Mars, with its ancient history of long-lived habitable environments, continues to captivate researchers exploring the potential for extant life. This study investigates the biosignature potential of Martian methane by assessing the viability of hydrogenotrophic methanogenesis in Methanosarcina barkeri MS under simulated Martian surface conditions. We expose M. barkeri to sustained hypobaria (7-12 mbar), low temperature (0˚C), and a CO-dominated gas mixture mimicking the Martian atmosphere. The results demonstrate statistically quantifiable CH production under all tested conditions, including at 7-12 mbar. Transcriptomics reveal that low total pressure and temperature did not significantly impact gene expression, highlighting the resilience of M. barkeri. However, atmospheric gas composition, specifically Mars gas with 2.9% pH, led to significant down-regulation of methanogenesis genes, hindering growth over 14 days. Notably, CH production scaled with the partial pressure of H, revealing that hydrogen uptake affinity is a stronger predictor of habitability and methanogenic potential than favorable Gibbs free energy of reaction. Our findings suggest that Mars' subsurface could harbor habitable refugia capable of supporting methanogenesis, sustaining microbial life at low metabolic steady states. These insights challenge assumptions about Martian habitability and have implications for astrobiological exploration, planetary protection, and in situ resource utilization for future human missions.
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http://dx.doi.org/10.1038/s41598-025-86145-1 | DOI Listing |
Sci Rep
January 2025
Department of Plant Pathology, Space Life Sciences Lab, University of Florida, 505 Odyssey Way, Exploration Park,, Merritt Island, FL, 32953, USA.
Mars, with its ancient history of long-lived habitable environments, continues to captivate researchers exploring the potential for extant life. This study investigates the biosignature potential of Martian methane by assessing the viability of hydrogenotrophic methanogenesis in Methanosarcina barkeri MS under simulated Martian surface conditions. We expose M.
View Article and Find Full Text PDFJ Surg Res
March 2016
Department of Visceral, Thoracic and Vascular Surgery, Giessen and Marburg University Hospital (UKGM), Marburg, Germany.
Background: Small arteries and veins up to 7 mm can be sealed safe and divided with a bipolar sealing instrument. The results for the safe sealing of larger vessels were unsatisfactory in the past. Using an ex vivo pulmonary artery model, we aimed to investigate, if a higher compression force and duration will improve the bursting pressures in case of vessels >7 mm.
View Article and Find Full Text PDFElectrophoresis
May 2016
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan, P. R. China.
An effective dual preconcentration method involving off-line membrane supported liquid-liquid-liquid microextraction (MS-LLLME) and on-line field-amplified sample injection (FASI) was proposed for the extraction of six cardiovascular drugs, including mexiletine, xylocaine, propafenone, propranolol, metoprolol, and carvedilol from aqueous solution prior to CE-UV. In MS-LLLME, the analytes were extracted from 9 mL sample solution into toluene, and then back extracted into a drop of acceptor phase of 10 μL 20 mmol/L acetic acid. After that, the acceptor phase was directly introduced into CE for FASI without any modification.
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