Bioprospecting microwave-alkaline hydrolysate cocktail of defatted soybean meal and jackfruit peel biomass as carrier additive of molasses-alginate-bead biofertilizer

The extraction of soluble hydrolysate protein and sugar from a biomass cocktail of defatted soybean meal (DSM) and jackfruit peel (JP) was examined using microwave-alkaline hydrolysis by varying the NaOH concentrations (0.04–0.11 M) and residence times (2–11 min). Based on the central composite design, the optimized parameters were achieved at 0.084 M NaOH concentration (100 mL), for 8.7 min at 300 W microwave power level to obtain the highest protein (5.31 mg/mL) and sugar concentrations (8.07 mg/mL) with > 75% recovery. Both raw and detoxified hydrolysate (using activated carbon) were correspondingly biocompatible with Enterobacter hormaechei strain 40a (P > 0.05) resulting in maximal cell counts of > 10 log CFU/mL. The optimized hydrolysate was prepared as an additive in molasses-alginate bead encapsulation of strain 40a. Further evaluation on phosphate and potassium solubilization performance of the encapsulated strain 40a exhibited comparable results with those of free cell counterpart (P > 0.05). The DSM-JP hydrolysate cocktail holds potential as a carrier additive of encapsulated-cell bead biofertilizers in order to sustain bacterial cell quality and consequently improve crop growth and productivity.

Characteristics of Cesium Adsorption by Alginate Bead Adsorbent with Layer-by-Layer Synthesis of Prussian Blue

Objectives : The purpose of this study was to develop an adsorbent to which Prussian blue (PB) is stably immobilized to remove radioactive cesium (Cs).Methods : Prussian blue-Alginate (PA) bead and Prussian blue-Alginate with Layer-by-layer synthesis (PAL) bead were synthesized by immobilizing PB respectively.Results and Discussion : As a results of XRD and FT-IR analysis, PB was successfuuly immobilized in alginate bead and PA, PAL bead. SEM (EDS) and TG analysis data were confirmed that the PB content of the PAL bead to which the LBL synthesis method was applied was improved by 6.31%. It was confirmed that the Cs adsorption capacity was improved through the LBL assembly process. The maximum adsorption amount (qm) of PA bead was 25.783 mg/g, and PAL bead was mg/g. In addition, as a result of UV-vis analysis of washing water after synthesis of PA bead and PAL bead, it was confirmed that the PB desorption of the PAL bead was lower indicating that the stability was also improved by LBL synthesis.Conclusions : We developed an adsorbent which prussianblue immobilized on alginate bead for selective removal cesium in aqueous solution. PB was immobilized by LBL synthesis method qm of PAL beads was 28.294 mg/g. It was expected to applied effectively and stably to radioactive cesium contaminated water.

Fabrication of porous composites based on alginate to improve the adsorption capacity of Ni(II)

Calcium alginate bead (CAB) is a good adsorbent of heavy metal ions; however, CAB has a small specific surface area, limiting its applications in the removal of heavy metals in water treatment. In this study, alginate is denatured with activated carbon and surfactants to increase the porosity of the material and improve the adsorption capacity of the Ni(II) ion. Initial undenatured calcium alginate bead is almost no pores and a very small specific surface area (~0.04 m2/g). After modification, the porous composite made from alginate combined with active carbon and surfactant (P-CAB) has a large specific surface area ~160 m2/g, 4,000 times higher than CAB. The results of the Ni(II) ion adsorption study also showed that the maximum adsorption capacity of porous composite (qmax of 53.76 mg/g) significantly improved by 8.3 times than the adsorption capacity of CAB (6.48 mg/g).

Preparation of Highly Porous Thiophene-Containing DUT-68 Beads for Adsorption of CO2 and Iodine Vapor

Zirconium-based metal-organic frameworks (Zr-MOFs) have great structural stability and offer great promise in the application of gas capture. However, the powder nature of MOF microcrystallines hinders their further industrial-scale applications in fluid-phase separations. Here, Zr-based DUT-68 was structured into nontoxic and eco-friendly alginate beads, and the gas capture properties were evaluated by CO2 and volatile iodine. DUT-68 beads were synthesized via a facile and versatile cross-linked polymerization of sodium alginate with calcium ions. The composite beads keep the structural integrity and most of the pore accessibility of DUT-68. The resulting DUT-68@Alginate (2:1) porous bead processes a surface area of 541 m2/g and compressive strength as high as 1.2 MPa, and the DUT-68 crystals were well-dispersed in the alginate networks without agglomeration. The DUT-68@Alginate bead with a 60% weight ratio of MOFs exhibits a high carbon dioxide capacity (1.25 mmol/g at 273 K), as well as an excellent high adsorption capacity for iodine, reaching up to 0.65 g/g at 353 K. This work provides a method to construct thiophene-contained composite beads with millimeter sizes for the capture of gases in potential industrial applications.

Alginate Bead Biosystem for the Determination of Lactate in Sweat Using Image Analysis

Lactate is present in sweat at high concentrations, being a metabolite of high interest in sport science and medicine. Therefore, the potential to determine lactate concentrations in physiological fluids, at the point of need with minimal invasiveness, is very valuable. In this work, the synthesis and performance of an alginate bead biosystem was investigated. Artificial sweat with different lactate concentrations was used as a proof of concept. The lactate detection was based on a colorimetric assay and an image analysis method using lactate oxidase, horseradish peroxidase and tetramethyl benzidine as the reaction mix. Lactate in artificial sweat was detected with a R² = 0.9907 in a linear range from 10 mM to 100 mM, with a limit of detection of 6.4 mM and a limit of quantification of 21.2 mM. Real sweat samples were used as a proof of concept to test the performance of the biosystem, obtaining a lactate concentration of 48 ± 3 mM. This novel sensing configuration, using alginate beads, gives a fast and reliable method for lactate sensing, which could be integrated into more complex analytical systems.

The Specific Gravity-Free Method for the Isolation of Circulating Tumor KRAS Mutant DNA and Exosome in Colorectal Cancer

Background: Circulating tumor DNA (ctDNA) and exosome have been widely researched in the field of medical technology and diagnosis platforms. The purpose of our study was to improve the capturing properties of ctDNA and exosome, which involved combining two beads using approaches that may provide a new method for cancer diagnoses. Methods: We present a dual isolation system including a polydopamine (PDA)–silica-coated alginate bead for circulating tumor DNA (ctDNA) capture and an anti-CD63 immobilized bead for exosome capture. We examined the ctDNA mutation in pre-operative plasma samples obtained from 91 colorectal cancer (CRC) patients using a droplet digital PCR (ddPCR). Results: The area under the curve (AUROC) of ctKRAS G12D mutation in the buffy coat was 0.718 (95% CI: 0.598−0.838; p = 0.001). Patients with CRC that had unmethylation of MLH1 and MSH2 showed significantly higher buffy coat ctKRAS G12D mutations, ascites ctKRAS G12D mutations, miR-31-5, and mixed scores than the patients with a methylation of MLH1 and MSH2. Conclusion: Our proposed alginate bead using the specific gravity-free method suggests that the screening of mutated ctKRAS DNA and miR-31-5 by liquid biopsy aids in identifying the patients, predicting a primary tumor, and monitoring in the early detection of a tumor.

Treatment of Pesticide-Contaminated Water Using a Selected Fungal Consortium: Study in a Batch and Packed-Bed Bioreactor

This study provides the basis for implementing a continuous treatment system for wastewater containing a pesticide mixture formed by atrazine, iprodione, and chlorpyrifos. Two fungal strains (Verticilium sp. H5 and Metacordyceps sp. H12) isolated from a biomixture of a biopurification system were able to remove different pesticide concentrations (10 to 50 mg L−1) efficiently from the liquid medium; however, the half-life of the pesticides was reduced and characterized by a T1/2 of 5.4 to 9.2 d for atrazine, 3.7 to 5.8 d for iprodione, and 2.6 to 2.9 d for chlorpyrifos using the fungal consortium. The immobilization of the fungal consortium in alginate bead was effective, with the highest pesticide removal observed using an inoculum concentration of 30% wv−1. The packed-bed reactor with the immobilized fungal consortium, which was operated in the continuous mode at different flow rates (30, 60, and 90 mL h−1), required approximately 10 d to achieve removal efficiency (atrazine: 59%; iprodione: 96%; chlorpyrifos: ~85%). The bioreactor was sensitive to flow rate fluctuations but was able to recover performance quickly. The pesticide metabolites hydroxyatrazine, 3,5-dichloroaniline, and 3,5,6-trichloro-2-pyridinol were produced, and a slight accumulation of 3,5,6-trichloro-2-pyridinol was observed. Nevertheless, reactor removal efficiency was maintained until the study ended (60 d).