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Isolation, characterization and optimization of EPSs produced by a cold-adapted Marinobacter isolate from Antarctic seawater

Published online by Cambridge University Press:  18 March 2019

Consolazione Caruso
Affiliation:
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy
Carmen Rizzo
Affiliation:
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy
Santina Mangano
Affiliation:
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy
Annarita Poli
Affiliation:
Institute of Biomolecular Chemistry, National Research Council (ICB-CNR), Pozzuoli (NA), Italy
Paola Di Donato
Affiliation:
Institute of Biomolecular Chemistry, National Research Council (ICB-CNR), Pozzuoli (NA), Italy Department of Science and Technology, University of Naples Parthenope – Centro Direzionale, Isola C4, 80143 Napoli, Italy
Barbara Nicolaus
Affiliation:
Institute of Biomolecular Chemistry, National Research Council (ICB-CNR), Pozzuoli (NA), Italy
Ilaria Finore
Affiliation:
Institute of Biomolecular Chemistry, National Research Council (ICB-CNR), Pozzuoli (NA), Italy
Gaetano Di Marco
Affiliation:
Institute for Chemical-Physical Processes, National Research Council (IPCF-CNR), Messina, Italy
Luigi Michaud
Affiliation:
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy
Angelina Lo Giudice*
Affiliation:
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy Institute for the Biological Resources and Marine Biotechnologies National Research Council (IRBIM-CNR), Messina, Italy

Abstract

Marinobacter sp. W1-16 from Antarctic surface seawater was analysed for the production of extracellular polymeric substances (EPSs). Enhancement of the EPS biosynthesis was carried out by evaluating the influences of the carbon source (type and concentration), temperature, pH and salinity. EPS yields varied strongly depending on sugar substrate and temperature, while pH and salinity did not strongly affect levels of EPS production. Marinobacter sp. W1-16 produced the highest quantity of EPSs when growing at 15°C and pH 8, in the presence of 2% glucose and 3% NaCl. The EPS chemical characterization revealed a molecular weight of about 260 kDa. Colorimetric assays determined a higher quantity of carbohydrate than of proteins and uronic acids, as well as the presence of sulphate, in the extracted EPSs. The monosaccharidic composition resulted in Glc:Man:Gal:GalN:GalA:GlcA in relative molar proportions of 1:0.9:0.2:0.1:0.1:0.01. Some biotechnological potentialities (i.e. emulsifying and cryoprotective actions, and heavy metal binding properties) of the EPSs were proved, suggesting possible industrial and bioremediation applications.

Type
Biological Sciences
Copyright
Copyright © Antarctic Science Ltd 2019 

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Footnotes

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Posthumous

References

Arias, S., Moral, A.D., Ferrer, M.R., Tallon, R., Quesada, E. & Bejar, V. 2003. Mauran, an exopolysaccharide produced by the halophilic bacterium Halomonas maura, with a novel composition and interesting properties for biotechnology. Extremophiles, 7, 319326.Google Scholar
Banat, I.M., Makkar, R.S. & Cameotra, S.S. 2000. Potential commercial applications of microbial surfactants. Applied Microbiology and Biotechnology, 53, 495508.Google Scholar
Bargagli, R., Nelli, L., Ancora, S. & Focardi, S. 1996. Elevated cadmium accumulation in marine organisms from Terra Nova Bay (Antarctica). Polar Biology, 16, 513520.Google Scholar
Bhaskar, P. & Bhosle, N.B. 2006. Bacterial extracellular polymeric substance (EPS): a carrier of heavy metals in the marine food-chain, Environment International, 32, 191198.Google Scholar
Carrion, O., Delgado, L. & Mercade, E. 2015. New emulsifying and cryoprotective exopolysaccharides from Antarctic Pseudomonas sp. ID1. Carbohydrate Polymers, 117, 10281034.Google Scholar
Caruso, C., Rizzo, C., Mangano, S., Poli, A., Di Donato, P., Finore, I. et al. 2018a. Production and biotechnological potential of extracellular polymeric substances from sponge-associated Antarctic bacteria. Applied and Environmental Microbiology, 84, e01624-17.Google Scholar
Caruso, C., Rizzo, C., Mangano, S., Poli, A., Di Donato, P., Nicolaus, B., et al. 2018b. Extracellular polymeric substances with metal adsorption capacity produced by Pseudoalteromonas sp. MER144 from Antarctic seawater. Environmental Science and Pollution Research, 25, 46674677.Google Scholar
Chua, M.J., Campen, R.L., Wahl, L., Grzymski, J.J. & Mikucki, J.A. 2018. Genomic and physiological characterization and description of Marinobacter gelidimuriae sp. nov., a psychrophilic, moderate halophile from Blood Falls, an Antarctic subglacial brine. FEMS Microbiology Ecology, 1, 94, 10.1093/femsec/fiy021.Google Scholar
Costa, O.Y.A., Raaijmakers, J.M. & Kuramae, E.E. 2018. Microbial extracellular polymeric substances: ecological function and impact on soil aggregation. Frontiers in Microbiology, 9, 10.3389/fmicb.2018.01636.Google Scholar
Filisetti-Cozzi, T.M.C.C. & Carpita, N.C. 1991. Measurement of uronic acids without interference from neutral sugars. Analytical Biochemistry, 197, 157162.Google Scholar
Finore, I., Orlando, P., Di Donato, P., Leone, L., Nicolaus, B. & Poli, A. 2016. Nesterenkonia aurantiaca sp. nov., an alkaliphilic actinobacterium isolated from Antarctica. International Journal of Systematic and Evolutionary Microbiology, 66, 15541560.Google Scholar
Gauthier, M.J., Lafay, B., Christen, R., Fernandez, L., Acquaviva, M., Bonin, P. & Bertrand, J.C. 1992. Marinobacter hydrocarbonoclasticus gen. nov., sp. nov., a new, extremely halotolerant, hydrocarbon-degrading marine bacterium. International Journal of Systematic Bacteriology, 42, 568576.Google Scholar
Gupta, P. & Diwan, B. 2017. Bacterial exopolysaccharide mediated heavy metal removal: a review on biosynthesis, mechanism and remediation strategies. Biotechnology Reports, 13, 5871.Google Scholar
Handley, K.M. & Lloyd, J.R. 2013. Biogeochemical implications of the ubiquitous colonization of marine habitats and redox gradients by Marinobacter species. Frontiers in Microbiology, 4, 110.Google Scholar
Kumar, A.S., Mody, K. & Jha, B. 2007. Bacterial exopolysaccharides - a perception. Journal of Basic Microbiology, 47, 103117.Google Scholar
Lijour, Y., Gentric, E., Deslandes, E, Guezennec, J. 1994. Estimation of the sulfate content of hydrothermal vent bacteria polysaccharides by Fourier transformed infrared spectroscopy. Analytical Biochemistry, 220, 244248.Google Scholar
Liu, C., Chen, C.X., Zhang, X.Y., Yu, Y., Liu, A., Li, G.W., et al. 2012. Marinobacter antarcticus sp. nov., a halotolerant bacterium isolated from Antarctic intertidal sandy sediment. International Journal of Systematic and Evolutionary Microbiology, 62, 18381844.Google Scholar
Lo Giudice, A. & Rizzo, C. 2018. Bacteria associated with marine benthic invertebrates from polar environments: unexplored frontiers for biodiscovery? Diversity, 10, 10.3390/d10030080.Google Scholar
Lo Giudice, A., Bruni, V. & Michaud, L. 2007. Characterization of Antarctic psychrotrophic bacteria with antibacterial activities against terrestrial microorganisms. Journal of Basic Microbiology (Special Issue: Bio-Geo-Interactions), 47, 496505.Google Scholar
Lo Giudice, A., Caruso, C., Mangano, S., Bruni, V., De Domenico, M. & Michaud, L. 2012. Marine bacterioplankton diversity and community composition in an Antarctic coastal environment. Microbial Ecology, 63, 210223.Google Scholar
Lo Giudice, A., Casella, P., Bruni, V. & Michaud, L. 2013. Response of bacterial isolates from Antarctic shallow sediments towards heavy metals, antibiotics and polychlorinated biphenyls. Ecotoxicology, 22, 240250.Google Scholar
Lo Giudice, A. & Fani, R. 2015. Cold-adapted bacteria from the coastal Ross Sea (Antarctica): linking microbial ecology to biotechnology. Hydrobiologia, 761, 417441.Google Scholar
Mancuso Nichols, C.A., Garron, S., Bowman, J.P., Raguénès, G. & Guèzennec, J. 2004. Production of exopolysaccharides by Antarctic marine bacterial isolates. Journal of Applied Microbiology, 96, 10571066.Google Scholar
Mancuso Nichols, C., Bowman, J.P. & Guézennec, J. 2005a. Effects of incubation temperature on growth and production of exopolysaccharides by an Antarctic sea ice bacterium grown in batch culture. Applied and Environmental Microbiology, 71, 35193523.Google Scholar
Mancuso Nichols, C., Bowman, J.P. & Guézennec, J. 2005b. Olleya marilimosa gen nov, sp nov, an exopolysaccharide-producing marine bacterium from the family Flavobacteriaceae, isolated from the Southern Ocean. International Journal of Systematic and Evolutionary Microbiology, 55, 15571561.Google Scholar
Mancuso Nichols, C.A., Garon Lardiere, S., Bowman, J.P., Nichols, P.D., Gibson, J.A.E. & Guézennec, J. 2005c. Chemical characterization of exopolysaccharides from Antarctic marine bacteria. Microbial Ecology, 49, 578589.Google Scholar
Mangano, S., Michaud, L., Caruso, C. & Lo Giudice, A. 2014. Metal and antibiotic resistance in psychrotrophic bacteria associated with the Antarctic sponge Hemigellius pilosus (Kirkpatrick, 1907). Polar Biology, 37, 227235.Google Scholar
Manzoni, M. & Rollini, M. 2001. Isolation and characterization of the exopolysaccharide produced by Daedalea quercina. Biotechnology Letters, 23, 14911497.Google Scholar
Marx, J.G., Carpenter, S.D. & Deming, J.W. 2009. Production of cryoprotectant extracellular polysaccharide substance (EPS) by the marine psychrophilic bacterium Colwellia psychrerythraea strain 34H under extreme conditions. Canadian Journal of Microbiology, 55, 6372.Google Scholar
Michaud, L., Di Cello, F., Brilli, M., Fani, R., Lo Giudice, A. & Bruni, V. 2004. Biodiversity of cultivable Antarctic psychrotrophic marine bacteria isolated from Terra Nova Bay (Ross Sea). FEMS Microbiology Letters, 230, 6371.Google Scholar
Montes, M.J., Bozal, N. & Mercade, E. 2008. Marinobacter guinea sp. nov., a novel moderately halophilic bacterium from an Antarctic environment. International of Journal and Systematic Evolutionary Microbiology, 58, 13461349.Google Scholar
Nicolaus, B., Panico, A., Manca, M.C., Lama, L., Gambacorta, A., Maugeri, T., et al. 2000. A thermophilic Bacillus isolated from an Eolian shallow hydrothermal vent, able to produce exopolysaccharides. Systematic and Applied Microbiology, 23, 426432.Google Scholar
Ozturk, S. & Aslim, B. 2008. Relationship between chromium (VI) resistance and extracellular polymeric substances (EPS) concentration by some cyanobacterial isolates. Environmental Sciences and Pollution Research, 15, 478480.Google Scholar
Poli, A., Finore, I., Romano, I., Gioiello, A., Lama, L. & Nicolaus, B. 2017. Microbial diversity in extreme marine habitats and their biomolecules. Microorganisms, 5, 25.Google Scholar
Qin, G., Zhu, L., Chen, X., Wang, P.G. & Zhang, Y. 2007. Structural characterization and ecological roles of a novel exopolysaccharide from deep-sea psychrotolerant bacterium Pseudoalteromonas sp. SM9913. Microbiology, 153, 15661572.Google Scholar
Sand, W. & Gehrke, T. 2006. Extracellular polymeric substances mediate bioleaching/biocorrosion via interfacial processes involving iron (III) ions and acidophilic bacteria. Research in Microbiology, 157, 4956.Google Scholar
Sheng, G.P., Yu, H.Q. & Li, X.Y. 2010. Extracellular polymeric substances (EPS) of microbial aggregates in biological wastewater treatment systems: a review. Biotechnology Advances, 28, 882894.Google Scholar
Yildiz, S.Y., Anzelmo, G., Ozer, T., Radchenkova, N., Genc, S., Di Donato, P., et al. 2014. Brevibacillus themoruber: a promising microbial cell factory for exopolysaccharide production. Journal of Applied Microbiology, 116, 314324.Google Scholar