Fabrication and Experimental Analysis of Axially Oriented Nanofibers.

A novel design of a laboratory built axially rotating collector (ARC) having capability to align electrospun nanofibers have been described. A detailed morphological comparison of such nanofibers orientation and their geometry is done using scanning electron microscopy (SEM). For comparison various polymeric solutions were electrospun on conventional static collector as well as ARC. The average diameter of polyvinyl alcohol (PVA) nanofibers was found to be 250 nm while polycaprolactone (PCL) nanofibers were found to be within a range of 600-800 nm. Conducting nanoparticles such as graphene and multi-walled carbon nanotubes (MWNTs) mixed with polymer solutions shown to have a significant influence on the overall geometry of these nanofibers and their diameter distribution. It is evident from the SEM analysis that both graphene and MWNTs in polymer solution play a crucial role in achieving a uniform diameter of nanofibers. Lastly, the formation of the aligned nanofibers using ARC has been mathematically modeled and the electromagnetic field governing the process has been simulated.

Strontium Manganese Oxide Getter for Capturing Airborne Cr and S Contaminants in High-Temperature Electrochemical Systems.

Traces (ppm to ppb level) of airborne contaminants such as CrO2(OH)2 and SO2 irreversibly degrade the electrochemical activity of air electrodes in high-temperature electrochemical devices such as solid oxide fuel cells by retarding oxygen reduction reactions. The use of getter has been proposed as a cost-effective strategy to mitigate the electrode poisoning. However, owing to the harsh operating conditions (i.e., exposure to heat and moisture), the long-term durability of getter materials remains a considerable challenge. In this study, we report our findings on strontium manganese oxide (SMO) as a robust getter material for cocapture of airborne Cr and S contaminants. The SMO getter with a 3D honeycomb architecture, fabricated via slurry dip-coating, successfully maintains the electrochemical activity of solid oxide cells under the flow of gaseous Cr and S species, validating the getter's capability of capturing traces of Cr and S contaminants. Investigations found that both Sr and Mn cations contribute to the absorption reaction and that the reaction processes are accompanied by morphological elongation in the form of SrSO4 nanorods and SrCrO4 whiskers, which favors continued absorption and reaction of incoming S and Cr contaminants. The SMO getter also displays robust stability at high temperatures and in humid environments without phase transformation and hydrolysis. These results demonstrate the feasibility of the use of SMO getter under severe operating conditions representative of high-temperature electrochemical systems.

An experimental modeling of trinomial bioengineering- crp, rDNA, and transporter engineering within single cell factory for maximizing two-phase bioreduction.

A carbonyl reductase (cr) gene from Candida glabrata CBS138 has been heterologously expressed in cofactor regenerating E. coli host to convert Ethyl-4-chloro-3-oxobutanoate (COBE) into Ethyl-4-chloro-3-hydroxybutanoate (CHBE). The CR enzyme exhibited marked velocity at substrate concentration as high as 363mM with highest turnover number (112.77±3.95s-1). Solitary recombineering of such catalytic cell reproduced CHBE 161.04g/L per g of dry cell weight (DCW). Introduction of combinatorially engineered crp (crp*, F136I) into this heterologous E. coli host yielded CHBE 477.54g/L/gDCW. Furthermore, using nerolidol as exogenous cell transporter, the CHBE productivity has been towered to 710.88g/L/gDCW. The CHBE production has thus been upscaled to 8-12 times than those reported so far. qRT-PCR studies revealed that both membrane efflux channels such as acrAB as well as ROS scavenger genes such as ahpCF have been activated by engineering crp. Moreover, membrane protecting genes such as manXYZ together with solvent extrusion associated genes such as glpC have been upregulated inside mutant host. Although numerous proteins have been investigated to convert COBE to CHBE; this is the first approach to use engineering triad involving crp engineering, recombinant DNA engineering and transporter engineering together for improving cell performance during two-phase biocatalysis.

Graphene oxide as a quencher for fluorescent assay of amino acids, peptides, and proteins.

Understanding the interaction between graphene oxide (GO) and the biomolecules is fundamentally essential, especially for disease- and drug-related peptides and proteins. In this study, GO was found to strongly interact with amino acids (tryptophan and tyrosine), peptides (Alzheimer's disease related amyloid beta 1-40 and type 2 diabetes related human islet amyloid polypeptide), and proteins (drug-related bovine and human serum albumin) by fluorescence quenching, indicating GO was a universal quencher for tryptophan or tyrosine related peptides and proteins. The quenching mechanism between GO and tryptophan (Trp) or tyrosine (Tyr) was determined as mainly static quenching, combined with dynamic quenching (Förster resonance energy transfer). Different quenching efficiency between GO and Trp or Tyr at different pHs indicated the importance of electrostatic interaction during quenching. Hydrophobic interaction also participated in quenching, which was proved by the presence of nonionic amphiphilic copolymer Pluronic F127 (PF127) in GO dispersion. The strong hydrophobic interaction between GO and PF127 efficiently blocked the hydrophobic interaction between GO and Trp or Tyr, lowering the quenching efficiency.