Search Results (3)

Nitric oxide (NO) is a widely recognized signaling molecule found across various organisms, yet its specific effects on fungal growth and development under anaerobic conditions remain underexplored. This study investigates how NO influences the growth and development of Schizophyllum commune 20R-7-F01 under anaerobic environments. The results demonstrated an increase in endogenous NO levels during mycelial growth and basidiospore germination. The addition of cPTIO, a NO scavenger, inhibited mycelial growth, delayed basidiospore germination, and reduced the expression of genes involved in basidiospore germination, highlighting the critical role of NO in fungal growth and development. On the other hand, exogenous NO supplementation accelerated mycelial growth and facilitated the formation of primordia, suggesting NO’s potential as a key regulator of fungal development. These findings deepen our understanding of NO’s contribution to fungal growth in anaerobic conditions and offer new perspectives on its role as a signaling molecule in the development of S. commune communities, shedding light on the metabolic regulation of anaerobic microorganisms. Full article

Schizophyllum commune is an edible fungus with high medicinal value, but exposure to heavy-metal pollution poses significant health risks. Cadmium (Cd) toxicity inhibits fungal growth and leads to Cd accumulation in the mycelium. However, the regulatory mechanisms of Cd-induced growth inhibition and Cd accumulation remain poorly understood. Here, S. commune 20R-7-F01 was cultured in Cd-supplemented minimal medium (MM) to investigate the response of S. commune 20R-7-F01 to Cd exposure. We found that Cd exposure resulted in growth inhibition and a Cd-dependent increase in endogenous nitric oxide (NO) levels. NO production was primarily mediated by the nitrate reductase (NR) pathway. Cd-induced growth inhibition was alleviated by inhibiting NR activity or scavenging NO, highlighting the role of NO in stress responses. Furthermore, NO was found to enhance chitinase activity, thereby promoting Cd accumulation in the fungal cell wall and leading to growth inhibition. These results reveal a novel mechanism by which S. commune copes with Cd stress. This study highlights the potential of manipulating NO levels as a strategy to enhance fungal tolerance to heavy-metal pollution, providing a new avenue for managing environmental stresses in edible fungi and protecting human health. Full article

Fungi inhabiting deep subseafloor sediments have been shown to possess anaerobic methane (CH₄) production capabilities under atmospheric conditions. However, their ability to produce CH₄ under in situ conditions with high hydrostatic pressure (HHP) remains unclear. Here, Schizophyllum commune 20R-7-F01, isolated from ~2 km below the seafloor, was cultured in Seawater Medium (SM) in culture bottles fitted with sterile syringes for pressure equilibration. Subsequently, these culture bottles were transferred into 1 L stainless steel pressure vessels at 30 °C for 5 days to simulate in situ HHP and anaerobic environments. Our comprehensive analysis of bioactivity, biomass, and transcriptomics revealed that the S. commune not only survived but significantly enhanced CH₄ production, reaching approximately 2.5 times higher levels under 35 MPa HHP compared to 0.1 MPa standard atmospheric pressure. Pathways associated with carbohydrate metabolism, methylation, hydrolase activity, cysteine and methionine metabolism, and oxidoreductase activity were notably activated under HHP. Specifically, key genes involved in fungal anaerobic CH₄ synthesis, including methyltransferase mct1 and dehalogenase dh3, were upregulated 7.9- and 12.5-fold, respectively, under HHP. Enhanced CH₄ production under HHP was primarily attributed to oxidative stress induced by pressure, supported by intracellular reactive oxygen species (ROS) levels and comparative treatments with cadmium chloride and hydrogen peroxide. These results may provide a strong theoretical basis and practical guidance for future studies on the contribution of fungi to global CH₄ flux. Full article