It is estimated that over 700,000 tons of synthetic dyes are produced annually, 15% of which are emitted as effluents. These highly stable dyes enter the world water ecosystems and stay in the environment, and eventually cause adverse impacts to the environment. Current wastewater treatment methods, such as filtration, coagulation, and chemical oxidation, have sideeffects, including toxic residue formation, membrane fouling, bioaccumulation, and secondary pollutant formation. Given the issues mentioned, it is necessary to study how to improve the degradation of synthetic dye with a cost-effective and ecofriendly approach. Natural oxidation provides a greener option. Recently, Deuteromycetes fungus Myrothecium verrucaria G-1 (M. verrucaria G-1) has shown great potential in producing high level of dye oxidase. This study aims to generate a dye oxidase hyperproducer, 3H6 from M. verrucaria G-1 by using atmospheric and room temperature plasma (ARTP) coupled with ultraviolet (UV) irradiation. This method increases oxidase production by nearly 106.15%. After a simple precipitation and dialysis, this mutant oxidase increases by 1.97-fold in a specific activity with dye degradation rates at 70% for Mmethylene blue (MB) and 85% for Congo red (CR). It is found that the genetic stability of 3H6 remains active for ten generations. The size of oxidase is 65 kDa, and optimum temperature for reaction is 30 °C with 4.5 pH. This study presents that the first combined mutagenesis approach by ARPT-UV on fungus species generates an impressive increment of acid dye oxidases production. As such, this method presents a cost-effective alternative to mitigate hazardous dye pollution.

Fungal growth within the structure of buildings or in ventilation filters generates “hidden contamination”, which cannot be detected only through visual inspection. At the beginning of development, the fungi release fungal volatile organic compounds (FVOCs) into the atmosphere, which can originate from metabolic pathways or from the enzymatic degradation of materials. This study analyzed the air quality of a public referral hospital in Fortaleza, Ceará, Brazil in terms of FVOCs, to establish ways to improve methods of monitoring and control of specific sectors in the hospital. For that, we created and validated a protocol for detection of FVOCs, using GC/MS, while fungal samples were identified by analysis of macro and micromorphology. In total, 48 samples (60.5% positive) were analyzed for FVOCs; 7 were detected in at least one of the sectors analyzed, with 2-heptanone (179.5 μg/m3) and 2-methyl-1-propanol (121.5 μg/m3) as the most abundant. With respect to fungal findings, 24 samples were analyzed, with a high number of colony-forming units per cubic meter (CFU/m3) observed in all sectors. The airborne fungal spectrum revealed the existence of 19 genera, composed predominantly by hyaline filamentous deuteromycetes. Analysis with periodic monitoring is still needed to allow improvement in the data quality. Also, further discussion on the subject in the academic and legislative environment is needed to contribute to the systematic study of aerobiology.