TY - JOUR A1 - Kaplan, Aaron A1 - Harel, Moshe A1 - Kaplan-Levy, Ruth N. A1 - Hadas, Ora A1 - Sukenik, Assaf A1 - Dittmann-Thünemann, Elke T1 - The languages spoken in the water body (or the biological role of cyanobacterial toxins) JF - Frontiers in microbiology N2 - Although intensification of toxic cyanobacterial blooms over the last decade is a matter of growing concern due to bloom impact on water quality, the biological role of most of the toxins produced is not known. In this critical review we focus primarily on the biological role of two toxins, microcystins and cylindrospermopsin, in inter- and intra-species communication and in nutrient acquisition. We examine the experimental evidence supporting some of the dogmas in the field and raise several open questions to be dealt with in future research. We do not discuss the health and environmental implications of toxin presence in the water body. KW - aoa KW - cylindrospermopsin KW - microcystin KW - cyr KW - mcy Y1 - 2012 U6 - https://doi.org/10.3389/fmicb.2012.00138 SN - 1664-302X VL - 3 PB - Frontiers Research Foundation CY - Lausanne ER - TY - JOUR A1 - Welker, Martin A1 - Dittmann-Thünemann, Elke A1 - von Doehren, Hans ED - Hopwood, DA T1 - Cyanobacteria as a source of natural products JF - Methods in enzymology JF - Methods in Enzymology N2 - Cyanobacteria or blue-green algae from various environments have been recognized as sources of a variety of bioactive metabolites. Strategies of strain isolation from aquatic habitats, and cultivation and harvesting for metabolite production are described. Strategies for screening of compounds are discussed, including their direct MALDI-TOF mass spectrometric detection in whole cells. Genetic approaches including genomic mining, mutagenesis including transcriptional activation, heterologous expression, and in vitro. reconstitution of pathways are presented. Y1 - 2012 SN - 978-0-12-404634-4 U6 - https://doi.org/10.1016/B978-0-12-404634-4.00002-4 SN - 0076-6879 VL - 517 IS - 1 SP - 23 EP - 46 PB - Elsevier CY - San Diego ER - TY - JOUR A1 - Guljamow, Arthur A1 - Delissen, Friedmar A1 - Baumann, Otto A1 - Thuenemann, Andreas F. A1 - Dittmann-Thünemann, Elke T1 - Unique properties of eukaryote-type actin and profilin horizontally transferred to cyanobacteria JF - PLoS one N2 - A eukaryote-type actin and its binding protein profilin encoded on a genomic island in the cyanobacterium Microcystis aeruginosa PCC 7806 co-localize to form a hollow, spherical enclosure occupying a considerable intracellular space as shown by in vivo fluorescence microscopy. Biochemical and biophysical characterization reveals key differences between these proteins and their eukaryotic homologs. Small-angle X-ray scattering shows that the actin assembles into elongated, filamentous polymers which can be visualized microscopically with fluorescent phalloidin. Whereas rabbit actin forms thin cylindrical filaments about 100 mu m in length, cyanobacterial actin polymers resemble a ribbon, arrest polymerization at 510 lam and tend to form irregular multi-strand assemblies. While eukaryotic profilin is a specific actin monomer binding protein, cyanobacterial profilin shows the unprecedented property of decorating actin filaments. Electron micrographs show that cyanobacterial profilin stimulates actin filament bundling and stabilizes their lateral alignment into heteropolymeric sheets from which the observed hollow enclosure may be formed. We hypothesize that adaptation to the confined space of a bacterial cell devoid of binding proteins usually regulating actin polymerization in eukaryotes has driven the co-evolution of cyanobacterial actin and profilin, giving rise to an intracellular entity. Y1 - 2012 U6 - https://doi.org/10.1371/journal.pone.0029926 SN - 1932-6203 VL - 7 IS - 1 SP - 221 EP - 231 PB - PLoS CY - San Fransisco ER - TY - JOUR A1 - Harel, Moshe A1 - Weiss, Gad A1 - Daniel, Einat A1 - Wilenz, Avraham A1 - Hadas, Ora A1 - Sukenik, Assaf A1 - Sedmak, Bojan A1 - Dittmann-Thünemann, Elke A1 - Braun, Sergei A1 - Kaplan, Aaron T1 - Casting a net fibres produced by Microcystis sp in field and laboratory populations JF - Environmental microbiology reports N2 - The reasons for the apparent dominance of the toxic cyanobacterium Microcystis sp., reflected by its massive blooms in many fresh water bodies, are poorly understood. We show that in addition to a large array of secondary metabolites, some of which are toxic to eukaryotes, Microcystis sp. secretes large amounts of fibrous exopolysaccharides that form extremely long fibres several millimetres in length. This phenomenon was detected in field and laboratory cultures of various Microcystis strains. In addition, we have identified and characterized three of the proteins associated with the fibres and the genes encoding them in Microcystis sp. PCC 7806 but were unable to completely delete them from its genome. Phylogenetic analysis of the most abundant one, designated IPF-469, showed its presence only in cyanobacteria. Its closest relatives were detected in Synechocystis sp. PCC 6803 and in Cyanothece sp. strains; in the latter the genomic organization of the IPF-469 was highly conserved. IPF-469 and the other two proteins identified here, a haloperoxidase and a haemolysin-type calcium-binding protein, may be part of the fibres secretion pathway. The biological role of the fibres in Microcystis sp. is discussed. Y1 - 2012 U6 - https://doi.org/10.1111/j.1758-2229.2012.00339.x SN - 1758-2229 VL - 4 IS - 3 SP - 342 EP - 349 PB - Wiley-Blackwell CY - Malden ER -