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1.
J Eukaryot Microbiol ; 71(4): e13039, 2024.
Article in English | MEDLINE | ID: mdl-38956983

ABSTRACT

The planktonic dinoflagellate Prorocentrum compressum is widespread in warm and temperate seas. A strain identified as P. cf. compressum BEA 0681B isolated from the island of Gran Canaria, NE Atlantic Ocean, showed a divergence in rDNA/ITS phylogenies with respect to P. compressum. The Canarian strain was oval, with an average length-to-width ratio of 1.35, smooth thecal surface with less than 150 thecal pores, including oblique pores, sometimes with a bifurcated opening. In contrast, P. compressum was rounder, with a length-to-width ratio < 1.2, with reticulate-foveate ornamentation and 200-300 pores per valve. We propose Prorocentrum canariense sp. nov. These species clustered as the most early-branching lineage in the clade Prorocentrum sensu stricto. Although this clade mainly contains planktonic species, the closer relatives were the benthic species P. tsawwassenense and P. elegans. Interestingly, P. compressum and P. canariense sp. nov. are widely distributed in temperate and warm seas without an apparent morphological adaptation to planktonic life. The formation of two concentric hyaline mucilaginous walls could contribute to this success. We discuss the use of Prorocentrum bidens to solve the nomenclature issue of P. compressum that was described citing a diatom as basionym.


Subject(s)
DNA, Protozoan , DNA, Ribosomal , Dinoflagellida , Phylogeny , Dinoflagellida/classification , Dinoflagellida/genetics , DNA, Ribosomal/genetics , DNA, Protozoan/genetics , Atlantic Ocean , Sequence Analysis, DNA , DNA, Ribosomal Spacer/genetics , DNA, Ribosomal Spacer/analysis , Molecular Sequence Data
2.
Mar Drugs ; 21(5)2023 Apr 29.
Article in English | MEDLINE | ID: mdl-37233478

ABSTRACT

Nocuolin A (1), an oxadiazine, was isolated from the cyanobacterium Nostoc sp. Its chemical structure was elucidated using NMR and mass spectroscopic data. From this compound, two new oxadiazines, 3-[(6R)-5,6-dihydro-4,6-dipentyl-2H-1,2,3-oxadiazin-2-yl]-3-oxopropyl acetate (2) and 4-{3-[(6R)-5,6-dihydro-4,6-dipentyl-2H-1,2,3-oxadiazin-2-yl]-3-oxopropoxy}-4-oxobutanoic acid (3), were synthesised. The chemical structures of these two compounds were elucidated by a combination of NMR and MS analysis. Compound 3 showed cytotoxicity against the ACHN (0.73 ± 0.10 µM) and Hepa-1c1c7 (0.91 ± 0.08 µM) tumour cell lines. Similarly, compound 3 significantly decreased cathepsin B activity in ACHN and Hepa-1c1c7 tumour cell lines at concentrations of 1.52 ± 0.13 nM and 1.76 ± 0.24 nM, respectively. In addition, compound 3 showed no in vivo toxicity in a murine model treated with a dose of 4 mg/kg body weight.


Subject(s)
Cathepsin B , Nostoc , Animals , Mice , Molecular Docking Simulation , Cell Line, Tumor , Molecular Structure
3.
Bioresour Technol ; 363: 127979, 2022 Nov.
Article in English | MEDLINE | ID: mdl-36126844

ABSTRACT

Centrate is a low-cost alternative to synthetic fertilizers for microalgal cultivation, reducing environmental burdens and remediation costs. Adapted microalgae need to be selected and characterised to maximise biomass production and depuration efficiency. Here, the performance and composition of six microalgal communities cultivated both on synthetic media and centrate within semi-open tubular photobioreactors were investigated through Illumina sequencing. Biomass grown on centrate, exposed to a high concentration of ammonium, showed a higher quantity of nitrogen (5.6% dry weight) than the biomass grown on the synthetic media nitrate (3.9% dry weight). Eukaryotic inocula were replaced by other microalgae while cyanobacterial inocula were maintained. Communities were generally similar for the same inoculum between media, however, inoculation with cyanobacteria led to variability within the eukaryotic community. Where communities differed, centrate resulted in a higher richness and diversity. The higher nitrogen of centrate possibly led to higher abundance of genes coding for N metabolism enzymes.


Subject(s)
Ammonium Compounds , Cyanobacteria , Microalgae , Ammonium Compounds/metabolism , Biomass , Fertilizers , Microalgae/metabolism , Nitrates/metabolism , Nitrogen/metabolism , Photobioreactors/microbiology , Sustainable Growth , Wastewater
4.
Mar Drugs ; 17(5)2019 May 20.
Article in English | MEDLINE | ID: mdl-31137530

ABSTRACT

Water extracts and polysaccharides from Anabaena sp., Ecklonia sp., and Jania sp. were tested for their activity against the fungal plant pathogen Botrytis cinerea. Water extracts at 2.5, 5.0, and 10.0 mg/mL inhibited B. cinerea growth in vitro. Antifungal activity of polysaccharides obtained by N-cetylpyridinium bromide precipitation in water extracts was evaluated in vitro and in vitro at 0.5, 2.0, and 3.5 mg/mL. These concentrations were tested against fungal colony growth, spore germination, colony forming units (CFUs), CFU growth, and on strawberry fruits against B. cinerea infection with pre- and post-harvest application. In in vitro experiments, polysaccharides from Anabaena sp. and from Ecklonia sp. inhibited B. cinerea colony growth, CFUs, and CFU growth, while those extracted from Jania sp. reduced only the pathogen spore germination. In in vitro experiments, all concentrations of polysaccharides from Anabaena sp., Ecklonia sp., and Jania sp. reduced both the strawberry fruits infected area and the pathogen sporulation in the pre-harvest treatment, suggesting that they might be good candidates as preventive products in crop protection.


Subject(s)
Anabaena/chemistry , Antifungal Agents/pharmacology , Botrytis/drug effects , Fragaria/drug effects , Fragaria/microbiology , Phaeophyceae/chemistry , Rhodophyta/chemistry , Antifungal Agents/isolation & purification , Botrytis/physiology , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Spores, Fungal/drug effects , Water/chemistry
5.
J Nat Prod ; 81(2): 410-413, 2018 02 23.
Article in English | MEDLINE | ID: mdl-29432010

ABSTRACT

Cybastacines A (1) and B (2) were discovered as a novel pentacyclic sesterterpenoid-alkaloid skeleton structure, with a guanidinium group. These molecules were isolated from a Nostoc sp. cyanobacterium collected in the Canary Islands. Their structures were elucidated primarily by a combination of spectroscopic analyses and X-ray diffraction. These compounds showed antibiotic activities against several clinically relevant bacterial strains.


Subject(s)
Anti-Bacterial Agents/chemistry , Nostoc/chemistry , Sesterterpenes/chemistry , Guanidine/chemistry , Spain
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