Role of macrophyte life forms in driving periphytic microalgal assemblages in a Brazilian reservoir

Macrophytes play several roles in aquatic ecosystems, including the provision of habitat for many aquatic organisms, especially the periphyton. The aims of this study were to characterize the structure of periphytic microalgal assemblages on different aquatic macrophyte life forms in order to establish similarities between assemblages from nearby sampling sites. We hypothesized that i) aquatic macrophytes with different life forms and morphological characteristics could differently influence the structure of the periphyton and that ii) the greatest similarity in periphyton composition should be observed among macrophytes that occupy the same sampling site. The study was conducted from 2006 to 2008 in the Thomaz Osterne de Alencar reservoir (Crato City, Ceará State, Brazil) and involved the taxonomic surveying of microalgae attached to five different macrophytes with the application of structural descriptors (richness, abundance, frequency, diversity and equitability). A total of 127 taxa, of which 44% belonged to the Chlorophyta, were identified. The microalgae assemblages showed high species richness on Salvinia auriculata Aubl., a free-floating macrophyte, and large abundance on Apalanthe granatensis (Humb. & Bonpl.) Planch., a submerged anchored macrophyte. ANOVA indicated that periphyton significantly varied among the macrophytes investigated, and nearby sampling sites showed no structural similarities in microalgal assemblages. In general, we can conclude that the structure of periphyton assemblages is influenced by the substrate (i.e., macrophyte organ), as this can not only promote high diversity and equitability but can also be a predictor of dissimilarity in the distribution and frequency of occurrence of microalgae. These results reinforce the findings of other studies that have shown that macrophytes play an important role in structuring the periphyton assemblages

Detection, purification and characterization of a lectin from freshwater green algae Spirogyra spp.

<div><p>ABSTRACT Freshwater algae are rich sources of structurally biologically active metabolites, such as fatty acids, steroids, carotenoids and polysaccharides. Among these metabolites, lectins stand out. Lectins are proteins or glycoproteins of non-immune origin which bind to carbohydrates or glycoconjugates, without changing ligand structure. Many studies have reported on the use of Spirogyra spp. as effective bioindicators of heavy metals; however, reports on Spirogyra molecular bioprospecting are quite limited. Therefore, this study aimed to detect, isolate, purify and characterize a lectin present in the freshwater green algae Spirogyra. Presence of the lectin protein in the extract was detected by hemagglutination assays. Subsequently, the protein extract was subjected to a sugar inhibition assay to identify the lectin-specific carbohydrate. Following this, the extract was applied to a guar gum column to afford the pure lectin. The lectin was inhibited by N-acetyl-glucosamine and N-acetyl-beta-D-mannose, but more strongly by D-galactose. The apparent molecular mass of the purified lectin was evaluated by Polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate (SDS-PAGE). Electrophoretic analysis revealed a single protein band with an apparent molecular mass of 56 kDa. Thus, it could be concluded that a lectin was purified from Spirogyra spp.</p></div