Cooperative Communication Enabled Cognitive Radio in a Home-Care Application

Wireless Personal Communications - In this paper, cooperative communication (CC) assisted cognitive wireless sensor network (CWSN) is presented for monitoring health and activity of an end-user in...     

Chitosan–silver nanocomposites: New functional biomaterial for health-care applications

Chitosan–silver nanocomposites (CS-HDA-AgNCs) was prepared using chitosan, biogenic silver nanocomposites, and crosslinker, hexamethylene 1,6-di(amino carboxysulfonate) (HDA). The film is flexible and transparent. Its physical, mechanical, thermal, hydrophilicity, and swelling properties were improved by HDA (2.5%). The antimicrobial activity of CS-HDA-AgNCs were not displayed any remarkable zone of inhibition but showed toxic effect in the presence of normal 3T3 fibroblasts and cancer HeLa cells. It decreases to ca. 5–7% for both cell lines. In conclusion, it can be mentioned that the CS-HDA-AgNCs, a kind of new functional biomaterial, could be useful for health-care applications.     

MADE3D: Enabling the next generation of high-torque density wind generators by additive design and 3D printing

Forschung im Ingenieurwesen - Direct-drive wind turbine generators are increasing in popularity, thanks to recent project developments—especially offshore, where reliability and efficiency...     

Insights into discrepancy in power generation among glucose and malate grown Rubrivivax benzoatilyticus JA2 microbial fuel cells

In this study, Rubrivivax benzoatilyticus JA2^T (=ATCC BAA-35^T = JCM 13220^T = MTCC 7087^T), an anoxygenic photosynthetic bacterium, was subjected to altered conditions and observed for changes in power outcome in the two chambered microbial fuel cells (MFCs), the basis of which was established using metabolomic studies. This is an extension to our previous studies, which showed that, under photo heterotrophic conditions, glucose in the form of a solitary carbon resource in minimal media, caused the strain JA2 to exhibit altered growth rates, progressive loss of pigmentation and reduced cell size (3–4 μm), compared to malate grown cells (6–7 μm). When R. benzoatilyticus JA2 cells were grown in malate bio-anodes, they presented higher potentials (289.22 ± 4.6 mV or 436.22 OCV per mg dry weight) compared to glucose bioanodes (163 ± 5.5 mv or 188.98 OCV per mg dry weight). Insights from the metabolomic footprints and fingerprints have revealed differential regulation of key components in the central metabolic pathway such as fumarate, citrate and succinate, which are significantly increased in malate grown bio anodes. Strain JA2 cells when grown with malate as substrate are densely grown on the electrodes and exhibited reduced size, when observed under SEM, which contrasts with control cells grown on malate broth. The artificial selection pressure of the MFC and the different metabolic pathways followed by these bacteria are the reasons for such discrepancy in the power production by the strain JA2. These adaptations may indicate survival advantage during the electron transfer and growth in bio anodes. The study throws light on what types of effluents would be more suitable as substrates for R. benzoatilyticus JA2 microbial fuel cells.     

Development of Phosphodiesterase–Protein-Kinase Complexes as Novel Targets for Discovery of Inhibitors with Enhanced Specificity

Phosphodiesterases (PDEs) hydrolyze cyclic nucleotides to modulate multiple signaling events in cells. PDEs are recognized to actively associate with cyclic nucleotide receptors (protein kinases, PKs) in larger macromolecular assemblies referred to as signalosomes. Complexation of PDEs with PKs generates an expanded active site that enhances PDE activity. This facilitates signalosome-associated PDEs to preferentially catalyze active hydrolysis of cyclic nucleotides bound to PKs and aid in signal termination. PDEs are important drug targets, and current strategies for inhibitor discovery are based entirely on targeting conserved PDE catalytic domains. This often results in inhibitors with cross-reactivity amongst closely related PDEs and attendant unwanted side effects. Here, our approach targeted PDE–PK complexes as they would occur in signalosomes, thereby offering greater specificity. Our developed fluorescence polarization assay was adapted to identify inhibitors that block cyclic nucleotide pockets in PDE–PK complexes in one mode and disrupt protein-protein interactions between PDEs and PKs in a second mode. We tested this approach with three different systems—cAMP-specific PDE8–PKAR, cGMP-specific PDE5–PKG, and dual-specificity RegA–R_D complexes—and ranked inhibitors according to their inhibition potency. Targeting PDE–PK complexes offers biochemical tools for describing the exquisite specificity of cyclic nucleotide signaling networks in cells.     

Editorial

Innovations in Systems and Software Engineering -     

Dual role of grass clippings as buffering agent and biomass during anaerobic co-digestion with food waste

Clean Technologies and Environmental Policy - There is a dire need to replace the chemical buffers that regulate the redox environment in single-stage anaerobic digestion of food waste. Hence, the...     

Stereovision based force estimation with stiffness mapping in surgical tool insertion using recurrent neural network

The Journal of Supercomputing - This paper proposes a novel method for estimating the reaction force, the Stereovision Based Force Estimation Method (SBFEM), with deep learning techniques to...     

Structure‐Guided Design of Thiazolidine Derivatives as Mycobacterium tuberculosis Pantothenate Synthetase Inhibitors

The pantothenate biosynthetic pathway is essential for the persistent growth and virulence of Mycobacterium tuberculosis (Mtb) and one of the enzymes in the pathway, pantothenate synthetase (PS, EC: 6.3.2.1), encoded by the panC gene, has become an appropriate target for new therapeutics to treat tuberculosis. Herein, we report nanomolar thiazolidine inhibitors of Mtb PS developed by a rational inhibitor design approach. The thiazolidine compounds were discovered by using energy‐based pharmacophore modelling and subsequent in vitro screening, which resulted in compounds with a half maximal inhibitory concentration (IC₅₀) value of (1.12±0.12) μM . These compounds were subsequently optimised by a combination of modelling and synthetic chemistry. Hit expansion of the lead by chemical synthesis led to an improved inhibitor with an IC₅₀ value of 350 nM and an Mtb minimum inhibitory concentration (MIC) of 1.55 μM . Some of these compounds also showed good activity against dormant Mtb cells.     

Performance investigation in modified and improved augmented power generation Kalina cycle using Python

In the generation of electricity and cogeneration, Kalina cycle is considered as one of the competitors to organic Rankine cycle. With the simplicity and identical components of the binary mixture, Kalina system makes it more prominent to get developed and implemented as well with its environmental friendly associate. This work proposes a new improved Kalina cycle system to convert the natural source from sun to useful work. The proposed system utilizes heat source suitable to medium temperature heat applications. The proposed cycle have 2 units of solar collector, favoring an additional heat recovery and higher performance. Solar hot source temperature and pressure are 190°C and 45 bar with additional flow to the turbine of 1.15 kg/s. Energy and second law analysis have considered in evaluating the performance of the proposed plant. The energy analysis shows minimum value of net power, energy efficiency and plant efficiency as 241 kW, 15.5% and 5.7. The exergy analysis defines that, to the proposed cycle, the exergy efficiency initializes at 77% with more exergy destruction at turbine with 31%. With the parametric analysis, the system is amended to have the maximum values of energy and exergy performances as 18.5%, 7.1% and 85%. The parametric study identifies the optimum value of the inlet temperature and pressure of the pump and turbine.