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Within the Svalbard archipelago, Kongsfjorden is an important marine ecosystem that is recognised as one of the main representative Arctic glacial fjords. Prokaryotic organisms are key drivers of important ecological processes such as carbon fluxes, nutrient mineralisation, and energy transfer, as well as sentinels of environmental pollution, especially in sediments, that are a repository of contaminants. In some areas of the Arctic, the structure and metabolic activity of the microbial community in the organic matter turnover and globally in the functioning of the benthic domain are mostly still unknown. A snapshot of the main microbial parameters such as bacterial abundance (by microscopic and plate counts), structure (by 16S rRNA sequencing), and metabolic activity was provided in Ny-Ålesund harbour, contextually in seawater and sediment samples. Fluorogenic substrates were used to assess the microbial ability to utilise organic substrates such as proteins, polysaccharides, and organic phosphates through specific enzymatic assays (leucine aminopeptidase—LAP, beta-glucosidase—ß-GLU, and alkaline phosphatase—AP, respectively). The metabolic profiles of psychrophilic heterotrophic bacterial isolates were also screened using a qualitative assay. The phylogenetic analysis of the microbial community revealed that Proteobacteria prevailed among the observed taxonomic groups. Several of the observed sequences were assigned to clones found in harbours, microbial biofilms, antifouling paints, or oil-polluted facilities of cold environments, highlighting a signature of human pressure on the polar habitat of Ny-Ålesund harbour.

Five psychrotolerant Alcanivorax spp. strains were isolated from Antarctic coastal waters. Strains were screened for molecular and physiological properties and analyzed regarding their growth capacity. Partial 16S rDNA, alk-B1, and P450 gene sequencing was performed. Biolog EcoPlates and the API 20E test were used to evaluate metabolic and biochemical profiles. Bacterial growth in sodium acetate was determined at 4, 15, 20, and 25 °C to evaluate the optimal temperature. Furthermore, the ability of each strain to grow in a hydrocarbon mixture at 4 and 25 °C was assayed. Biosurfactant production tests (drop-collapse and oil spreading) and emulsification activity tests (E24) were also performed. Concerning results of partial gene sequencing (16S rDNA, alk-B1, and P450), a high similarity of the isolates with the same genes isolated from other Alcanivorax spp. strains was observed. The metabolic profiles obtained by Biolog assays showed no significant differences in the isolates compared to the Alcanivorax borkumensis wild type. The results of biodegradative tests showed their capability to grow at different temperatures. All strains showed biosurfactant production and emulsification activity. Our findings underline the importance to proceed in the isolation and characterization of Antarctic hydrocarbon-degrading bacterial strains since their biotechnological and environmental applications could be useful even for pollution remediation in polar areas.