Survivability and growth kinetics of methanogenic archaea at various pHs and pressures: Implications for deep subsurface life on Mars

Abstract Life as we know it requires liquid water and sufficient liquid water is highly unlikely on the surface of present-day Mars. However, according to thermal models there is a possibility of liquid water in the deep subsurface of Mars. Thus, the martian subsurface, where the pressure and temperature is higher, could potentially provide a hospitable environment for a biosphere. Also, methane has been detected in the Mars’ atmosphere. Analogous to Earth’s atmospheric methane, martian methane could also be biological in origin. The carbon and energy sources for methanogenesis in the subsurface of Mars could be available by downwelling of atmospheric CO2 into the regolith and water-rock reactions such as serpentinization, respectively. Corresponding analogs of the martian subsurface on Earth might be the active sites of serpentinization at depths where methanogenic thermophilic archaea are the dominant species. Methanogens residing in Earth’s hydrothermal environments are usually exposed to a variety of physiological stresses including a wide range of pressures, temperatures, and pHs. Martian geochemical models imply that the pH of probable groundwater varies from 4.96 to 9.13. In this work, we used the thermophilic methanogen, Methanothermobacter wolfeii, which grows optimally at 55oC. Therefore, a temperature of 55oC was chosen for these experiments, possibly simulating Mars’ subsurface temperature. A martian geophysical model suggests depth and pressure corresponding to a temperature of 55 °C would be between 1–30 km and 100-3,000 atm respectively. Here, we have simulated Mars deep subsurface pH, pressure, and temperature conditions and have investigated the survivability, growth rate, and morphology of M. wolfeii after exposure to a wide range of pH 5–9) and pressure (1−1200 atm) at a temperature of 55 °C. Interestingly, in this study we have found that M. wolfeii was able to survive at all the pressures and pHs tested at 55 °C. In order to understand the effect of different pHs and pressures on the metabolic activities of M. wolfeii, we also calculated their growth rate by measuring methane concentration in the headspace gas samples at regular intervals. In acidic conditions, the growth rate (γ) of M. wolfeii increased with the increase in pressure. In neutral and alkaline conditions, the growth rate (γ) of M. wolfeii initially increased with pressure, but decreased upon further increase of pressure. To investigate the effect of combined pH, pressure, and temperature on the morphology of M. wolfeii, we took phase contrast images of the cells. We did not find any obvious significant alteration in the morphology of M. wolfeii cells. Methanogens, chemolithoautotrophic anaerobic microorganisms, are considered as ideal model microorganisms for Mars. In light of research presented here, we suggest that at least one methanogen, M. wolfeii, could survive in the deep subsurface environment of Mars.

[1]  Charles H Lineweaver,et al.  An extensive phase space for the potential martian biosphere. , 2011, Astrobiology.

[2]  Tobias Owen,et al.  Detection of methane in the martian atmosphere: evidence for life? , 2004 .

[3]  Andrew Steele,et al.  Mars methane detection and variability at Gale crater , 2015, Science.

[4]  R. Mancinelli Accessing the Martian deep subsurface to search for life , 2000 .

[5]  B. Jakosky,et al.  Biological potential of Martian hydrothermal systems. , 2002, Astrobiology.

[6]  M. Malin,et al.  Evidence for recent groundwater seepage and surface runoff on Mars. , 2000, Science.

[7]  Andrew C. Schuerger,et al.  Low pressure and desiccation effects on methanogens: Implications for life on Mars , 2011 .

[8]  Manish R. Patel,et al.  Numerical modelling of the transport of trace gases including methane in the subsurface of Mars , 2015 .

[9]  D. Blake,et al.  Serpentinization and its implications for life on the early Earth and Mars. , 2006, Astrobiology.

[10]  Alfred S. McEwen,et al.  Corrigendum: Spectral evidence for hydrated salts in recurring slope lineae on Mars , 2015 .

[11]  C. Cockell,et al.  The ultraviolet environment of Mars: biological implications past, present, and future. , 2000, Icarus.

[12]  W. Brazelton,et al.  Record of archaeal activity at the serpentinite‐hosted Lost City Hydrothermal Field , 2013, Geobiology.

[13]  C P McKay,et al.  On the possibility of chemosynthetic ecosystems in subsurface habitats on Mars. , 1992, Icarus.

[14]  Barry L. Lutz,et al.  Deuterium on Mars: The Abundance of HDO and the Value of D/H , 1988, Science.

[15]  Donald M. Hunten,et al.  Possible oxidant sources in the atmosphere and surface of Mars , 1979, Journal of Molecular Evolution.

[16]  C. Oze,et al.  Have olivine, will gas: Serpentinization and the abiogenic production of methane on Mars , 2005 .

[17]  V. Baker Water and the martian landscape , 2001, Nature.

[18]  N. Sinha,et al.  Stable carbon isotope fractionation by methanogens growing on different Mars regolith analogs , 2015 .

[19]  John Parnell,et al.  Groundwater activity on Mars and implications for a deep biosphere , 2013 .

[20]  Marco Giuranna,et al.  Detection of Methane in the Atmosphere of Mars , 2004, Science.

[21]  Michael D. Smith,et al.  Strong Release of Methane on Mars in Northern Summer 2003 , 2009, Science.

[22]  Michael J. Mumma,et al.  Detection and Mapping of Methane and Water on Mars , 2004 .

[23]  Andrew Steele,et al.  Isotope Ratios of H, C, and O in CO2 and H2O of the Martian Atmosphere , 2013, Science.

[24]  A. Libchaber,et al.  Pressure and temperature dependence of growth and morphology of Escherichia coli: experiments and stochastic model. , 2012, Biophysical journal.

[25]  S. Giovannoni,et al.  Sources of nutrients and energy for a deep biosphere on Mars , 1999 .

[26]  R. Cavicchioli Extremophiles and the search for extraterrestrial life. , 2002, Astrobiology.

[27]  D. Clark,et al.  Pressure and Temperature Effects on Growth and Methane Production of the Extreme Thermophile Methanococcus jannaschii , 1988, Applied and environmental microbiology.

[28]  T. Kral,et al.  Potential use of highly insoluble carbonates as carbon sources by methanogens in the subsurface of Mars , 2014 .

[29]  L. Rothschild,et al.  Life in extreme environments , 2001, Nature.

[30]  S. Murchie,et al.  Geologic setting of serpentine deposits on Mars , 2010 .

[31]  Gerald G. Owenson,et al.  Microbial diversity of soda lakes , 1998, Extremophiles.

[32]  C. Schleper,et al.  Picrophilus gen. nov., fam. nov.: a novel aerobic, heterotrophic, thermoacidophilic genus and family comprising archaea capable of growth around pH 0 , 1995, Journal of bacteriology.

[33]  Christopher R. Webster,et al.  Abundance and Isotopic Composition of Gases in the Martian Atmosphere from the Curiosity Rover , 2013, Science.

[34]  T. Kral,et al.  Survival of methanogens during desiccation: implications for life on Mars. , 2006, Astrobiology.

[35]  R. Jaenicke,et al.  High Pressure Enhances the Growth Rate of the Thermophilic Archaebacterium Methanococcus thermolithotrophicus without Extending Its Temperature Range , 1988, Applied and environmental microbiology.

[36]  F. Nimmo,et al.  Formation of methane on Mars by fluid‐rock interaction in the crust , 2005 .

[37]  K. Lloyd,et al.  Effects of Dissolved Sulfide, pH, and Temperature on Growth and Survival of Marine Hyperthermophilic Archaea , 2005, Applied and Environmental Microbiology.

[38]  D. Clark,et al.  Pressure effects on the composition and thermal behavior of lipids from the deep-sea thermophile Methanococcus jannaschii , 1995, Journal of bacteriology.

[39]  Paul R. Mahaffy,et al.  Methane and related trace species on Mars: Origin, loss, implications for life, and habitability , 2007 .

[40]  D. Boone,et al.  Diffusion of the Interspecies Electron Carriers H2 and Formate in Methanogenic Ecosystems and Its Implications in the Measurement of Km for H2 or Formate Uptake , 1989, Applied and environmental microbiology.

[41]  D. R. Rushneck,et al.  The search for organic substances and inorganic volatile compounds in the surface of Mars , 1977 .

[42]  D. Lovley,et al.  A hydrogen-based subsurface microbial community dominated by methanogens , 2002, Nature.

[43]  Barbara Sherwood Lollar,et al.  Is Mars alive , 2006 .

[44]  P. McGovern,et al.  Depth of the Martian cryosphere: Revised estimates and implications for the existence and detection of subpermafrost groundwater , 2010 .

[45]  T. Kral,et al.  Sensitivity and adaptability of methanogens to perchlorates: Implications for life on Mars , 2016 .

[46]  J D Farmer,et al.  Hydrothermal systems on Mars: an assessment of present evidence. , 1996, Ciba Foundation symposium.

[47]  D. Boone,et al.  Control of the Life Cycle of Methanosarcina mazei S-6 by Manipulation of Growth Conditions , 1988, Applied and environmental microbiology.

[48]  K. Nealson,et al.  Atmospheric energy for subsurface life on Mars? , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[49]  Christopher P. McKay,et al.  Growth of Methanogens on a Mars Soil Simulant , 2004, Origins of life and evolution of the biosphere.

[50]  D. Montgomery,et al.  Continental-scale salt tectonics on Mars and the origin of Valles Marineris and associated outflow channels , 2006 .