A stable delivery system for curcumin: Fabrication and characterization of self-assembling acylated kidney bean protein isolate nanogels.

The construction of protein-based nano-gels as curcumin delivery system effectively enhances the stability and bioavailability of curcumin. In this study, acylation modification and self-assembly techniques were jointly employed to construct acylated kidney bean protein isolate (AKBPI)-nanogels. Optimal conditions for AKBPI-nanogels were determined to be pH 7, concentration of 2 mg/mL, and temperature at 90℃ for 30 min. The optimized AKBPI-nanogels exhibited excellent uniformity as evidenced by decreasing average particle size (137.35 nm) and polydispersity index (0.38). Acylation enhanced the intermolecular interactions within the nanogel by reducing the polarity of tyrosine microenvironment and free sulfhydryl groups. AKBPI-nanogels demonstrated remarkable characteristics in terms of pH sensitivity, salt concentration, and storage tolerance. The curcumin-loaded AKBPI-nanogels exhibited an encapsulation efficiency of 92.30 % and maintained high antioxidant activity. In simulated gastrointestinal digestion, AKBPI-nanogels facilitated the controlled release and higher bioavailability of curcumin. Therefore, AKBPI-nanogels can be a stable tool for delivering curcumin.

Enhancement of chlortetracycline biodegradation with Trichoderma harzianum LJ245 and its spore-producing mutants using co-metabolism.

Chlortetracycline (CTC) has been widely used in veterinary medicine in recent years, which has resulted in severe environmental issues due to its low degradation rate and high risk to induce antibiotic resistance bacteria and genes. In previous studies, CTC could be efficiently degraded by Trichoderma harzianum LJ245. Nevertheless, the strain itself suffers from relatively poor adaptability due to the limited number of spores produced. In this paper, ultraviolet (UV) mutagenesis was conducted on LJ245, and various mutants with high sporulation rate were generated to expand the environmental adaptability and enhance CTC degradation. An OmniLog-based method, where 95 types of carbon sources were applied, was first proposed to acquire the carbon metabolic profile of the strains. Several controlled experiments were performed to evaluate the impact of co-substrate metabolism on strain growth, CTC biodegradation, and metabolites biotoxicity removal. The result shows that produced mutants could significantly broaden the carbon metabolic profile and expand the environmental adaptability compared to the original LJ245, where the mutants obtained remarkable increase in total number of usable carbon sources. Meanwhile, as the sole carbon source, CTC could not be fully degraded by the strains. However, the use of co-metabolism could considerably enhance CTC degradation and completely remove CTC degradation products biotoxicity by all strains. Specifically, amino acids and carboxylic acids had the best performance on both strain growth and CTC degradation among all carbon source categories. The results can be applied to the biodegradation treatment of CTC in solid residue, waste water and other environments.