Search

Huanglongbing (HLB) is a highly destructive disease that inflicts significant economic losses on the citrus industry worldwide but with no cure available. However, microbiomes formulated by citrus plants may serve as disease antagonists, increasing the level of HLB tolerance. This study established an integrated analysis of untargeted metabolomics and microbiomics data for different citrus cultivars, providing critical insights into the interactions between plant metabolism and plant-associated bacteria in the development of HLB. Machine learning models were applied to screen important metabolites and bacteria in multiple citrus materials, and the selected metabolites were then analyzed to identify essential pathways enriched in the plant and to correlate with the selected bacteria. Results demonstrated that the regulation of plant pathways, especially ABC transporters and ubiquinone and other terpene-ubiquinone biosynthesis pathways, could affect the microbial community structure, indicating potential solutions for controlling HLB by modulating bacteria in citrus plants or breeding tolerant citrus cultivars.

A magnetic nanocomposite film with the capability of reversibly collecting functionalized magnetic particles was fabricated by simultaneously imposing two orthogonal stimuli (electrical and magnetic). We demonstrate that cathodic codeposition of chitosan and Fe3O4 nanoparticles while simultaneously applying a magnetic field during codeposition can (i) organize structure, (ii) confer magnetic properties, and (iii) yield magnetic films that can perform reversible collection/assembly functions. The magnetic field triggered the self-assembly of Fe3O4 nanoparticles into hierarchical "chains" and "fibers" in the chitosan film. For controlled magnetic properties, the Fe3O4-chitosan film was electrodeposited in the presence of various strength magnetic fields and different deposition times. The magnetic properties of the resulting films should enable broad applications in complex devices. As a proof of concept, we demonstrate the reversible capture and release of green fluorescent protein (EGFP)-conjugated magnetic microparticles by the magnetic chitosan film. Moreover, antibody-functionalized magnetic microparticles were applied to capture cells from a sample, and these cells were collected, analyzed, and released by the magnetic chitosan film, paving the way for applications such as reusable biosensor interfaces (e.g., for pathogen detection). To our knowledge, this is the first report to apply a magnetic field during the electrodeposition of a hydrogel to generate magnetic soft matter. Importantly, the simple, rapid, and reagentless fabrication methodologies demonstrated here are valuable features for creating a magnetic device interface.

We have developed a two-step replica molding method for rapid fabrication of biomimetically patterned plant surfaces (BPS) using polydimethylsiloxane (PDMS-BPS) and agarose (AGAR-BPS). Beyond providing multiple identical specimens that faithfully reproduce leaf surface microstructure, this approach also offers unique chemical, physical, and biological features. PDMS-BPS provide good structural durability for SEM examination, have surface wettability comparable to plant surfaces for coating development, and allow for real-time monitoring of biosynthesis through incorporation into microfluidic devices. AGAR-BPS are compatible with bacterial growth, recovery, and quantification, and enable investigation of the effects of surface topography on spatially varying survival and inactivation of Escherichia coli cells during biocide treatment. Further development and application of these biomimetically patterned surfaces to study (and possibly modify) other aspects of plant-bacteria interactions can provide insight into controlling pathogen contamination in a wide range of applications.

Cationic β-lactoglobulin (CBLG) was developed as a bioavailability enhancer for poorly absorbed bioactives. At most 11 anionic amino acid residues of β-lactoglobulin (BLG) were substituted by ethylenediamine (EDA), resulting in a highly positive surface charge (zeta potential up to 39 mV at pH 7.0) and significantly increased surface hydrophobicity. These changes conferred CBLG with desirable water solubility and improved mucoadhesion by at most 252%, according to quartz crystal microbalance (QCM) study. Furthermore, CBLG inherited the unique resistance to gastric digestion from BLG, while the digestion under simulated intestinal condition was significantly improved. The latter was possibly due to the formation of aspartic acid-EDA conjugates, together with the randomization of protein conformation related with decreased percentage of β-sheet. Compared to BLG, CBLG formed smaller (75-94 nm), more uniform nanoparticles by the acetone-desolvation method. These merits made CBLG a useful material that provides desirable solubility, controlled release, and enhanced absorption to nutraceuticals or drugs.

In this study, soy protein isolate (SPI) was conjugated with folic acid (FA) to prepare nanoparticles for target-specific drug delivery. Successful conjugation was evidenced by UV spectrophotometry and primary amino group analysis. An increase in count rate by at least 142% was observed in FA-SPI nanoparticles compared to the nonconjugated ones, whereas the particle size was decreased upon FA conjugation. This was probably attributed to the substitution of positively charged lysine residues by the FA backbone. The ζ-potential ranged from -36 to -42 mV depending on the conjugation degree, indicating desirable dispersion stability. Curcumin as a model drug was encapsulated successfully into FA-SPI nanoparticles, evidenced by X-ray diffraction study. The highest encapsulation and loading efficiencies were around 92.7% and 5.4%, respectively, which were significantly higher (P < 0.05) than those with nonconjugated SPI nanoparticles. In addition, a faster and more complete release of curcumin was observed for FA-SPI nanoparticles in PBS/Tween 20 buffer. Cell culture study showed that conjugation of FA resulted in an increase in cellular uptake by at most 93% in Caco-2 cells. These results suggested that FA-SPI is a potential wall material for encapsulation and enhanced delivery of anticancer drugs.

Zein is a corn prolamin that has broad industrial applications because of its unique physical properties. Currently, the high cost of extraction and purification, which is directly related to the dispersion of zein in different solvents, is the major bottleneck of the zein industry. Solution behaviors of zein have been studied for a long time. However, the physical nature of zein in different solvents remains unclear. In this study, small-angle X-ray scattering (SAXS), static light scattering (SLS), and rheology were combined to study the structure and protein-solvent interaction of α-zein in both acetic acid and aqueous ethanol solutions. We found that the like-dissolve-like rule, the partial unfolding, and the protonation of zein are all critical to understanding the solution behaviors. Zein holds an elongated conformation (i.e., prolate ellipsoid) in all solutions, as revealed from SAXS data. There is an "aging effect" for zein in aqueous ethanol solutions, as evidenced by the transition of Newtonian rheological profiles for fresh zein solutions to the non-Newtonian shear thinning behavior for zein solutions after storage at room temperature for 24 h. Such shear thinning behavior becomes more pronounced for zein solutions at higher concentrations. The SLS results clearly show that acetic acid is a better solvent to dissolve zein than aqueous ethanol solution, as supported by a more negative second virial coefficient. This is majorly caused by the protonation of the protein, which was further verified by the dissolution of zein in water (a nonsolvent for zein) with the addition of acids.

It has been a long-lasting challenge to prepare highly ordered biopolymer nanocomposites to optimize or tune the desired mechanical and barrier properties of the nanocomposite film. In this study, we developed a simple and cost-effective method to synthesize highly ordered zein nanocomposites. The method involved the synthesis of magnetic iron oxide (Fe(3)O(4)) nanofiller and the preparation of a highly ordered structure by in situ nanofiller reorientation under an external magnetic field. The successful preparation of Fe(3)O(4) magnetic nanoplatelets together with exfoliated and highly ordered zein resin nanocomposites was confirmed by scanning electron microscopy, X-ray diffraction, and a vibrating sample magnetometer. As a result, in comparison to zein resin film, the exfoliated zein nanocomposites (Fe-Zein) showed dramatic improvement on mechanical and barrier properties. The tensile strength, elongation, and Young's modulus of Fe-Zein were increased by 218, 48, and 264%, respectively, while the water vapor and oxygen permeability decreased by 68 and 29%. More importantly, the highly ordered zein nanocomposites (Fe-Zein-Mag) showed additional improvement on the mechanical and gas barrier properties. In comparison to Fe-Zein, the tensile strength and elongation of Fe-Zein-Mag were increased by 10 and 48%, respectively, and a 30% decrease in Young's Modulus was observed, indicating the Fe-Zein-Mag film was more elastic. Besides, the water vapor and oxygen permeability of Fe-Zein-Mag were also decreased by an additional 48 and 17%, respectively.

Recently, silver, a traditional broad-spectrum antiseptic, drew increasing attentions as a solution against antibiotic resistant bacteria. Various synthetic polymers and nature polymers were applied to form silver polymer composites to cope with the defects (e.g., low hemocompatibility) of silver-loaded antimicrobial agents. In this study, an alcohol-soluble prolamine, zein, was applied to prepare silver-zein composites as novel antiseptics. Both zein in silver (Z]A) and silver nanoparticles (AgNP) in zein (A']Z) structures at two pH conditions (i.e., pH = 3.3 and 6.5) were successfully prepared. Several characterization methods (i.e., zeta potential, FTIR, SEM, and turbidity) confirmed the formation of silver-zein composites through a nitrogen-silver coordination bond and electrostatic interaction. It was found that low pH was critical in facilitating formation and increasing stability of the silver-zein composites, probably by inducing electrostatic interaction between silver and zein. The antiseptic activities (i.e., growth inhibition and bactericidal activity) of different silver-zein composites were studied against Gram negative E. coli and Gram positive S. aureus . It was revealed that the silver-zein composites showed similar or better results against both types of bacteria compared to those of AgNO(3) and AgNP, except for the sample of A']Z-Ac. It had better growth inhibition activity but inferior bactericidal activity than that of AgNP because of its decreased solubility in aqueous medium. Furthermore, addition of zein was proven to be capable of dramatically increasing hemocompatibility of silver-loaded antiseptic agents. Therefore, silver-zein composites prepared in this work may find applications in wound care and food packaging areas.

The hydroxypropylated psyllium derivatives were successfully prepared with propylene oxide under the alkaline condition for the first time. Four hydroxypropylated psyllium derivatives, denoted as HP1, HP2, HP3, and HP4, were characterized for their hydroxypropyl content, molar substitution, and IR spectra. The hydroxypropyl derivatives were also evaluated for their surface structure, gelling properties, water uptake capacities, swelling volumes, and in vitro bile acid-binding abilities. The results showed that hydroxypropylation significantly reduced the gelling properties of psyllium. Psyllium derivatives with a relatively low hydroxypropyl substitution degree had greater in vitro binding capacities against cholic and chenodeoxycholic acids and higher swelling ability. The results from this study suggested that hydroxypropylation may be a possible approach for obtaining novel psyllium derivatives with improved physicochemical, functional, and biological properties for utilization in functional foods or supplemental and pharmaceutical products.

The sulfation of psyllium was carried out with sulfur trioxide-pyridine in dimethyl formamide. Three sulfated psyllium derivatives, named SP1, SP2, and SP3, were characterized by sulfur content determination, elemental analysis, FT-IR, and surface charge analysis. The sulfated derivatives were also evaluated for their morphological and rheological properties, water uptake capacities, swelling volumes, and in vitro bile acid-binding abilities. The results showed that sulfation reduced the gelling capacity of psyllium and the viscosity of its solution, and significantly increased its bile acid-binding capacity. Sulfation might also increase the water uptake ability of psyllium but might decrease its swelling capacity. The three sulfated psyllium derivatives had in vitro binding capacities against cholic and chenodeoxycholic acids comparable to that of cholestyramine resin on a per same as it is weight basis. The bile acid-binding capacity of SP1 was about 8.4-fold of that observed for the original psyllium preparation under the same assay conditions. The results from this study suggest that sulfation is a possible approach to obtain novel psyllium derivatives with desirable physicochemical, functional, and biological properties for utilization in functional foods or supplemental and pharmaceutical products.

Highly uniform Cu2S nanocrystals with controllable sizes and shapes (circular and elongated) have been synthesized through a novel water-oil interface confined reaction. They can self-assemble into highly ordered multilayer superlattices. By controlling the size and shape of building block nanocrystals, the packing symmetry of the superlattice can be engineered. For circular nanocrystals, both fcc and hcp multilayer superlattices are found in the sample. For elongated nanocrystals, they can also generate a close-packed layer and further stack into a multilayer superlattice. The dipole moment of the inner nanocrystals is useful for their stacking. This work provides a simple bottom-up approach to integrate nanocrystals, as well as to adjust the packing symmetry of the final superlattice, which may have potential applications for nanomaterials and nanodevices in the future.