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Evolutionary relationships among photosynthetic bacteria

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Abstract

To understand the evolution of photosynthetic bacteria it is necessary to understand how the main groups within Bacteria have evolved from a common ancestor, a critical issue that has not been resolved in the past. Recent analysis of shared conserved inserts or deletions (indels) in protein sequences has provided a powerful means to resolve this long-standing problem in microbiology. Based on a set of 25 indels in highly conserved and widely distributed proteins, all main groups within bacteria can now be defined in clear molecular terms and their relative branching orders logically deduced. For the 82 presently completed bacterial genomes, the presence or absence of these signatures in various proteins was found to be almost exactly as predicted by the indel model, with only 11 exceptions observed in 1842 observations. The branching order of different bacterial groups as deduced using this approach is as follows: low G+C Gram-positive (Heliobacterium chlorum) ↔ high G+C Gram-positive ↔ Clostridium–Fusobacterium–ThermotogaDeinococcus–Thermus ↔ green nonsulfur bacteria (Chloroflexus aurantiacus) ↔ Cyanobacteria ↔ SpirochetesChlamydia–Cytophaga–Flavobacteria–green sulfur bacteria (Chlorobium tepidum) ↔ AquifexProteobacteria (δ and ∈) ↔ Proteobacteria (α) ↔ Proteobacteria (β) and ↔ Proteobacteria (γ). The Heliobacterium species, which contain an Fe–S type of reaction center (RC 1) and represent the sole photosynthetic phylum from the Gram-positive or monoderm bacteria (i.e., bounded by only a single membrane), is indicated to be the most ancestral of the photosynthetic lineages. Among the Gram-negative or diderm bacteria (containing both inner and outer cell membranes) the green nonsulfur bacteria, which contain a pheophytin-quinone type of reaction center (RC 2), are indicated to have evolved first. The later emerging photosynthetic groups which contain either one or both of these reaction centers could have acquired such genes from the earlier branching lineages by either direct descent or by means of lateral gene transfer.

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References

  • Blankenship RE (1992) Origin and early evolution of photosynthesis. Photosynth Res 33: 91–111

    Article  PubMed  CAS  Google Scholar 

  • Blankenship RE (1994) Protein structure, electron transfer and evolution of prokaryotic photosynthetic reaction centers. Antonie van Leeuwenhoek 65: 311–329

    Article  PubMed  CAS  Google Scholar 

  • Brown JR and Doolittle WF (1997) Archaea and the prokaryote-toeukaryote transition. Microbiol Mol Biol Rev 61: 456–502

    PubMed  CAS  Google Scholar 

  • Burke DH, Hearst JE and Sidow A (1993) Early evolution of photosynthesis: clues from nitrogenase and chlorophyll iron proteins. Proc Natl Acad Sci USA 90: 7134–7138

    Article  PubMed  CAS  Google Scholar 

  • Doolittle WF (1999) Phylogenetic classification and the universal tree. Science 284: 2124–2128

    Article  PubMed  CAS  Google Scholar 

  • Eisen JA (1995) The RecA protein as a model molecule for molecular systematic studies of bacteria: comparison of trees of RecAs and 16S rRNAs from the same species. J Mol Evol 41: 1105–1123

    Article  PubMed  CAS  Google Scholar 

  • Eisen JA, Nelson KE, Paulsen IT, Heidelberg JF, Wu M, Dodson RJ, DeBoy R, Gwinn ML, Nelson WC, Haft DH, Hickey EK, Peterson JD, Durkin AS, Kolonay JL, Yang F, Holt I, Umayam LA, Mason T, Brenner M, Shea TP, Parksey D, Nierman WC, Feldblyum TV, Hansen CL, Craven MB, Radune D, Vamathevan J, Khouri H, White O, Gruber TM, Ketchum KA, Venter JC, Tettelin H, Bryant DA and Fraser CM (2002) The complete genome sequence of Chlorobium tepidum TLS, a photosynthetic, anaerobic, green-sulfur bacterium. Proc Natl Acad Sci USA 99: 9509–9514

    Article  PubMed  CAS  Google Scholar 

  • Gest H and Favinger J (1983) Heliobacterium chlorum, an anoxygenic brownish-green photosynthetic bacterium containing a ‘new’ form of bacteriochlorophyll. Arch Microbiol 136: 11–16

    Article  CAS  Google Scholar 

  • Golbeck JH (1993) Shared thematic elements in photochemical reaction centers. Proc Natl Acad Sci USA 90: 1642–1646

    Article  PubMed  CAS  Google Scholar 

  • Gupta RS (1998) Protein phylogenies and signature sequences: a reappraisal of evolutionary relationships among archaebacteria, eubacteria, and eukaryotes. Microbiol Mol Biol Rev 62: 1435–1491

    PubMed  CAS  Google Scholar 

  • Gupta RS (2000a) The phylogeny of proteobacteria: relationships to other eubacterial phyla and eukaryotes. FEMS Microbiol Rev 24: 367–402

    Article  PubMed  CAS  Google Scholar 

  • Gupta RS (2000b) The natural evolutionary relationships among prokaryotes. Crit Rev Microbiol 26: 111–131

    Article  PubMed  CAS  Google Scholar 

  • Gupta RS (2001) The branching order and phylogenetic placement of species from completed bacterial genomes, based on conserved indels found in various proteins. Int Microbiol 4: 187–202

    Article  PubMed  CAS  Google Scholar 

  • Gupta RS (2002) Phylogeny of Bacteria: are we now close to understanding it? ASM News 68: 284–291

    Google Scholar 

  • Gupta RS and Griffiths E (2002) Critical issues in bacterial phylogeny. Theor Popul Biol 61: 423–434

    Article  PubMed  Google Scholar 

  • Gupta RS, Mukhtar T and Singh B (1999) Evolutionary relationships among photosynthetic prokaryotes (Heliobacterium chlorum, Chloroflexus aurantiacus, cyanobacteria, Chlorobium tepidum and proteobacteria): implications regarding the origin of photosynthesis. Mol Microbiol 32: 893–906

    Article  PubMed  CAS  Google Scholar 

  • Igarashi N, Harada J, Nagashima S, Matsuura K, Shimada K and Nagashima KV (2001) Horizontal transfer of the photosynthesis gene cluster and operon rearrangement in purple bacteria. J Mol Evol 52: 333–341

    PubMed  CAS  Google Scholar 

  • Jain R, Rivera M and Lake JA (1999) Horizontal gene transfer among genomes: the complexity hypothesis. Proc Natl Acad Sci USA 96: 3801–3806

    Article  PubMed  CAS  Google Scholar 

  • Klenk H-P, Meier T-D, Durovic P, Schwass V, Lottspeich F, Dennis PP and Zillig W (1999) RNA Polymerase of Aquifex pyrophilus: Implications for the evolution of the bacterial rpoBC operon and extremely thermophilic bacteria. J Mol Evol 48: 528–541

    Article  PubMed  CAS  Google Scholar 

  • Kondratieva EN, Pfennig N and Truper HG (1992) The phototrophic prokaryotes. In: Balows A, Truper HG, Dworkin M, Harder W and Schleifer KH (eds) The Prokaryotes, pp 312–330. Springer-Verlag, New York

    Google Scholar 

  • Koonin EV, Makarova KS and Aravind L (2001) Horizontal gene transfer in prokaryotes: quantification and classification. Annu Rev Microbiol 55: 709–742

    Article  PubMed  CAS  Google Scholar 

  • Ludwig W and Klenk H-P (2001) Overview: a phylogenetic backbone and taxonomic framework for prokaryotic systamatics. In: Boone DR and Castenholz RW (eds) Bergey's Manual of Systematic Bacteriology, Vol 1, 2nd ed: The Archaea and the Deeply Branching and Phototrophic Bacteria, pp 49–65. Springer-Verlag, Berlin

    Google Scholar 

  • Mulkidjanian AY and Junge W (1997) On the origin of photosynthesis as inferred from sequence analysis. Photosynth Res 51: 27–42

    Article  CAS  Google Scholar 

  • Murray RGE (1986) Family II.Deinococcaceae Brooks and Murray 1981, 356VP. In: Sneath PHA, Mair NS, Sharpe ME and Holt JG (eds) Bergey's Manual of Systematic Bacteriology, Vol 2, pp 1035–1043. Williams and Wilkins, Baltimore, Maryland

    Google Scholar 

  • Nelson N and Ben-Shem A (2002) Photosystem I reaction center: past and future. Photosynth Res 73: 193–206

    Article  PubMed  CAS  Google Scholar 

  • Nitschke W and Rutherford AW(1991) Photosynthetic reaction centers: variation on a common structural theme? Trends Biochem Sci 16: 241–245

    Article  PubMed  CAS  Google Scholar 

  • Olsen GJ, Woese CR and Overbeek R (1994) The winds of (evolutionary) change: breathing new life into microbiology. J Bacteriol 176: 1–6

    PubMed  CAS  Google Scholar 

  • Olson JM and Pierson BK (1987) Evolution of reaction centers in photosynthetic prokaryotes. Int Rev Cytol 108: 209–248

    Article  PubMed  CAS  Google Scholar 

  • Raymond J, Zhaxybayeva O, Gogarten JP, Gerdes SY and Blankenship RE (2002)Whole-genome analysis of photosynthetic prokaryotes. Science 298: 1616–1620

    Article  PubMed  CAS  Google Scholar 

  • Vermaas WF (1994) Evolution of heliobacteria: Implications for photosynthetic reaction center complexes. Photosynth Res 41: 285–294

    Article  PubMed  CAS  Google Scholar 

  • Woese CR (1987) Bacterial evolution. Microbiol Rev 51:221–271

    PubMed  CAS  Google Scholar 

  • Woese CR (2002) On the evolution of cells. Proc Natl Acad Sci USA 99: 8742–8747

    Article  PubMed  CAS  Google Scholar 

  • Xiong J, Inoue K and Bauer CE (1998) Tracking molecular evolution of photosynthesis by characterizaton of a major photosynthesis gene cluster from Heliobacillus mobilis. Proc Natl Acad Sci USA 95: 14851–14856

    Article  PubMed  CAS  Google Scholar 

  • Xiong J, Fischer WM, Inoue K, Nakahara M and Bauer CE (2000) Molecular evidence for the early evolution of photosynthesis. Science 289: 1724–1730

    Article  PubMed  CAS  Google Scholar 

  • Yurkov VV and Beatty JT (1998) Aerobic anoxygenic phototropic bacteria. Microbiol Mol Biol Rev 62: 695–724

    PubMed  CAS  Google Scholar 

Download references

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Gupta, R.S. Evolutionary relationships among photosynthetic bacteria. Photosynthesis Research 76, 173–183 (2003). https://doi.org/10.1023/A:1024999314839

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