Studies on the decomposition of keratin wastes by saprotrophic microfungi. I. Criteria for evaluating keratinolytic activity

The abilities and keratinolytic activity of saprotrophic microfungi (37 strains) have been investigated. Uniform criteria for the evaluation of this activity have been established

Biodecolorization of anthraquinone dyes using immobilised mycelium of

The aim of this study was to characterize the activity of oxidoreductases during biotransformation of 0.01% anthraquinone dyes: Alizarin Blue Black B (ABBB) and Acid Blue 129 (AB129), Carminic Acid (CA), Remazol Brilliant Blue R (RBBR), Acid Green 25 (AG25) and Poly R-478 by immobilized strain of Bjerkandera adusta CCBAS 930. Phenolic compounds, phytotoxicity (Lepidium sativum L.), biotoxicity were evaluated to determine the toxicity of anthraquinone dyes before and after the treatment with immobilized B. adusta CCBAS 930. More than 60% of CA and AB129 were removed by immobilized B. adusta CCBAS after 7 days. No secondary products toxic to plants and bacteria were formed during immobilized cultures of B. adusta CCBAS 930

Correlation between the abundance of cellulolitic fungi and selected soil properties

The study conducted has revealed the general abundance of cellulolytic fungi in the soil is significantly correlated only with the phosphors content. The correlation with specific soil properties was found in the case of the genera Humicola, Penicillium, Fusarium and Chrysosporium of the 10 genera of these fungi isolated most often

Possibility to Biotransform Anthracyclines by Peroxidases Produced by <i>Bjerkandera adusta</i> CCBAS 930 with Reduction of Geno- and Cytotoxicity and Pro-Oxidative Activity

The aim of this study was to evaluate the bioremoval mechanism of anthracycline antibiotics by the white-rot fungus B. adusta CCBAS 930. The activity of oxidoreductases and levels of phenolic compounds and free radicals were determined during the biotransformation of anthraquinone antibiotics: daunomycin (DNR) and doxorubicin (DOX) by B. adusta strain CCBAS 930. Moreover, phytotoxicity (Lepidium sativum L.), ecotoxicity (Vibrio fischeri), genotoxicity and cytotoxicity of anthraquinone dyes were evaluated before and after biological treatment. More than 80% and 90% of DNR and DOX were removed by biodegradation (decolorization). Initial solutions of DNR and DOX were characterized by eco-, phyto-, geno- and cytotoxicity. Despite efficient decolorization, secondary metabolites, toxic to bacteria, formed during biotransformation of anthracycline antibiotics in B. adusta CCBAS 930 cultures. DNR and DOX metabolites did not increase reactive oxygen species (ROS) production in human fibroblasts and resazurin reduction. DNR metabolites did not change caspase-3 activity

Impact of the Cultivation System and Plant Cultivar on Arbuscular Mycorrhizal Fungi of Spelt (<em>Triticum aestivum</em> ssp. <em>Spelta</em> L.) in a Short-Term Monoculture

Native communities of arbuscular mycorrhizal fungi (AMF) constitute a natural biofertilization, biocontrol, and bioprotection factor for most agricultural crops, including cereals. The present study investigated the native AMF population in cultivated spelt, i.e., a cereal that has not been analyzed in this respect to date. In particular, the aim of the study was to determine the number of spores and the degree of AMF root colonization in two spelt cultivars (Franckenkorn and Badengold) from a 3-year monoculture grown in two different cultivation systems: conventional tillage and no-tillage systems. The study showed considerable accumulation of AMF spores in the soil (on average 1325 in 100 g of air-dry soil), with a wide range of their numbers, and not a very high degree of endomycorrhizal colonization (on average from 3.0% to 31%). The intensity of AMF growth in the subsequent cultivation years gradually increased and depended on the cultivation system as well as the growth stage and cultivar of the spelt. It was found that both analyzed AMF growth indices in the no-tillage system were positively correlated with each other. Moreover, their values were higher in the no-tillage system than in the conventional system, with statistical significance only for the number of spores. This was mainly observed in the variant with the Franckenkorn cultivar. The effect of the growing season was evident in both cultivation systems and spelt cultivars. It was reflected by intensification of sporulation and mycorrhization of spelt roots by AMF in summer (maturation stage) compared with the spring period (flowering stage)

Impact of Ecological Factors on the Occurrence and Spatial-Taxonomic Structure of Keratinophilic Fungi and Their Co-Occurrence in Arable Soils

Fungi that decompose keratinized animal remains are an important component of the arable soil microbiome. The aim of the study is to characterize the communities of keratinophilic and co-inhabiting (non-keratinophilic) fungi in four cultivated soils that differ in physico-chemical properties, with particular emphasis on granulometric fractions, which have so far been omitted from studies concerning the ecology of these micromycetes. Fungi were isolated using the keratin-baiting method. Fungal species identification was carried out on the basis of their macro- and micromorphological features. The Simpson diversity index and Marczewski–Steinhaus similarity index were calculated for precise determination of the relationships between fungal communities. In the studied soils, Trichophyton ajelloi and Ctenomyces serratus dominated among keratinophilic fungi, while Purpureocillium lilacinum and Metacordyceps chlamydosporia, from the orders Eurotiales and Hypocreales, were dominant among non-keratinophilic fungi. The frequency of keratinophilic fungi was significantly positively correlated with pH and the content of two granulometric fractions, as opposed to non-keratinophilic fungi. This was reflected in the higher growth rates of keratinomycetes in loamy soil, chernozem, and rendzina, i.e., soils with a higher content of silt and clay fractions compared to sandy soil characterized by a high content of sand fractions. The species composition of both groups of fungi was most similar between loamy soil and chernozem, whereas the greatest differences were found for sandy soil and rendzina. Chernozem was characterized by the highest diversity of fungal species from both groups of fungi. The study, in addition to providing information about ecological factors, provided a collection of keratinomycete strains that can be used as a starting material for subsequent research stages regarding keratinolytic activity of these fungi and their potential use in agricultural practices

Possibility to Biotransform Anthracyclines by Peroxidases Produced by Bjerkandera adusta CCBAS 930 with Reduction of Geno- and Cytotoxicity and Pro-Oxidative Activity

The aim of this study was to evaluate the bioremoval mechanism of anthracycline antibiotics by the white-rot fungus B. adusta CCBAS 930. The activity of oxidoreductases and levels of phenolic compounds and free radicals were determined during the biotransformation of anthraquinone antibiotics: daunomycin (DNR) and doxorubicin (DOX) by B. adusta strain CCBAS 930. Moreover, phytotoxicity (Lepidium sativum L.), ecotoxicity (Vibrio fischeri), genotoxicity and cytotoxicity of anthraquinone dyes were evaluated before and after biological treatment. More than 80% and 90% of DNR and DOX were removed by biodegradation (decolorization). Initial solutions of DNR and DOX were characterized by eco-, phyto-, geno- and cytotoxicity. Despite efficient decolorization, secondary metabolites, toxic to bacteria, formed during biotransformation of anthracycline antibiotics in B. adusta CCBAS 930 cultures. DNR and DOX metabolites did not increase reactive oxygen species (ROS) production in human fibroblasts and resazurin reduction. DNR metabolites did not change caspase-3 activity