Diversity and ecology of psychrophilic microorganisms

Prokaryotes: The unseen majority

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Cold-Adapted Enzymes

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Geographic Barriers Isolate Endemic Populations of Hyperthermophilic Archaea

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Psychrophilic microorganisms: challenges for life

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Fungal diversity in the Antarctic active layer

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Antarctic DNA moving forward: genomic plasticity and biotechnological potential

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New insights into the structure and function of the prokaryotic communities colonizing plastic debris collected in King George Island (Antarctica): Preliminary observations from two plastic fragments

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Himalayan Microbiomes for Agro-environmental Sustainability: Current Perspectives and Future Challenges

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Microarray transcriptional profiling of Arctic Mesorhizobium strain N33 at low temperature provides insights into cold adaption strategies

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Cold‐adapted bacteria for bioremediation of crude oil‐contaminated soil

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Alpine headwaters emerging from glaciers and rock glaciers host different bacterial communities: Ecological implications for the future

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Overview of extremophiles and their food and medical applications

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Relative Roles of Deterministic and Stochastic Processes in Driving the Vertical Distribution of Bacterial Communities in a Permafrost Core from the Qinghai-Tibet Plateau, China

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Improvement in extracellular protease production by the marine antarctic yeast Rhodotorula mucilaginosa L7

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Variation with depth of the abundance, diversity and pigmentation of culturable bacteria in a deep ice core from the Yuzhufeng Glacier, Tibetan Plateau

Shen, L., Liu, Y., Wang, N., Jiao, N., Xu, B., & Liu, X. (2017) · Extremophiles · doi:10.1007/s00792-017-0973-8 · Cited by 39

Tolerance to Ultraviolet Radiation of Psychrotolerant Yeasts and Analysis of Their Carotenoid, Mycosporine, and Ergosterol Content

Villarreal, P. D., Carrasco, M., Barahona, S., Alcaı́no, J., Cifuentes, V., & Baeza, M. (2015) · Current Microbiology · doi:10.1007/s00284-015-0928-1 · Cited by 38

Isolation and genome sequencing of four Arctic marine Psychrobacter strains exhibiting multicopper oxidase activity

Moghadam, M. S., Albersmeier, A., Winkler, A., Cimmino, L., Rise, K., Hohmann‐Marriott, M. F., Kalinowski, J., Rückert, C., Wentzel, A., & Lale, R. R. (2016) · BMC Genomics · doi:10.1186/s12864-016-2445-4 · Cited by 38

Cold adaptation of the Antarctic haloarchaea Halohasta litchfieldiae and Halorubrum lacusprofundi

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Manganese-Oxidizing Antarctic Bacteria (Mn-Oxb) Release Reactive Oxygen Species (ROS) as Secondary Mn(II) Oxidation Mechanisms to Avoid Toxicity

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Characterization of amylase produced by cold-adapted bacteria from Antarctic samples

Ottoni, J. R., Silva, T. R. E., de Oliveira, V. M., & Passarini, M. R. Z. (2019) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2019.101452 · Cited by 37

Whole-genome sequencing of the endemic Antarctic fungus Antarctomyces pellizariae reveals an ice-binding protein, a scarce set of secondary metabolites gene clusters and provides insights on Thelebolales phylogeny

Batista, T. M., Hilário, H. O., Mendes, G. A., Moreira, R. G., Furtado, C., de Menezes, G. C. A., Rosa, C. A., Rosa, L. H., & Franco, G. R. (2020) · Genomics · doi:10.1016/j.ygeno.2020.05.004 · Cited by 37

Soil Microbiomes With the Genetic Capacity for Atmospheric Chemosynthesis Are Widespread Across the Poles and Are Associated With Moisture, Carbon, and Nitrogen Limitation

Ray, A. E., Zhang, E., Terauds, A., Ji, M., Kong, W., & Ferrari, B. C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01936 · Cited by 37

Soil freezing-thawing induces immediate shifts in microbial and resource stoichiometry in Luvisol soils along a postmining agricultural chronosequence in Western Germany

Rosinger, C., Clayton, J., Baron, K., & Bonkowski, M. (2021) · Geoderma · doi:10.1016/j.geoderma.2021.115596 · Cited by 36

Amplicon-Metagenomic Analysis of Fungi from Antarctic Terrestrial Habitats

Baeza, M., Barahona, S., Alcaı́no, J., & Cifuentes, V. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02235 · Cited by 37

Cryptic diversity within the choanoflagellate morphospecies complex Codosiga botrytis – Phylogeny and morphology of ancient and modern isolates

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Genetic and biochemical characterization of yeasts isolated from Antarctic soil samples

Białkowska, A. M., Szulczewska, K. M., Krysiak, J. M., Florczak, T., Gromek, E., Kassassir, H., Kur, J., & Turkiewicz, M. (2017) · Polar Biology · doi:10.1007/s00300-017-2102-7 · Cited by 36

High diversity and distinctive community structure of bacteria on glaciers in China revealed by 454 pyrosequencing

Liu, Q. F., Zhou, Y., & Xin, Y. (2015) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2015.09.005 · Cited by 35

Psychrophilic yeasts and their biotechnological applications - A review

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Fate of glacier surface snow‐originating bacteria in the glacier‐fed hydrologic continuums

Liu, K., Liu, Y., Hu, A., Wang, F., Zhang, Z., Yan, Q., Ji, M., & Vick‐Majors, T. J. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15788 · Cited by 35

The microbial diversity, distribution, and ecology of permafrost in China: a review

Hu, W., Zhang, Q., Tian, T., Cheng, G., An, L., & Feng, H. (2015) · Extremophiles · doi:10.1007/s00792-015-0749-y · Cited by 35

Biodegradation of Petroleum Oil in Cold Marine Environments

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Cold Adaptation Mechanisms of a Snow Alga Chlamydomonas nivalis During Temperature Fluctuations

Peng, Z., Liu, G., & Huang, K. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.611080 · Cited by 34

Diversified diazotrophs associated with the rhizosphere of Western Indian Himalayan native red kidney beans (Phaseolus vulgaris L.)

Suyal, D. C., Yadav, A., Shouche, Y. S., & Goel, R. (2014) · 3 Biotech · doi:10.1007/s13205-014-0238-5 · Cited by 34

Cold-Adapted Yeasts: A Lesson from the Cold and a Challenge for the XXI Century

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Psychrotrophic plant beneficial bacteria from the glacial ecosystem of Sikkim Himalaya: Genomic evidence for the cold adaptation and plant growth promotion

Mukhia, S., Kumar, A., V, Kumari, P., & Kumar, R. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127049 · Cited by 38

Microbial abundance and community structure in a melting alpine snowpack

Lazzaro, A., Wismer, A., Schneebeli, M., Erny, I., & Zeyer, J. (2015) · Extremophiles · doi:10.1007/s00792-015-0744-3 · Cited by 34

Microbial diversity and activity in hypersaline high Arctic spring channels

Lay, C.-Y., Mykytczuk, N., Niederberger, T. D., Martineau, C., Greer, C. W., & Whyte, L. G. (2012) · Extremophiles · doi:10.1007/s00792-011-0417-9 · Cited by 32

Evidence of in situ microbial activity and sulphidogenesis in perennially sub-0 °C and hypersaline sediments of a high Arctic permafrost spring

Lamarche‐Gagnon, G., Comery, R., Greer, C. W., & Whyte, L. G. (2014) · Extremophiles · doi:10.1007/s00792-014-0703-4 · Cited by 34

Identification and characterization of yeasts isolated from the South Shetland Islands and the Antarctic Peninsula

Troncoso, E., Barahona, S., Carrasco, M., Villarreal, P. D., Alcaı́no, J., Cifuentes, V., & Baeza, M. (2016) · Polar Biology · doi:10.1007/s00300-016-1988-9 · Cited by 32

Species interactions and distinct microbial communities in high Arctic permafrost affected cryosols are associated with the CH 4 and CO 2 gas fluxes

Altshuler, I., Hamel, J., Turney, S., Magnuson, E., Lévesque, R. C., Greer, C. W., & Whyte, L. G. (2019) · Environmental Microbiology · doi:10.1111/1462-2920.14715 · Cited by 33

Bacterial community structure of a glacio-marine system in the Arctic (Ny-Ålesund, Svalbard)

Thomas, F. A., Sinha, R. K., & Krishnan, K. P. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.135264 · Cited by 32

Cryptococcus vaughanmartiniae sp. nov. and Cryptococcus onofrii sp. nov.: two new species isolated from worldwide cold environments

Turchetti, B., Selbmann, L., Blanchette, R. A., Mauro, S. D., Marchegiani, E., Zucconi, L., Arenz, B. E., & Buzzini, P. (2014) · Extremophiles · doi:10.1007/s00792-014-0692-3 · Cited by 32

The gut microbiota facilitate their host tolerance to extreme temperatures

Wang, Z., Wu, Y., Li, X., Ji, X., & Liu, W. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03277-6 · Cited by 35

Lipidomic analysis of psychrophilic yeasts cultivated at different temperatures

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Isolation and characterization of fast‐growing green snow bacteria from coastal East Antarctica

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A thin ice layer segregates two distinct fungal communities in Antarctic brines from Tarn Flat (Northern Victoria Land)

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Hibernation Leads to Altered Gut Communities in Bumblebee Queens (Bombus terrestris)

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Potential feedback mediated by soil microbiome response to warming in a glacier forefield

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Bacterial Diversity and Communities Structural Dynamics in Soil and Meltwater Runoff at the Frontier of Baishui Glacier No.1, China

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Antarctic psychrophiles: models for understanding the molecular basis of survival at low temperature and responses to climate change

Verde, C., di Prisco, G., Giordano, D., Russo, R., Anderson, D. E., & Cowan, D. A. (2012) · Biodiversity · doi:10.1080/14888386.2012.706703 · Cited by 29

Biohydrogen production using psychrophilic bacteria isolated from Antarctica

Alvarado-Cuevas, Z. D., Lopez-Hidalgo, A. M., Ordóñez, L. G., Oceguera-Contreras, E., Ornelas-Salas, J. T., & León‐Rodríguez, A. D. (2014) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2014.10.063 · Cited by 29

Microbial distribution and turnover in Antarctic microbial mats highlight the relevance of heterotrophic bacteria in low-nutrient environments

Valdespino-Castillo, P. M., Cerqueda‐García, D., Espinosa, A. C., Batista, S. B., Ibarra, M. M., Taş, N., Alcántara‐Hernández, R., & Falcón, L. I. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy129 · Cited by 29

Fungi in perennial ice from Scărișoara Ice Cave (Romania)

Brad, T., Iţcuş, C., Pascu, M.-D., Perşoiu, A., Hillebrand‐Voiculescu, A., Iancu, L., & Purcărea, C. (2018) · Scientific Reports · doi:10.1038/s41598-018-28401-1 · Cited by 29

Isolation of oligotrophic yeasts from supraglacial environments of different altitude on the Gulkana Glacier (Alaska)

Uetake, J., Yoshimura, Y., Nagatsuka, N., & Kanda, H. (2012) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2012.01323.x · Cited by 29

Soil microbial legacies influence freeze–thaw responses of soil

Pastore, M. A., Classen, A. T., English, M., Frey, S. D., Knorr, M. A., Rand, K., & Adair, E. C. (2023) · Functional Ecology · doi:10.1111/1365-2435.14273 · Cited by 28

Diversity of cultured bacteria from the perennial ice block of Scarisoara Ice Cave, Romania

Iţcuş, C., Pascu, M.-D., Brad, T., Perşoiu, A., & Purcărea, C. (2016) · International Journal of Speleology · doi:10.5038/1827-806x.45.1.1948 · Cited by 28

Characterization of a temperature-responsive two component regulatory system from the Antarctic archaeon, Methanococcoides burtonii

Najnin, T., Siddiqui, K. S., Taha, Elkaid, N., Kornfeld, G., Curmi, P. M. G., & Cavicchioli, R. (2016) · Scientific Reports · doi:10.1038/srep24278 · Cited by 28

Psychrophiles and Psychrotrophs

Moyer, C. L., Collins, R. E., & Morita, R. Y. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.02282-2 · Cited by 28

Extremophiles: Cold Environments

Deming, J. W. (2009) · Elsevier eBooks · doi:10.1016/b978-012373944-5.00280-7 · Cited by 28

Comparison of Bacterial and Fungal Composition and Their Chemical Interaction in Free Tropospheric Air and Snow Over an Entire Winter Season at Mount Sonnblick, Austria

Els, N., Greilinger, M., Reisecker, M., Tignat‐Perrier, R., Baumann‐Stanzer, K., Kasper‐Giebl, A., Sattler, B. I., & Larose, C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00980 · Cited by 27

Eco-evolutionary feedbacks mediated by bacterial membrane vesicles

Zlatkov, N., Nadeem, A., Uhlin, B. E., & Wai, S. N. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa047 · Cited by 28

Unique genomic traits for cold adaptation inNaganishia vishniacii, a polyextremophile yeast isolated from Antarctica

Nizovoy, P., Bellora, N., Haridas, S., Sun, H., Daum, C. G., Barry, K., Grigoriev, I. V., Libkind, D., Connell, L. B., & Moliné, M. (2020) · FEMS Yeast Research · doi:10.1093/femsyr/foaa056 · Cited by 32

Novel cold temperature active β-glucosidase from Pseudomonas lutea BG8 suitable for simultaneous saccharification and fermentation

Tiwari, R., Singh, S., Shukla, P., & Nain, L. (2014) · RSC Advances · doi:10.1039/c4ra09784j · Cited by 27

Nutrient Cycling at Higher Altitudes

Packialakshmi, J. S., Dash, B., Singh, A. K., Suyal, D. C., & Soni, R. (2020) · Rhizosphere biology · doi:10.1007/978-981-15-1902-4_15 · Cited by 26

Fighting plant pathogens with cold-active microorganisms: biopesticide development and agriculture intensification in cold climates

Torracchi-Carrasco, E., Morel, M. A., Tapia‐Vázquez, I., Castro‐Sowinski, S., Batista‐García, R. A., & Yarzábal, L. A. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10812-8 · Cited by 26

Archaeal Distribution in Moonmilk Deposits from Alpine Caves and Their Ecophysiological Potential

Reitschuler, C., Spötl, C., Hofmann, K., Wagner, A. O., & Illmer, P. (2016) · Microbial Ecology · doi:10.1007/s00248-015-0727-z · Cited by 26

Resource capture and competitive ability of non-pathogenic Pseudogymnoascus spp. and P. destructans, the cause of white-nose syndrome in bats

Wilson, M. B., Held, B. W., Freiborg, A. H., Blanchette, R. A., & Salomon, C. E. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178968 · Cited by 25

Psychrophilic endophytic fungi with biological activity inhabit Cupressaceae plant family

Moghaddam, M. S. H., & Soltani, J. (2014) · Symbiosis · doi:10.1007/s13199-014-0290-2 · Cited by 25

Unusual Lipid A from a Cold‐Adapted Bacterium: Detailed Structural Characterization

Casillo, A., Ziaco, M., Lindner, B., Parrilli, E., Schwudke, D., Holgado, A., Verstrepen, L., Sannino, F., Beyaert, R., Lanzetta, R., et al. (2017) · ChemBioChem · doi:10.1002/cbic.201700287 · Cited by 24

Culturable bacteria isolated from seven high-altitude ice cores on the Tibetan Plateau

Liu, Y., Priscu, J. C., Yao, T., Vick‐Majors, T. J., Michaud, A. B., & Sheng, L. (2018) · Journal of Glaciology · doi:10.1017/jog.2018.86 · Cited by 24

Geochemistry and Bacterial Recovery from Hindu Kush Range Glacier and Their Potential for Metal Resistance and Antibiotic Production

Rafiq, M., Hayat, M., Zada, S., Sajjad, W., Hassan, N., & Hasan, F. (2019) · Geomicrobiology Journal · doi:10.1080/01490451.2018.1551947 · Cited by 24

Bacteria recovered from a high-altitude, tropical glacier in Venezuelan Andes

Ball, M. M., Gómez, W., Magallanes, X., Rosales, R., Melfo, A., & Yarzábal, L. A. (2013) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-013-1511-1 · Cited by 24

Geochemical and Microbiological Studies of Nitrous Oxide Variations within the New NEEM Greenland Ice Core during the Last Glacial Period

Miteva, V. I., Sowers, T., Schüpbach, S., Fischer, H., & Brenchley, J. E. (2015) · Geomicrobiology Journal · doi:10.1080/01490451.2015.1074321 · Cited by 24

Characterization of the prokaryotic diversity through a stratigraphic permafrost core profile from the Qinghai-Tibet Plateau

Hu, W., Zhang, Q., Tian, T., Li, D., Cheng, G., Mu, J., Wu, Q., Niu, F., An, L., & Feng, H. (2016) · Extremophiles · doi:10.1007/s00792-016-0825-y · Cited by 24

Prokaryotic assemblages within permafrost active layer at Edmonson Point (Northern Victoria Land, Antarctica)

Papale, M., Conte, A., Mikkonen, A., Michaud, L., Ferla, R. L., Azzaro, M., Caruso, G., Paranhos, R., Anderson, S. C., Maimone, G., et al. (2018) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2018.05.004 · Cited by 24

Adaptation Mechanisms and Applications of Psychrophilic Fungi

Rafiq, M., Hassan, N., Rehman, M., & Hasan, F. (2019) · Springer eBooks · doi:10.1007/978-3-030-19030-9_9 · Cited by 25

Characterization of heavy metals resistant heterotrophic bacteria from soils in the Windmill Islands region, Wilkes Land, East Antarctica

Tomova, I., Stoilova-Disheva, M. M., & Vasileva−Tonkova, E. (2014) · Polish Polar Research · doi:10.2478/popore-2014-0028 · Cited by 24

Distribution of CO2 fixation and acetate mineralization pathways in microorganisms from extremophilic anaerobic biotopes

Montoya, L., Celis, L. B., Razo‐Flores, E., & Alpuche-Solis, A. G. (2012) · Extremophiles · doi:10.1007/s00792-012-0487-3 · Cited by 26

Genomic and physiological characterization and description of Marinobacter gelidimuriae sp. nov., a psychrophilic, moderate halophile from Blood Falls, an antarctic subglacial brine

Chua, M. J., Campen, R., Wahl, L., Grzymski, J. J., & Mikucki, J. A. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy021 · Cited by 23

Soil age and soil organic carbon content shape biochemical responses to multiple freeze–thaw events in soils along a postmining agricultural chronosequence

Rosinger, C., & Bonkowski, M. (2021) · Biogeochemistry · doi:10.1007/s10533-021-00816-5 · Cited by 23

Biotechnological potential of microorganisms from textile effluent: isolation, enzymatic activity and dye discoloration

Bernal, S. P. F., LIRA, M. M. A., Jean-Baptiste, J., Garcia, P. E., Batista, E., Ottoni, J. R., & Passarini, M. R. Z. (2021) · Anais da Academia Brasileira de Ciências · doi:10.1590/0001-3765202120191581 · Cited by 23

Yeasts in Nonpolar Cold Habitats

Sannino, C., Tasselli, G., Filippucci, S., Turchetti, B., & Buzzini, P. (2017) · Springer eBooks · doi:10.1007/978-3-319-62683-3_12 · Cited by 23

Structural analyses of adenylate kinases from Antarctic and tropical fishes for understanding cold adaptation of enzymes

Moon, S., Kim, J., & Bae, E. (2017) · Scientific Reports · doi:10.1038/s41598-017-16266-9 · Cited by 23

Cystobasidium alpinum sp. nov. and Rhodosporidiobolus oreadorum sp. nov. from European Cold Environments and Arctic Region

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Subsurface In Situ Detection of Microbes and Diverse Organic Matter Hotspots in the Greenland Ice Sheet

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Biodiversity, Ecological, and Commercial Importance of Psychrophilic Microorganisms

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