A Brief Review of Graphene-Based Biosensors Developed for Rapid Detection of COVID-19 Biomarkers.

The prevalence of mutated species of COVID-19 antigens has provided a strong impetus for identifying a cost-effective, rapid and facile strategy for identifying the viral loads in public places. The ever-changing genetic make-up of SARS-CoV-2 posts a significant challenfge for the research community to identify a robust mechanism to target, bind and confirm the presence of a viral load before it spreads. Synthetic DNA constructs are a novel strategy to design complementary DNA sequences specific for antigens of interest as in this review's case SARS-CoV-2 antigens. Small molecules, complementary DNA and protein-DNA complexes have been known to target analytes in minimal concentrations. This phenomenon can be exploited by nanomaterials which have unique electronic properties such as ballistic conduction. Graphene is one such candidate for designing a device with a very low LOD in the order of zeptomolar and attomolar concentrations. Surface modification will be the significant aspect of the device which needs to have a high degree of sensitivity at the same time as providing a rapid signaling mechanism.

An energy efficient production of high moisture barrier nanocellulose/carboxymethyl cellulose films via spray-deposition technique.

Nanocellulose (NC) films are considered as a prospective alternative to non-sustainable packaging materials, however, their higher embodied energy and limited moisture barrier properties are regarded as a huge constraint regarding their commercialization. This study aims to produce films with relatively low environmental impact and improved barrier performance. For this purpose, carboxymethyl cellulose (CMC) and NC were combined, and this resulted in multidimensional advantages. The mass production of films could be achieved in only 2 h (requiring at least 24 h under ambient conditions) when dried in an oven at 75 °C with enhanced mechanical properties and without compromising their dimensional stability. The moisture barrier properties of the NC/CMC films were improved up to 92 % compared with the NC films alone and the results achieved are comparable with packaging materials such as polyethylene terephthalate (PET), polycarbonates (PC) etc. Finally, the NC/CMC (1:1) films have low environmental impact compared with PET films.

Cloning and expression of S-Adenosyl Methionine Synthetase gene in recombinant E. coli strain for large scale production of SAMe

S-Adenosyl Methionine (SAMe) Synthetase is an enzyme which catalyses the synthesis of S-Adenosyl Methionine using methionine and ATP. It is also known as AdoMet which is well known methyl donor, which modifies DNA, RNA, histones and other proteins, dictating replicational, transcriptional and translational fidelity, mismatch repair, chromatin modeling, epigenetic modifications and imprinting. The objective of the present work is to clone the SAMe Synthetase gene in recombinant E. coli strain in order to express, characterize and purify it for further synthesis of SAMe in a large scale fermentation. Expression was induced by 1 mM IPTG and expressed protein was characterized by SDS-PAGE. The recombinant E. coli cells were used for the production of SAMe through batch and fed batch fermentation operations. The produced SAMe was purified through paper chromatography in order to use it in our future studies.

Porous keratin scaffold-promising biomaterial for tissue engineering and drug delivery.

A porous keratin scaffold, prepared from the reduced keratin solution, has shown good cell viability which makes it a potential candidate for cell seeding. An aqueous solution of reduced keratin was extracted from horn meal using a mixture of urea, sodium dodecyl sulfate, mercaptoethanol, and water at 60 degrees C. The molecular mass of the extracted keratin is found to be ranging between 225 and 150 KDa. The CD spectrum of aqueous solution of keratin shows the presence of infinity-helical structure with beta-turns as negative absorption band at 225 nm and as positive absorption band at 195 nm. The FTIR spectrum of the same confirms infinity-helical structure with beta-turns. Its characteristic absorption bands are assigned mainly to the peptide bonds for amide I, II, and III respectively. DSC and TGA data of the reduced keratin peaks fall in region 200 degrees C-250 degrees C and 200 degrees C-400 degrees C temperatures, respectively. They correspond to the infinity-helix denaturation of the material.