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      Detection of Macromolecules in Desert Cyanobacteria Mixed with a Lunar Mineral Analogue After Space Simulations

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          Abstract

          In the context of future exposure missions in Low Earth Orbit and possibly on the Moon, two desert strains of the cyanobacterium Chroococcidiopsis, strains CCMEE 029 and 057, mixed or not with a lunar mineral analogue, were exposed to fractionated fluencies of UVC and polychromatic UV (200–400 nm) and to space vacuum. These experiments were carried out within the framework of the BIOMEX (BIOlogy and Mars EXperiment) project, which aims at broadening our knowledge of mineral-microorganism interaction and the stability/degradation of their macromolecules when exposed to space and simulated Martian conditions. The presence of mineral analogues provided a protective effect, preserving survivability and integrity of DNA and photosynthetic pigments, as revealed by testing colony-forming abilities, performing PCR-based assays and using confocal laser scanning microscopy. In particular, DNA and pigments were still detectable after 500 kJ/m 2 of polychromatic UV and space vacuum (10 −4 Pa), corresponding to conditions expected during one-year exposure in Low Earth Orbit on board the EXPOSE-R2 platform in the presence of 0.1 % Neutral Density (ND) filter. After exposure to high UV fluencies (800 MJ/m 2) in the presence of minerals, however, altered fluorescence emission spectrum of the photosynthetic pigments were detected, whereas DNA was still amplified by PCR. The present paper considers the implications of such findings for the detection of biosignatures in extraterrestrial conditions and for putative future lunar missions.

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          Most cited references30

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          The Sample Analysis at Mars Investigation and Instrument Suite

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            The ultraviolet environment of Mars: biological implications past, present, and future.

            A radiative transfer model is used to quantitatively investigate aspects of the martian ultraviolet radiation environment, past and present. Biological action spectra for DNA inactivation and chloroplast (photosystem) inhibition are used to estimate biologically effective irradiances for the martian surface under cloudless skies. Over time Mars has probably experienced an increasingly inhospitable photobiological environment, with present instantaneous DNA weighted irradiances 3.5-fold higher than they may have been on early Mars. This is in contrast to the surface of Earth, which experienced an ozone amelioration of the photobiological environment during the Proterozoic and now has DNA weighted irradiances almost three orders of magnitude lower than early Earth. Although the present-day martian UV flux is similar to that of early Earth and thus may not be a critical limitation to life in the evolutionary context, it is a constraint to an unadapted biota and will rapidly kill spacecraft-borne microbes not covered by a martian dust layer. Microbial strategies for protection against UV radiation are considered in the light of martian photobiological calculations, past and present. Data are also presented for the effects of hypothetical planetary atmospheric manipulations on the martian UV radiation environment with estimates of the biological consequences of such manipulations.
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              Ionizing-radiation resistance in the desiccation-tolerant cyanobacterium Chroococcidiopsis.

              The effect of X-ray irradiation on cell survival, induction, and repair of DNA damage was studied by using 10 Chroococcidiopsis strains isolated from desert and hypersaline environments. After exposure to 2.5 kGy, the percentages of survival for the strains ranged from 80 to 35%. In the four most resistant strains, the levels of survival were reduced by 1 or 2 orders of magnitude after irradiation with 5 kGy; viable cells were recovered after exposure to 15 kGy but not after exposure to 20 kGy. The severe DNA damage evident after exposure to 2.5 kGy was repaired within 3 h, and the severe DNA damage evident after exposure to 5 kGy was repaired within 24 h. The increase in trichloroacetic acid-precipitable radioactivity in the culture supernatant after irradiation with 2.5 kGy might have been due to cell lysis and/or an excision process involved in DNA repair. The radiation resistance of Chroococcidiopsis strains may reflect the ability of these cyanobacteria to survive prolonged desiccation through efficient repair of the DNA damage that accumulates during dehydration.
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                Author and article information

                Contributors
                +39 0672594341 , billi@uniroma2.it
                Journal
                Orig Life Evol Biosph
                Orig Life Evol Biosph
                Origins of Life and Evolution of the Biosphere
                Springer Netherlands (Dordrecht )
                0169-6149
                1573-0875
                30 October 2014
                2014
                : 44
                : 3
                : 209-221
                Affiliations
                [ ]Department of Biology, University of Rome “Tor Vergata”, Rome, Italy
                [ ]Institute of Planetary Research, German Aerospace Center (DLR) Berlin, Berlin, Germany
                [ ]Radiation Biology Department, Institute of Aerospace Medicine, German Aerospace Center (DLR), Cologne, Germany
                Article
                9367
                10.1007/s11084-014-9367-4
                4669540
                25351683
                ded9c2ad-228a-4903-a01a-a0205b068941
                © Springer Science+Business Media Dordrecht 2014
                History
                : 30 January 2014
                : 16 September 2014
                Categories
                Astrobiology
                Custom metadata
                © Springer Science+Business Media Dordrecht 2014

                Evolutionary Biology
                astrobiology,extreme environments,expose-r2,biosignatures,lunar regolith
                Evolutionary Biology
                astrobiology, extreme environments, expose-r2, biosignatures, lunar regolith

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