Search Results (749)

This study aimed to evaluate the effect of selenium concentrations in mitigating salt stress on the physiology, growth, and yield of okra plants irrigated with brackish water. Treatments consisted of four irrigation water salinity levels (ECw: 0.4, 1.3, 2.2, and 3.1 dS m⁻¹) combined with four selenium concentrations (0, 5, 10, and 15 mg L⁻¹), arranged in a randomized block design in a 4 × 4 factorial scheme, with three replicates and one plant per plot. Increasing irrigation water salinity from 0.4 dS m⁻¹ reduced relative water content, gas exchange, initial chlorophyll a fluorescence, plant growth, and production of okra, while increasing the percentage of electrolyte leakage. Irrigation Water salinity levels above 0.4 dS m⁻¹ impaired plant water status, gas exchange, growth, chlorophyll a fluorescence, yield, and water-use efficiency, while increasing electrolyte leakage. Salinity above 1.0 dS m⁻¹ also inhibited photosynthetic pigment synthesis. Selenium did not mitigate salinity-induced reductions in chlorophyll and carotenoids. However, foliar Se at 8.6–15 mg L⁻¹ enhanced gas exchange, chlorophyll a fluorescence, growth, and fruit yield under salinity up to 3.1 dS m⁻¹. These results support Se induced attenuation of salinity stress, warranting further mechanistic studies. Full article

This study evaluated the effect of different sprouting methods on the morphological traits, pigmentation, and bioactive compound content of radish sprouts (Raphanus sativus L.). The following four sprouting techniques were compared: tray (T), sprouter (S), jar (J5–J20), and tank (R5–R20), varying in seed density and aeration conditions. The results demonstrated that the sprouting method significantly influenced growth parameters and phytochemical profiles. Sprouts produced using the tray (T) and sprouter (S) methods exhibited the highest mass and lowest dry matter content, reflecting favorable hydration and aeration. Sprouter-grown sprouts were particularly rich in chlorophyll (47.6 mg/100 g DW) and ascorbic acid (11.36 mg/100 g DW), indicating optimal photosynthetic and antioxidant metabolism. Tray-grown sprouts showed the highest polyphenol (919.8 mg GAE/100 g DW) and anthocyanin (217.0 mg C3G/100 g DW) concentrations, suggesting enhanced synthesis of secondary metabolites under mild abiotic stress. A comparative assessment using a three-point scale confirmed that sprouter, tray, and low-density tank methods provided the most favorable nutritional and sensory attributes. Overall, both technological factors and genetic background determine the nutritional quality of radish sprouts, offering practical guidance for optimizing sprout production and developing functional foods. Full article

Background: Anthocyanins and proanthocyanidins (PAs), as flavonoid compounds with potent antioxidant activity, exhibit significant health-promoting and medicinal properties. Black wolfberry (Lycium ruthenicum Murr.) is renowned for its exceptional anthocyanin content; however, the regulatory mechanisms of anthocyanin biosynthesis remain poorly understood, limiting its biotechnological potential. This study aimed to elucidate the transcriptional regulatory function of LrMYB30 in anthocyanin biosynthesis in black wolfberry. Methods: The regulatory function of LrMYB30 was investigated using virus-induced gene silencing (VIGS), yeast one-hybrid assays, and dual-luciferase reporter assays in black wolfberry. Results: VIGS demonstrated that silencing LrMYB30 promoted anthocyanin accumulation while reducing PA content, establishing that the LrMYB30 transcription factor as a negative regulator of anthocyanin synthesis. Yeast one-hybrid and dual-luciferase reporter assays confirmed that LrMYB30 directly binds to and activates the promoter of LrANR, a key structural gene in PA biosynthesis. In contrast, LrMYB30 neither binds to nor suppresses the promoters of the critical anthocyanin biosynthesis genes LrUF3GT and LrDFR. Conclusions: Thus, LrMYB30 redirects the flavonoid metabolic flux from anthocyanin to PA synthesis through transcriptional activation of LrANR during later fruit development, reducing anthocyanin accumulation and delaying coloration. These findings reveal a novel regulatory mechanism in black wolfberry pigmentation and maturation, providing genetic targets for molecular breeding of high-anthocyanin cultivars. Full article

Copper (Cu) pollution poses environmental and health risks. Owing to its adaptability and potential for water purification, Nymphoides peltata (N. peltata) is being considered for use in the remediation of Cu pollution. However, the feasibility of using N. peltata for the remediation of Cu-polluted water bodies has not yet been assessed. Here, the physiological response of N. peltata to Cu stress was determined. N. peltata samples were exposed to varying Cu concentrations (0.2, 0.4, 0.6 and 0.8 mg∙L⁻¹), and the activities of glutamine synthetase (GS), nitrate reductase (NR), nitrite reductase (NiR), ribulose-1,5-diphosphate carboxylase (Rubisco), and glycolate oxidase (GO) were measured together with the concentrations of photosynthetic pigments. The results revealed that under Cu stress, NR and GS activities significantly decreased, while NiR activity significantly increased. Exposure to 0.2 mg∙L⁻¹ Cu promoted chlorophyll synthesis and enhanced Rubisco and GO activities; in contrast, exposure to Cu concentrations above 0.4 mg∙L⁻¹ significantly inhibited the aforementioned parameters. These findings indicate that Cu stress, regardless of concentration, significantly affects nitrogen metabolism in N. peltata by decelerating nitrate reduction and impairing the ammonification process. Meanwhile, only high Cu concentrations significantly affected photosynthesis. N. peltata can survive low Cu stress by regulating its photosynthetic enzymes. Therefore, N. peltata has potential for the ecological restoration of water bodies polluted with low Cu concentrations. Full article

In response to environmental concerns and the depletion of fossil resources, transitioning coatings toward sustainability is imperative. Bio-based coatings, derived from renewable biomass, represent a highly promising development pathway. This review comprehensively summarizes recent advances, prevailing challenges, and future prospects of bio-based coatings, with a focus on bio-based polymer resins—serving as the primary film-forming materials—and key auxiliary components such as pigments and fillers, additives, and solvents. This review systematically elaborates on the definition of bio-based coatings, their raw material sources, and international standards for bio-based carbon content determination. The core strategies for converting biomass into coating components are critically analyzed, namely direct utilization, physical blending, chemical modification, and biosynthesis. Furthermore, the synthesis, properties, and applications of key bio-based polymer systems—including epoxy, polyurethane, alkyd, and acrylic resins—are critically discussed, with particular emphasis on how molecular engineering enhances their performance and functionality. Despite significant progress, bio-based coatings still face several challenges, such as balancing performance and cost, ensuring the stability of raw material supply chains, and establishing globally unified standards. This review concludes that the integration of chemical modification and biosynthesis technologies, coupled with the establishment of a unified bio-based content standard system, constitutes two core drivers for advancing bio-based coatings from “green alternatives” toward “high-performance dominance” in the future. Full article

Background/Objectives: Staphylococcus aureus is a well-known opportunistic pathogen that causes a wide range of infections, from cutaneous blemishes to potentially fatal systemic diseases. The increasing prevalence of antibiotic-resistant bacteria highlights the critical need for alternative therapeutic methods that target virulence factors rather than growth. Methods: The antibacterial activity of 3-fluorocatechol (3-FC) against bacterial and fungal pathogens (e.g., Candida albicans) was determined by broth microdilution to establish the lowest inhibitory concentration. The antibiofilm impact of 3-FC against S. aureus was evaluated using crystal violet staining and viable colony counts, followed by scanning electron microscopy to visualize the biofilm architecture. The methanol extraction method was used to quantify staphyloxanthin synthesis in S. aureus cells. Furthermore, in silico molecular docking was used to evaluate 3-FC binding interactions and provide mechanistic insight into its impacts on S. aureus biofilms and virulence-associated factors. Results: Although the study showed that 3-FC exhibits weak antibacterial activity against S. aureus (MIC > 2048 µg/mL), it shows effective inhibition of up to 86.5% at sub-inhibitory doses during the initial stage of biofilm formation. The CFU enumeration also confirms the significant reduction of viable cell count of S. aureus in the presence of sub-MIC of 3-FC. The SEM analysis confirms disruption of the S. aureus biofilm architecture in the presence of a sub-MIC of 3-FC. Furthermore, the eradication of mature S. aureus biofilm at a sub-MIC dose of 3-FC was 60.6%. 3-FC significantly reduced staphyloxanthin formation, a vital antioxidant pigment that contributes to bacterial pathogenicity, with a maximal suppression of 66.3% at 2048 µg/mL. Molecular docking analyses provide further insight into the molecular basis of 3-FC activity, revealing strong binding affinities with numerous S. aureus virulence regulators and enzymes, suggesting interference with quorum-sensing, adhesion, and oxidative-stress response pathways. Conclusions: Collectively, our findings indicate that 3-FC has antibiofilm and antivirulence properties against S. aureus. Furthermore, this study suggests 3-FC as a viable structural scaffold for the development of a novel anti-infective agent to treat chronic staphylococcal infections. Full article

A novel bacterial strain, Lysinibacillus sp. JNUCC 51, was isolated from volcanic soil collected at Baengnokdam Crater Lake, Mt. Halla, Jeju Island, Republic of Korea. Phylogenetic, ANI (88.76%), and dDDH (70.4%) analyses indicated that the strain represents a distinct genomic lineage closely related to L. xylanilyticus. The complete genome (5.12 Mb; 37% G+C) encoded 4912 genes, including ten biosynthetic gene clusters (NRPS, β-lactone, RiPP, terpene, and T3PKS types), suggesting strong metabolic versatility. Cells were Gram-positive rods (1.5–3.0 × 0.5–0.7 µm) growing at pH 4.0–9.0 and up to 5% NaCl. Chemotaxonomic profiles revealed iso-C₁₅:₀, iso-C₁₇:₀, and iso-C₁₆:₀ as dominant fatty acids; MK-6/MK-7 as major quinones; and phosphatidylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, and phosphatidylcholine as main polar lipids. Bioactivity-guided fractionation of the culture extract led to the isolation of Diolmycin A2 (phenolic polyketide) and maculosin (diketopiperazine), both exhibiting anti-inflammatory and melanogenesis-inhibitory effects consistent with their PKS/NRPS gene clusters. The culture broth suppressed nitric oxide production in LPS-stimulated RAW 264.7 macrophages and reduced melanin synthesis in α-MSH–induced B16F10 melanocytes. A human patch test (5% extract) confirmed dermatological safety. Overall, Lysinibacillus sp. JNUCC 51 is a volcanic-origin bacterium producing structurally diverse bioactive metabolites with promising postbiotic and cosmeceutical potential, particularly for skin inflammation and pigmentation control. Full article

This study’s objective was to evaluate the effect of the glucose transporter GLTP1 in Monascus ruber CICC41233 on Monascus pigment biosynthesis. The gltp1 gene in M. ruber CICC41233 was cloned to construct the overexpression vector pNeo0380-gltp1, resulting in complementation and overexpression strains, and its upstream and downstream homologous arms were used to construct the gene knockout plasmid pHph0380G/Gltp1::hph, resulting in a mutant strain. The results showed that the gltp1 gene knockout strain M. ruber GLTP24 exhibited dramatically accelerated starch degradation and a significant increase (74.1% higher) in the yield of alcohol-soluble pigments compared to the wild-type. Reverse genetic experiments confirmed this phenotype: complementation strains restored wild-type pigment production levels, while overexpression strains showed reduced pigment synthesis. Integrated transcriptomic analyses revealed that gltp1 deletion triggered extensive metabolic reprogramming. This included the downregulation of key components in the carbon-sensing GprD-cAMP/PKA signaling pathway and the concerted upregulation of multiple amino acid metabolic pathways, which supply essential precursors and amino groups for Monascus pigment synthesis. This study provides novel insights into the molecular link between carbon transport, signaling, and Monascus pigments in Monascus ruber. Full article

This study investigated muscle quality differences between wild-type (WT) and yellow-mutant (YM) Triplophysa siluroides. Texture analysis showed WT T. siluroides had significantly greater hardness, gumminess, and resilience than YM. Histological and biochemical analyses ruled out myofiber diameter/density as drivers, instead identifying reduced collagen in YM as key, as confirmed by Picrosirius red staining, collagen quantification, and transmission electron microscopy. Transcriptomic and proteomic analyses revealed that TGF-β/BMP pathway suppression in YM resulted in downregulation of core molecules (e.g., BMP2 and SMAD1), collagen-related genes (e.g., COL1A1a and COL1A1b), and ECM-related genes (e.g., TNC and FN1), potentially influencing collagen synthesis and ECM homeostasis. Notably, melanin gene TYRP1 was also downregulated in YM T. siluroides, suggesting a link between pathway suppression, muscle quality alteration, and body pigmentation. The potential role of the BMP2-SMAD1-TYRP1 axis in the association between muscle quality and body colour provides novel mechanistic insights, offering molecular targets for the breeding of T. siluroides with superior commercial traits. Full article

Genome modification of legumes, peas in particular, is accompanied by significant challenges. Establishing a reliable reporter system to identify tissue that expresses foreign DNA may help to optimize and develop transformation protocols for these species. The RUBY system, based on the synthesis of red betalain from tyrosine, offers a convenient solution for monitoring the efficiency of transgene introduction. To evaluate the effectiveness of RUBY application in pea tissue culture, we combined agrobacterial transformation with an in vitro cultivation system, inducing callus development. Transformed explants demonstrated RUBY pigmentation, but it disappeared during cultivation. We hypothesized that this issue is caused by tyrosine depletion. To check this suggestion, we tested whether tyrosine supplementation could maintain RUBY coloring. In the later stages, pigmentation still could not be preserved. However, our modified conditions increased the percent of colored shoot apex explants during the early cultivation stages. Thus, it is likely that some explants transformed with the RUBY cassette do not synthesize a sufficient amount of betalain due to the deficit of endogenous tyrosine. In this case, adding exogenous tyrosine would enhance betalain production and improve the detectability of tissues containing the RUBY cassette. These data can be used for the optimization of RUBY application conditions for peas and other species. Full article

The current interest in microalgal biomass does not subside but continues to intensify due to the emergence of new trends in the use of this bioresource in various biotechnological and environmental processes. The rather slow growth rate of phototrophs compared to other microorganisms limits more active application of the biomass for various purposes. Stimulation of the Quorum Sensing formation in the cells due to the appearance of their own quorum molecules or those produced by other co-cultured microorganisms in the medium is one of the efficient approaches for overcoming this limitation. This review discusses the immobilization or co-immobilization of phototrophic cells with other microorganisms as an effective way to maintain accumulation of the target biomass for long-term period at improved rates. The 40% increase in the use of co-immobilized phototrophs for biomass obtaining and its use in wastewater treatment has been observed over the past five years. The level of investigations of co-immobilized microalgae cells is four times higher than that of the immobilized single cultures. Among the main trends in the new investigations of immobilized forms of microalgae, the predominant application of Chlorella genus cells in immobilized samples of individual cultures and the involvement of diatom microalgae and cyanobacteria, in addition to Chlorella cells, in co-immobilization with other microorganisms, was ascertained. The most significant increase in the rate of microalgal biomass accumulation uncovered in cases of co-immobilization of microalgae with bacteria. In several cases, in the presence of bacteria, co-immobilization has led to the emergence of new characteristics in microalgal cells (increased synthesis of pigments, polysaccharides, biofilm formation, etc.), which opens new directions for their further practical use as biopesticides, components of packaging and building materials, etc. Full article

In this study, titanium dioxide nanoparticles (TiO₂-NPs) were produced via green routes using blueberry extracts obtained with isopropanol (I-TiO₂-NPs) and methanol (M-TiO₂ NPs). HPLC-DAD confirmed phenolic/flavonoid profiles in the extracts, and spectroscopy/microscopy established anatase, polyhedral, mesoporous TiO₂-NPs with Eg ≈ 3.0 eV, hydrodynamic sizes ≈ 130–150 nm and negative ζ-potentials (−33 to −50 mV). The in vitro compatibility between TiO₂-NPs and the plant-growth-promoting microorganisms (PGPMs) Bacillus subtilis (Bs), Bacillus thuringiensis (B), and Trichoderma harzianum (T) sustained increased growth up to 150 µg/mL without visible negative effects. In greenhouse experimentation of Capsicum annuum exposed to low-moderate TiO₂-NPs, an increased leaf number and plant height were observed, while root length did not exceed the controls. I-TiO₂ at moderate concentrations, particularly with a single PGPM (B or T), promoted fresh and dry biomass accumulation. Biochemically, peroxidase rose sharply for M-TiO₂ at a low dose with consortium, whereas I-TiO₂ elicited broader antioxidant responses; total protein increased at higher doses for both formulations, and total chlorophyll was highest with I-TiO₂ (high dose with or without PGPMS). Collectively, the nano-bio system shows a formulation- and dose-dependent biphasic behavior: (I) I-TiO₂ enhances biomass and photosynthetic pigments; (II) M-TiO₂ favors strong POX induction under specific microorganism-dose combinations; and (III) single PGPM co-application with I-TiO₂-NPs or M-TiO₂ NPs outperforms consortia under our experimental conditions. Green synthesis thus provides surface functionalities that improve dispersion, microbial compatibility, and predictable physiological/biochemical outcomes for precision agriculture. Full article

Anthocyanins pigment plant tissues, mitigate biotic and abiotic stresses, and deliver human health benefits; raising their content in mung bean (Vigna radiata) sprouts is a long-standing research target. Transcriptome analysis identified VrNAC25, a NAC transcription factor whose expression closely parallels anthocyanin accumulation; functional validation in mung bean confirmed that VrNAC25 acts as a positive regulator of the pathway. Although VrNAC25 does not bind to the promoters of the key structural genes VrDFR or VrLDOX, it indirectly controls anthocyanin synthesis by interacting with the core R2R3-MYB activator VrMYB90, previously established as the central regulator of anthocyanin production in mung beans. This interaction operates at both transcriptional and protein levels, thereby amplifying the expression of downstream structural genes and boosting pigment accumulation. Our findings refine the molecular network governing anthocyanin biosynthesis in sprouts and provide a clear theoretical basis for breeding or biotechnological strategies aimed at enhancing the nutritional quality and commercial value of mung bean products through light treatment or by selecting an anthocyanin-rich mung bean variety. Full article

11-cis-retinal, the indispensable chromophore of photoreceptor opsins, is fundamental for light detection and the initiation of visual signal transduction. Its synthesis and regeneration through the visual cycle are critical not only for phototransduction but also for maintaining retinal homeostasis. Disruption of key enzymes, such as retinal pigment epithelium (RPE)65 and retinol dehydrogenases, results in toxic retinoid accumulation, oxidative stress, and progressive photoreceptor degeneration. These pathological mechanisms contribute to inherited and acquired retinal diseases, including Stargardt disease type 1, age-related macular degeneration, Leber congenital amaurosis, retinitis pigmentosa, and fundus albipunctatus. Recent therapeutic advances, ranging from gene replacement therapy with RPE65 (voretigene neparvovec, Luxturna^®) to small-molecule modulators and antioxidant strategies, underscore the translational potential of targeting chromophore metabolism. This review outlines molecular processes underlying chromophore synthesis and regeneration, elucidates how disruptions in these processes contribute to inherited and acquired retinal pathologies, and evaluates existing and emerging therapeutic strategies that target chromophore metabolism. We highlight ongoing challenges and critical knowledge gaps to guide future investigations on basic science, translational research, and clinical practice. This review provides a comprehensive overview of the molecular mechanisms, current therapeutic approaches, and outstanding challenges, with a focus on future intervention directions. Full article

Objectives: Pseudomonas aeruginosa is an opportunistic pathogen of high clinical relevance due to its ability to form biofilms, its inherent virulence regulated by quorum-sensing systems, and its multidrug resistance. In the present study, we evaluated the inhibitory potential of nine extracts from Inula species (chloroform and methanolic fractions, including a sesquiterpene lactone-enriched fraction) against biofilm formation and virulence-associated traits of P. aeruginosa PAO1 and three multidrug-resistant clinical isolates, as well as their cytotoxicity, biocompatibility, and ability to affect cytokine and nitric oxide production in infected skin explants. Methods: The following methods were applied: fractionation and extraction of plant extracts; cytotoxicity assessment on HFF cells; crystal violet assay for determining antibiofilm activity; fluorescence microscopy for evaluating biofilm viability; electron microscopy for assessing the 3D structure of biofilms and morphological alterations; inhibition assays of pyocyanin pigment, protease activity, bacterial motility, interleukin-17, and nitric oxide production; histological analysis of mouse skin explants. Results: Quantitative analyses of antibiofilm activity revealed that five of the tested extracts inhibited biofilm formation by more than 50%. Structural and functional analyses using confocal laser scanning microscopy and scanning electron microscopy demonstrated a substantial reduction in biofilm thickness, exfoliation of biofilm biomass, the presence of isolated bacterial clusters, metabolically inactive cell populations, and morphological abnormalities associated with cell elongation, invaginations, and polar deformations as a consequence of treatment. In addition, the plant extracts strongly affected virulence factors regulated by quorum sensing. The methanolic fractions from I. britannica and I. bifrons significantly suppressed pyocyanin synthesis. In contrast, the chloroform fractions from I. helenium and I. spiraeifolia produced the largest inhibition zones in assays for extracellular protease activity. Furthermore, all chloroform extracts suppressed bacterial motility, with the lowest swarming diameter observed for the chloroform and lactone-enriched fractions from I. britannica. The chloroform extracts of I. helenium and I. bifrons, methanolic extracts of I. britannica, and chloroform and methanolic extracts of I. spiraeifolia showed relatively low toxicity to normal diploid human fibroblasts. Methanolic and chloroform fractions from I. britannica disrupted biofilm integrity and reduced IL-17A and nitric oxide production in infected skin explants. Conclusions: All these findings indicate a possible synergistic action of the chemical constituents within the fractions on quorum-sensing regulation, biofilm formation, cellular viability, and modulation of host inflammatory responses. Full article