Metabolism of Mycosporine-Glutamicol in the Lichen Cladonia arbuscula subsp. squarrosa under Seasonal Changes and Elevated Exposure to UV-B or PAR Irradiation.

Cladonia arbuscula in its environmental niches is regularly affected by daily and annual variations in solar radiation. Mycosporine-glutamicol, Myc-Glu(OH), which it synthesizes, may act as a significant cellular UV-protector. Therefore, we studied this compound concentration in lichen thalli concerning seasonal changes and increased exposure to UV-B and photosynthetically active radiation (PAR) with/without simultaneous CO2 deprivation. Myc-Glu(OH) occurred year-round and exhibited a strong seasonality. The most crucial role in the control of its synthesis played UV-B radiation, although its high concentration was also found after PAR irradiation at 1000 µmol m-2 s-1. As PAR intensity increased to 2000 µmol m-2 s-1, the rate of Myc-Glu(OH) synthesis slowed down. In turn, under dark/PAR irradiation with simultaneous deprivation of CO2 in the atmosphere surrounding C. arbuscula and during darkness with continuous access to atmospheric CO2, its production was insignificant. Obtained data confirmed that Myc-Glu(OH) plays an important role in protecting C. arbuscula from UV damage and favours its adaptation to environmental stress in its natural habitat. They also suggest that its synthesis is a synergism of multiple factors. Consequently, further studies should focus on their evaluation and the identification of a lichen partner actively involved in Myc-Glu(OH) biogenesis.

Inhibition of growth rate and cylindrospermopsin synthesis by Raphidiopsis raciborskii upon exposure to macrophyte Lemna trisulca (L).

Impact of macrophyte Lemna trisulca on the growth rate and synthesis of cylindrospermopsin (CYN) by cyanobacterium Raphidiopsis raciborskii was determined. The presence of L. trisulca inhibited the biomass accumulation of the cyanobacterium by 25% compared to the control during co-cultivation. The simultaneous cultivation of these organisms slightly affected the inhibition of macrophyte growth rate by 5.5% compared to the control. However, no morphological changes of L. trisulca after incubation with cyanobacteria were observed. It was also shown that the long-term (35 days) co-cultivation of R. raciborskii and L. trisulca led to a decrease in CYN concentration in media and cyanobacterial cells by 32 and 38%, respectively, compared to the values obtained for independent cultivation of cyanobacterium. Excessive absorption of phosphate ions by L. trisulca from the medium compared to nitrate ions led to a significant increase in the nitrate:phosphate ratio in the media, which inhibits the development of cyanobacterium. The obtained results indicate that L. trisulca in the natural environment may affect the physiology of cyanobacteria. The presented study is the first assessment of the allelopathic interaction of macrophyte and R. raciborskii.

Anatoxin-a degradation by using titanium dioxide.

Advanced oxidation processes, such as using titanium dioxide (TiO2) photocatalysis, are being developed to reduce or eliminate the toxicity of treated water. In this study, the removal of purified anatoxin-a (ANTX-a), live Dolichospermum flos-aquae cells, and a cell extract of this organism under UV-A/TiO2 photocatalysis, creation of decomposition products and their toxicity were investigated. Total degradation of purified ANTX-a from the initial concentration of 10 mg·L-1 with the addition of TiO2 under UV-A irradiation was achieved in 30 min. Under these conditions several decomposition products were noted with m/z ratio from 156.11 to 216.1. Analysis of the completely degraded ANTX-a sample using Thamnotoxkit F™ toxicity test showed that it was no longer toxic. TiO2 photocatalysis was also efficient in the decomposition of the living cyanobacterial cells. Degradation of their cell structures and degradation of released toxin was also achieved in 30 min. Earlier homogenization of cyanobacteria culture significantly accelerated degradation of ANTX-a to 10 min.