Hydrogen Peroxide Stress Induced in the Marine Cyanobacterium Synechococcus aeruginosus and Phormidium valdarianum.

Biochemical markers against hydrogen peroxide-induced oxidative stress were developed in marine cyanobacteria under standard laboratory conditions. To find out the ability to cope with different concentrations of hydrogen peroxide, two species of marine cyanobacteria including unicellular and filamentous forms were exposed for shorter duration. Synechococcus aeruginosus and Phormidium valderianum tolerated hydrogen peroxide by showing the highest growth of Superoxide dismutase in Synechococcus aeruginosus and Phormidium valderianum, catalase in Synechococcus aeruginosus, peroxidase in Synechococcus aeruginosus and Phormidium valderianum, Glutathione S-transferase in Synechococcus aeruginosus and Phormidium valderianum which were identified as biochemical markers of oxidative stress against H2O2 in marine cyanobacteria. Synechococcus aeruginosus showed new isoforms for Superoxide dismutase, catalase, peroxidase, Glutathione peroxidase, and Glutathione S-transferase and Phormidium valderianum for Superoxide dismutase, peroxidase, and Glutathione S-transferase. Synechococcus aeruginosus is suggested as the indicator species for biochemical markers against hydrogen peroxide in marine cyanobacteria. Peroxidase is suggested as biochemical enzyme marker. The present investigated on these new isoenzymes were identified as biochemical markers for oxidative stress.

Hydrogen peroxide can be a plausible biomarker in cyanobacterial bloom treatment.

The effect of combined stresses, photoinhibition, and nutrient depletion on the oxidative stress of cyanobacteria was measured in laboratory experiments to develop the biomass prediction model. Phormidium ambiguum was exposed to various photosynthetically active radiation (PAR) intensities and phosphorous (P) concentrations with fixed nitrogen concentrations. The samples were subjected to stress assays by detecting the hydrogen peroxide (H2O2) concentration and antioxidant activities of catalase (CAT) and superoxide dismutase (SOD). H2O2 concentrations decreased to 30 µmol m-2 s-1 of PAR, then increased with higher PAR intensities. Regarding P concentrations, H2O2 concentrations (nmol L-1) generally decreased with increasing P concentrations. SOD and CAT activities were proportionate to the H2O2 protein-1. No H2O2 concentrations detected outside cells indicated the biological production of H2O2, and the accumulated H2O2 concentration inside cells was parameterized with H2O2 concentration protein-1. With over 30 µmol m-2 s-1 of PAR, H2O2 concentration protein-1 had a similar increasing trend with PAR intensity, independently of P concentration. Meanwhile, with increasing P concentration, H2O2 protein-1 decreased in a similar pattern regardless of PAR intensity. Protein content decreased with gradually increasing H2O2 up to 4 nmol H2O2 mg-1 protein, which provides a threshold to restrict the growth of cyanobacteria. With these results, an empirical formula-protein (mg L-1) = - 192*Log((H2O2/protein)/4.1), where H2O2/protein (nmol mg-1) = - 0.312*PAR2/(502 + PAR2)*((25/PAR)4 + 1)*Log(P/133,100), as a function of total phosphorus concentration, P (µg L-1)-was developed to obtain the cyanobacteria biomass.

Silver nanoparticles green synthesis via cyanobacterium Phormidium sp.: characterization, wound healing, antioxidant, antibacterial, and anti-inflammatory activities.

OBJECTIVE: Green synthesis of silver nanoparticles (AgNPs) using cyanobacterial platforms is becoming more popular nowadays. In this study, the filamentous non-heterocystous cyanobacterium Phormidium sp. was used for AgNPs production. Then, it was investigated for its antibacterial and wound-healing properties. MATERIALS AND METHODS: The cyanobacterium cultures were challenged by AgNO3, and the obtained nanoparticles were characterized using UV and FTIR spectrometric methods. The antimicrobial activity of AgNPs was scrutinized against MRSA either alone or in combination 0.5% chloramphenicol. The green synthesized AgNPs were tested for their skin wound healing activity using several wound models at different concentrations. RESULTS: The cyanobacterial culture extract showed the characteristic surface plasmon resonance peak at 440 nm for AgNPs. Different functional groups that could contribute to the reduction of Ag+ to AgNPs or the stabilization of the nanoparticles were identified by the FTIR. AgNPs potentiated the antimicrobial activity of chloramphenicol against MRSA. Green synthesized silver nanoparticles have demonstrated topical effectiveness in different wound models, including excision, incision, and burn. Significant wound improvement and the increase in wound closure rate, hydroxyproline content, and the reduction in epithelialization period confirmed the wound healing potency of AgNPs. The enzymatic antioxidant level escalation and inflammatory cytokines attenuation supported the AgNPs substantial effect on wound repairing. CONCLUSIONS: Biogenic AgNPs produced by Phormidium sp. showed significant antimicrobial together with wound healing abilities.

Bioseparation of phycocyanin from Phormidium tergestinum using an aqueous two-phase system.

This study aimed at purification of phycocyanin (PC) from Phormidium tergestinum using an aqueous two-phase system (ATPS) comprised of polyethylene glycol (PEG) and salts. The partitioning efficiency of PC in ATPS and the effect of phase composition, pH, crude loading, and neutral salts on purification factor and yield were investigated. Results showed that PC was selectively partitioned toward bottom phase of the system containing potassium phosphate. Under optimum conditions of 20% (w/w) PEG 4000, 10% (w/w) potassium phosphate, 20% (v/v) crude load at pH 7, with addition of 0.5% (w/w) NaCl, PC from P. tergestinum was partially purified up to 5.34-fold with a yield of 87.8%. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that the molecular weight of PC was ∼19 kDa. Results from this study demonstrated ATPS could be used as a potential approach for the purification of PC from P. tergestinum.