Improvement of fermentative production of exopolysaccharides from Aureobasidium pullulans under various conditions

The optimization of exopolysaccharide (EPS) production was investigated in the polymorphic fungal strain of Aureobasidium pullulans (KCTC 6081) with varying pH, nutrients concentration, and mixing parameters in batch fermentation condition. The maximum production of EPS (～7.5 g/L) was observed at pH 4, while optimum nutrient concentration of carbon (sucrose), nitrogen (NaNO₃), phosphorous (K₂HPO₄), and ascorbic acid was 50 g/L, 5 g/L, 1 g/L and 2 g/L, respectively. Interestingly, EPS productivity under non pH controlled fermentation conditions was 0.12 g/L/h with 400 rpm mixing, while under a controlled pH of 4, the EPS productivity was 0.21 g/L/h with 600 rpm, respectively. The fed-batch fermentation increased the EPS productivity up to 0.345 g/L/h with changing mixing conditions from 200 to 600 rpm and reached 47 g/L with 88% pullulan. Thus, pH and mixing were the key parameters for enhancing EPS production from A. pullulans. It is expected that these optimized parameters can be well used for enhanced industrial production of pullulan.     

Mass Spectrometric Confirmation of γ-Linolenic Acid Ester-Linked Ceramide 1 in the Epidermis of Borage Oil Fed Guinea Pigs

Ceramide 1 (Cer1), a Cer species with eicosasphingenine (d20:1) amide‐linked to two different ω‐hydroxy fatty acids (C30wh:0:C32wh:1), which are, in turn, ester‐linked to linoleic acid (LNA; 18:2n‐6), plays a critical role in maintaining the structural integrity of the epidermal barrier. Prompted by the recovery of a disrupted epidermal barrier with dietary borage oil [BO: 36.5 % LNA and 23.5 % γ‐linolenic acid (GLA; 18:3n‐6)], in essential fatty acid (EFA)‐deficient guinea pigs, we further investigated the effects of BO on the substitution of ester‐linked GLA for LNA in these two epidermal Cer1 species by LC–MS in positive and negative modes. Dietary supplementation of BO for 2 weeks in EFA‐deficient guinea pigs increased LNA ester‐linked to C32wh:1/d20:1 and C30wh:0/d20:1 of Cer1. Moreover, GLA ester‐linked to C32wh:1/d20:1, but not to C30wh:0/d20:1, of Cer1 was detected, which was further confirmed by the product ions of m/z 277.2 for ester‐linked GLA and m/z 802.3 for the deprotonated C32wh:1/d20:1. C20‐Metabolized fatty acids of LNA or GLA were not ester‐linked to these Cer1 species. Dietary BO induced GLA ester‐linked to C32wh:1/d20:1 of epidermal Cer1.     

Cybotactic nematic phase in main-chain polyesters with bent-core mesogens

New six main-chain polyesters containing bent-core mesogens with various central units (Ar = 1,2- or 1,3-phenylene and 1,6-, 1,7-, 2,3- or 2,7-naphthylene) were synthesized. All of the polymers were soluble in a mixture of phenol/p-chlorophenol/TCE (25/40/35 w/w/w). The inherent viscosities were in the range of 0.18–0.38 dL/g. Despite the existence of bent-core mesogens eliciting a remarkable diminution of molecular packing, polymer with Ar = 2,7-naphthylene formed a smectic phase, and polymers with both Ar = 1,2-phenylene and 2,3-naphthylene formed nematic phases. Moreover, most of the polymers were distinctly semi-crystalline. Herein, we report our findings regarding the first detection of cybotactic groups from the nematic phases of main-chain polyesters with bent-core mesogens.     

Combustion Synthesis of BiOCl with Tunable Percentage of Exposed {001} Facets and Enhanced Photocatalytic Properties

Bismuth oxychloride (BiOCl) was synthesized by a simple combustion method. The structures, morphologies, absorbance, optical, and photocatalytic properties of the samples were studied by X‐ray powder diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet–visible spectrophotometry, and photoluminescence. The experimental results show that BiOCl microsheet with high percentage of exposed {001} facets was obtained. It is interesting to note that the thickness of BiOCl sheets, in other words, the percentage of exposed {001} facets can be modulated through changing the added amount of ammonium chloride. The sample with the thinnest BiOCl sheets shows the best photodegradation performance of Rhodamine B under ultraviolet light irradiation, which can be attributed to the cooperative effect between the high percentage of exposed {001} facets and high‐specific surface area. Moreover, the corresponding influencing mechanism on the percentage of exposed {001} facets of BiOCl was discussed.     

Enzymatic Synthesis of Galactosylated Serine/Threonine Derivatives by β-Galactosidase from Escherichia coli

The transgalactosylations of serine/threonine derivatives were investigated using β-galactosidase from Escherichia coli as biocatalyst. Using ortho-nitrophenyl-β-d-galactoside as donor, the highest bioconversion yield of transgalactosylated N-carboxy benzyl l-serine benzyl ester (23.2%) was achieved in heptane:buffer medium (70:30), whereas with the lactose, the highest bioconversion yield (3.94%) was obtained in the buffer reaction system. The structures of most abundant galactosylated serine products were characterized by MS/MS. The molecular docking simulation revealed that the binding of serine/threonine derivatives to the enzyme’s active site was stronger (−4.6~−7.9 kcal/mol) than that of the natural acceptor, glucose, and mainly occurred through interactions with aromatic residues. For N-tert-butoxycarbonyl serine methyl ester (6.8%) and N-carboxybenzyl serine benzyl ester (3.4%), their binding affinities and the distances between their hydroxyl side chain and the 1′-OH group of galactose moiety were in good accordance with the quantified bioconversion yields. Despite its lower predicted bioconversion yield, the high experimental bioconversion yield obtained with N-carboxybenzyl serine methyl ester (23.2%) demonstrated the importance of the thermodynamically-driven nature of the transgalactosylation reaction.     

Superoxide Dismutase 3-Transduced Mesenchymal Stem Cells Preserve Epithelial Tight Junction Barrier in Murine Colitis and Attenuate Inflammatory Damage in Epithelial Organoids

Superoxide dismutase 3 (SOD3), also known as extracellular superoxide dismutase, is an enzyme that scavenges reactive oxygen species (ROS). It has been reported that SOD3 exerts anti-inflammatory abilities in several immune disorders. However, the effect of SOD3 and the underlying mechanism in inflammatory bowel disease (IBD) have not been uncovered. Therefore, in the present study, we investigated whether SOD3 can protect intestinal cells or organoids from inflammation-mediated epithelial damage. Cells or mice were treated with SOD3 protein or SOD3-transduced mesenchymal stem cells (MSCs). Caco-2 cells or intestinal organoids stimulated with pro-inflammatory cytokines were used to evaluate the protective effect of SOD3 on epithelial junctional integrity. Dextran sulfate sodium (DSS)-induced colitis mice received SOD3 or SOD3-transduced MSCs (SOD3-MSCs), and were assessed for severity of disease and junctional protein expression. The activation of the mitogen-activated protein kinase (MAPK) pathway and elevated expression of cytokine-encoding genes decreased in TNF-α-treated Caco-2 cells or DSS-induced colitis mice when treated with SOD3 or SOD3-MSCs. Moreover, the SOD3 supply preserved the expression of tight junction (ZO-1, occludin) or adherence junction (E-cadherin) proteins when inflammation was induced. SOD3 also exerted a protective effect against cytokine- or ROS-mediated damage to intestinal organoids. These results indicate that SOD3 can effectively alleviate enteritis symptoms by maintaining the integrity of epithelial junctions and regulating inflammatory- and oxidative stress.     

Application of Upstream Open Reading Frames (uORFs) Editing for the Development of Stress-Tolerant Crops

Global population growth and climate change are posing increasing challenges to the production of a stable crop supply using current agricultural practices. The generation of genetically modified (GM) crops has contributed to improving crop stress tolerance and productivity; however, many regulations are still in place that limit their commercialization. Recently, alternative biotechnology-based strategies, such as gene-edited (GE) crops, have been in the spotlight. Gene-editing technology, based on the clustered regularly interspaced short palindromic repeats (CRISPR) platform, has emerged as a revolutionary tool for targeted gene mutation, and has received attention as a game changer in the global biotechnology market. Here, we briefly introduce the concept of upstream open reading frames (uORFs) editing, which allows for control of the translation of downstream ORFs, and outline the potential for enhancing target gene expression by mutating uORFs. We discuss the current status of developing stress-tolerant crops, and discuss uORF targets associated with salt stress-responsive genes in rice that have already been verified by transgenic research. Finally, we overview the strategy for developing GE crops using uORF editing via the CRISPR-Cas9 system. A case is therefore made that the mutation of uORFs represents an efficient method for developing GE crops and an expansion of the scope of application of genome editing technology.     

Effects of calcination temperature on morphological and crystallographic properties of oyster shell as biocidal agent

To develop biocompatible antimicrobial agent, oyster shell wastes were thermally calcined at different temperatures ranging from 300 to 1000 °C. The chemical compositions and properties of oyster shells were characterized. As such, crystallographic analysis presented that oyster shells had a hexagonal crystalline shape, and calcination process reduced their crystalline size, volume (grain dimension), and bond length, which strongly affected antimicrobial efficacy. Results showed that the main components of uncalcined and calcined oyster shells were CaCO₃ and CaO, by which CaO was found to be the main antimicrobial component. Notably, calcined oyster shells showed antimicrobial potency against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus). Furthermore, cytotoxicity analysis proved that calcined oyster shells had good cell viability and low cytotoxicity. Results highlighted that calcined oyster shells, particularly those treated at 750°C, could be a biocompatible alternative to synthetic biocidal and antimicrobial agents using in food packaging, biomedical, and cosmetic industries.     

Liquid-phase degradation of HDPE over alkali-treated natural zeolite catalysts

Catalytic performance of alkali-treated natural zeolites was studied in the liquid-phase catalytic degradation of HDPE. Alkali treatment of natural zeolite with a moderate NaOH solution brought about the formation of mesopores and a decrease in acid site density, resulting in a considerable improvement of its catalytic activity. However, alkali treatment with highly concentrated NaOH solutions induced zeolite structure destruction, resulting in lower activity. HDPE conversion and product selectivity of alkali-treated natural zeolites were discussed in terms of their pore structures, acidities and the diffusion properties of large molecules.     

SO2 oxidation over the V2O5/TiO2 SCR catalyst

The effects of V₂O₅ loading of the V₂O₅/TiO₂ SCR catalyst on SO₂ oxidation activity were examined by infrared spectroscopy (DRIFT) and SO₂ oxidation measurement. Vanadium oxide added to the catalyst was found to be well dispersed over the TiO₂ carrier until covered with monolayer V₂O₅. The rate of SO₂ oxidation increased almost linearly with V₂O₅ loading below the monolayer capacity and attained saturation with further increase. The hydroxyl groups bonded to vanadium atoms, V–OH, might be altered by SO₂ oxidation. Both V=O and V–OH groups are likely involved in the adsorption and desorption of SO₂ and SO₃.