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Genomics of an extreme psychrophile, Psychromonas ingrahamii
Open accessAbstract
BACKGROUND: The genome sequence of the sea-ice bacterium Psychromonas ingrahamii 37, which grows exponentially at -12C, may reveal features that help to explain how this extreme psychrophile is able to grow at such low temperatures. Determination of the whole genome sequence allows comparison with genes of other psychrophiles and mesophiles. RESULTS: Correspondence analysis of the composition of all P. ingrahamii proteins showed that (1) there are 6 classes of proteins, at least one more than other bacteria, (2) integral inner membrane proteins are not sharply separated from bulk proteins suggesting that, overall, they may have a lower hydrophobic character, and (3) there is strong opposition between asparagine and the oxygen-sensitive amino acids methionine, arginine, cysteine and histidine and (4) one of the previously unseen clusters of proteins has a high proportion of "orphan" hypothetical proteins, raising the possibility these are cold-specific proteins. Based on annotation of proteins by sequence similarity, (1) P. ingrahamii has a large number (61) of regulators of cyclic GDP, suggesting that this bacterium produces an extracellular polysaccharide that may help sequester water or lower the freezing point in the vicinity of the cell. (2) P. ingrahamii has genes for production of the osmolyte, betaine choline, which may balance the osmotic pressure as sea ice freezes. (3) P. ingrahamii has a large number (11) of three-subunit TRAP systems that may play an important role in the transport of nutrients into the cell at low temperatures. (4) Chaperones and stress proteins may play a critical role in transforming nascent polypeptides into 3-dimensional configurations that permit low temperature growth. (5) Metabolic properties of P. ingrahamii were deduced. Finally, a few small sets of proteins of unknown function which may play a role in psychrophily have been singled out as worthy of future study. CONCLUSION: The results of this genomic analysis provide a springboard for further investigations into mechanisms of psychrophily. Focus on the role of asparagine excess in proteins, targeted phenotypic characterizations and gene expression investigations are needed to ascertain if and how the organism regulates various proteins in response to growth at lower temperatures.
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Cites
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy AssessmentPreprint
Ewing, B., Hillier, L., Wendl, M. C., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.175 · Cited by 6,993
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
Ewing, B., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.186 · Cited by 5,439
Atlas of protein sequence and structure
Chang, M.-Y., Dayhoff, M. O., Eck, R. V., & Sochard, M. R. (1965) · NASA Technical Reports Server (NASA) · Cited by 4,383
Consed: a graphical tool for sequence finishing.Preprint
Gordon, D., Abajian, C., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.195 · Cited by 3,706
National Center for Biotechnology Information
Gressner, A. M., & Arndt, T. (2019) · Springer Reference Medizin · doi:10.1007/978-3-662-48986-4_301184 · Cited by 1,412
rRNA Operon Copy Number Reflects Ecological Strategies of Bacteria
Klappenbach, J. A., Dunbar, J., & Schmidt, T. M. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.4.1328-1333.2000 · Cited by 1,140
Siddiqui, K. S., & Cavicchioli, R. (2006) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.75.103004.142723 · Cited by 899
Quorum sensing controls biofilm formation in Vibrio cholerae
Hammer, B. K., & Bassler, B. L. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03688.x · Cited by 888
Correspondence Analysis: A Neglected Multivariate Method
Hill, M. O. (1974) · Journal of the Royal Statistical Society Series C (Applied Statistics) · doi:10.2307/2347127 · Cited by 830
Amino acid substitution matrices from an information theoretic perspective
Altschul, S. F. (1991) · Journal of Molecular Biology · doi:10.1016/0022-2836(91)90193-a · Cited by 630
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Margesin, R., & Miteva, V. (2011) · Research in Microbiology · doi:10.1016/j.resmic.2010.12.004 · Cited by 518
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Mykytczuk, N., Foote, S. J., Omelon, C. R., Southam, G., Greer, C. W., & Whyte, L. G. (2013) · The ISME Journal · doi:10.1038/ismej.2013.8 · Cited by 327
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Zhou, J., Lyu, Y., Richlen, M. L., Anderson, D. M., & Cai, Z. (2016) · Critical Reviews in Plant Sciences · doi:10.1080/07352689.2016.1172461 · Cited by 217
Ayala-del-Rı́o, H. L., Chain, P., Grzymski, J. J., Ponder, M. A., Ivanova, N., Bergholz, P. W., Bartolo, G. D., Hauser, L., Land, M., Bakermans, C., et al. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.02101-09 · Cited by 193
Self-citationVarin, T. V., Lovejoy, C., Jungblut, A. D., Vincent, W. F., & Corbeil, J. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.06354-11 · Cited by 179
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Allen, M. A., Lauro, F. M., Williams, T. J., Burg, D. W., Siddiqui, K. S., Francisci, D. D., Chong, K., Pilak, O., Chew, H. H., DeMaere, M. Z., et al. (2009) · The ISME Journal · doi:10.1038/ismej.2009.45 · Cited by 166
Self-citationRodrigues, D. F., Ivanova, N., He, Z., Huebner, M., Zhou, J. Z., & Tiedje, J. M. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-547 · Cited by 147
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Akindolire, M. A., Rama, H., & Roopnarain, A. (2022) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2022.112394 · Cited by 107
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Piette, F., D’Amico, S., Struvay, C., Mazzucchelli, G., Renaut, J., Tutino, M. L., Danchin, A., Leprince, P., & Feller, G. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07084.x · Cited by 95
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Lauritano, C., Rizzo, C., Giudice, A. L., & Saggiomo, M. (2020) · Microorganisms · doi:10.3390/microorganisms8121957 · Cited by 84
Qin, Q., Xie, B., Yu, Y., Shu, Y., Rong, J., Zhang, Y., Zhao, D., Chen, X., Zhang, X., Chen, B., et al. (2013) · Environmental Microbiology · doi:10.1111/1462-2920.12318 · Cited by 75
Mocali, S., Chiellini, C., Fabiani, A., Decuzzi, S., de Pascale, D., Parrilli, E., Tutino, M. L., Perrin, E., Bosi, E., Fondi, M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-00876-4 · Cited by 75
Shi, F., Powell, S. M., Wilson, R., & Bowman, J. P. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evt209 · Cited by 71
Firdaus‐Raih, M., Hashim, N. H. F., Bharudin, I., Bakar, M. F. A., Huang, K. K., Alias, H., Lee, B. K. B., Isa, M. N. M., Mat-Sharani, S., Sulaiman, S., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0189947 · Cited by 69
Pacchioni, R. G., de Carvalho, F. M., Thompson, C. E., Faustino, A. L. F., Nicolini, F., Pereira, T. D. S., Silva-Portela, R. D. C. B., Cantão, M. E., Gerber, A. L., de Vasconcelos, A. T. R., et al. (2014) · MicrobiologyOpen · doi:10.1002/mbo3.169 · Cited by 63
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He, L., Zhang, P.-W., Huang, J., Zhu, F.-C., Danchin, A., & Wang, Y. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01965-17 · Cited by 58
Self-citationDanchin, A., Ouzounis, C., Tokuyasu, T., & Zucker, J. (2018) · Microbial Biotechnology · doi:10.1111/1751-7915.13284 · Cited by 56
Self-citationVincent, A. T., Trudel, M. V., Freschi, L., Nagar, V., Gagné-Thivierge, C., Lévesque, R. C., & Charette, S. J. (2016) · BMC Genomics · doi:10.1186/s12864-016-2381-3 · Cited by 55
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Hoffmann, K., Hassenrück, C., Salman-Carvalho, V., Holtappels, M., & Bienhold, C. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00266 · Cited by 54
Kumar, R., Acharya, V., Mukhia, S., Singh, D. P., & Kumar, S. (2018) · Genomics · doi:10.1016/j.ygeno.2018.03.008 · Cited by 50
Liu, Q. F., Liu, H., Zhou, Y., & Xin, Y. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01069 · Cited by 49
Fuchs, T. M., Neuhaus, K., & Scherer, S. (2013) · Springer eBooks · doi:10.1007/978-3-642-30123-0_56 · Cited by 48
Aliyu, H., Maayer, P. D., & Cowan, D. A. (2016) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiw032 · Cited by 47
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Scott, K. M., Williams, J. T., Porter, C. M. B., Russel, S., Harmer, T. L., Paul, J. H., Antonen, K., Bridges, M. K., Camper, G. J., Campla, C. K., et al. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14090 · Cited by 41
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Self-citationBowman, J. S. (2015) · Elementa Science of the Anthropocene · doi:10.12952/journal.elementa.000072 · Cited by 39
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Espinola, F. J., Dionisi, H. M., Borglin, S. E., Brislawn, C., Jansson, J. K., Cormack, W. P. M., Carroll, J., Sjöling, S., & Lozada, M. (2017) · Microbial Ecology · doi:10.1007/s00248-017-1028-5 · Cited by 36
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Carrier, T. J., & Reitzel, A. M. (2019) · Marine Ecology Progress Series · doi:10.3354/meps12872 · Cited by 33
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Novak, H. R., Sayer, C., Panning, J., & Littlechild, J. A. (2013) · Marine Biotechnology · doi:10.1007/s10126-013-9522-3 · Cited by 31
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Shen, L., Liu, Y., Xu, B., Wang, N., Zhao, H., Liu, X., & Liu, F. (2017) · Scientific Reports · doi:10.1038/s41598-017-02191-4 · Cited by 32
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Auman, A. J., Breezee, J. L., Gosink, J. J., Schümann, P., Barnes, C. R., Kämpfer, P., & Staley, J. T. (2009) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.007773-0 · Cited by 28
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Bharudin, I., Bakar, M. F. A., Hashim, N. H. F., Isa, M. N. M., Alias, H., Firdaus‐Raih, M., Illias, R. M., Najimudin, N., Mahadi, N. M., Bakar, F. D. A., et al. (2018) · Marine Environmental Research · doi:10.1016/j.marenvres.2018.03.007 · Cited by 26
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Kahlke, T., & Thorvaldsen, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051761 · Cited by 25
Possmayer, M., Berardi, G., Beall, B. F. N., Trick, C. G., Hüner, N. P. A., & Maxwell, D. P. (2011) · Journal of Phycology · doi:10.1111/j.1529-8817.2011.01047.x · Cited by 24
Baker, J. M., Riester, C., Skinner, B., Newell, A., Swingley, W. D., Madigan, M. T., Jung, D. O., Asao, M., Chen, M., Loughlin, P. C., et al. (2017) · Microorganisms · doi:10.3390/microorganisms5010008 · Cited by 23
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
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Arias, P. M., Butler, J., Randhawa, G. S., Soltysiak, M. P. M., Hill, K. A., & Lila Kari, A. (2023) · Scientific Reports · doi:10.1038/s41598-023-42518-y · Cited by 22
Bowman, J. P. (2013) · Springer eBooks · doi:10.1007/978-3-642-30123-0_46 · Cited by 22
Diversity of Psychrophilic Bacteria from Sea Ice - and Glacial Ice Communities
Junge, K., Christner, B. C., & Staley, J. T. (2010) · Springer eBooks · doi:10.1007/978-4-431-53898-1_39 · Cited by 22
Self-citationRusso, R., Giordano, D., Riccio, A., di Prisco, G., & Verde, C. (2010) · Marine Genomics · doi:10.1016/j.margen.2010.09.001 · Cited by 22
Perfumo, A., Elsaesser, A., Littmann, S., Foster, R. A., Kuypers, M. M. M., Cockell, C. S., & Kminek, G. (2014) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12443 · Cited by 21
Junge, K., Cameron, K. A., & Nunn, B. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814849-5.00012-5 · Cited by 20
Cross-tolerance between osmotic and freeze-thaw stress in microbial assemblages from temperate lakes
Wilson, S. L., Frazer, C., Cumming, B. F., Nuin, P. A. S., & Walker, V. K. (2012) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2012.01404.x · Cited by 19
Growth and Metabolism of Extremophilic Microorganisms
Tse, C., & Ma, K. (2016) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-319-13521-2_1 · Cited by 19
Characterizing the surface-exposed proteome of Planococcus halocryophilus during cryophilic growth
Ronholm, J., Raymond‐Bouchard, I., Creskey, M., Cyr, T. D., Cloutis, E. A., & Whyte, L. G. (2015) · Extremophiles · doi:10.1007/s00792-015-0743-4 · Cited by 19
Chiu, L., Wang, M., Tseng, K.-Y., Wei, C., Lin, H., Yang, S., & Tseng, Y. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.976255 · Cited by 17
Psychrophiles: Genetics, Genomics, Evolution
Lauro, F. M., Allen, M. A., Wilkins, D. E., Williams, T. J., & Cavicchioli, R. (2010) · Springer eBooks · doi:10.1007/978-4-431-53898-1_42 · Cited by 16
Giordano, D., Coppola, D., Russo, R., Tinajero‐Trejo, M., di Prisco, G., Lauro, F. M., Ascenzi, P., & Verde, C. (2013) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-407693-8.00008-x · Cited by 15
Román, E. A., Faraj, S. E., Cousido-Siah, A., Mitschler, A., PODJARNY, A. D., & Santos, J. (2013) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2013.02.015 · Cited by 15
Mohanty, A., Shilpa, S., & Meena, S. S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90274-8.00009-5 · Cited by 14
Nowak, M., Olszewski, M., Śpibida, M., & Kur, J. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-91 · Cited by 14
Complete Genome Sequence of the Deep-Sea Bacterium Psychromonas Strain CNPT3
Lauro, F. M., Stratton, T. K., Chastain, R. A., Ferriera, S., Johnson, J. H., Goldberg, S. M. D., Yayanos, A. A., & Bartlett, D. H. (2013) · Genome Announcements · doi:10.1128/genomea.00304-13 · Cited by 14
Maciejewska, N., Walkusz, R., Olszewski, M., & Szymańska, A. (2018) · Molecular Biotechnology · doi:10.1007/s12033-018-0142-z · Cited by 14
Psychrophilic Microorganisms in Alpine Soils
Margesin, R. (2011) · Springer eBooks · doi:10.1007/978-3-7091-0136-0_14 · Cited by 14
Psychrophilic microorganisms as important source for biotechnological processes
Fendrihan, S., & Negoiţă, T. G. (2012) · Springer eBooks · doi:10.1007/978-3-211-99691-1_7 · Cited by 13
Baeza, M., Zúñiga, S., Peragallo, V., Barahona, S., Alcaı́no, J., & Cifuentes, V. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.623171 · Cited by 12
Response to Cold: A Comparative Transcriptomic Analysis in Eight Cold-Adapted Yeasts
Baeza, M., Zúñiga, S., Peragallo, V., Gutierrez, F., Barahona, S., Alcaı́no, J., & Cifuentes, V. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.828536 · Cited by 12
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Noguera, M. E., Román, E. A., Rigal, J. B., Cousido-Siah, A., Mitschler, A., PODJARNY, A. D., & Santos, J. (2015) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-015-1251-9 · Cited by 11
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Abbamondi, G. R., Kambourova, M. S., Poli, A., Finore, I., & Nicolaus, B. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814905-8.00004-6 · Cited by 11
Differential expression of catalases in Vibrio parahaemolyticus under various stress conditions
Lin, L., Lin, G.-H., Wang, Z., Tseng, Y.-H., & Yu, M.-S. (2015) · Research in Microbiology · doi:10.1016/j.resmic.2015.07.001 · Cited by 11
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Turchetti, B., Buzzini, P., & Baeza, M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1026102 · Cited by 10
Wu, Z., Yu, X., Fu, Y., Guo, J., Pan, M., Guo, Y., Liu, J., Mai, K., & Zhang, W. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.739871 · Cited by 10
NADP+-dependent isocitrate dehydrogenase from a psychrophilic bacterium, Psychromonas marina
Hirota, R., Tsubouchi, K., & Takada, Y. (2017) · Extremophiles · doi:10.1007/s00792-017-0936-0 · Cited by 10
Temperature‐Dependent Molecular Adaptations, Microbial Proteins
Kumar, S., Singh, S. K., & Gromiha, M. M. (2010) · Wiley eBooks · doi:10.1002/9780470054581.eib516 · Cited by 9
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García-Descalzo, L., Alcázar, A., Baquero, F., & Cid, C. (2012) · Extremophiles · doi:10.1002/9781118394144.ch6 · Cited by 9
Life in icy habitats: new insights supporting panspermia theory
Parrilli, E., Sannino, F., Marino, G., & Tutino, M. L. (2011) · RENDICONTI LINCEI · doi:10.1007/s12210-011-0136-2 · Cited by 8
Miyazaki, M., & Nogi, Y. (2014) · Springer eBooks · doi:10.1007/978-3-642-38922-1_228 · Cited by 8
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Metadata
- Authors
- Riley, M., Staley, J. T., Danchin, A., Wang, T. Z., Brettin, T. S., Hauser, L. J., Land, M. L., & Thompson, L. S.
- Affiliations
- Marine Biological Laboratory (US)
- University of Washington (US)
- Centre National de la Recherche Scientifique (FR)
- Los Alamos National Laboratory (US)
- Oak Ridge National Laboratory (US)
- Corresponding author
- Riley, Monica
- Venue
- BMC Genomics
- Published
- 2008
- Volume
- 9
- Issue
- 1
- Pages
- 210
- ISSN
- 1471-2164 (ISSN-L)
- PMC
- PMC2405808
- OpenAlex
- W1970019238
- Cited by
- 126
- References
- 39
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 2 · 2023: 3 · 2022: 7 · 2021: 8 · 2020: 2 · 2019: 5 · 2018: 9 · 2017: 12 · 2016: 7 · 2015: 6 · 2014: 10 · 2013: 12 · 2012: 11
- FWCI
- 7.79
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- BMC Genomics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Open Access Server of the Woods Hole Scientific Community (Woods Hole Scientific Community) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- National Science Foundation (DEAC02-05CH11231, DEAC05- 00OR22725, 00OR22725, W-7405-ENG-36)
- U.S. Department of Energy (-AC02-05CH11231, AC05-00OR22725, W-7405, Contract No. DE-AC02-05-CH11231, DE--AC05--00OR22725, DE‐FG02‐, DE-AC05?, Contract No. DE-AC05-00OR22725, 05CH11231, FG02-04ER63940, No. DE-AC02-05-CH11231, DE AC02 05CH11231, -7405-ENG-48, W‐7405‐ENG‐48, No. DE-AC05-00OR22725, W-7405-ENG-36, 00OR22725, DE-AC02-)
- National Aeronautics and Space Administration (DE-AC02-05CH11231, DE-AC05-00OR22725)
- University of Washington
- European Commission (DE-AC05-00OR22725, DE-AC02-05CH11231)
- Office of Science (DEAC05- 00OR22725, No. DE-AC02- 05-CH11231, No. DE-AC05-00OR22725, DEAC02–05CH11231, AC02-05CH11231, DE-AC02, 05CH11231, Contract No. DE-AC02-05CH11231, AC05-00OR22725)
- Biological and Environmental Research (W-7405-Eng-48, 05CH11231, No. DE-AC02-05CH11231, DE-AC02 − 05CH11231, 00OR22725, Contract No. DE-AC02-05CH11231, DE‐AC05–00OR22725, AC02-05CH11231)
- Lawrence Livermore National Laboratory (W-7405-ENG 48, -7405-Eng-48, DE-AC05-00OR22725, W-7405-ENG-36, W-7405-ENG, DE-AC02-05CH11231)
- Oak Ridge National Laboratory (AC05-00OR22725, Contract No. DE-AC05-00OR22725, DE-AC0205CH11231, DE-AC05-00OR22725)
- Lawrence Berkeley National Laboratory (AC02‐05CH11231, DE-AC02-05CH11231, No. DE-AC02-05CH11231, DE-AC05-00OR22725, Contract No. DE-AC02-05CH11231, 05CH11231)
- Los Alamos National Laboratory (W‐7405‐ENG‐36, DE-AC05-00OR22725, W-7405-Eng-48, DE-AC02-05CH11231)
- Topics
- Physical Sciences › Environmental Science › Ecology › Polar Research and Ecology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- sea ice bacteria, cold adaptation, protein composition, exopolysaccharides, osmolytes, nutrient transport, molecular chaperones, stress proteins, genome annotation
- MeSH terms
- Amino Acids, Bacterial Proteins, Base Composition, Cold Climate, DNA, Bacterial, Energy Metabolism, Fatty Acids, Genes, Bacterial, Multigene Family, Glucose, Heat-Shock Proteins, Ice, Molecular Weight, Seawater, Genome, Bacterial, Molecular Chaperones, Gammaproteobacteria, GC Rich Sequence, Genomics
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