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Early evolution of life on Earth Wachtershauser. Miller and Urey experiment.

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Presentation on theme: "Early evolution of life on Earth Wachtershauser. Miller and Urey experiment."— Presentation transcript:

1 Early evolution of life on Earth Wachtershauser

2 Miller and Urey experiment

3 Early catabolism

4 Evolution of cell types

5 Primitive Metabolism Early catabolism must make use of chemical disequilibria Later, photosynthetic energetics may have evolved –First photosynthetics were undoubtedly anaerobic photosynthetic bacteria –Later, oxygenic photosynthesis changed the chemistry of the Earth In addition to O 2 being an electron acceptor for respiration, it caused development of an O 3 layer

6 Summary First evidence for potential life 3.8 billion yrs ago other fossil evidence molecular fossils chemolithotrophy vs heterotrophs, who came first? anoxygenic photosynthesis oxygenic photosynthesis Banded iron formations (BIFs)-red beds

7 Evolution of cell types

8 Endosymbiosis

9 Taxonomy Until recently, life on Earth in 5 kingdoms: –Bacteria –Fungi –Protists –Plants –Animals Division between Bacteria, Archaea, and Eukarya more profound than former kingdoms: level called domains

10 Taxonomic Ranks Empire or Domain Kingdoms (Bacteria and Eukarya not yet divided into kingdoms) Phylum Class Order Family Genus Species (name is binomial: genus + epithet)

11 Bacterial Taxonomy Bacterial species is the base unit for taxonomy –Definition of any given species is subjective –>70% sequence similarity of genome –>98% sequence similarity of rRNA –Each species is phenotypically distinct

12 Evolutionary Chronometers Phenotypic characteristics Mole percent Guanine + Cytosine DNA sequence similarity (gross sequence similarity) –Good at the species level Small-subunit RNA (16S rRNA of prokaryotes; 18S of eukaryotes)

13 Phenotypic Taxonomies Phenotype determination is classic taxonomic method Today more reliance on molecular methods for taxonomies above the genus level –Still, phenotypic differentiation is considered requirement for separation of species Some methods collect large amounts of phenotypic data quickly –FAME analysis –Pyrolysis/GC –Automated testing of enzymatic activities

14 Range of G+C contents

15 DNA hybridization

16 16S rRNA as evolutionary chronometer

17 Evolution of sequences

18 Evolutionary distance and correction for back- or multiple mutations

19 Generation of evolutionary trees

20 Molecular microbial ecology Signature sequences identify phylogenetic groups –16S & 18S sequences identify Bacteria, Archaea, and Eucarya Probes can be developed for FISH (fluorescent in situ hybridization)

21 Community analysis by molecular methods


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