The medicinal administration of Aloe vera gel has become promising in pharmaceutical and cosmetic applications particularly with the development of the nanotechnology concept. Nowadays, effective H. pylori treatment is a global problem; therefore, the development of natural products with nanopolymers such as chitosan nanoparticles (CSNPs) could represent a novel strategy for the treatment of gastric infection of H. pylori. HPLC analysis of A. vera gel indicated the presence of chlorogenic acid as the main constituent (1637.09 µg/mL) with other compounds pyrocatechol (1637.09 µg/mL), catechin (1552.92 µg/mL), naringenin (528.78 µg/mL), rutin (194.39 µg/mL), quercetin (295.25 µg/mL), and cinnamic acid (37.50 µg/mL). CSNPs and A. vera gel incorporated with CSNPs were examined via TEM, indicating mean sizes of 83.46 nm and 36.54 nm, respectively. FTIR spectra showed various and different functional groups in CSNPs, A. vera gel, and A. vera gel incorporated with CSNPs. Two strains of H. pylori were inhibited using A. vera gel with inhibition zones of 16 and 16.5 mm, while A. vera gel incorporated with CSNPs exhibited the highest inhibition zones of 28 and 30 nm with resistant and sensitive strains, respectively. The minimal inhibitory concentration (MIC) was 15.62 and 3.9 µg/mL, while the minimal bactericidal concentration (MBC) was 15.60 and 7.8 µg/mL with MBC/MIC 1 and 2 indexes using A. vera gel and A. vera gel incorporated with CSNPs, respectively, against the resistance strain. DPPH Scavenging (%) of the antioxidant activity exhibited an IC₅₀ of 138.82 μg/mL using A.vera gel extract, and 81.7 μg/mL when A.vera gel was incorporated with CSNPs. A.vera gel incorporated with CSNPs enhanced the hemolysis inhibition (%) compared to using A.vera gel alone. Molecular docking studies through the interaction of chlorogenic acid and pyrocatechol as the main components of A. vera gel and CSNPs with the crystal structure of the H. pylori (4HI0) protein supported the results of anti-H. pylori activity.

Nowadays, endophytic fungi represent a rich source of biological active compounds. In the current study, twelve endophytic fungal species were isolated from Avicennia marina leaves. From the isolates, Aspergillus niger, Penicillium rubens and Alternaria alternata recorded the highest isolation frequency (80%), relative density (12.5%) and antimicrobial activity. The antimicrobial and anticancer activities of P. rubens were more effective than those of A. niger and A. alternata; therefore, its identification was confirmed via the ITS rRNA gene. Filtrate extracts of P. rubens, A. alternata and A. niger were analyzed using GC-MS and showed different detected constituents, such as acetic acid ethyl ester, N-(4,6-Dimethyl-2-pyrimidinyl)-4-(4-nitrobenzylideneamino) benzenesulfonamide, 1,2-benzenedicarboxylic acid, hexadecanoic acid and octadecanoic acid. Filtrate extract of P. rubens exhibited the presence of more compounds than A. alternata and A. niger. Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Candida albicans and Aspergillus fumigatus were more inhibited by P. rubens extract than A. alternata or A. niger, with inhibition zones of 27.2 mm, 22.21 mm, 26.26 mm, 27.33 mm, 28.25 mm and 8.5 mm, respectively. We observed negligible cytotoxicity of P. rubens extract against normal cells of human lung fibroblasts (WI-38 cell line), unlike A. alternata and A. niger extracts. Proliferation of prostate cancer (PC-3) was inhibited using P. rubens extract, exhibiting mortality levels of 75.91% and 76.2% at 200 µg/mL and 400 µg/mL of the extract. Molecular docking studies against the crystal structures of C. albicans (6TZ6) and the cryo-EM structure of B. subtilis (7CKQ) showed significant interactions with benzenedicarboxylic acid and N-(4,6-dimethyl-2-pyrimidinyl)-4-(4-nitrobenzylideneamino) benzenesulfonamide as a constituent of P. rubens extract. N-(4,6-dimethyl-2-pyrimidinyl)-4-(4-nitrobenzylideneamino) benzenesulfonamide had the highest scores of −6.04905 kcal/mol and −6.590 kcal/mol towards (6tz6) and (7CKQ), respectively.

In nanotechnology, fungi have been identified as excellent candidates for the synthesis of nanoparticles, thus presenting a cleaner alternative to produce new materials with a wide range of potential applications in biomedicine and industry. In this respect, A novel biological approach Penicillium olsonii have demonstrated excellent synthesis capacity to produce copper nanoparticles (CuNPs). Their properties were determined by ultraviolet-visible (UV-Vis) absorption spectrum, Fourier transform infrared spectroscopy (FT-IR), and Scanning Electron Microscopy (SEM) images. UV-Vis spectra with characteristic absorption peak was observed at 565nm. Biomolecules mediating the synthesis and stabilizing the nanobactericides was studied with FTIR that showed different functional groups. SEM investigations confirmed that size of CuNPs were varied from 6-26 nm. The antifungal activity of CuNPs was evaluated by testing against three phytopathogenic fungi including Fusarium oxysporum, Fusarium solani and Curvularia curvulatat with growth inhibition 86.25, 32.92 and 68.42%, respectively at 200ppm. F. oxysporum was more affected by CuNPs followed by C. curvulata and F. solani. The present work demonstrated that it is possible to perform the biogenic synthesis of CuNPs using P. olsonii as appropriate fungicide.

The growing need for sturdy lumber in many applications has made wood preservation more crucial. Nanoparticles (NPs) have been considered to improve the functionality of wood. This review article focuses on how NPs can be used to enhance the qualities of wood and wood-based products and provide them with anti-microbial protection. The ability of nano-based substances to permeate deeply into wood surfaces, which in turn causes a shift in their exterior chemistry, is the primary driver behind the nanotechnology application in lumber development. The microbial enzymes secreted by microbes is a major factor that can alter the structure of wood, especially during storage before use. This review illustrates various examples of microorganisms which secrete enzymes which impact wood structure through various mechanisms. The increased interface region created by the treatment serves as the reason for any prospective changes in the wood’s characteristics via NPs application. To a certain extent, the NPs change the original characteristics of wood, thus improving its qualities. There are challenges and limitations for using NPs in wood preservation. The potential effect of NPs on human health and the ecosystem should be considered using techniques such as life-cycle evaluations to avoid harmful consequences.

Guar (Cyamopsis tetragonoloba L. Taub.) is a significant summer legume used as food for both humans and livestock. In Saudi Arabia, the root nodule bacteria of guar have not been studied. The present work investigated the phenotypic and genetic diversity of guar microsymbionts. Eighty-eight bacterial strains were isolated from the root nodules of guar grown in different locations of Jazan region of Saudi Arabia. The strains were analyzed based on their phenotypic characteristics and variations in their 16S rRNA gene sequences. A significant proportion of the isolates (90%) were fast-growing rhizobia, with 77% showing tolerance to 3–4% NaCl and 91% capable of thriving at temperatures reaching 40 °C. Several isolates exhibited strong plant growth-promoting traits, particularly in IAA production and phosphate solubilization. Genetic analysis indicated considerable diversity, with isolates classified under the genera Rhizobium, Ensifer, Mesorhizobium, Bradyrhizobium, and Agrobacterium. To the best of our knowledge, this study is the first to report on the phenotypic and genetic diversity of guar microsymbionts in Saudi Arabia.

Acalypha indica, a plant used in traditional medicine, was evaluated for its phenolic composition and bioactivity. The methanolic extract of its aerial parts (stem and leaves) was analyzed using high-performance liquid chromatography (HPLC), identifying 17 phenolic compounds, including rutin (53.8 µg mL⁻¹), chlorogenic acid (53.3 µg mL⁻¹), gallic acid (36.3 µg mL⁻¹), and ferulic acid (33.3 µg mL⁻¹) as the primary constituents. These compounds correlated with the extract’s antioxidant activity, confirmed by the DPPH radical-scavenging assay, yielding an IC₅₀ of 6.8 µg mL⁻¹. The extract showed significant antimicrobial activity against Gram-positive bacteria, including Bacillus subtilis and Staphylococcus aureus, with inhibition zones exceeding that of Gentamycin. It also demonstrated moderate activity against Gram-negative bacteria, such as Salmonella typhi and Klebsiella pneumoniae, and antifungal activity against Candida albicans. Minimum inhibitory concentration (MIC) and bactericidal concentration (MBC) assays showed bactericidal effects at 7.8 µg mL⁻¹. Additionally, the extract inhibited biofilm formation and hemolysin production, suggesting anti-virulence potential. The Cyclooxygenase (COX) inhibition assays indicated anti-inflammatory effects (IC₅₀ = 11 µg mL⁻¹). Cytotoxicity tests on PC-3 prostate and SKOV-3 ovarian cancer cells revealed reductions in cell viability, with IC₅₀ values of 11.52 and 10.31 µg mL⁻¹, highlighting the therapeutic potential of Acalypha indica.