Cyanobacteria synthesize secondary metabolites with antifungal activity, making them potential biopesticide agents for sustainable, eco-friendly agriculture. Programmes to identify Cyanobacterial strains with effective bioactivity generally screen strains maintained in culture collections. These strains are often monoclonal but non-axenic and this may potentially influence the bioactivity of the generated biomass. The present study investigated in vitro antifungal activity of Nostoc muscorum MACC-189 and N. linckia MACC-612 strains co-isolated with fungal co-partners and maintained in the Mosonmagyaróvár Algal Culture Collection (MACC). The fungal co-partners were isolated from the Cyanobacterial stock cultures and identified as Purpureocillium lilacinum and Sarocladium sp., respectively. The cultures were tested against seven phytopathogens. The phytopathogenic fungi were grown on potato dextrose agar plates and suspension cultures of the Cyanobacteria-fungi and isolated fungal co-partners were placed in the centre of the plate. Antifungal effects were assessed semi-quantitatively after 10 days of incubation. The Cyanobacteria-fungal co-cultures had antifungal activity against Monilinia fructigena and Aspergillus sp. with the N. muscorum/P. lilacinum culture being the most effective. The fungal isolates inhibited M. fructigena with P. lilacinum having a dose-dependent response but did not inhibit Aspergillus sp. This suggested that the antifungal effect of the Cyanobacterial cultures on M. fructigena was due to the fungal partner rather than the cyanobacterium while the antifungal effect on Aspergillus sp. was due to the cyanobacterium partner. As it was not possible to maintain living axenic N. muscorum and N. linckia cultures, this could not be conclusively confirmed. These results highlight the importance of either using axenic cultures or identifying the co-isolates when testing Cyanobacteria cultures for antifungal bioactivity.

Highly saline conditions represent a strong challenge for most microorganisms in freshwater ecosystems. Eukaryotic freshwater green algae from the Chlorophyta clade were investigated for their ability to survive in and adapt to increased salt concentration in the growth medium. Striking differences were detected between the responses of the various algae species to the elevated salt concentrations. The investigated Chlamydomonas reinhardtii cc124 and Coelastrella sp. MACC-549 algae showed a moderate resistance to increased salt concentration, while Chlorella sp. MACC-360 exhibited high salt tolerance, showed unaltered growth characteristics and photosynthetic efficiency compared to the saline-free control conditions even at 600 mM NaCl concentration. Diverse physiological responses to elevated salt concentrations were described for the tested algae including variations in their growth capacity, characteristic morphological changes, alterations in the structure and function of the photosynthetic machinery and differences in the production of reactive oxygen species. Special alterations were identified in the lipid and exopolysaccharide production patterns of the tested algal strains in response to high salinity. As a conclusion Chlorella sp. MACC-360 algae showed outstanding salt tolerance features. Together with the concomitant lipid-producing phenotype under highly saline conditions this unicellular green alga is a promising candidate for biotechnological applications.

The nuclear, chloroplast and mitochondrial genomes of a unicellular green algal species of the Coelastrella genus was sequenced, assembled and annotated. The strain was previously classified as Chlamydomonas sp. MACC-549 based on morphology and partial 18S rDNA analysis. However, the proposed multi-loci phylogenomic approach described in this paper placed this strain within the Coelastrella genus, therefore it was re-named to Coelastrella vacuolata MACC-549. The strain was selected for de novo sequencing based on its potential value in biohydrogen production as revealed in earlier studies. This is the first thorough report and characterization for green algae from the Coelastrella genus. The whole genome annotation of Coelastrella vacuolata MACC-549 (including nuclear, chloroplast and mitochondrial genomes) shed light on interesting metabolic and sexual breeding features of this algae and served as a basis to taxonomically classify this strain.

Systematic studies on 70 MACC isolates previously identified as ‘Chlamydomonas’, a unicellular flagellate, were carried out based on partial 18S rRNA. The aim of this study was to determine the phylogenetic affiliations of Chlamydomonas strains in the MACC collection. The study found that most of the strains were not Chlamydomonas. Nine clusters of phylogenetically similar taxa were identified. The previous determinations were completed with their new phylogenetic affiliations (partly due to changes in green algae classification). Molecular data revealed that 3 of the 70 strains are from Arenicolinia, 14 are members of the phylogroup Stephanosphaerinia, 11 are Oogamochlamydinia, 1 is Chloromonadinia, 19 are Reinhardtinia, 2 are Polytominia, 9 are Scenedesmaceae, 5 are Moewusinia, and 6 are Chlorella. Clades were established by 18S rRNA similarity and p-distances. This study reveals the need to revise established culture collections whose isolates are solely identified with morphology.

Study on 37 MACC isolates previously identified as “Anabaena,” a freshwater filamentous heterocytous taxon, were carried out using the 16S rRNA. The study found that most of the strains were misidentified at genus level. Three clusters of phylogenetically and morphologically similar taxa were identified. The previous determinations were amended with their new taxonomic classifications (partly due to changes in cyanobacterial classification). Some morphological structures could not be found in the cultures (e.g. akinetes). Molecular data revealed that 6 of the 37 strains are Desmonostoc, 8 are members of the genus Nostoc, 19 strains bear genetic resemblance to the genus Trichormus and 4 strains remain unresolved. Clades were established by 16S rRNA similarity and p-distances. The goal of this study was to amend the strain designations in this collection. This study reveals the necessity to revisit established culture collections that originally used only morphological classifications for species identification.