Inorganic pollutants in Colombian cocoa (Theobroma cacao L.) agrosystems cause problems in the production, quality, and exportation of this raw material. There has been an increased interest in bioprospecting studies of different fungal species focused on the biosorption of heavy metals. Furthermore, fungi constitute a valuable, profitable, ecological, and efficient natural soil resource that could be considered in the integrated management of cadmium mitigation. In this study, we report a new species of Talaromyces, isolated from cocoa soil from San Vicente de Chucurí-Colombia. The characterization of the culture was performed on six different standardized media and was distinguished by characteristic colony morphology: biverticillate and monoverticillate penicilli, acerose phialides, and slightly globose smooth-walled conidia. Culture was featured by bright yellow mycelium in young culture on CYA and CYAS medium. Colonies grew faster on Malt and Oat agar, attaining 36 and 32 mm diameter after seven days at 20 ºC. High acid production on CREA medium at 20-30 ºC was observed. Phylogenetic analysis was based on the ITS region and the RPB2, Calmodulin (CaM) and β-Tubulin genes that indicate that it is new to science and is named Talaromyces santanderensis sp. nov. This new species belongs to the Talaromyces section and is closely related to T. lentulus and related to T. soli, T. tumuli and T. pratensis (inside the T. pinophilus species complex) in the inferred phylogeny. Mycelia growth of the fungal strains was subjected to a range of 0-400 ppm Cd and incorporated into malt extract agar (MEA) in triplicates. Fungal radial growth was recorded every three days over a 13-days incubation period and In vitro cadmium tolerance tests showed a high tolerance index = 0,81 when the mycelium was exposed to 300 ppm of Cd. Results suggest T. santanderensis showed tolerance to Cd concentrations that exceed the permissible limits for contaminated soils, and it is promising for its use in bioremediation strategies to eliminate Cd from highly contaminated agricultural soils.

Endophytic fungi isolated from plants of different ecosystems have an impressive ability to produce diverse chemical classes of bioactive secondary metabolites. In this study, the cytotoxic activity and chemical composition of the ethyl acetate extract of the white beans culture of the endophytic fungus (FWBC), Talaromyces wortmannii isolated from the widespread reed grass, Arundo donax L. were investigated. A new ceramide named talaramide (1), along with other four known compounds; stigmasterol (2), thymine (3), uracil (4), and stigmasterol-3-O-β-D-glucoside (5) were identified. The structure of compound 1 was elucidated based on extensive 1D and 2D NMR spectroscopic techniques in combination with HR-ESI-MS. The produced FWBC extract exhibited cytotoxic activity against three cancer cell lines viz., MCF7, HepG2, and A549 (IC50; 54.57 ±0.27, 57.12 ± 0.59 and 84.33 ± 1.07 µg/mL, respectively) compared to methotrexate (IC50; 80.25 ± 1.11, 83.83 ± 0.74 and 153.20 ± 2.03 µg/mL, respectively) as a positive control. It showed selectivity indices with values ranging from 1.37 to 2.11 using the normal cell line, WI38 (IC50; 115.43 ± 1.92 µg/mL). The observed cytotoxicity, combined with acceptable selectivity indices, suggests the potential of this endophyte as a source of anticancer agents. Based on previous reports, it was also suggested that the identified ceramide could be responsible for the observed cytotoxic activity of the investigated extract.

Panax notoginseng is a traditional Chinese medicine, and saponins are its main active ingredients. The content of saponins in flower of P. notoginseng is the highest in the whole plant. Minor ginsenosides have stronger pharmacological activity than main ginsenosides, but its content in nature is very low. We can use extracted total saponins from P. notoginseng flower as the substrate to produce minor ginsenosides by biotransformation method. In this study, we used the fungus Talaromyces flavus and its crude enzymes to transform the extracted total saponins of P. notoginseng flower. Through the qualitative and quantitative analysis of the transformation substrates and products, it was found that minor ginsenosides Gyp-XVII, ginsenosides C-Mc1, C-Mx1, F2, Rg3, 20(R)-Rg3, Rk1 and Rg5 were found in the products and the conversion rate of the major saponins in P. notoginseng flower ranged from 44.16 to 55.22%, the yields of the minor ginsenosides ranged from 0.05 to 3.24%. This study provided a good experimental idea, greatly increased the utilization rate of total saponins in P. notoginseng flower, and laid a foundation for promoting the wide application of minor saponins.