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This work is a systematic review that reports state-of-the-art in removal of pharmaceuticals from water and wastewater by photosynthetic organisms in photobioreactors. The PRISMA protocol-based review of the most recent literature data from the last 10 years (2011–2021) was reported. Articles were searched by the combination of the following keywords: photobioreactor, pharmaceuticals, drugs, hormones, antibiotics, biodegradation, removal, wastewater treatment. The review focuses on original research papers (not reviews), collected in 3 scientific databases: Scopus, Web of Knowledge, PubMed. The review considered the following factors: type of microorganisms, type of micropollutants removed, degradation efficiency and associated products, types of photosynthetic organisms and photobioreactor types. The conclusion from the systematic review is that the main factors that limit widespread pharmaceuticals removal in photobioreactors are high costs and the problem of low efficiency related with low concentrations of pharmaceuticals. The review indicated a need for further research in this area due to increasing amounts of metabolites in the food chain, such as p-aminophenol and estrone, which can cause harm to people and ichthyofauna. Pharmaceuticals removal can be improved by adapting the type of microorganism used to the type of contamination and implementing photoperiods, which increase the removal efficiency of e.g. sulfamethazine by up to 28%. In the future, it is necessary to search for new solutions in terms of the construction of photobioreactors, as well as for more effective species in terms of pharmaceuticals biodegradation that can survive the competition with other strains during water and wastewater treatment.

In the current situation of a serious raw material crisis related to the disruption of supply chains, the bioeconomy is of particular significance. Rising prices and the problem with the availability of natural gas have made N fertilizers production very expensive. It is expected that due to natural gas shortages, conventional production of nitrogen fertilizers by chemical synthesis will be hindered in the coming season. An important alternative and an opportunity to solve the problems of fertilizer nitrogen availability are biological wastewater treatment plants, which can be treated as a renewable biological nitrogen mines. Sewage sludge (including activated sludge) contains up to 6-8% DM. N. Considering the quantity of sewage sludge generated in wastewater treatment plants, it can become an important raw material for the sustainable production of organic-mineral fertilizers from renewable resources available locally, with a low carbon footprint. Furthermore, the sewage sludge management method should take nitrogen retention into account and should not allow the emission of greenhouse gases containing nitrogen. This article analyzes the technological solutions of nitrogen recovery for fertilization purposes from biological wastewater treatment plants in the context of a new and difficult resource situation. Conventional and new nitrogen recovery methods were analyzed from the perspective of the current legal situation. An attempt was made to evaluate the possibility of implementing the assumptions of the circular economy through the recovery of renewable nitrogen resources from municipal wastewater treatment plants.

The leather tannery industry generates about 33 Mt/year of solid waste with different properties, turning its management into a challenge. One of the valorization methods of tannery wastes is the production of biochar by pyrolysis of leather scratches. Biochar's sorption properties and its high nitrogen content (10%) make it suitable for its application as a soil conditioner or carrier of microelements for fertilizers. The paper presents an innovative spray method to enrich biochar with cationic micronutrients: Cu, Mn, Zn. Enriched biochar contained 1095 mg/kg Cu(II), 1334 mg/kg Mn(II) and 1205 mg/kg Zn(II). The high bioavailability of nutrients and the effectiveness of the new fertilizer were demonstrated in extraction in vitro tests - the analysis of leachability of elements to water and bioavailability of micro-nutrients. The functional properties of enriched biochar were examined in vivo (germination, pot) tests. A high biomass increase (approximately 10%) was observed compared to the group fertilized with a commercial product. The proposed solution benefits the environment in that it is made from alternative resources from which innovative fertilizers are produced according to the circular economy concept.

The increase in livestock production creates a serious problem of managing animal waste and by-products. Among the wide range of waste valorization methods available, anaerobic digestion is very promising. It is a form of material recycling that also produces renewable energy in the form of biogas, which is reminiscent of energy recycling. The effluent and digestate from the anaerobic digestion process need to be processed further. These materials are widely used in agriculture due to their composition. Both the liquid and solid fractions of digestate are high in nitrogen, making them a valuable source for plants. Before soil or foliar application, conditioning (e.g., with inorganic acids) and neutralization (e.g., with potassium hydroxide) is required to eliminate odorous compounds and microorganisms. Various methods of conducting the process by anaerobic digestion (use of additives increasing activity of microorganisms, co-digestion, multiple techniques of substrate preparation) and the possibility of controlling process parameters such as optimal C/N ratio (15-30), optimal temperature (psychrophilic (20 °C), mesophilic (35-37 °C) and thermophilic (55 °C) for microorganism activity ensure high efficiency of the process. Literature data describing tests of various digestates on different plants prove high efficiency, determined by yield increase (even by 28%), nitrogen uptake (by 20%) or phosphorus recovery rate (by 43%) or increase of biometric parameters (e.g., leaf area).

The article summarizes over 20 years of experience of a reference lab in fragile X mental retardation 1 gene (FMR1) molecular analysis in the molecular diagnosis of fragile X spectrum disorders. This includes fragile X syndrome (FXS), fragile X-associated primary ovarian insufficiency (FXPOI) and fragile X-associated tremor/ataxia syndrome (FXTAS), which are three different clinical conditions with the same molecular background. They are all associated with an expansion of CGG repeats in the 5'UTR of FMR1 gene. Until 2016, the FMR1 gene was tested in 9185 individuals with the pre-screening PCR, supplemented with Southern blot analysis and/or Triplet Repeat Primed PCR based method. This approach allowed us to confirm the diagnosis of FXS, FXPOI FXTAS in 636/9131 (6.96%), 4/43 (9.3%) and 3/11 (27.3%) of the studied cases, respectively. Moreover, the FXS carrier status was established in 389 individuals. The technical aspect of the molecular analysis is very important in diagnosis of FXS-related disorders. The new methods were subsequently implemented in our laboratory. This allowed the significance of the Southern blot technique to be decreased until its complete withdrawal. Our experience points out the necessity of implementation of the GeneScan based methods to simplify the testing procedure as well as to obtain more information for the patient, especially if TP-PCR based methods are used.

Mastitis is an economically important disease in which fungi belonging to the genusCandidamay participate as etiological agents. This study focused on determining the frequency of fungal isolation and differentiation of fungal species isolated from milk of mastitic cows. Sixty-six milk samples from mastitic cows were studied, and 55 strains of fungi were isolated. Seven different species classified asCandidawere identified basing on phenotypic properties, and the dominating species wasC. parapsilosis. Genomic DNA was isolated and amplified in PCR with ITS1 and NL2 primers. Amplification products were digested with restriction enzymesHpaII andEcoRI. Amplification of DNA with ITS1 and NL2 primers resulted in products of different sizes. Comparison of product sizes in restriction fragment PCR REA confirmed differences among species. Strains grouped together on the basis of phenotype characteristics differed in restriction fragment profiles. None of the investigated species showed similar genetic profiles.