Stability of immobilized biosorbent and its influence on biosorption of copper

Biomass immobilization in a polymeric matrix may improve biosorption capacity and facilitate the separation of biomass from metal-bearing solutions. Many polymers are studied as immobilizing agents for biosorption including biopolymers such as sodium alginate. In the article swelling behaviour of gel and dry beads has been studied in aqueous solutions with different acid-base character. Swelling of gel or dry calcium alginate beads was found in all acidic and basic solutions except of the gel beads in strong acidic solutions, which exhibited the tendency to shrink. Dry beads in diluted acidic solutions had the greatest stability because they exhibited minimum swelling. Dry and gel beads were completely dissolved in concentrated solutions of sodium and potassium hydroxides. The potential use of immobilized algal biomass in Ca-alginate beads for removal of copper ions from aqueous solution was also investigated. The results of the kinetic studies showed that the sorption of copper ions on gel immobilized beads are the most suitable.

Immobilization of Metanil Yellow Decolorizing Mixed Culture FN3 Using Gelling Gum as Matrix for Bioremediation Application

In this study, the Metanil Yellow (MY) decolorizing mixed culture, namely FN3, has been isolated from agriculture soil. The mixed culture was immobilized using gellan gum. In order to optimize the immobilization process for maximal dye decolorization, Response Surface Methodology (RSM) was performed. The optimal conditions for immobilization predicted by desirability function are 130 mg/L of MY dye concentration, 1.478% of gellan gum concentration, 50 beads and 0.6 cm of beads size with the percentage of decolorization of 90.378%. The correlation coefficients of the model (R2 and R2 adj) are 0.9767 and 0.9533, respectively. This indicates that the established model is suitable to predict the effectiveness of dye decolorization under the investigated condition. The immobilized beads of mixed culture FN3 were able to be reused up to 15 batches of decolorization. The immobilized cells also have high tolerance towards heavy metals. This was proven by higher dye decolorization rate by the immobilized cells even with the addition of heavy metals in the media. The decolorization potential of the mixed culture indicates that it could be useful for future bioremediation of soil contaminated sites and treatment solutions of water bodies polluted with MY dye.

Application of peptides with an affinity for phospholipid membranes during the automated purification of extracellular vesicles

Extracellular vesicles (EVs), such as exosomes, have garnered increasing interest because of their potential clinical applications that range from diagnostics to therapeutics. The development of an automated and reproducible EV purification platform would therefore aid the introduction of EV biomarkers and therapies into the clinic. Here, we demonstrate that K8- as well as K-16 peptides (containing 8 and 16 lysine residues with dissociation constants of 102 nM and 11.6 nM for phosphatidylserine, respectively) immobilized on magnetic beads can capture small EVs (< 0.2 µm) from culture supernatants of MCF7 human breast cancer cells. Importantly, the bound EVs could be dissociated from the beads under mild conditions (e.g. 0.5 M NaCl), and the isolated EVs had the typical shapes of EVs under SEM and TEM with a mean particle size of 99 nm. Using the peptide-immobilized beads, we adapted a pre-existing bench top instrument for magnetic separation to perform automated EV purification with higher purity and yield than that obtained using the standard ultracentrifugation method.

Production of chitosan from Oyster mushroom for α-amylase immobilization

Experiments were carried out to produce chitosan from a locally available mushroom and to use the produced chitosan as a matrix to immobilize α-amylase. On the basis of morphological characteristics and the sequence of the internal transcribed spacer region of the nuclear rDNA, the fungal sample was identified as Pleurotus ostreatus. The average crude chitin content in the dried fruit body of P. ostreatus was 24.11%. The average yield of chitosan from P. ostreatus was 163.3 mg/g dry weight and the degree of deacetylation of the produced chitosan was 73.42%. This chitosan was used as a matrix to immobilize α-amylase. The diameter of the α-amylase immobilized beads ranged from 1839 - 2273 μm. The amount of reducing sugar produced from starch by using free α-amylase and chitosan-immobilized α-amylase was 1.710 and 1.508 mg/ml, respectively. Immobilized enzyme produced only 11.81% less reducing sugar than that of the soluble enzyme in the first cycle. However, immobilized α-amylase was easily recovered from the product and reused for two more cycles which was not possible with the same soluble free enzyme. Considering the total production of reducing sugar in three cycles, chitosan-immobilized α-amylase was found to be more productive and cost-effective than conventional soluble enzymatic reaction.

Effective decolorization of anthraquinone dye reactive blue 19 using immobilized Bacillus sp. JF4 isolated by resuscitation-promoting factor strategy

Given the highly complex recalcitrant nature of synthetic dyes, biological treatment of textile wastewater using efficient bacterial species is still considered as an environmentally friendly manner. In this study, a reactive blue 19 (RB19)-degrading strain, Bacillus sp. JF4, which was isolated by resuscitation-promoting factor (Rpf) strategy, was immobilized into polyvinyl alcohol–calcium alginate–activated carbon beads (JF4-immobilized beads) for RB19 decolorization. Results suggest that the JF4-immobilized beads, which were capable of simultaneous adsorption and biodegradation, showed a high decolorization activity, while they exhibited better tolerability towards high RB19 concentrations. The JF4-immobilized beads could almost completely decolorize 100 mg/L RB19 within 10 d, while only 92.1% was decolorized by free bacteria within 12 d. Further investigation on the equilibrium and kinetics of the adsorption process suggests that the pseudo-second-order model best fit the adsorption kinetics data, and the Freundlich isotherm was the most suitable for the description of the equilibrium data. Notably, the repeated batch cycles indicated that complete decolorization of 100 mg/L RB19 by JF4-immobilized beads can be maintained for at least three cycles without much reduction in efficiency. These findings suggest that immobilizing Rpf-resuscitated strain into beads was an effective strategy for textile wastewater treatment.

Magnetophoretic Harvesting of Nannochloropsis oculata Using Iron Oxide Immobilized Beads

In this work, the harvesting of Nannochloropsis oculata microalgae through the use of nanosized Fe3O4 immobilized in polyvinyl alcohol (PVA)/sodium alginate (SA) as a flocculant (Fe3O4/PS) is investigated. Using the Fe3O4/PS immobilized beads could reduce the amount of soluble ferrous ions (Fe2+) released from naked Fe3O4 in acid treatment, leading to easy recovery. The characterization was performed under different dosages and pH values of Fe3O4/PS. The results show that the Fe3O4/PS, when applied to the algae culture (500 mg dry cell weight/L), achieves a 96% harvesting efficiency under conditions of a pH of 4 with 200 mT magnetic field intensity. Fe3O4/PS can be directly reused without adjusting the pH value. The recycled Fe3O4/PS shows stability in terms of its surface properties, maintaining more than 80% harvesting efficiency after five recycles. Magnetophoretic harvesting, using immobilized magnetic iron oxide as a particle-based flocculant, is a potential method to reduce challenges related to the cost-effective microalgae-harvesting method.

Identification of candidate molecular targets of the novel antineoplastic antimitotic NP-10

We previously reported the identification of a novel antimitotic agent with carbazole and benzohydrazide structures: N′-[(9-ethyl-9H-carbazol-3-yl)methylene]-2-iodobenzohydrazide (code number NP-10). However, the mechanism(s) underlying the cancer cell-selective inhibition of mitotic progression by NP-10 remains unclear. Here, we identified NP-10-interacting proteins by affinity purification from HeLa cell lysates using NP-10-immobilized beads followed by mass spectrometry. The results showed that several mitosis-associated factors specifically bind to active NP-10, but not to an inactive NP-10 derivative. Among them, NUP155 and importin β may be involved in NP-10-mediated mitotic arrest. Because NP-10 did not show antitumor activity in vivo in a previous study, we synthesized 19 NP-10 derivatives to identify more effective NP-10-related compounds. HMI83-2, an NP-10-related compound with a Cl moiety, inhibited HCT116 cell tumor formation in nude mice without significant loss of body weight, suggesting that HMI83-2 is a promising lead compound for the development of novel antimitotic agents.