Pulsed electric field treatment of soymilk: Impact on Kunitz trypsin inhibitor allergenicity, antinutritional factor, and aroma characteristics.

Allergens, antinutritional factors, and lipoxygenase (LOX) enzyme present in soymilk limit its consumption as vegan milk. Therefore, the present study focuses on reducing these limiting factors using pulsed electric field (PEF) treatment. In this regard, 20-40 kV/cm electric field was applied to soymilk for the effective treatment periods of 450, 1350, and 2250 ms. After the treatment, a reduction in pH (6.60 ± 0.10 to 6.47 ± 0.12) and an increase in the conductivity (173.03 ± 0.40 to 177.33 ± 0.72 µS) were observed. Furthermore, FTIR (Fourier Transform Infrared Spectroscopy), UV (Ultra Violet) intrinsic spectra, and CD (Circular Dichroism) spectra (α-helix reduction and ß-sheet increase) data indicated mild structural changes in the proteins of soymilk. As a result, PEF treatment reduced the soymilk allergenicity (67.33 ± 20.48%), LOX activity (69.45 ± 9.38%), and trypsin inhibitor activity (75.61 ± 4.04%). Apart from that, the color, viscosity, and volatiles of soymilk also had significant changes due to PEF treatment. The aroma changes in PEF-treated soymilk were highly influenced by two major principal component (PC1 & PC2) groups and they accounted for about 70% of the aroma variations. However, these changes were mild and did not induce any off-flavors and the treatment remained effective against the quality hazards like allergens, antinutritional factors, and LOX enzyme. PRACTICAL APPLICATION: PEF treatment of soymilk reduces the possible allergic reactions in human body at least by 30%. Further, it reduces the antinutritional factor and off-odor inducing compounds. Therefore, the PEF treatment can be used in industries as a pre-treatment to produce allergen and antinutritional compounds free protein isolates from soybeans.

An amide to thioamide substitution improves the permeability and bioavailability of macrocyclic peptides.

Solvent shielding of the amide hydrogen bond donor (NH groups) through chemical modification or conformational control has been successfully utilized to impart membrane permeability to macrocyclic peptides. We demonstrate that passive membrane permeability can also be conferred by masking the amide hydrogen bond acceptor (>C = O) through a thioamide substitution (>C = S). The membrane permeability is a consequence of the lower desolvation penalty of the macrocycle resulting from a concerted effect of conformational restriction, local desolvation of the thioamide bond, and solvent shielding of the amide NH groups. The enhanced permeability and metabolic stability on thioamidation improve the bioavailability of a macrocyclic peptide composed of hydrophobic amino acids when administered through the oral route in rats. Thioamidation of a bioactive macrocyclic peptide composed of polar amino acids results in analogs with longer duration of action in rats when delivered subcutaneously. These results highlight the potential of O to S substitution as a stable backbone modification in improving the pharmacological properties of peptide macrocycles.

Study on the characteristics of gluten/alginate-cellulose/onion waste extracts composite film and its food packaging application.

The study aimed to improve the properties of SA-CMC film by gluten (G) blends and bioactive compounds from onion waste extracts (OWEs) peel (OPE) and stalk (OSE). The applicability of film on the quality of peeled shallot onion during storage was also examined. Water barrier (0.62 g/msPa × 10-14) and tensile strength (11.50 MPa) of G/SA-CMC film improved more than SA-CMC film (1.55 g/msPa × 10-13 and 7.05 MPa). OPE and OSE increase the total phenolic content (43.86 and 38.35 mgGAE/g) and radical scavenging activity (88.74 and 68.30 %) of G/SA-CMC film than control (20.33 mgGAE/g and 39.20 %). Microbial load (logCFU/g) in terms of total bacterial count, yeast and mold count of shallot onion packed in OPE (5.34 and 5.21) and OSE (4.26 and 4.21) film was reduced than control (6.03 and 4.68). Thus, the G/SA-CMC/OWEs film had improved properties than SA-CMC film and can be used to store peeled onion at 4℃ for 21 days.

Bio-energy generation and treatment of tannery effluent using microbial fuel cell.

In this study, Graphite Particle (GP) and Carbon Cloth (CC) are employed as anode electrodes to study both bio-energy generation, and decrease of Chemical Oxygen Demand (COD) simultaneously using tannery effluent. The influence of electrodes distance (10 cm and 20 cm) on electricity production was evaluated. COD removal level of GP (75%) and CC (60%), maximum power outputs for 10 cm distance (600 ± 5 mW m-2) & (500 ± 10 mW m-2) and for 20 cm distance (520 ± 5 mW m-2) and also (430 ± 20 mW m-2) GP and CC were noted correspondingly. The outcomes of different parameters of MFC namely pH, conductivity, COD concentration, membrane thickness and size of bio-energy generation from tannery effluent in the MFC were investigated. The experimental results reveal that electrode provides highest power output with 10 cm distance between anode and cathode chamber. As a result, GP electrode is gradually viable, biocompatible, effective and adaptable for field application in MFC. The GP electrode has high potential for more power output, when compared to the CC electrode. The MFC system performance was improved with increasing effluent COD concentration (2340-4720 ppm), anolyte conductivity (1.6-8.1 mS cm-1) and membrane area (9-20 cm2). The system working with conductivity of 8.1 mS cm-1 and its effluent COD concentration of 4720 ppm generated the maximum peak power density of 44.69 mW m-2 with respective current density of 109 mA m-2. The findings thus show that considerable power production and effluent treatment can be achieved by MFC.

Development of active packaging film from sodium alginate/carboxymethyl cellulose containing shallot waste extracts for anti-browning of fresh-cut produce.

Owing to growing concerns about making pollution-free sustainable environment by reducing the dumping of agricultural waste and convert it into valuable product is a key to carry out the present study. The ultimate goal of this study is to convert shallot onion wastes (SOWs) into active packaging and evaluating the anti-browning effect due to the SOWs holding rich polyphenols and antioxidants. The active packaging film was fabricated by using sodium alginate (SA) and carboxymethyl cellulose (CMC) along with shallot onion waste extract (SOWEs) such as peel and stalk at 0.2% and 0.5% concentration. The film made with SA/CMC/SOWEs had good physical, mechanical, optical and barrier property, higher phenolic and antioxidant activity compared to control. In addition, the effect of SA/CMC/SOWEs film packaging on anti-browning and quality of fresh-cut apple and potato stored at 4 °C was studied. The results show the SA/CMC/SOWEs film had better effect on controlling browning index in fresh-cut apple and potato over the storage of 12 days and 5 days. This study concludes that the SA/CMC film developed with shallot stalk extract can be used for wrapping of fresh-cut fruits and vegetables. It also prevents browning and maintains the overall quality than control and shallot peel incorporated film.

Design, synthesis, anticancer, antimicrobial activities and molecular docking studies of novel quinoline bearing dihydropyridines.

A new series of eight quinoline bearing dihydropyridine derivatives (A1-A8) were synthesized in high yield and in short reaction time by a four component reaction of 2-chloro-3-fomyl quinoline, malononitrile, arylamines and dimethyl acetylenedicarboxylate in the presence of a catalytic amount of triethylamine. The compounds were fully characterized by IR, NMR and GC-MS. These compounds were screened for potential biological activity in an A549 lung cancer cell line and were also evaluated for their antibacterial activities against Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 29213 whilst their molecular docking properties in an enzymatic system were also determined. Compounds A2, A3, A4 and A8 showed anti-proliferative activity; with A4 having the highest toxicity at 250µg/mL and A8 has high toxicity at 125, 250 and 500µg/mL, respectively. Antibacterial results indicated that A4 have significant activity against tested microorganisms at the minimum inhibitory concentration (MIC) values of 32µg/mL against Pseudomonas aeruginosa and Escherichia coli, and 16µg/mL against Staphylococcus aureus. Docking of A1 with human mdm2 indicated the lowest binding energy (-6.111Kcal/mol) thereby showing strong affinity of the ligand molecule with the receptor which has been stabilized by strong hydrogen bond interactions in the binding pocket. This confirms that A1 is a better inhibitor for E3 ubiquitin-protein ligase mdm2.

Stainless steel surface functionalization for immobilization of antibody fragments for cardiovascular applications.

Stainless steel 316 L material is commonly used for the production of coronary and peripheral vessel stents. Effective biofunctionalization is a key to improving the performance and safety of the stents after implantation. This paper reports the method for the immobilization of recombinant antibody fragments (scFv) on stainless steel 316 L to facilitate human endothelial progenitor cell (EPC) growth and thus improve cell viability of the implanted stents for cardiovascular applications. The modification of stent surface was conducted in three steps. First the stent surface was coated with titania based coating to increase the density of hydroxyl groups for successful silanization. Then silanization with 3 aminopropyltriethoxysilane (APTS) was performed to provide the surface with amine groups which presence was verified using FTIR, XPS, and fluorescence microscopy. The maximum density of amine groups (4.8*10(-5) mol/cm(2)) on the surface was reached after reaction taking place in ethanol for 1 h at 60 °C and 0.04M APTS. On such prepared surface the glycosylated scFv were subsequently successfully immobilized. The influence of oxidation of scFv glycan moieties and the temperature on scFv coating were investigated. The fluorescence and confocal microscopy study indicated that the densest and most uniformly coated surface with scFv was obtained at 37 °C after oxidation of glycan chain. The results demonstrate that the scFv cannot be efficiently immobilized without prior aminosilanization of the surface. The effect of the chemical modification on the cell viability of EPC line 55.1 (HucPEC-55.1) was performed indicating that the modifications to the 316 L stainless steel are non-toxic to EPCs.

Selective binding and detection of magnetic labels using PHR sensor via photoresist micro-wells.

We have developed a novel platform for selective binding of magnetic labels on planar Hall resistance sensor (PHR) for biosensing applications. The photoresist (PR) micro wells were prepared on the PHR sensor junctions to trap the magnetic bead at specified locations on the sensor surface and thin layer of Au was sputtered in the PR wells immobilize bimolecular. The Au surface is functionalized with single-stranded oligonucleotide and further biotin was used to immobilize streptavidin coated magnetic labels (Dynabeads Myone 1.0 microm, Invitrogen Co.). After removal of the PR wells on the sensor surface the non specific binding magnetic labels were successfully removed and only the chemically bounded magnetic labels were remained on the Au surface for detection of biomolecules using PHR sensor. We controlled the number of magnetic labels on the PHR sensor surface by using different sizes of the PR well on the junctions. The specifically bounded magnetic labels were successfully detected by characterizing the individual PHR sensor junctions. This technique enables the complete control over the magnetic labels for selective binding of biomolecules on the sensor surface for increasing the sensitivity of the PHR sensor as well as removal of the non specific bindings on the sensor surface.

Translocation of bio-functionalized magnetic beads using smart magnetophoresis.

We demonstrate real time on-chip translocation of bio-functionalized superparamagnetic beads on a silicon surface in a solution using a magnetophoresis technique. The superparamagnetic beads act as biomolecule carriers. Fluorescent-labeled Atto-520 biotin was loaded to streptavidin-coated magnetic beads (Dynabead(®) M-280) by means of ligand-receptor interactions. The magnetic pathways were patterned lithographically such that semi-elliptical Ni(80)Fe(20) elements were arranged sequentially for a few hundred micrometers in length. An external rotating magnetic field was used to drive translational forces on the magnetic beads that were proportional to the product of the field strength and its gradient. The translational force at the curving edge of the pathway element of 6 µm diameter was calculated to be ∼1.2 pN for an applied field of 7.9 kA m(-1). However, the force at the flat edge was calculated to be ∼0.16 pN. The translational force was larger than the drag force and thus allowed the magnetic beads to move in a directional way along the curving edge of the pathway. However, the force was not sufficient to move the beads along the flat edge. The top and bottom curving edge semi-elliptical NiFe pathways were obliquely-arranged on the left and right sides of the converging site, respectively. This caused a central translational force that allowed the converging and diverging of the Atto-520 biotin loaded streptavidin magnetic beads at a particular site.