Balancing mechanical property and swelling behavior of bacterial cellulose film by in-situ adding chitosan oligosaccharide and covalent crosslinking with γ-PGA.

Bacterial cellulose (BC) is an ideal candidate material for drug delivery, but the disbalance between the swelling behavior and mechanical properties limits its application. In this work, covalent crosslinking of γ-polyglutamic acid (γ-PGA) with the chitosan oligosaccharide (COS) embedded in BC was designed to remove the limitation. As a result, the dosage, time, and batch of COS addition significantly affected the mechanical properties and the yield of bacterial cellulose complex film (BCCF). The addition of 2.25 % COS at the incubation time of 0.5, 1.5, and 2 d increased the Young's modulus and the yield by 5.65 and 1.42 times, respectively, but decreased the swelling behavior to 1774 %, 46 % of that of native BC. Covalent γ-PGA transformed the dendritic structure of BCCF into a spider network, decreasing the porosity and increasing the swelling behavior by 3.46 times. The strategy balanced the swelling behavior and mechanical properties through tunning hydrogen bond, electrostatic interaction, and amido bond. The modified BCCF exhibited a desired behavior of benzalkonium chlorides transport, competent for drug delivery. Thereby, the strategy will be a competent candidate to modify BC for such potential applications as wound dressing, artificial skin, scar-inhibiting patch, and so on.

ß-Alanine enhancing the crosslink of chitosan/poly-(γ-glutamic acid) hydrogel for a potential alkaline-adapted wound dressing.

Tiny crosslink in chitosan (CS)/poly-(γ-glutamic acid) (γ-PGA) hydrogel leads to some disadvantages including low mechanical strength and high swelling. To enhance the crosslink of CS/γ-PGA hydrogel, amino acid (AA) was introduced to remove the drawbacks. The results indicated that AA can dramatically increase the crosslink and mechanical properties of CS/γ-PGA hydrogel, and AA chain length and concentration have a drastic effect on them. Particularly, 0.5 % ß-Alanine (ß-Ala) decreased the hydrogel by 70 % in porosity, 52 % in water solubility, and 30 % in swelling, but increased by 2.2-fold in elastic modulus, 2.08-fold in stress, and 1.53-fold in water retention. The porosity of the hydrogel correlates positively with the elastic modulus but negatively with the crosslinking degree. The effect of pH on CS/ß-Ala/γ-PGA hydrogel was investigated in the load and release of benzalkonium chlorides (BAC). ß-Ala strengthened pH response of the hydrogel in BAC load and release. The loading capacity increased with pH value, and 0.5 % ß-Ala increased the hydrogel by 1.25-fold in the release capacity in alkaline environment, suggesting a good buffering effect of ß-Ala on pH variation to accelerate the transportation of BAC. CS/ß-Ala/γ-PGA hydrogel will be competently applied as a potential material for wound dressing in alkaline environment.

Dendrobium officinale Enzyme Changing the Structure and Behaviors of Chitosan/γ-poly(glutamic acid) Hydrogel for Potential Skin Care.

Hydrogels have been widespreadly used in various fields. But weak toughness has limited their further applications. In this study, Dendrobium officinale enzyme (DOE) was explored to improve chitosan/γ-poly(glutamic acid) (CS/γ-PGA) hydrogel in the structure and properties. The results indicated that DOE with various sizes of ingredients can make multiple noncovalent crosslinks with the skeleton network of CS/γ-PGA, significantly changing the self-assembly of CS/γ-PGA/DOE hydrogel to form regular protuberance nanostructures, which exhibits stronger toughness and better behaviors for skin care. Particularly, 4% DOE enhanced the toughness of CS/γ-PGA/DOE hydrogel, increasing it by 116%. Meanwhile, water absorption, antioxygenation, antibacterial behavior and air permeability were increased by 39%, 97%, 27% and 52%.

GpemDB: A Scalable Database Architecture with the Multi-omics Entity-relationship Model to Integrate Heterogeneous Big-data for Precise Crop Breeding.

BACKGROUND: With the development of high-throughput genome sequencing and phenotype screening techniques, there is a possibility of leveraging multi-omics to speed up the breeding process. However, the heterogeneity of big data handicaps the progress and the lack of a comprehensive database supporting end-to-end association analysis impedes the efficient use of these data. METHODS: In response to this problem, a scalable entity-relationship model and a database architecture are firstly proposed in this paper to manage the cross-platform data sets and explore the relationship among multi-omics, and finally accelerate our breeding efficiency. First, the targeted omics data of crops should be normalized before being stored in the database. A typical breeding data content and structure is demonstrated with the case study of rice (Oryza sativa L). Second, the structure, patterns and hierarchy of multi-omics data are described with the entity-relationship modeling technique. Third, some statistical tools used frequently in the agricultural analysis have been embedded into the database to help breeding. RESULTS: As a result, a general-purpose scalable database, called GpemDB integrating genomics, phenomics, enviromics and management, is developed. It is the first database designed to manage all these four omics data together. The GpemDB involving Gpem metadata-level layer and informative-level layer provides a visualized scheme to display the content of the database and facilitates users to manage, analyze and share breeding data. CONCLUSIONS: GpemDB has been successfully applied to a rice population, which demonstrates this database architecture and model are promising to serve as a powerful tool to utilize the big data for high precise and efficient research and breeding of crops.

Preparation of pH-sensitive carboxymethyl cellulose/chitosan/alginate hydrogel beads with reticulated shell structure to deliver Bacillus subtilis natto.

pH-sensitive hydrogels have been applied in delivering probiotics and drugs. However, pH sensitivity has been found to be contradictory with structural stability in hydrogel preparation. In this work, a novel strategy based on two systems of sodium carboxymethyl cellulose (CMC)/chitosan (CS) and sodium alginate (SA)/calcium chloride was designed to construct a reticulated shell structure stable for 3 h in simulated gastric fluid (pH 1.2) but began to break up at 2 h in simulated intestinal fluid (pH 6.8), exhibiting obvious pH sensitivity. The embedding rate of Bacillus subtilis natto reached to 67.3%, and the sustained release lasted for more than 10 h. It is implicated that the reticulated shell structure has harmoniously balanced the two incompatible properties of pH sensitivity and sustained release of CMC/CS/SA beads.

Harnessing digital imaging to detect the transmittance coupled with the uniformity of transparent optical materials.

A digital image (DI) method is reported to determine the transmittance and the uniformity of transparent optical materials (TOMs) at the same time, in which an objective image (OI) with a two dimensional (2D) entropy of 3.45 is scanned using a scanner with a black background. The OI pictures covered without and with a TOM went through gamma correction and color correction. The two corrected pictures were transformed into two matrixes, between which the transparency ratio and the correlation coefficient refer to the transmittance and the uniformity of TOMs. As a result, a p-value of 0.97 and an r value of 0.92 were achieved from the paired T-test between the DI method and the ultraviolet spectrometry (UVS) method, indicating a similar accuracy in determining the transmittance of TOMs between them. In addition, the DI method is a simple and rapid method to evaluate the uniformity of TOMs and to reveal the correlation among transmittance, uniformity and thickness of TOMs, particularly applicable for inhomogeneous TOMs.

A rapid and rapid method to quantify poly (γ-glutamic acid) content via copper ion complexation.

Presently, there have been some limitations in most of methods to determine poly (γ-glutamic acid) (γ-PGA) content because of many impurities in test specimens. It is necessary to establish a rapid and accurate method to quantify γ-PGA content. In this work, γ-PGA and some impurities commonly seen in fermented broth like glucose, glutamic acid and proteins were used to complex with copper ions. The results show that only γ-PGA can make copper ion precipitated, which content linearly correlates with the precipitate amount. From the study on the validity of the method, it is found that the accuracy and precision are 95.82% and 99.29%, much higher than the ones of method UV and weighing. Therefore, the method via the complexation of copper ion will be popularized to determine γ-PGA content in crude biological samples.

Inhibition of nattokinase against the production of poly (γ-glutamic Acid) in Bacillus subtilis natto.

OBJECTIVE: To study the effect of nattokinse (NK) on the synthesis of poly(γ-glutamic acid) (γ-PGA) in Bacillus subtilis natto. RESULTS: γ-PGA yield significantly decreased as NK was added in the original medium. With the increment of NK dosage, the yield decreased increasingly, but biomass increased instead of decreasing. The fact that cell density triggers the synthesis of γ-PGA is a controversial issue. γ-PGA yield and biomass closely correlate with addition time of NK. The later the addition of NK, the more γ-PGA yield decreased but the more biomass increased. It is concluded that cell hunger is a key factor to trigger the transmission of the cell density signal, and NK may inhibit γ-PGA synthesis by alleviating cell hunger. Besides, NK may reduce γ-PGA yield by degrading extracellular γ-PGA molecules. The study of adding L-glutamate of 0-20 g/L to the original medium showed that low concentration of L-glutamate (less than 5 g/L) could promote the synthesis of NK and γ-PGA, and thus NK may inhibit γ-PGA synthesis through strengthening substrate competition. CONCLUSIONS: NK mainly inhibits γ-PGA synthesis in Bacillus subtilis natto through alleviating cell starvation and strengthening substrate competition, and reduces γ-PGA yield through degrading extracellular γ-PGA molecules.