s suspicions, that DNA replicated by splitting down the middle and using each half as a template. Thus, each DNA is half-old and half-new.

Srb-Horowitz Experiment

AspectDescription
QuestionWhat do genes do?
HypothesisEach gene contains information needed to make one enzyme.
Null HypothesisGenes do not have a one-to-one correspondence with enzymes.
Experimental StrategyProduce mutants unable to synthesize arginine, then test different steps in the mtabolic pathway for synthesizing arginine.
Experimental SetupIsolate Neurospora crassa that cannot synthesize arginine in four environments: no supplement, supplemented with only ornithine, supplemented only with citrulline, supplemented only with arginine
Prediction of HypothesisThere will be 3 distinct types of mutants corresponding to defects in enzyme 1, 2, and 3 in the pathway for synthesizing arginine. Each mutant will be able to grow on different combinations.
Prediction of Null HypothesisThere will not be a simple correspondence between a particular mutation and a particular enzyme.
ResultsThree types of mutants arg1, arg2, arg3. They are able to grow in the metabolic pathway from orthinine, citrulline, and arginine, respectively. arg1 cells lack enzyme 1 from precursor to orthinine, arg2 cells lack enzyme 2 from orthinine to citrulline, etc.
ConclusionThe one-gene, one-enzyme hypothesis is supported.

Zamecnik et al Experiment

AspectDescription
QuestionWhat happens to amino acids attached to tRNAs?
HypothesisAminoacyl tRNAs transfer amino acids to growing polypeptides.
Null HypothesisAminoacyl tRNAs do not transfer amino acids to growing polypeptides.
Experimental SetupAttach radioactive leucine molecules to tRNAs. Attach aminoacyl tRNAs to an in vitro system that allows protein synthesis. Follow the path of radioactive amino acids.
Prediction of HypothesisRadioactive amino acids will be found in the polypeptides.
Prediction of Null HypothesisRadioactive amino acids will not be found in the polypeptides.
ResultsRadioactive signal of tRNA and polypeptides are inversely proportional to each other. When there is low radioactive signal in tRNA, there is high radioactive signal in the polypeptides, and vice versa.
ConclusionAminoacyl tRNAs transfer amino acids to growing polypeptides.