White pitaya, a popular tropical fruit, is known for its high nutritional value. It is commercially cultivated worldwide for its potential use in the food and pharmaceutical industries. This study aims to assess the nutritional and phytochemical contents and biological potential of the South Chinese White Pitaya (SCWP) peel, flesh, and seed extracts. Extract fractions with increasing polarity (ethyl acetate < acetone < ethanol < methanol < aqueous) were prepared. Antibacterial potential was tested against multidrug-resistant (MDR) bacteria, and antioxidant activity was determined using, 2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assays, and cytotoxic activity against human keratinocyte cells using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. Pharmacological screening and molecular docking simulations were conducted to identify potential antibacterial compounds with druggable characteristics. Molecular dynamics simulation (MDS) was employed to validate the binding stability of the promising ligand-protein complexes. All parts of the fruit exhibited a substantial amount of crucial nutrients (minerals, sugars, proteins, vitamins, and fatty acids). The ethanol (ET) and acetone (AC) fractions of all samples demonstrated notable inhibitory effects against tested MDR bacteria, with MIC₅₀ ranges of 74–925 μg/mL. Both ET and AC fractions also displayed remarkable antioxidant activity, with MIC₅₀ ranges of 3–39 μg/mL. Cytotoxicity assays on HaCaT cells revealed no adverse effects from the crude extract fractions. LC-MS/MS analyses identified a diverse array of compounds, known and unknown, with antibacterial and antioxidant activities. Molecular docking simulations and pharmacological property screening highlighted two active compounds, baicalein (BCN) and lenticin (LTN), showing strong binding affinity with selected target proteins and adhering to pharmacological parameters. MDS indicated a stable interaction between the ligands (BCN and LTN) and the receptor proteins over a 100-ns simulation period. Our study provides essential information on the nutritional profile and pharmacological potential of the peel, flesh, and seeds of SCWP. Furthermore, our findings contribute to the identification of novel antioxidants and antibacterial agents that could be capable of overcoming the resistance barrier posed by MDR bacteria.

Zinc finger proteins (ZFPs) are a diverse group of plant transcription factors essential for regulating development, signaling, and stress responses. In this study, we performed a genome-wide identification and integrative analysis of 140 C3H-type zinc finger transcription factor genes in the soybean genome, exhibiting an uneven distribution across all 20 chromosomes. These C3H-ZFPs contained one (37), two (58), three (19), four (7), five (17), or six (2) C3H domains and were classified into 14 subsets based on their domain architecture. All C3H genes encoding proteins harbored the conserved C3H-ZFP domain and displayed various physicochemical characteristics. Phylogenetic analysis grouped them into 10 clades, closely related to other species like Arabidopsis, rice and alfalfa. Promoter analysis revealed cis-elements associated with stress response (~39.1%), light response (~37.3%), phytohormones (~18.5%), and development (~4.97%). Duplication analysis revealed 78 pairs of segmental and eight tandem duplication events, with purifying selection indicated by Ka/Ks (nonsynonymous/synonymous) ratios, indicating that these C3H-ZFP duplicates were largely maintained under purifying selection. A total of 388 miRNAs from 196 gene families were predicted to target 140 C3H-ZFP genes, with most enriched miRNAs targeting C3H-ZFP genes, including the miR156, miR395, and miR396 families. Transcription factor binding sites for MYB, AP2, MIKC_MADS, BBR-BPC, ERF, C2H2, and Dof were found upstream of most C3H-ZFP genes. RNA-Seq and qRT-PCR analyses showed tissue-specific expression and stress-responsive expression patterns, with several C3H-ZFP genes, especially GmC3H1, GmC3H63, GmC3H124, and GmC3H127, being significantly upregulated under abiotic stress conditions. Together, these results provide a comprehensive overview of soybean C3H-ZFP genes and identify promising candidates for future functional studies on development and abiotic stress adaptation.

Monosaccharide transporters (MSTs) are important plant glucose transporters that play roles in carbon allocation, growth, development, and stress regulation. However, research on MST regulatory genes in soybeans remains unexplored. In this study, we identified 110 MST-like candidate genes in the Glycine max L. (soybean) genome. The MST genes were distributed throughout 20 chromosomes, with many undergoing segmental duplication. The majority of MST group proteins exhibit significant preservation in Arabidopsis and soybean, and phylogenetic analysis reveals seven main categories. The promoters of the GmMST genes comprise cis-acting elements associated with plant responses to abscisic acid, auxin signaling, methyl jasmonate, low temperatures, and abiotic stresses. The RNA-seq data demonstrated diverse expression levels of MST genes across various tissues or organs, categorizing them into 11 primary clusters. The co-expression study of the network complex indicated that the GmMST genes encode proteins that interact with many essential genes associated with gibberellin, which are pivotal in seed and stamen development. A qPCR study validated the expression patterns of seven MST genes with exposure to copper (Cu) and cadmium (Cd) stress. Certain MST genes were notably stimulated by both Cu and Cd stress treatments, suggesting their involvement in defense responsiveness. Therefore, we provide a comprehensive analysis of the MST genes in soybeans and emphasize their substantial role in plant development and tolerance to metal ion stressors.

The plant homeodomain (PHD) finger constitutes a subgroup of transcription factors that contribute to the coordination of plant growth, morphogenesis, and adaptation to environmental stress mechanisms. In this study, we identified and functionally characterized the BrPHD58 gene from Brassica rapa . Using sequence analysis, subcellular localization of BrPHD58–GFP fusion proteins, and transgenic Arabidopsis thaliana lines ectopically expressing BrPHD58, we investigated its role in salt stress responses, including seedling phenotypes and expression of salt-responsive genes. Subcellular localization analysis indicated that BrPHD58 predominantly accumulates within the nuclear compartment. Ectopic expression of BrPHD58 in A. thaliana significantly reduced seedling survival rates and root lengths under varying concentrations of NaCl compared to wild-type (WT) plants. Under soil-grown conditions, transgenic lines overexpressing BrPHD58 exhibited markedly decreased tolerance to salt stress. Moreover, ectopic expression of BrPHD58 led to a down regulation of key salt-responsive genes, AtRD22, AtRD29A , and AtLEA14 , under salt stress conditions. Collectively, all these findings indicate that BrPHD58 acts as a negative modulator of salt stress tolerance in transgenic plants. Further investigation involving the development and analysis of BrPHD58 loss-of-function mutants in B. rapa is necessary to fully elucidate its physiological role in salinity adaptation.