Cargando…
Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions
Nitrate-dependent Fe(2+) oxidation (NDFO) is a microbially mediated process observed in many anaerobic, low-nutrient (oligotrophic) neutral–alkaline environments on Earth, which describes oxidation of Fe(2+) to Fe(3+) in tandem with microbial nitrate reduction. Evidence suggests that similar environ...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997339/ https://www.ncbi.nlm.nih.gov/pubmed/35418959 http://dx.doi.org/10.3389/fmicb.2022.800219 |
_version_ | 1784684680199536640 |
---|---|
author | Price, Alex Macey, Michael C. Pearson, Victoria K. Schwenzer, Susanne P. Ramkissoon, Nisha K. Olsson-Francis, Karen |
author_facet | Price, Alex Macey, Michael C. Pearson, Victoria K. Schwenzer, Susanne P. Ramkissoon, Nisha K. Olsson-Francis, Karen |
author_sort | Price, Alex |
collection | PubMed |
description | Nitrate-dependent Fe(2+) oxidation (NDFO) is a microbially mediated process observed in many anaerobic, low-nutrient (oligotrophic) neutral–alkaline environments on Earth, which describes oxidation of Fe(2+) to Fe(3+) in tandem with microbial nitrate reduction. Evidence suggests that similar environments existed on Mars during the Noachian epoch (4.1–3.7 Ga) and in periodic, localised environments more recently, indicating that NDFO metabolism could have played a role in a potential early martian biosphere. In this paper, three NDFO microorganisms, Acidovorax sp. strain BoFeN1, Pseudogulbenkiania sp. strain 2002 and Paracoccus sp. strain KS1, were assessed for their ability to grow oligotrophically in simulated martian brines and in a minimal medium with olivine as a solid Fe(2+) source. These simulant-derived media were developed from modelled fluids based on the geochemistry of Mars sample locations at Rocknest (contemporary Mars soil), Paso Robles (sulphur-rich soil), Haematite Slope (haematite-rich soil) and a Shergottite meteorite (common basalt). The Shergottite medium was able to support growth of all three organisms, while the contemporary Mars medium supported growth of Acidovorax sp. strain BoFeN1 and Pseudogulbenkiania sp. strain 2002; however, growth was not accompanied by significant Fe(2+) oxidation. Each of the strains was also able to grow in oligotrophic minimal media with olivine as the sole Fe(2+) source. Biomineralised cells of Pseudogulbenkiania sp. strain 2002 were identified on the surface of the olivine, representing a potential biosignature for NDFO microorganisms in martian samples. The results suggest that NDFO microorganisms could have thrived in early martian groundwaters under oligotrophic conditions, depending on the local lithology. This can guide missions in identifying palaeoenvironments of interest for biosignature detection. Indeed, biomineralised cells identified on the olivine surface provide a previously unexplored mechanism for the preservation of morphological biosignatures in the martian geological record. |
format | Online Article Text |
id | pubmed-8997339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89973392022-04-12 Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions Price, Alex Macey, Michael C. Pearson, Victoria K. Schwenzer, Susanne P. Ramkissoon, Nisha K. Olsson-Francis, Karen Front Microbiol Microbiology Nitrate-dependent Fe(2+) oxidation (NDFO) is a microbially mediated process observed in many anaerobic, low-nutrient (oligotrophic) neutral–alkaline environments on Earth, which describes oxidation of Fe(2+) to Fe(3+) in tandem with microbial nitrate reduction. Evidence suggests that similar environments existed on Mars during the Noachian epoch (4.1–3.7 Ga) and in periodic, localised environments more recently, indicating that NDFO metabolism could have played a role in a potential early martian biosphere. In this paper, three NDFO microorganisms, Acidovorax sp. strain BoFeN1, Pseudogulbenkiania sp. strain 2002 and Paracoccus sp. strain KS1, were assessed for their ability to grow oligotrophically in simulated martian brines and in a minimal medium with olivine as a solid Fe(2+) source. These simulant-derived media were developed from modelled fluids based on the geochemistry of Mars sample locations at Rocknest (contemporary Mars soil), Paso Robles (sulphur-rich soil), Haematite Slope (haematite-rich soil) and a Shergottite meteorite (common basalt). The Shergottite medium was able to support growth of all three organisms, while the contemporary Mars medium supported growth of Acidovorax sp. strain BoFeN1 and Pseudogulbenkiania sp. strain 2002; however, growth was not accompanied by significant Fe(2+) oxidation. Each of the strains was also able to grow in oligotrophic minimal media with olivine as the sole Fe(2+) source. Biomineralised cells of Pseudogulbenkiania sp. strain 2002 were identified on the surface of the olivine, representing a potential biosignature for NDFO microorganisms in martian samples. The results suggest that NDFO microorganisms could have thrived in early martian groundwaters under oligotrophic conditions, depending on the local lithology. This can guide missions in identifying palaeoenvironments of interest for biosignature detection. Indeed, biomineralised cells identified on the olivine surface provide a previously unexplored mechanism for the preservation of morphological biosignatures in the martian geological record. Frontiers Media S.A. 2022-03-28 /pmc/articles/PMC8997339/ /pubmed/35418959 http://dx.doi.org/10.3389/fmicb.2022.800219 Text en Copyright © 2022 Price, Macey, Pearson, Schwenzer, Ramkissoon and Olsson-Francis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Price, Alex Macey, Michael C. Pearson, Victoria K. Schwenzer, Susanne P. Ramkissoon, Nisha K. Olsson-Francis, Karen Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title | Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title_full | Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title_fullStr | Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title_full_unstemmed | Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title_short | Oligotrophic Growth of Nitrate-Dependent Fe(2+)-Oxidising Microorganisms Under Simulated Early Martian Conditions |
title_sort | oligotrophic growth of nitrate-dependent fe(2+)-oxidising microorganisms under simulated early martian conditions |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997339/ https://www.ncbi.nlm.nih.gov/pubmed/35418959 http://dx.doi.org/10.3389/fmicb.2022.800219 |
work_keys_str_mv | AT pricealex oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions AT maceymichaelc oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions AT pearsonvictoriak oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions AT schwenzersusannep oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions AT ramkissoonnishak oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions AT olssonfranciskaren oligotrophicgrowthofnitratedependentfe2oxidisingmicroorganismsundersimulatedearlymartianconditions |