Potato scab, a global soil-borne disease caused by Streptomyces, is pivotal in developing resistant cultivars due to its complex resistance mechanisms. This study investigates the transcriptomic responses in potato to common scab using resistant variety CS10 and susceptible CS11 post S. scabie inoculation (0 d and 10 d, 12 cDNA libraries). Differential expression analysis identified 147 key DEGs (Differentially Expressed Genes) essential in disease recognition, signal transduction, and defense. GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) enrichment analyses revealed several significant metabolic pathways, such as ADP binding, heme binding, chloroplast thylakoid membrane, photosynthesis, glutathione metabolism, and homologous recombination, among others. Notably, the correlation between chloroplast pathways (GO:0019745) and photosynthesis (map00195) highlights photosynthesis’s role in potato scab response, while the oxygen transport (GO:0031408)-related glutathione metabolism pathway (map00480) emphasizes antioxidant defenses. Furthermore, three potential resistance genes were validated: Ethylene Response Factor ERF010 (LOC102589042), Disease Resistance Protein RPP13 (LOC102605863), and Cytochrome P450 83B1 (LOC102604056), demonstrating the linkage between metabolic pathways and pathogen response. These findings offer insights into potato’s molecular resistance mechanisms against potato scab, supporting the breeding of resistant varieties and comprehensive disease management, thus advancing sustainable agriculture.

Physalis philadelphica, a member of the Solanaceae family, commonly known as Physalis, is a one-year-old herbaceous plant with both medicinal and edible properties, as well as ornamental value. At present, only limited research is available on the flower color of P. philadelphica. This study aimed to elucidate the metabolic characteristics underlying the flower color of P. philadelphica and to identify key genes associated with flower color metabolism. We selected two representative varieties of P. philadelphica with significant differences in flower color, namely, “Tieba” (yellow flower) and “Qingjin” (yellow-purple flower), as the experimental materials. The analysis of related pigment components and the determination of relative content by high-performance liquid chromatography were conducted to investigate the flower color-related metabolic pathways of P. philadelphica. Through next-generation sequencing, these pathways were further investigated for the characteristics and differentially expressed genes (DEGs) associated with flower color formation. The results of the research show that: Anthocyanin is the main component of petal coloring of P. philadelphica var. Qingjin, while malvidin pigment, pelargonidin, delphinidin, and cyanidin are the main components of flower color intensity. Carotenoids are the main components of the petal coloring of P. philadelphica var. Tieba and β-carotene is the main component of flower color intensity. Comparing different developmental stages of these two kinds of Physalis pubescens, we identified two key transcription factors (TFs) (eBP and STAT) that were involved in the inhibition of anthocyanin synthesis and regulate the inhibition of pf05G124640 (dihydroflavonol 4-reductase) and pf09G224140 (anthocyanin synthase) in anthocyanin synthesis. One heat shock transcription factor was found to regulate the flavonoid and flavonol synthesis pathway of pf01G020090 (anthocyanin 3-O-glucosyltransferase); two key TFs (NAC and G2-Like), pf10G255070 (isoricin dehydrogenase) and pf09G237080 (abscisic acid 8′-hydroxylase), played important roles in carotene biosynthesis. This study provides new insights for further exploration of the genetic diversity of petal coloring in P. philadelphica and establishes a foundation for subsequent molecular breeding efforts.

The potato is a pivotal food crop on a global scale. Nitrate reductase (NR) and nitrite reductase (NiR) are the key enzymes in nitrogen assimilation. In previous research, we found that the nitrogen assimilation process was effectively regulat...

Panax ginseng (ginseng) is an important herbal medicine plant; however, successive ginseng cultivation causes intense acidification and active aluminum (Al) dissolution in ginseng bed soil. High Al retention in the root epidermis has been well documented to associate with the occurrence of red skin root syndrome of ginseng. The present study aimed to clarify the origins and effects of this Al accumulation patterns. Healthy and red skin ginseng were collected to compare Al concentrations in whole plants and root epidermis cell wall modification from physiological parameters, transcriptional expression, and the sugar-targeted-metabolome perspectives. In healthy ginseng plants, around 50 % of Al content was distributed in the aboveground parts, while red skin ginseng of comparable ages had markedly higher Al concentrations in the main root epidermis and fibrous roots than those in healthy plants. Isolated red skin ginseng root epidermis showed strong Al-morin fluorescence staining, lower cell wall Al adsorption ability, lower hemicellulose and pectin content, and altered monosaccharide concentrations, relative to those from healthy plants. Fibrous roots from red skin ginseng had higher transcriptional abundance of several cell wall degradation-related genes. Overall, comparable Al concentrations were transported to discarded organs, such as leaves and stems, of healthy ginseng plants. Conversely, in red skin ginseng, higher Al concentrations were detained in the root epidermis, resulting from epidermal cell wall degradation.