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Lecture 23 PMB

Candice Young Biology English 34 cards

Lecture 23 PMB

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  1. 1Layers of living stromatolitessedimentary layers of limestone accreted by centuries of microbial growth
    Oxygenic phototrophs on top --> red light-induced H2S photolysis to sulfate -->
    sulfate reducers on bottom
  2. 2microfossilsto form these, minerals precipitate & fill in forms of ancient microbial cells
    Must show regular 3D patterns that cannot be explained by abiotic processes
    --> this is subjective and can be wrong
  3. 3Biosignaturesspecific organic molecules (that can only be made by microbes!!) found within the rocks
    Ex: hopanoids
  4. 4problems with biosignatures1) biosignatures may not actually be as specific to an organism as we believe
    2) hard to rule out abiotic sources of the biosignature
    3) the oldest biosignatures probably have already been destroyed
  5. 5isotope ratios as evidence for lifeenzymes favor metabolizing substrates containing C12, while abiotic processes use C13 and C12 equally
    CO2 converted to CaCO3 in sedimentary rock, will contain less C13/C12 ratio in biologically derived CaCO3
    these ratios depend on WHERE you are
  6. 6problems with using isotope ratios as evidence for life1) tells us nothing about the actual early FORMS of life
    2) can't necessarily prove that abiotic processes uses the isotopes equally
    3) a false positive could form if enzymes depleted isotopes the other way around
  7. 7Hadeon era"hell" era, all a vocanic soupy mess
  8. 8Archaean erafirst period with liquid water forming stable oceans, oldest stromatolites from here
    cyanobacterial hopanoids found at the END --> molecular oxygen waste product changes everything
  9. 9Paleoproterozoicenough atmospheric oxygen to support a little aerobic respiration --> colonial cyanobacteria, eukaryotic microbes, ozone layer!
  10. 10Neoproterozoic eraO2 reaches present day levels, early multicellular life
  11. 11Possible energy sources for earliest life1) Light driven ion pumps AKA bacteriorhodopsins
    2) Redox reactions involving available substrates
    3) Methanogenesis
    4) Primitive hydrogenase that splits H2 across membrane
  12. 12earliest conditions for living things on earthno atmospheric protection from UV light, so everything had to live underwater
    really cold or really hot?
  13. 13redox reactions involving available substrates during the Archaean eraoxidized substances diffuse down into water from atmosphere, reduced substances diffuse up from ocean floor
    --> redox reactions at interface include cyanobacteria, anoxygenic photosynthesizers, methanotrophs and fermenters, FeS bacteria, methanogens
  14. 14Oxygenic Photosynthesis of Cyanobacteriaafter a lot of Fe2+ oxidized to Fe3+, metabolism began to accumulate oxygen in atmosphere --> evolution of aerobic respirators, ozone layer created to shield life from UV light
  15. 15Evolutionary relationshipsdescribed by phylogenetic trees:
    - a monophyletic group shares a common ancestor not shared by anyone else
  16. 16Possible phenotypic characteristics (not DNA) that were used to determine evolutionary relatednessshape, gram stain, oxygen use, carbon use (autotroph or heterotroph), temperature, living conditions
  17. 17problems of using phenotypic similarities to determine evolutionary relatedness-can't really determine which phenotypic difference is important --> conflicting trees
    -little fossil record
    -lack of complex structures
    -metabolic characteristics may change according to how a strain is cultured
    -can’t define species as a group capable of interbreeding/having fertile offspring
  18. 18Assumptions of using DNA as molecular clocks1) Mutations in DNA accumulate randomly due to errors in replication
    2) Mutations can cause phenotypic changes subject to natural selection
    3) Random mutations with neutral effects accumulate at a steady rate
    4) More sequence differences between two organisms means that they diverged from each other further in the past!!!
  19. 19what type of DNA can we look at?can't use "junk DNA" that doesn't contain a known gene/function
    can't pick DNA with no selective constraints, since these will lose their coherent identity throughout recent brancings
  20. 20Why is 16S rRNA a good choice of DNA to study evolutionary relatedness?1) does not face different selective pressures in different organisms
    2) has highly conserved regions that make it easier to align and amplify 2 sequences
    3) has less conserved regions where sequence variability occurs
    4) didn't evolve twice through convergent evolution, present in ALL organisms
  21. 21Methods of comparing two 16S rRNA sequences1) Isolate genomic DNA from organisms to be compared
    2) PCR 16S rRNA genes using universal primers based on conserved nucleotides
    3) Obtain & align sequences
    4) Compute number of differences
    5) Repeat for all other sequence pairs --> create a distance matrix
    6) Use these distances to make a tree that reflects evolutionary relationships
  22. 22correlation factorconsiders that whatever sequence changes we see are considered to be the minimum, because a sequence could have mutated forward and backward, or forward twice
    depends on mutation rate at time of divergence
  23. 23endosymbiosishypothesis that mitochondria/chloroplasts originated as proteobacteria/cyanobacteria
    that were engulfed by a protist and came to live as permanent symbionts
    believed eukaryotes evolved FROM prokaryotes, rather than alongside them
  24. 24evidence for endosymbiosismitochondria and chloroplasts resemble bacteria; have own circular genomes, ribosomes, and tRNAs; make own proteins
  25. 25discovery of three domains16S rRNA sequencing led to discovery of three distinct groups (Bacteria, Archaea, Eukaryotes) all equidistant in sequence differences
  26. 26evolutionary tree LUCAsLBCA = last bacterial common ancestor
    LACA = last archaeal common ancestor
    LECA = last eukaryal common ancestor
    FME = first eukaryotic ancestor with a mitochondrion
  27. 27relationship between archaea and eukaryotespreviously thought up to be sister domains, but new sequences has led to conclusions that eukaryotes emerged from WITHIN archaea (*Korarchaeota, Agiarchaeota,
    and Thaumarchaeota*)
  28. 28Major groups of Archaea1) Euryarchaeota
    2) Crenarchaeota
    3) Thaumarchaeota
  29. 29EuryarchaeotaMethanogens: synthesize methane, are autotrophic obligate aerobes, found in stagnant water, sewage treatment plants,
    intestinal tracts, ocean bottom, hot springs
    Extreme halophiles: optimal growth in water much more salty than the sea (ocean borders/etc), are aerobic heterotrophs, use bacteriorhodopsin in low O2 environments,
    pump K+ into cell as a compatible solute to maintain water balance
  30. 30CrenarchaeotaExtreme thermophiles: some have temperature optima above 80C, ALL are obligate/facultative anaerobes and chemolithotrophs/chemoorganotrophs
    use diverse electron acceptors and donors, can either be autotrophs or heterotrophs
  31. 31ThaumoarchaeotaAmmonia oxidizers: really abundant and widespread, NH3 = donor, O2 = acceptor
    can grow in really low concentrations of NH3/in acidic soils where only archaea can grow --> key part of biological N cycle!!
  32. 32memorize key differences between domains!!!memorize key differences between domains!!!
  33. 33When are evolutionary trees a good model of relationships?When:
    1) DNA you have used for the tree is passed from “parents”
    2) Genes change by accumulation of point mutations
  34. 34Limitations of using phylogenetic trees1) More than one tree can sometimes be drawn using the same data!
    2) Similar sequences result from convergent evolution at the sequence level (homoplasmy), rather than inheritance of the same allele
    3) DNA not always passed down by parents
    (horizontal gene transfer)

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Evolution
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Candice Young
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