ArticleFrontiers in microbiology2017
Nutrient Acquisition and the Metabolic Potential of Photoferrotrophic Chlorobi.
Article in Frontiers in microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 40 citations in OpenAlex.
- Recent origin of iron oxidation in extant microbial groups and low clade fidelity of iron metabolisms.Applied and environmental microbiology · 2025Article
- Cryptic iron cycling influenced by organic carbon availability in a seasonally stratified lake.FEMS microbiology ecology · 2025Article
- Late acquisition of the rTCA carbon fixation pathway by Chlorobi.Nature ecology & evolution · 2023Article
- Article
- "Frontiers in microbiology · 2021Article
- Anoxygenic photosynthesis and iron-sulfur metabolic potential of Chlorobia populations from seasonally anoxic Boreal Shield lakes.The ISME journal · 2020Article
- Diazotroph Genomes and Their Seasonal Dynamics in a Stratified Humic Bog Lake.Frontiers in microbiology · 2020Article
- Anoxygenic photosynthesis and the delayed oxygenation of Earth's atmosphere.Nature communications · 2019Article
- Proteome Response of a Metabolically Flexible Anoxygenic Phototroph to Fe(II) Oxidation.Applied and environmental microbiology · 2018Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Anoxygenic photosynthesis evolved prior to oxygenic photosynthesis and harnessed energy from sunlight to support biomass production on the early Earth. Models that consider the availability of electron donors predict that anoxygenic photosynthesis using Fe(II), known as photoferrotrophy, would have supported most global primary production before the proliferation of oxygenic phototrophs at approximately 2.3 billion years ago. These photoferrotrophs have also been implicated in the deposition of banded iron formations, the world's largest sedimentary iron ore deposits that formed mostly in late Archean and early Proterozoic Eons. In this work we present new data and analyses that illuminate the metabolic capacity of photoferrotrophy in the phylum Chlorobi. Our laboratory growth experiments and biochemical analyses demonstrate that photoferrotrophic Chlorobi are capable of assimilatory sulfate reduction and nitrogen fixation under sulfate and nitrogen limiting conditions, respectively. Furthermore, the evolutionary histories of key enzymes in both sulfur (CysH and CysD) and nitrogen fixation (NifDKH) pathways are convoluted; protein phylogenies, however, suggest that early Chlorobi could have had the capacity to assimilate sulfur and fix nitrogen. We argue, then, that the capacity for photoferrotrophic Chlorobi to acquire these key nutrients enabled them to support primary production and underpin global biogeochemical cycles in the Precambrian.
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