Characterization of true-branching cyanobacteria from geothermal sites and hot springs of Costa Rica.

Costa Rica is at the centre of the Mesoamerican biodiversity hotspot. Little is known about cyanobacteria from this region so far. Here, four isolates of the order Stigonematales (section V) were characterized in a polyphasic approach. All strains were isolated from geothermal sites and hot springs of Costa Rica. However, one of them, identified as Westiellopsis sp. Ar73, did not grow at more than 40 degrees C. Based on its identical 16S rRNA to several previously isolated Westiellopsis sp. and Fischerella muscicola strains, a ubiquitous distribution throughout tropical and subtropical regions can be implied. In contrast, the isolates MV9, MV11 and RV14 grew well up to 50-55 degrees C. Based on morphologic, ultrastructural, molecular and physiologic data, MV9, MV11 and RV14 were identified to belong to the genus Fischerella. Two distinct intergenic transcribed spacer (ITS) types, with or without tRNA genes, were detected for all Stigonematales analysed here, indicating ITS polymorphism as a characteristic feature of heterocystous cyanobacteria. In phylogenetic trees, these Fischerella spp. formed a new and distinct clade within the wider lineage of thermophilic Fischerella (Mastigocladus cf. laminosus), which might represent a geographic lineage. Thus, geographic isolation may be an underestimated aspect of microbial evolution. The strains presented here are suitable as new models to study this group of cyanobacteria.

Binding structure of the leucine aminopeptidase inhibitor microginin FR1.

Natural bioactive compounds are of general interest for pharmaceutical research because they may serve as leads in drug development campaigns. Among them, microginins are linear peptides known to inhibit various exopeptidases. The crystal structure of microginin FR1 from Microcystis sp. bound to bovine lens leucine aminopeptidase was established at 1.73 Angstrom resolution. The observed binding structure could be beneficial for the design of potent aminopeptidase inhibitors.

Cianobacterias y riesgos potenciales de toxicidad en aguas continentales de Chile / Cyanobacteria and potential risks of toxicity in continental waters of Chile

Las cianobacterias son microorganismos fototróficos oxigénicos, con una amplia distribución, ya que han sido reportados en aguas dulces o saladas de los cinco continentes. Eventualmente pueden desarrollarse en grandes masas, denominadas ®blooms (florecimientos), generados, usualmente, por efectos antropogénicos. Varias especies de cianobacterias pueden producir potentes neurotoxinas y hepatotoxinas, las cuales presentan serias dificultades para ser eliminadas del agua. La intoxicación con algunas de estas toxinas puede ser grave causando la muerte de animales o el hombre y se sospecha que la ingestión aún de microdosis, pueda inducir la formación de tumores. La distribución de cianobacterias de aguas continentales de Chile, se presenta desde el extremo Norte hasta el territorio Antártico. Se ha determinado en diferentes regiones la presencia de especies tóxicas y la formación de florecimientos. Mediante cromatografía líquida de alta presión (HPLC) y espectrometría de masas (MALDITOF) (PSD), se ha determinado en diferentes cuerpos de agua la cianotoxina microcistina. Finalmente se sugieren recomendaciones para tomar conocimiento y establecer controles que eviten el riesgo a su exposición.

Cyanobacteria are phototropic and oxygenic microorganisms that are widely distributed and reported to be present in freshwater or seawater from the five continents. They can eventually develop into large masses called ®blooms¼ which are usually generated by anthropogenic effects. Several species of cyanobacteriacan produce potent neurotoxins and hepatotoxins, which are difficult to eliminate from water. The intoxicationwith some of these toxins can become severe causing death in animals and man and it is suspected that ingestion of even microdoses of them can induce tumor appearance. The distribution of cyanobacteria in continental waters of Chile has been recorded from uppermost north of Chile up to the Antarctic territory. The presence of toxic species as well as the development of blooms have been detected in different regions.The mycrocystin cyanotoxin has been assessed in different masses of water by means of high pressure liquidchromatography (HPLC) together with mass spectrometry (MALDI-TOF) (PSD). Finally it is recommended to make analysis in order to establish controls that avoid risk of exposure to these cyanotoxins.

Characterization of proteases in guts of Daphnia magna and their inhibition by Microcystis aeruginosa PCC 7806.

Many cyanobacteria produce peptides that inhibit mammalian proteases. The hypothesis that inhibitors of mammalian proteases produced by cyanobacteria also interfere with digestive proteases of natural cladoceran grazers was tested by comparing the effects of cyanobacterial protease inhibitors on digestive proteases from Daphnia magna and on commercially available bovine proteases. The major digestive proteases of D. magna are trypsins and chymotrypsins, which differ from those of bovine origin in substrate specificity and susceptibility to synthetic inhibitors. An extract from Microcystis aeruginosa strain PCC 7806 inhibited both types of D. magna proteases. Subsequent fractionation of the extract by high-performance liquid chromatography indicated that several inhibitors are produced by M. aeruginosa that differ in their specificity for the trypsins and chymotrypsins of D. magna. Two fractions differed in their inhibitory effect on proteases of D. magna and bovine origin; therefore, assessment of the impact of cyanobacterial protease inhibitors on natural communities requires the use of digestive proteases from ecologically relevant grazers.

Channel-forming (Porin) activity in Herpetosiphon aurantiacus Hp a2.

Detergent extracts of cell envelopes of the gliding bacterium Herpetosiphon aurantiacus formed channels in lipid bilayers. Fast protein liquid chromatography across a HiTrap-Q cation-exchange column demonstrated that a 45-kDa protein forms the channel. The observation of a channel-forming protein suggests that Herpetosiphon aurantiacus Hp a2 has a permeability barrier on its surface.

Binding structure of elastase inhibitor scyptolin A.

Natural bioactive compounds are of general interest to pharmaceutical research because they may be used as leads in drug development campaigns. Among them, scyptolin A and B from Scytonema hofmanni PCC 7110 are known to inhibit porcine pancreatic elastase, which in turn resembles the attractive drug target neutrophil elastase. The crystal structure of scyptolin A as bound to pancreatic elastase was solved at 2.8 A resolution. The inhibitor occupies the most prominent subsites S1 through S4 of the elastase and prevents a hydrolytic attack by covering the active center with its rigid ring structure. The observed binding structure may help to design potent elastase inhibitors.

Hofmannolin, a cyanopeptolin from Scytonema hofmanni PCC 7110.

Two depsipeptide metabolites, scyptolin A and B, were reported recently from the axenically grown terrestrial cyanobacterium Scytonema hofmanni PCC 7110. A related, novel depsipeptide was isolated from this Scytonema and designated hofmannolin. The amino acid analysis in context with infrared, mass and 1H/13C-NMR spectroscopies revealed a cyclic depsipeptide structure of M(r) 1073 belonging to the class of cyanopeptolins. Two peculiar features distinguish hofmannolin from other cyanopeptolins: O-methylated tyrosine forms the sixth moiety from the amino terminus, and the N-terminus is blocked by 2-hydroxy-3-methyl-valeric acid, a residue that has not yet been reported as a component in other cyanopeptolins. Preliminary assays of peptidase inhibitory and antimicrobial activities suggested negligible bioactivities for hofmannolin.

Characterization of a photosynthetic Euglena strain isolated from an acidic hot mud pool of a volcanic area of Costa Rica.

Abstract Conspicuous green patches on the surface of an acidic hot mud pool located near the Rincón de la Vieja volcano (northwestern Costa Rica) consisted of apparently unialgal populations of a chloroplast-bearing euglenoid. Morphological and physiological studies showed that it is a non-flagellated photosynthetic Euglena strain able to grow in defined mineral media at temperatures up to 40 degrees C and exhibiting higher thermotolerance than Euglena gracilis SAG 5/15 in photosynthetic activity analyses. Molecular phylogeny studies using 18S rDNA and GapC genes indicated that this strain is closely related to Euglena mutabilis, another acid-tolerant photosynthetic euglenoid, forming a clade deeply rooted in the Euglenales lineage. To our knowledge this is the most thermotolerant euglenoid described so far and the first Euglenozoan strain reported to inhabit acidic hot aquatic habitats.

Biologically active peptides in cyanobacteria

Las cianobacterias se encuentran en el medio natural tanto en aguas dulces como saladas. Ellas pueden desarrollarse en grandes masas formando "blooms" (florecimientos) en aguas dulces y saladas en diferentes partes del mundo, incluyendo América del Sur. Tales florecimientos, así como crecimientos axénicos de cianobacterias, pueden ser una rica fuente de péptidos lineales o cíclicos únicos, muchos de los cuales presentan actividad biológica. En el pasado la mayor atención ha sido puesta en las toxinas microcistina y nodulatoria. Estos péptidos ciclicos son hepatotoxinas que inhíben la proteína fosfatasa 1 y 2A, después de ingresar específicamente al hepatocito mediante la captación de las sales biliares. Sin embargo, en cianobacterias se están encontrando péptidos con otras actividades biológicas. No obstante, auque no se consideren tóxicos, estos péptidos tienen actividades biológicas tales como: una fuerte y específica inhibición de las proteasas (tripsina, quimo-tripsina, elastasa, trombina, plasmina y la enzima procesadora angiotensina), anticianobacterias, antialgas, antihongos, inmunosupresores y promotores de diferenciación celular. Ejemplos de péptidos cianobacteriales inhibidores de proteasas son las cianopeptolina. Las interacciones de microcistina/proteína fosfatasa y de cianopeptolina/proteasa, han sido bien estudiadas por difracción de rayos x en cocristales y la determinación de microcistina y de otros péptidos puede ser realizada por métodos químicos y biológicos. Ambas, microcistina y cianopeptolina han sido recientemente determinadas en blooms producidos en cuerpos de agua en Chile, utilizando cromatografía líquida de alta resolución (HPLC), espectrometría de masas (MALDI-TOF) (PSD), además de bioensayos de inhibición enzimática

Lipopolysaccharide and porin of Roseobacter denitrificans, confirming its phylogenetic relationship to the alpha-3 subgroup of Proteobacteria.

Roseobacter denitrificans has rough (R)-type lipopolysaccharide, containing 2-keto-3-deoxyoctonate but no hepatoses. Its lipid A has a glucosamine-containing, phosphorylated backbone. It contains the rare 3-oxotetradecanoic (3-oxomyristic) acid as the only amide-bound fatty acid and ester-bound 3-hydroxydecanoic acid, this pattern being characteristic for the alpha-3 subgroup of Proteobacteria. Treatment of the major outer-membrane protein (porin, apparent molecular mass 88 kDa) of Roseobacter denitrificans with EDTA (2 mM, 30 degrees C, 20 min) resulted in the dissociation of the oligomers into monomers (apparent molecular mass 35 kDa). EDTA-sensitive dissociation has so far been observed only within the alpha-3 subgroup of Proteobacteria. The 12 N-terminal amino acids of the monomers exhibit sequence homology with the porins of Rhodobacter capsulatus, Rhodobacter sphaeroides and Rhodopseudomonas blastica. Renaming of Roseobacter denitrificans as Rhodobacter denitrificans is suggested.