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Native yeasts are a promising microbial resource for the development of sustainable biorefineries. In this study, we isolated 30 yeast strains from soil, decaying wood, and tree bark in a preserved Araucaria Forest in Southern Brazil and characterized them phenotypically and taxonomically. All strains were able to grow on glucose, xylose, and cellobiose, and 50% of them could metabolize arabinose. Several isolates showed high growth rates on xylose (up to 0.47 h−1) and cellobiose (up to 0.45 h−1). Notably, 19 strains (63% of the analyzed yeasts) exhibited xylanase activity at 50 °C (up to 156.84 U/mL), and four strains (13%) showed significant cellulase production. β-Glucosidase activities were particularly high in permeabilized cells of CHAP-258, CHAP-277, and CHAP-278 (up to 584.33 U/mg DCW), with kinetic parameters indicating high enzymatic performance. Twelve strains (40% of the total) were classified as oleaginous, and three (10%) displayed both lipogenic and esterase activity. Lipase activity against p-nitrophenyl palmitate (pNPP) reached 55.55 U/mL in CHAP-260. Taxonomic identification revealed representatives of seven genera, including Meyerozyma, Papiliotrema, Scheffersomyces, and Sugiyamaella, with potential for biotechnological use. Overall, the biochemical diversity observed highlights the value of native yeasts from Araucaria Forests as biocatalysts for lignocellulose-based bioprocesses, particularly due to their ability to grow on pentoses, secrete hydrolytic enzymes, and accumulate lipids.

Visceral leishmaniasis is a reemerging neglected tropical disease with limitations for its diagnosis, including low concentration of antibodies in the serum of asymptomatic patients and cross-reactions. In this context, this work proposes an electrochemical immunosensor for the diagnosis of visceral leishmaniasis in a more sensitive way that is capable of avoiding cross-reaction with Chagas disease (CD). Crude Leishmania infantum antigens tested in the enzyme-linked immunosorbent assay (ELISA) were methodologically standardized to best engage to the sensor. The antibodies anti-Trypanosoma cruzi and anti-Leishmania sp. Present in serum from patients with diverse types of CD or leishmaniasis were chosen. A screen-printed carbon electrode modified with gold nanoparticles was the best platform to guarantee effective adsorption of all antigens so that the epitope of specific recognition for leishmaniasis occurred efficiently and without cross-reaction with the evaluated CD. The current peaks reduced linearly after the recognition, and still were able to notice the discrimination between different kinds of diseases (digestive, cardiac, undetermined Chagas/acute and visceral chronic leishmaniasis). Comparative analyses with ELISA were performed with the same groups, and a low specificity (44%) was verified due to cross-reactions (high number of false positives) on ELISA tests, while the proposed immunosensor presented high selectivity and specificity (100%) without any false positives or false negatives for the serum samples from isolated patients with different types of CD and visceral leishmaniasis. Furthermore, the biosensor was stable for 5 days and presented a detection limit of 200 ng mL−1.

•We compared 2 types of recombinant follicle stimulating hormone.•Fifty nanogram per liter of diluted rFSH induced higher rates of follicular survival and growth.•Diluted/dynamized FSH induced higher follicular diameter and survival rate.•Diluted/dynamized FSH may be used as an alternative to diluted rFSH. This study compared 2 types of recombinant follicle stimulating hormone (rFSH): diluted and diluted/dynamized, on in vitro development of ovine follicles. In experiment 1, ovarian fragments were cultured for 1 or 7 days in α-MEM+ in the absence or presence of different concentrations of diluted rFSH to determine the best concentration. In experiment 2, the effect of diluted and diluted/dynamized rFSH (rFSH 6 cH—ultradiluted and succussioned), alone or in combination, was studied. In experiment 1, compared to control, 50ng/mL of diluted rFSH induced higher rates of follicular survival after 7 days of culture and higher percentages of growing follicles at day 1 of culture (P<0.05). In experiment 2, compared to control, diluted/dynamized rFSH induced higher follicular diameter and survival rate after 7 days and early follicle activation at day 1 of culture (P<0.05). Compared to diluted rFSH, diluted/dynamized rFSH induced higher rates of follicle activation at day 1 of culture (P<0.05). In conclusion, compared to the control medium, diluted/dynamized rFSH promoted survival and early activation of follicles, while diluted rFSH promoted higher activation later in the culture. Thus, diluted/dynamized rFSH may be used as an alternative to diluted rFSH for the in vitro culture of ovine preantral follicles.