Soil microorganisms play important roles in nutrient mobilization and uptake of mineral nutrition in plants. Agricultural management, such as soil sterilization, can have adverse effects on plant growth because of the elimination of indigenous microorganisms. Arbuscular mycorrhizal (AM) fungi are one of the most important beneficial soil microorganisms for plant growth. However, whether AM fungi can compensate for the loss of indigenous microbial communities to support plant growth and metabolism is largely unknown. In this study, a pot experiment was conducted to investigate the effects of AM fungi on plant growth and secondary metabolism in sterilized and unsterilized soil. We used liquorice (Glycyrrhiza uralensis Fisch.), an important medicinal plant as the host, which was inoculated with the AM fungus Rhizophagus irregularis or not and grown in unsterilized or sterilized soil. Plant photosynthesis traits, plant growth and nutrition level, concentrations of the secondary metabolites, and expression levels of biosynthesis genes were determined. The results showed that soil sterilization decreased plant growth, photosynthesis, and glycyrrhizin and liquiritin accumulation, and moreover, downregulated the expression of related biosynthesis genes. Inoculation with R. irregularis in sterilized soil offset the loss of indigenous microbial communities, resulting in plant growth and glycyrrhizin and liquiritin concentrations similar to those of plants grown in unsterilized soil. Thus, AM fungi could compensate for the loss of indigenous microbial communities by soil sterilization to support plant growth and secondary metabolism.

Arbuscular mycorrhizal (AM) fungi establish mutualistic symbioses with plant roots, enhancing plant growth and improving soil fertility through nutrient exchange. Among these, soil nitrogen (N) and phosphorus (P) are critical for symbiosis formation, directly influencing nutrient uptake and translocation within the symbiotic system. This study aimed to examine the regulatory roles of N and P levels on AM fungal development and associated bacterial communities in culture. Sorghum was used as the host plant in pot experiments with two AM fungi, Rhizophagus irregularis and Funneliformis mosseae, under varying N and P concentrations. The analyzed parameters included mycorrhizal colonization, propagule production, plant biomass, nutrient contents (N, P, and K), and bacterial community diversity. N3P1 treatment (150 mg/L N, 30 mg/L P) yielded the highest colonization rate, spore production, and arbuscule abundance in both AM fungal symbionts. At equivalent N and P concentrations, the N, P, and K contents in inoculated plants were significantly higher than those in controls. AM fungal inoculation markedly increased the bacterial diversity in the culture (Shannon index raised by 15.2–28.7%) and enriched beneficial taxa, such as Bradyrhizobium and Pseudomonas. N and P concentrations substantially influenced AM fungal symbiosis, with optimal development observed under N3P1 conditions. By regulating AM symbiotic establishment, N and P levels reshaped microbial community composition, providing theoretical guidance for industrialized AM fungal cultivation and inoculant production.

To investigate how steam-explosion pretreatment affects humification during sawdust composting, an aerobic composting experiment was conducted using sawdust, chicken manure, and spent mushroom substrate as feedstocks. Two treatments were established—a steam-explosion-pretreated sawdust group (SEW) and an untreated sawdust control (CK)—each with three replicate reactors. Samples were collected dynamically at five key composting stages (initial, heating, thermophilic, cooling, and maturation) for physicochemical, enzymatic, and microbial community analyses. Linear mixed-effects model analysis revealed that enzyme activities were significantly affected by treatment, composting time, and their interaction. SEW significantly enhanced cellulase and polyphenol oxidase activities, and increased laccase and peroxidase activities at specific stages. Compared with CK (humic substances, 75.30 g/kg), SEW promoted higher humic substance accumulation (120.80 g/kg) and altered the dynamics of dissolved organic carbon. Microbial co-occurrence networks in SEW (50 nodes, 602 edges) were more complex than CK (49 nodes, 464 edges), indicating tighter microbial interactions. Path analysis revealed that HS in CK was mainly influenced by DOC and temperature, while HS in SEW was associated with enzyme activities, microbial diversity, and Pseudogracilibacillus. These results suggest that steam-explosion pretreatment enhances substrate transformation and humic substance formation during composting.