Genomic comparison and phenotypic profiling of small colony variants of Burkholderia pseudomallei

Burkholderia pseudomallei (B. pseudomallei) is an intracellular pathogen that causes melioidosis, a life-threatening infection in humans. The bacterium is able to form small colony variants (SCVs) as part of the adaptive features in response to environmental stress. In this study, we characterize the genomic characteristics, antimicrobial resistance (AMR), and metabolic phenotypes of B. pseudomallei SCV and wild type (WT) strains. Whole-genome sequence analysis was performed to characterize the genomic features of two SCVs (CS and OS) and their respective parental WT strains (CB and OB). Phylogenetic relationship between the four draft genomes in this study and 19 publicly available genomes from various countries was determined. The four draft genomes showed a close phylogenetic relationship with other genomes from Southeast Asia. Broth microdilution and phenotype microarray were conducted to determine the AMR profiles and metabolic features (carbon utilization, osmolytes sensitivity, and pH conditions) of all strains. The SCV strains exhibited identical AMR phenotype with their parental WT strains. A limited number of AMR-conferring genes were identified in the B. pseudomallei genomes. The SCVs and their respective parental WT strains generally shared similar carbon-utilization profiles, except for D,L-carnitine (CS), g-hydroxybutyric acid (OS), and succinamic acid (OS) which were utilized by the SCVs only. No difference was observed in the osmolytes sensitivity of all strains. In comparison, WT strains were more resistant to alkaline condition, while SCVs showed variable growth responses at higher acidity. Overall, the genomes of the colony morphology variants of B. pseudomallei were largely identical, and the phenotypic variations observed among the different morphotypes were strain-specific.

Probiotic Characterization And Safety Assessment of Lactococcus Lactis Subsp. Lactis R7 Isolated From Ricotta Cheese

The aim of this study was to identify and characterize in vitro Lactococcus lactis R7 isolated from commercial ricotta cheese. The results from phenotypic characterization demonstrated that L. lactis R7 had growth potential in a wide temperature range (15 °C and 45 °C), ability to tolerate high osmotic concentrations (sodium chloride 4.0 %), ability to growth in acidic and alkaline condition (pH 2.0 and 9.6), and ability to sugar fermentation (glucose, maltose and ribose). The findings confirm that L. lactis R7 belong to the genus Lactococcus. The results from molecular identification by 16S RNA identified the isolate as Lactococcus lactis subsp. lactis R7. The phenotypic characteristics combined with the molecular identification, indicate that the isolate R7 belongs to the lactis subspecies. The isolate L. lactis R7 was tolerant to acidity and bile salts. In the intestinal tract, cell concentrations were higher than 7.98 log CFU.mL-1 in the presence and absence of bile salts. L. lactis R7 showed antioxidant and inhibitory capacity for lipid peroxidation. It also demonstrated capacity for self-aggregation (25.8%), coaggregation (18.3%) and hydrophobicity (11.1%). The antagonist activity of the isolate was greater against Staphylococcus aureus (12.2 mm), when compared to Escherichia coli (11.1 mm) and Salmonella enteritidis (9.5 mm). In the MTT assays, L. lactis R7 did not show cytotoxicity to VERO cells at the evaluated concentrations. In conclusion, L. lactis R7 isolated from ricotta cheese presented probiotic characteristics and compatible safety aspects for use as a food technology culture.

Three-Phase Heterojunction NiMo-Based Nano-Needle for Water Splitting at Industrial Alkaline Condition

Constructing heterojunction is an effective strategy to develop high-performance non-precious-metal-based catalysts for electrochemical water splitting (WS). Herein, we design and prepare an N-doped-carbon-encapsulated Ni/MoO2 nano-needle with three-phase heterojunction (Ni/MoO2@CN) for accelerating the WS under industrial alkaline condition. Density functional theory calculations reveal that the electrons are redistributed at the three-phase heterojunction interface, which optimizes the adsorption energy of H- and O-containing intermediates to obtain the best ΔGH* for hydrogen evolution reaction (HER) and decrease the ΔG value of rate-determining step for oxygen evolution reaction (OER), thus enhancing the HER/OER catalytic activity. Electrochemical results confirm that Ni/MoO2@CN exhibits good activity for HER (ƞ-10 = 33 mV, ƞ-1000 = 267 mV) and OER (ƞ10 = 250 mV, ƞ1000 = 420 mV). It shows a low potential of 1.86 V at 1000 mA cm−2 for WS in 6.0 M KOH solution at 60 °C and can steadily operate for 330 h. This good HER/OER performance can be attributed to the three-phase heterojunction with high intrinsic activity and the self-supporting nano-needle with more active sites, faster mass diffusion, and bubbles release. This work provides a unique idea for designing high efficiency catalytic materials for WS.

Regulating oxygen vacancies in Co3O4 by combining solution reduction and Ni2+ impregnation for oxygen evolution reaction

Oxygen vacancies are considered to be an important factor to influence the electronic structure and charge transport of electrocatalysts in the field of energy chemistry. Various strategies focused on oxygen vacancy engineering are proved to be efficient for further improving the electrocatalytic performance of Co3O4. Herein, an optimal Co3O4 with rich oxygen vacancies have been synthesized via a two-step process combining solution reduction and Ni2+ impregnation. The as-prepared electrocatalyst exhibits an enhanced oxygen evolution performance with the overpotential of 330 mV at the current density of 10 mA cm−2 in alkaline condition, which is 84 mV lower than that of pristine one. With the increasing of oxygen vacancies , the charge transfer efficency and surface active area are relatively enhanced reflected by the Tafel slope and double-layer capacitance measurement. These results indicate that combining solution reduction and heteroatom doping can be a valid way for efficient metal oxides-based electrocatalyst development by constructing higher concentration of oxygen vacancy.

A multi-function textile with pH-induced switch wettability transition for controllable oil−water separation

The deterioration of water ecology caused by the discharge of oil spill wastewater, industrial sewage, and municipal sewage has attracted wide attention worldwide. Thus, it is significant to design a simple, environmentally friendly approach to separate oil–water mixtures. In this work, three different fabrics with pH-induced wettability transition were prepared by a dip-coating process for oil and water separation. The dip-coating fabrics had the advantages of oil–water separation, photocatalytic degradation, and recycling. Polyethylene terephthalate/polyamide nonwoven fabric was used as the substrate materials of the fabric. The carboxylic acid-modified TiO2 endowed the fabric with hydrophilicity–hydrophobicity and photocatalytic properties. The Fe3O4 nanoparticles obtained by the coprecipitation method provided magnetism for the fabric, facilitating the recycling of the fabric and improving the hydrophobicity of the fabric. The fabrics coated with dipping solutions were superhydrophobic in a neutral environment and hydrophilic in an alkaline environment. Among the three coated fabrics, the fabric coated with stearic acid/TiO2-Fe3O4 (FST) had the most satisfying oil–water separation performance and durability. Under the neutral condition, the contact angle of the FST was 151° and the separation efficiency was 98%. Under the alkaline condition, the underwater oil contact angle of the FST was 150° and the separation efficiency was 95%. After 15 cycles, the oil–water separation rate of the FST was still higher than 90%. Due to the presence of TiO2, the coated fabric had an exceptional performance in the photodegradation of organic pollutants (69.9%). In addition, the fabrics can be quickly recovered due to magnetism.

Efficient Hydrogen Generation and Total Nitrogen Removal for Urine Treatment in a Neutral Solution Based on a Self-Driving Nano Photoelectrocatalytic System

Urine is the main source of nitrogen pollution, while urea is a hydrogen-enriched carrier that has been ignored. Decomposition of urea to H2 and N2 is of great significance. Unfortunately, direct urea oxidation suffers from sluggish kinetics, and needs strong alkaline condition. Herein, we developed a self-driving nano photoelectrocatalytic (PEC) system to efficiently produce hydrogen and remove total nitrogen (TN) for urine treatment under neutral pH conditions. TiO2/WO3 nanosheets were used as photoanode to generate chlorine radicals (Cl•) to convert urea-nitrogen to N2, which can promote hydrogen generation, due to the kinetic advantage of Cl–/Cl• cyclic catalysis. Copper nanowire electrodes (Cu NWs/CF) were employed as the cathode to produce hydrogen and simultaneously eliminate the over-oxidized nitrate-nitrogen. The self-driving was achieved based on a self-bias photoanode, consisting of confronted TiO2/WO3 nanosheets and a rear Si photovoltaic cell (Si PVC). The experiment results showed that hydrogen generation with Cl• is 2.03 times higher than in urine treatment without Cl•, generating hydrogen at 66.71 μmol h−1. At the same time, this system achieved a decomposition rate of 98.33% for urea in 2 h, with a reaction rate constant of 0.0359 min−1. The removal rate of total nitrogen and total organic carbon (TOC) reached 75.3% and 48.4% in 2 h, respectively. This study proposes an efficient and potential urine treatment and energy recovery method in neutral solution.