Background: SNF-related Kinase 1 (SnRK1) is a key component of the cell signaling network. SnRK1 is known to respond to a wide variety of stresses, but its exact role in salt stress response and tolerance is still largely unknown.Results: In this study, we reported that overexpression of the gene encoding the α subunit ofPrunus persica SnRK1(PpSnRK1α) in tomato could improve salt stress tolerance. The increase in salt stress tolerance inPpSnRK1α-overexpressing plants was found to correlate with increasedPpSnRK1αexpression level and SnRK1 kinase activity. AndPpSnRK1αoverexpression lines exhibited a lower level of leaf damage as well as increased proline content and reduced malondialdehyde (MDA) compared with wild-type (WT) lines under salt stress. Furthermore,PpSnRK1αenhanced reactive oxygen species (ROS) metabolism by increasing the expression level of antioxidase genes and antioxidant enzyme activities. We further sequenced the transcriptomes of the WT and threePpSnRK1αoverexpression lines using RNA-seq and identified about 1000PpSnRK1α-regulated genes, including many antioxidant enzymes, and these genes were clearly enriched in the MAPK signaling pathway (plant), plant-pathogen interactions and plant hormone signaling transduction and can respond to stimuli, metabolic processes, and biological regulation. Furthermore, we identified the transcriptional levels of several salt stress-responsive genes,SlPP2C37,SlPYL4,SlPYL8,SlNAC022,SlNAC042,andSlSnRK2family were altered significantly byPpSnRK1α, signifying thatSnRK1αmay be involved in the ABA signaling pathway to improve tomato salt tolerance. Overall, these findings provided new evidence for the underlying mechanism ofSnRK1αconferment in plant salt tolerance phenotypes.Conclusions: Our findings demonstrated that plant salt stress resistance can be affected by the regulation of theSnRK1α. Further molecular and genetic approaches will accelerate our knowledge ofPpSnRK1αfunctions, and inform the genetic improvement of salt tolerance in tomato through genetic engineering and other related strategies.

Fruit quality depends largely on the type and amount of sugar accumulated in the fruit. In peach [Prunus persica (L.) Batsch], sorbitol is the main photosynthetic product and plays a crucial role in sugar metabolism. As a conserved energy sensor, SNF1-related kinase 1 (SnRK1) is involved in the regulation of carbon metabolism. In this study, SnRK1 was able to respond to induction by treatment with exogenous trehalose and sorbitol on ‘Ruipan 17’ peach fruit. After treatment with 100-mM trehalose for 3 h, the SnRK1 activity decreased by 18% and the activities of sorbitol dehydrogenase (SDH) and sucrose synthase (SS) also decreased significantly, but sucrose phosphate synthase (SPS) activity increased significantly; whereas sorbitol treatment under the same conditions resulted in a 12.6% increase in SnRK1 activity and the activities of SDH and SS synthase also increased significantly, compared with the control. The contents of glucose, fructose and sucrose in peach fruit increased significantly after 3 h of sorbitol treatment. In addition, the interactions between PpSnRK1α and enzymes PpSDH and PpSPS were confirmed by yeast two-hybrid method and the phosphorylation of PpSnRK1α and PpSDH was detected in vitro. Taken together, these results suggest that SnRK1 promotes sorbitol metabolism by activating SDH and it also regulates the activities of SS and SPS that enhance sucrose accumulation in peach fruit. SnRK1 protein kinase is involved in sugar metabolism and has the potential to be used for improving fruit quality.

Microbial fertilizers have a significant role in promoting plant growth, resistance to environmental stresses, and soil remediation. Microbial fertilizers are mainly composed of beneficial microorganisms that contain specific functions. Focusing on the peach tree rhizosphere region, this study aimed to isolate and screen bacteria with efficient phosphate-solubilizing capacity for application in microbial fertilizers, as well as to dig deeper into the other properties of the strains to further explore the roles of these phosphate-solubilizing bacteria (PSBs) in terms of plant growth in order to provide valuable microbial resources for microbial fertilizer development. By collecting soil samples from peach tree rhizospheres, we initially screened 86 PSB strains using the plate method and determined the phosphate-solubilizing capacity (ranged from 0 to 14 μg/mL). Afterwards, 51 strains with strong phosphate-solubilizing capacity were selected for molecular identification; the strains belonged to 12 genera, with Bacillus and Burkholderia accounting for the majority. Concurrent evaluation of iron carriers and indoleacetic-3-acid (IAA) production capabilities identified strain WPD85 as exhibiting dual functionality with strong performance in both parameters. Subsequently, we combined the analysis of phosphate-solubilizing capacity and growth-promoting properties to select eight strains of PSBs; characterized them physiologically, biochemically, and molecularly; determined the biofilm-forming capacity; and conducted potting experiments. Notably, strain WPD103 exhibited exceptional biofilm-forming capacity (OD₅₉₅ = 1.09). Of particular interest, strain WPD16 demonstrated both an elevated inorganic phosphate solubilization index (D/d = 2.99) and remarkable iron carriers production capacity, while peach seedlings treated with WPD16 exhibited 119% enhancement in plant height increment compared to the control. This study enhances our understanding of PSB traits and identifies Burkholderia sp. WPD16 as a strategic candidate for developing targeted microbial fertilizers, offering a sustainable solution to reduce reliance on chemical inputs in orchard management.

Trehalose-6-phosphate synthase (TPS) is essential for plant growth and development, linking trehalose-6-phosphate (T6P) to carbon metabolism. However, little is known about the TPS gene family in peaches and their potential roles in regulating carbohydrates in peach fruit. In this study, nine TPS genes were identified in the peach genome and named according to the homologous genes in Arabidopsis. Phylogenetic analysis showed that three subfamilies were identified, including TPSI, TPSII-1, and TPSII-2, which were also consistent with gene structure analysis. Considerable cis-elements were enriched in the promoters, including plant hormone-related elements. Tissue-specific analysis showed that these TPS genes were mainly expressed in leaves, stems, and fruit, showing different expression patterns for each gene. In addition, during fruit development, the content of trehalose-6-phosphate (T6P) was positively correlated with the expression of PpTPS7a and negatively with sucrose non-fermenting-1-related kinase 1 (SnRK1) activity. Transient overexpression and silencing of PpTPS7a in peach fruit validated its function in regulating T6P content and SnRK1 activity.

Background/Objectives: The sucrose non-fermentation-related kinase 1 (SnRK1) protein complex in plants plays an important role in energy metabolism, anabolism, growth, and stress resistance. SnRK1 is a heterotrimeric complex. The SnRK1 complex is mainly composed of α, β, βγ, and γ subunits. Studies on plant SnRK1 have primarily focused on the functional α subunit, with the β regulatory subunit remaining relatively unexplored. The present study aimed to elucidate the evolutionary relationship, structural prediction, and interaction with the core α subunit of peach SnRK1β3 (PpSnRK1) subunit. Methods: Bioinformatics analysis of PpSnRK1 was performed through software and website. We produced transgenic tomato plants overexpressing PpSnRK1 (OEPpSnRK1). Transcriptome analysis was performed on OEPpSnRK1 tomatoes. We mainly tested the growth index and drought resistance of transgenic tomato plants. Results: The results showed that PpSnRK1 has a 354 bp encoded protein sequence (cds), which is mainly located in the nucleus and cell membrane. Phylogenetic tree analysis showed that PpSnRK1β3 has similar domains to other woody plants. Transcriptome analysis of OEPpSnRK1β3 showed that PpSnRK1β3 is widely involved in biosynthetic and metabolic processes. Functional analyses of these transgenic plants revealed prolonged growth periods, enhanced growth potential, improved photosynthetic activity, and superior drought stress tolerance. Conclusions: The study findings provide insight into the function of the PpSnRK1 subunit and its potential role in regulating plant growth and drought responses. This comprehensive analysis of PpSnRK1 will contribute to further enhancing our understanding of the plant SnRK1 protein complex.