Currently, pectins are widely used in the cosmetic, pharmaceutical, and food industries, mainly as texturizing, emulsifying, stabilizing, and gelling agents. Pectins are polysaccharides composed of a large linear segment of α-(1,4) linked d-galactopyranosyluronic acids interrupted by β-(1,2)-linked l-rhamnoses and ramified by short chains composed of neutral hexoses and pentoses. The characteristics and applications of pectins are strongly influenced by their structures depending on plant species and tissues but also extraction methods. The aim of this review is therefore to highlight the structures of pectins and the various methods used to extract them, including conventional ones but also microwave heating, ultrasonic treatment, and dielectric barrier discharge techniques, assessing physico-chemical parameters which have significant effects on pectin characteristics and applications as techno-functional and bioactive agents.

Ultrasound pretreatment and microwave-assisted extraction (MAE) techniques were used to extract pectin from watermelon rind. This work investigated the effect of the power and time of pretreatment on the yield and characteristics of the extracted pectin. Imaging studies showed that ultrasonic pretreatment changed the morphology of the raw powder, leading to a greater porosity, and facilitated the extraction process. The highest extraction yield of pectin was 19.08% (w/w), for 5 min of extraction at 500 W ultrasonic pretreatment. Ultrasonic pretreatment affected the degree of esterification and the galacturonic acid content of pectin. The galacturonic acid content of all samples was higher than 69.0%. Extraction pretreatment reduced the surface tension value of the aqueous solution of pectin and affected the foam capacity of pectin and its monosaccharidic composition. The ultrasonic pretreatment caused significant changes in pectin characteristics, such as intrinsic viscosity, viscosity average, molecular weight, ratio of homogalacturonan to rhamnogalacturonan and the water holding capacity. In addition, kinetic studies showed that a kinetic empirical model adequately describes the effect of ultrasonic pretreatment on foam stability and its half-time.

Pseudomonas aeruginosa elastase LasB accelerates refrigerated food spoilage through proteolytic degradation of muscle and milk proteins. While Marrubium vulgare essential oil terpenes exhibit antimicrobial activity, their weak potency and nonspecificity limit direct food preservation applications. This computational study aimed to rationally redesign terpene scaffolds into predicted selective LasB inhibitors. A virtual library of 635 terpene–peptide–phosphinic acid hybrids (expanded to 3940 conformers) was evaluated using consensus molecular docking (Glide/Flare) against LasB (PDB: 3DBK) and three human off-target proteases. Top candidates underwent duplicate 150 ns molecular dynamics simulations with MM/GBSA binding free-energy calculations. Computational screening identified thymol–Leu–Trp–phosphinic acid as the lead candidate with predicted binding affinity of −12.12 kcal/mol, comparable to reference inhibitor phosphoramidon (−11.87 kcal/mol), and predicted selectivity index of +0.12 kcal/mol representing a 2.3 kcal/mol advantage over human proteases. Molecular dynamics simulations indicated exceptional stability (98.7% stable frames, 0.12 Å inter-replica RMSD) with consistent zinc coordination. Structure–activity analysis revealed phosphinic zinc-binding groups (+1.57 kcal/mol), Leu–Trp linkers (+2.47 kcal/mol), and phenolic scaffolds (+1.35 kcal/mol) as predicted optimal structural features. This in silico study provides a computational framework and prioritized candidate set for developing natural product-derived food preservatives. All findings represent computational predictions requiring experimental validation through enzymatic assays, food model studies, and toxicological evaluation.

This study explores a multi-resource approach for extracting and characterizing l-rhamnose-rich polysaccharides from nine natural biomasses, including green macroalgae (Ulva spp.), sumac species (Rhus spp.), and agro-industrial by-products such as sea buckthorn and sesame cakes. Hot-water and alkaline extractions were performed by biomass type, and the resulting fractions were analyzed using biochemical assays, monosaccharide profiling (HPAEC/PAD and GC/MS-EI), FTIR, and antioxidant activity tests. Extraction yields ranged from <1% in sea buckthorn residues to 15.48% in Ulva spp., which showed the highest recovery. l-rhamnose enrichment varied across biomasses: the highest proportions were found in Ulva extracts and Rhus semialata galls (PRS), reaching up to 44% of total sugars by HPAEC/PAD and 58% by GC/MS-EI. Antioxidant activities also differed markedly. In DPPH assays, the most active extracts were those from sea buckthorn berry cake (PTBA), Rhus coriaria seeds (PRC), and commercial sea buckthorn powder (PPA), with IC₅₀ values of 32, 43, and 42 µg/mL, respectively. Hydroxyl-radical inhibition was also substantial, reaching 83.0% for PTBA, 79.4% for PRC, and 79.9% for Ulva lactuca at 1 g/L, compared with 97.5% for ascorbic acid. These results highlight specific biomasses as promising dual sources of l-rhamnose and natural antioxidants for valorization within a circular bioeconomy.