TY - JOUR
T1 - A physiological perspective on the origin and evolution of photosynthesis
AU - Martin, William F.
AU - Bryant, Donald A.
AU - Beatty, J. Thomas
N1 - Funding Information:
We thank George Luther III, John F. Allen, Dianne Newman, Filipa Sousa, Christiane Dahl, Ines Periera, and Carlo Kleinermanns for discussions on aspects of the paper. We thank Verena Zimorski for help in preparing the manuscript. WFM thanks the ERC (666053 emicrobEvol) and the Volkswagen Foundation (93 046) for funding. DAB thanks the U. S. Dept. of Energy (DE-FG02-94ER20137), NASA Exobiology (NNX16AJ62G) and National Science Foundation (MCB-1613022) for support. JTB thanks Genome British Columbia (SOF153) and the Canadian Natural Sciences and Engineering Research Council (Discovery Grant 2796) for funding
Funding Information:
We thank George Luther III, John F. Allen, Dianne Newman, Filipa Sousa, Christiane Dahl, Ines Periera, and Carlo Klein-ermanns for discussions on aspects of the paper. We thank Verena Zimorski for help in preparing the manuscript. WFM thanks the ERC (666053 emicrobEvol) and the Volkswagen Foundation (93 046) for funding. DAB thanks the U. S. Dept. of Energy (DE-FG02-94ER20137), NASA Exobiology (NNX16AJ62G) and National Science Foundation (MCB-1613022) for support. JTB thanks Genome British Columbia (SOF153) and the Canadian Natural Sciences and Engineering Research Council (Discovery Grant 2796) for funding.
Publisher Copyright:
© FEMS 2017.
PY - 2018
Y1 - 2018
N2 - The origin and early evolution of photosynthesis are reviewed from an ecophysiological perspective. Earth's first ecosystems were chemotrophic, fueled by geological H2 at hydrothermal vents and, required flavin-based electron bifurcation to reduce ferredoxin for CO2 fixation. Chlorophyll-based phototrophy (chlorophototrophy) allowed autotrophs to generate reduced ferredoxin without electron bifurcation, providing them access to reductants other than H2. Because high-intensity, short-wavelength electromagnetic radiation at Earth's surface would have been damaging for the first chlorophyll (Chl)-containing cells, photosynthesis probably arose at hydrothermal vents under low-intensity, long-wavelength geothermal light. The first photochemically active pigments were possibly Zn-tetrapyrroles. We suggest that (i) after the evolution of red-absorbing Chl-like pigments, the first light-driven electron transport chains reduced ferredoxin via a type-1 reaction center (RC) progenitor with electrons from H2S; (ii) photothioautotrophy, first with one RC and then with two, was the bridge between H2-dependent chemolithoautotrophy and water-splitting photosynthesis; (iii) photothiotrophy sustained primary production in the photic zone of Archean oceans; (iv) photosynthesis arose in an anoxygenic cyanobacterial progenitor; (v) Chl a is the ancestral Chl; and (vi), anoxygenic chlorophototrophic lineages characterized so far acquired, by horizontal gene transfer, RCs and Chl biosynthesis with or without autotrophy, from the architects of chlorophototrophy-the cyanobacterial lineage.
AB - The origin and early evolution of photosynthesis are reviewed from an ecophysiological perspective. Earth's first ecosystems were chemotrophic, fueled by geological H2 at hydrothermal vents and, required flavin-based electron bifurcation to reduce ferredoxin for CO2 fixation. Chlorophyll-based phototrophy (chlorophototrophy) allowed autotrophs to generate reduced ferredoxin without electron bifurcation, providing them access to reductants other than H2. Because high-intensity, short-wavelength electromagnetic radiation at Earth's surface would have been damaging for the first chlorophyll (Chl)-containing cells, photosynthesis probably arose at hydrothermal vents under low-intensity, long-wavelength geothermal light. The first photochemically active pigments were possibly Zn-tetrapyrroles. We suggest that (i) after the evolution of red-absorbing Chl-like pigments, the first light-driven electron transport chains reduced ferredoxin via a type-1 reaction center (RC) progenitor with electrons from H2S; (ii) photothioautotrophy, first with one RC and then with two, was the bridge between H2-dependent chemolithoautotrophy and water-splitting photosynthesis; (iii) photothiotrophy sustained primary production in the photic zone of Archean oceans; (iv) photosynthesis arose in an anoxygenic cyanobacterial progenitor; (v) Chl a is the ancestral Chl; and (vi), anoxygenic chlorophototrophic lineages characterized so far acquired, by horizontal gene transfer, RCs and Chl biosynthesis with or without autotrophy, from the architects of chlorophototrophy-the cyanobacterial lineage.
UR - http://www.scopus.com/inward/record.url?scp=85046875868&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85046875868&partnerID=8YFLogxK
U2 - 10.1093/FEMSRE/FUX056
DO - 10.1093/FEMSRE/FUX056
M3 - Review article
C2 - 29177446
AN - SCOPUS:85046875868
SN - 0168-6445
VL - 42
SP - 205
EP - 231
JO - FEMS Microbiology Reviews
JF - FEMS Microbiology Reviews
IS - 2
ER -