Bajerski, Felizitas

Ganzert, L.

Lipski, A.

Mangelsdorf, K.

Wagner, Dirk

English

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Isolation and characterisation of heterotrophic microorganisms from mineral soils of Livingston Island (Antarctica) and Store Koldewey (Northeast-Greenland).1 1 2 3 1Felizitas Bajerski , Lars Ganzert , Kai Mangelsdorf , André Lipski  and Dirk WagnerMicrobial communities in extreme habitats like the Arctic and Antarctic are still insufficiently investigated. Only little information is available about diversity and function in such environments. Because of their geographic isolation, climatological specialities and the minor anthropogenic influence, polar regions provide a unique opportunity as a natural laboratory for studying the functional diversity of microbial life under extreme environmental conditions.1Alfred Wegener Institute for Polar and Marine Research, Research Department Potsdam, Telegraphenberg A45, 14473 Potsdam, Germany2Helmholtz Centre PotsdamGFZ German Research Centre for GeosciencesSection 4.3, Organic GeochemistryTelegrafenberg, B 42314473 Potsdam, Germany3Rheinische Friedrich-Wilhelms-Universität Bonn, Institute of Nutrition and Food Sciences, Department of Food Microbiology and Hygiene, Meckenheimer Allee 168, 53115 Bonn, GermanyStudy sitesThe polar climate on Store Koldewey is characterised by low temperatures varying between -24°C and 4°C and little precipitation around 150mm pa. Because of the harsh climate conditions only initial soil formation can be observed.The cold-maritime climate of Livingston Island is characterised by low temperatures from -10°C down to -35°C in winter and up to 10°C in summer. The annual precipitation averages around 500mm and is evenly distributed throughout the year. Environmental conditions and low input of organic material result in initial soil formation processes, e.g.  humus accumulation or clay formation. Store Koldewey (Arctic/Northeast-Greenland)Livingston Island (South Shetland Islands/Antarctica)Enrichment cultures from both study sites could be obtained by plating soil solutions on BR-media (Bunt-Rovira, 1955). Several heterotrophic aerobic bacteria were isolated and cultivated at 10°C. Amplification of the 16S rRNA genes was carried out using the primer pair E8F and 1492R to determine the molecular phenotype and for the phylogentic characterisation of selected isolates. Morphological, physiological and biochemical analyses were performed to describe the phenotype of certain strains.In the scope of this work we succeeded in enriching, isolating and characterising several heterotrophic bacteria in general, as well as an elaborate Tdescription of eight selected strains. Considering the current results of our research, we propose Arthrobacter livingstonensis sp. nov. LI-2  and TArthrobacter cryotolerans sp. nov. LI-3  as two novel species in the genus Arthrobacter. We report the isolation and identification of strain T TCryobacterium arcticum sp. nov. SK-1  as a novel psychrotolerant species in the genus Cryobacterium. Strain  LI-1  could be classified as a novel species in the genus Leifsonia, named Leifsonia psychrotolerans.Arthrobacter cryotolerans LI-3Cryobacterium arcticum SK-1Colonies and inoculumCell shape: Phase Contrast MicroscopyRaster Electron MicroscopyMethodsResults and conclusionF . B a j e r s k i F . B a j e r s k iF . B a j e r s k iF . B a j e r s k iF . B a j e r s k iF . B a j e r s k iF . B a j e r s k icharacter LI-1 LI-2 LI-3 LI-4 SK-1 SK-2 SK-3 SK-4 length (µm) 0.5-2.5 0.5-2.0 0.4-2.5 2.0-10.0 0.4-2.0 2.5-8.0 2.0-3.5 0.8-2.7 width (µm) 0.3-0.5 ~0.5 0.3-0.5 0.5-0.8 0.2-0.4 ~0.2 0.4-0.6 0.5-0.8 gram-reaction - + + + + - - - cell-form rods rods short rods rods short irregular  rods rods rods (form  v-shaped pairs) rods temperature- range -6 to 28°C -6 to 28°C -6 to 24°C 5 to 28°C -6 to 28°C 0 to 28°C -6 to 28°C 5 to 28°C temperatur- optimum 16°C 16°C 16°C 16°C 20°C 20°C 16°C 24°C pH-range 4.5 to 9.5 4.0 to 9.5 4.0 to 9.5 6.0 to 8.5 5.0 to 9.5 5.0 to 9.0 5.0 to 9.0 4.0 to 11.0 pH-optimum 5.5 to 6.5 7.5 to 8.0 6.5 7.5 6.5 to 7.5 6.5 8.0 6.0 to 6.5 NaCl- tolerance 0-4% 0-9% 0-9% 0-6% 0-3% 0-1.5% 0-4% 0-6% NaCl- optimum 1-2% 0-1% 0.5-3% 0-2% 0% 0.5% 0-1.5% 0% presence of O2 aerobic aerobic,  (fac. anaerobic) aerobic  (fac. anaerobic) aerobic (fac. anaerobic) aerobic aerobic,  (fac. anaerobic) obligate  aerobic aerobic amylase +/- - - - - + - - protease - +/- - +/- - ++ - ++ indol- production - - - - - - - - H2S- production + + + + + +/- - - urease - + - + - - - - catalase + + + + + - + +/- oxidase - - - - - + - +/- methylrot- test +/- - - - + - + + Soil profile T1-1 (0-14 cm depth) from Livingston Island: Silty sand in a bedrock depression, covered with a moss layerW a g n e r e t a l . ,  2 0 0 6http://www.uni-leipzig.de/~geologie/Forschung/ProjektSeiten/UmweltGroenl/Groenland1.jpg, modifiedhttp://lima.usgs.gov/documents/LIMA_overview_map.pdfhttp://en.wikipedia.org/wiki/File:South_Shetland_Islands_Map.pngBiochemical analyses: Methylred-test(LI-1, LI-2, LI-3, LI-4, positive control (pc), SK-1, SK-2. SK-3, SK-4, pc)Phenotypic characteristics of the eight selected strains                                                          (+  positive, - negative, +/- weak reaction, ++ strong reaction)Felizitas Bajerskihttp://www.awi.de/People/show.php?bajerskiwww.awi.de/en/go/geomicrobiologyFelizitas.Bajerski@awi.deBDP16DFG-Project: WA 1554/4-2

Isolation and characterisation of heterotrophic microorganisms from mineral soils of Livingston Island (Antarctica) and Store Koldewey (Northeast-Greenland).

Isolation and characterisation of heterotrophic microorganisms from mineral soils of Livingston Island (Antarctica) and Store Koldewey (Northeast-Greenland).

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