Abstract
While it is true that the chemistry of current life is well defined, 3.5 billion years ago, everything could have been different. Other elements may have been part of the chemical reactions that finally triggered an endless iteration with well-defined laws that gave way—and continue to give way—to the evolution of life. In this sense, arsenic could have been a key element for life back then. Its high reactivity and its abundance in the context of a reduced atmosphere could have given this element a key role, whereas nowadays it is so alien to the development of life. In this chapter, we address this question with a special emphasis on the description of one of the best natural laboratories to study early life that our planet presents: the Andean Puna.
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References
Albarracín VH, Kurth D, Ordoñez OF, Belfiore C, Luccini E, Salum GM et al (2015) High-up: a remote reservoir of microbial extremophiles in central Andean Wetlands. Front Microbiol 6:1404. https://doi.org/10.3389/fmicb.2015.01404
Andres J, Bertin PN (2016) The microbial genomics of arsenic. FEMS Microbiol Rev 40:299–322. https://doi.org/10.1093/femsre/fuv050
Belfiore C, Ordoñez OF, Farías ME (2013) Proteomic approach of adaptive response to arsenic stress in Exiguobacterium sp. S17, an extremophile strain isolated from a high-altitude Andean lake stromatolite. Extremophiles 17:421–431. https://doi.org/10.1007/s00792-013-0523-y
Benedetto JL (2010) El continente Gondwana a través del tiempo. Una introducción a la geología histórica. Academia Nacional de Ciencias. http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0002-70142010000200010. Accessed 11 Mar 2019
Bundschuh J, Gimene-Forcada E, Guerequiz E, Pérez Carrera A, García ME Mello J et al (2008) Fuentes geogénicas de arsénico y su liberación al medio ambiente. CYTED, Ciencia y Tecnología para el Desarrollo. https://eprints.usq.edu.au/26283/. Accessed 11 Mar 2019
Demergasso CS, Guillermo CD, Lorena EG, Mur JJP, Pedrós-Alió C (2007) Microbial precipitation of arsenic sulfides in Andean salt flats. Geomicrobiol J 24:111–123. https://doi.org/10.1080/01490450701266605
Escudero LV, Casamayor EO, Chong G, Pedrós-Alió C, Demergasso C (2013) Distribution of microbial arsenic reduction, oxidation and extrusion genes along a wide range of environmental arsenic concentrations. PLoS One 8:e78890. https://doi.org/10.1371/journal.pone.0078890
Farías ME, Contreras M, Rasuk MC, Kurth D, Flores MR, Poiré DG et al (2014) Characterization of bacterial diversity associated with microbial mats, gypsum evaporites and carbonate microbialites in thalassic wetlands: Tebenquiche and La Brava, Salar de Atacama, Chile. Extremophiles 18:311–329. https://doi.org/10.1007/s00792-013-0617-6
Farías ME, Rascovan N, Toneatti DM, Albarracín VH, Flores MR, Poiré DG et al (2013) The discovery of stromatolites developing at 3570 m above sea level in a high-altitude volcanic lake Socompa, Argentinean Andes. PLoS One 8:e53497. https://doi.org/10.1371/journal.pone.0053497
Fernandez AB, Rasuk MC, Visscher PT, Contreras M, Novoa F, Poire DG et al (2016) Microbial diversity in sediment ecosystems (evaporites domes, microbial mats, and crusts) of hypersaline Laguna Tebenquiche, Salar de Atacama, Chile. Front Microbiol 7:1284. https://doi.org/10.3389/fmicb.2016.01284
Goldford JE, Hartman H, Smith TF, Segrè D (2017) Remnants of an ancient metabolism without phosphate. Cell 168:1126–1134.e9. https://doi.org/10.1016/j.cell.2017.02.001
Hamaguchi H, Onuma N, Hirao Y, Yokoyama H, Bando S, Furukawa M (1969) The abundances of arsenic, tin and antimony in chondritic meteorites. Geochim Cosmochim Acta 33:507–518. https://doi.org/10.1016/0016-7037(69)90130-6
Holland HD (1994) Early Proterozoic atmospheric change. In: Bengston S (ed) Early life on Earth. Columbia University Press, New York, pp 237–244
Holland HD (1997) Evidence for life on Earth more than 3850 million years ago. Science 275:38–39. https://doi.org/10.1126/SCIENCE.275.5296.38
Karl DM (2000) Aquatic ecology: phosphorus, the staff of life. Nature 406:31–33. https://doi.org/10.1038/35017683.
Kasting JF (2001) Earth history: the rise of atmospheric oxygen. Science 293:819–820. https://doi.org/10.1126/science.1063811
Kornberg A, Rao NN, Ault-Riché D (1999) Inorganic polyphosphate: a molecule of many functions. Annu Rev Biochem 68:89–125. https://doi.org/10.1146/annurev.biochem.68.1.89
Kulp TR, Hoeft SE, Asao M, Madigan MT, Hollibaugh JT, Fisher JC et al (2008) Arsenic(III) fuels anoxygenic photosynthesis in hot spring biofilms from Mono Lake, California. Science. 321:967–970
Kurth D, Amadio A, Ordoñez OF, Albarracín VH, Gärtner W, Farías ME (2017) Arsenic metabolism in high altitude modern stromatolites revealed by metagenomic analysis. Sci Rep 7:1024. https://doi.org/10.1038/s41598-017-00896-0
Lahaye Y, Barnes S-J, Frick LR, Lambert DD (2001) Re-Os isotopic study of komatiitic volcanism and magmatic sulfide formation in the Southern Abitibi Greenstone Belt, Ontario, Canada. https://constellation.uqac.ca/2075/1/Yann_Lahaye.pdf. Accessed 11 Mar 2019
Lara J, Escudero González L, Ferrero M, Chong Díaz G, Pedrós-Alió C, Demergasso C (2012) Enrichment of arsenic transforming and resistant heterotrophic bacteria from sediments of two salt lakes in Northern Chile. Extremophiles 16:523–538. https://doi.org/10.1007/s00792-012-0452-1
Mandal BK, Suzuki KT (2002) Arsenic round the world: a review. Talanta 58:201–235. http://www.ncbi.nlm.nih.gov/pubmed/18968746. Accessed 8 Mar 2019
Muller D, Lievremont D, Simeonova DD, Hubert J-C, Lett M-C, Coppee J-Y et al (2003) Arsenite oxidase aox genes from a metal-resistant—proteobacterium. J Bacteriol 185:135–141. https://doi.org/10.1128/JB.185.1.135-141.2003
Olsen EJ, Kracher A, Davis AM, Steele IM, Hutcheon ID, Bunch TE (1999) The phosphates of IIIAB iron meteorites. Meteorit Planet Sci 34:285–300. https://doi.org/10.1111/j.1945-5100.1999.tb01752.x
Ordoñez OF, Lanzarotti E, Kurth D, Cortez N, Farías ME, Turjanski AG (2015) Genome comparison of two Exiguobacterium strains from high altitude Andean lakes with different arsenic resistance: identification and 3D modeling of the Acr3 efflux pump. Front Environ Sci 3:50. https://doi.org/10.3389/fenvs.2015.00050
Ordoñez OF, Lanzarotti E, Kurth D, Gorriti MF, Revale S, Cortez N et al (2013) Draft genome sequence of the polyextremophilic Exiguobacterium sp. strain S17, isolated from hyperarsenic lakes in the Argentinian Puna. Genome Announc 1:e00480–e00413. https://doi.org/10.1128/genomeA.00480-13
Ordoñez OF, Rasuk MC, Soria MN, Contreras M, Farías ME (2018) Haloarchaea from the Andean Puna: biological role in the energy metabolism of arsenic. Microb Ecol 76(3):695–705. https://doi.org/10.1007/s00248-018-1159-3
Oremland RS, Hoeft SE, Santini JM, Bano N, Hollibaugh RA, Hollibaugh JT (2002) Anaerobic oxidation of arsenite in Mono Lake water and by a facultative, arsenite-oxidizing chemoautotroph, strain MLHE-1. Appl Environ Microbiol 68:4795–4802. https://doi.org/10.1128/AEM.68.10.4795-4802.2002
Oremland RS, Saltikov CW, Wolfe-Simon F, Stolz JF (2009) Arsenic in the evolution of Earth and extraterrestrial ecosystems. Geomicrobiol. J. 26:522–536. https://doi.org/10.1080/01490450903102525
Oremland RS, Stolz JF (2003) The ecology of arsenic. Science 300:939–944. https://doi.org/10.1126/science.1081903
Páez-Espino D, Tamames J, de Lorenzo V, Cánovas D (2009) Microbial responses to environmental arsenic. Biometals 22:117–130. https://doi.org/10.1007/s10534-008-9195-y
Pasek M (2019) A role for phosphorus redox in emerging and modern biochemistry. Curr Opin Chem Biol 49:53–58. https://doi.org/10.1016/J.CBPA.2018.09.018
Pla-García J, Menor-Salván C (1990) La composición química de la atmósfera primitiva del planeta Tierra. Real Sociedad Española de Química. http://analesdequimica.es/index.php/AnalesQuimica/article/view/940. Accessed 11 Mar 2019
Rascovan N, Maldonado J, Vazquez MP, Eugenia Farías M (2016) Metagenomic study of red biofilms from Diamante Lake reveals ancient arsenic bioenergetics in haloarchaea. ISME J 10:299–309. https://doi.org/10.1038/ismej.2015.109
Rasuk MC, Fernández AB, Kurth D, Contreras M, Novoa F, Poiré D et al (2016) Bacterial diversity in microbial mats and sediments from the Atacama Desert. Microb Ecol 71:44–56. https://doi.org/10.1007/s00248-015-0649-9
Sancho-Tomás M, Somogyi A, Medjoubi K, Bergamaschi A, Visscher PT, Van Driessche AES et al (2018) Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de Atacama. Chem Geol 490:13–21. https://doi.org/10.1016/j.chemgeo.2018.04.029
Serrano AE, Escudero LV, Tebes-Cayo C, Acosta M, Encalada O, Fernández-Moroso S et al (2017) First draft genome sequence of a strain from the genus Fusibacter isolated from Salar de Ascotán in Northern Chile. Stand Genomic Sci 12:43. https://doi.org/10.1186/s40793-017-0252-4
Sforna MC, Philippot P, Somogyi A, van Zuilen MA, Medjoubi K, Schoepp-Cothenet B et al (2014) Evidence for arsenic metabolism and cycling by microorganisms 2.7 billion years ago. Nat Geosci 7:811–815. https://doi.org/10.1038/ngeo2276
Shih PM (2015) Photosynthesis and early Earth. Curr Biol 25:R855–R859. https://doi.org/10.1016/J.CUB.2015.04.046
Smedley P, Kinniburgh D (2002) A review of the source, behaviour and distribution of arsenic in natural waters. Appl Geochem 17:517–568. https://doi.org/10.1016/S0883-2927(02)00018-5
Summons RE, Jahnke LL, Hope JM, Logan GA (1999) 2-Methylhopanoids as biomarkers for cyanobacterial oxygenic photosynthesis. Nature 400:554–557. https://doi.org/10.1038/23005
Tawfik DS, Viola RE (2011) Arsenate replacing phosphate: alternative life chemistries and ion promiscuity. Biochemistry 50:1128–1134. https://doi.org/10.1021/bi200002a
Vanden Hoven RN, Santini JM (2004) Arsenite oxidation by the heterotroph Hydrogenophaga sp. str. NT-14: the arsenite oxidase and its physiological electron acceptor. Biochim Biophys Acta Bioenerg 1656:148–155. https://doi.org/10.1016/J.BBABIO.2004.03.001
Visscher P, Farias ME, Contreras M, Novoa-Cortez F, Rasuk MC, Patterson MM et al. (2014) The role of arsenic cycling in carbonate precipitation in microbialites through time. Paper presented at the 2014 Geological Society of America Annual Meeting, Vancouver, 19–22 Oct 2014
Wolfe-Simon F, Davies PCW, Anbar A (2008) Did nature also choose arsenic? Nat Prec. https://doi.org/10.1038/NPRE.2008.1482.1
Zannier F, Portero LR, Ordoñez OF, Martinez LJ, Farías ME, Albarracin VH (2019) Polyextremophilic bacteria from high altitude Andean lakes: arsenic resistance profiles and biofilm production. Biomed Res Int 2019:1–11. https://doi.org/10.1155/2019/1231975
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Saona Acuña, L.A., Soria, M.N., Villafañe, P.G., Stepanenko, T., Farías, M.E. (2020). Arsenic and Its Biological Role: From Early Earth to Current Andean Microbial Ecosystems. In: Farías, M. (eds) Microbial Ecosystems in Central Andes Extreme Environments. Springer, Cham. https://doi.org/10.1007/978-3-030-36192-1_19
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