SILVER NANOPARTICLES OF MORINGA OLEIFERA – GREEN SYNTHESIS,CHARACTERISATION AND ITS ANTIMICROBIAL EFFICACY

Abstract : The traditional medicinal plant Moringa oleifera is an integral part of the Indian diet and has notable beneficial effects in its leaves, stems, flowers, roots, bark and seeds. It has reported properties like antimicrobial, anti inflammatory, ant diabetic, anti oxidative, anti tumorogenic amongst many other properties. In the present study we have devised a new green method of synthesis of silver nanoparticles to evaluate its antimicrobial efficacy using the aqueous plant extract as the reductant as well as the stabilizer. A cold method of synthesis of silver nanoparticles using silver nitrate solution is performed. After the synthesis step, the nanoparticles are characterised using UV VIS spectroscopy, scanning electron microscopy and transmission electron microscopy. The results show the incorporation of the silver ions in the extract and also the reduction of the particle size to the nano range. The antimicrobial potential of these nanoparticles synthesized is tested against various gram positive and gram negative strains of bacteria keeping streptomycin as the standard positive control antibiotic. The antibiotic assay is performed using agar well diffusion method and comparable results are obtained in comparison to the standard antibiotic. It is seen that the nanoparticles have good antibacterial efficacy against the tested strains. Hence nanoparticles of Moringa oleifera aqueous extracts can be used as a potential alternative to traditional antibiotics using this non toxic safe way of green synthesis. Keywords: Moringa oleifera, silver nanoparticles, antimicrobia

Effects of disrupting the polyketide synthase gene WdPKS1 in Wangiella [Exophiala] dermatitidis on melanin production and resistance to killing by antifungal compounds, enzymatic degradation, and extremes in temperature

BACKGROUND: Wangiella dermatitidis is a human pathogenic fungus that is an etiologic agent of phaeohyphomycosis. W. dermatitidis produces a black pigment that has been identified as a dihydroxynaphthalene melanin and the production of this pigment is associated with its virulence. Cell wall pigmentation in W. dermatitidis depends on the WdPKS1 gene, which encodes a polyketide synthase required for generating the key precursor for dihydroxynaphthalene melanin biosynthesis. RESULTS: We analyzed the effects of disrupting WdPKS1 on dihydroxynaphthalene melanin production and resistance to antifungal compounds. Transmission electron microscopy revealed that wdpks1Δ-1 yeast had thinner cell walls that lacked an electron-opaque layer compared to wild-type cells. However, digestion of the wdpks1Δ-1 yeast revealed small black particles that were consistent with a melanin-like compound, because they were acid-resistant, reacted with melanin-binding antibody, and demonstrated a free radical signature by electron spin resonance analysis. Despite lacking the WdPKS1 gene, the mutant yeast were capable of catalyzing the formation of melanin from L-3,4-dihyroxyphenylalanine. The wdpks1Δ-1 cells were significantly more susceptible to killing by voriconazole, amphotericin B, NP-1 [a microbicidal peptide], heat and cold, and lysing enzymes than the heavily melanized parental or complemented strains. CONCLUSION: In summary, W. dermatitidis makes WdPKS-dependent and -independent melanins, and the WdPKS1-dependent deposition of melanin in the cell wall confers protection against antifungal agents and environmental stresses. The biological role of the WdPKS-independent melanin remains unclear

EVALUATING THE ANTI-MICROBIAL EFFECT OF EUGENOL EXTRACTED FROM OCIMUM SANCTUM

Eugenol is a phytochemical present in herbal and medicinal plants. It possess anti tubercular, anti-inflammatory, anti-mutagenic properties. Commercial or synthesised eugenol is used extensively in the market nowadays. The aim is to evaluate the anti-microbial property of eugenol extracted from both the powder and leaf samples of Ocimum sanctum (tulsi) and to have a comparative analysis of the synthetic eugenol and the naturally extracted eugenol from tulsi leaves. The eugenol is extracted from tulsi leaves by steam distillation. For quantitative analysis of the natural eugenol, HPLC and UV Spectroscopy are performed with commercial eugenol as the reference. While Raman Spectroscopy is performed for qualitative analysis of the constituents of tulsi leaves. Membrane casting is done with eugenol as the core ingredient and porosity of the membrane is checked by SEM. Further microbial assay is performed to evaluate the effect of eugenol. From the results it can be concluded that the eugenol extracted from the powder and fresh leaves of tulsi has anti-microbial effect and the membrane composed of eugenol has the capability to retain the eugenol. Keywords: Ocimum sanctum, eugenol, anti-microbial, membrane,anti-microbial

Heterotrimeric GAIT Complex Drives Transcript-Selective Translation Inhibition in Murine Macrophages

The gamma interferon (IFN-γ)-activated inhibitor of translation (GAIT) complex in human myeloid cells is heterotetrameric, consisting of glutamyl-prolyl-tRNA synthetase (EPRS), NS1-associated protein 1 (NSAP1), ribosomal protein L13a, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The complex binds a structural GAIT element in the 3′ untranslated region of VEGF-A and other inflammation-related transcripts and inhibits their translation. EPRS is dually phosphorylated by cyclin-dependent kinase 5 (Cdk5) at Ser(886) and then by a Cdk5-dependent-AGC kinase at Ser(999); L13a is phosphorylated at Ser(77) by death-associated protein kinases DAPK and ZIPK. Because profound differences in inflammatory responses between mice and humans are known, we investigated the GAIT system in mouse macrophages. The murine GAIT complex is heterotrimeric, lacking NSAP1. As in humans, IFN-γ activates the mouse macrophage GAIT system via induced phosphorylation of EPRS and L13a. Murine L13a is phosphorylated at Ser(77) by the DAPK-ZIPK cascade, but EPRS is phosphorylated only at Ser(999). Loss of EPRS Ser(886) phosphorylation prevents NSAP1 incorporation into the GAIT complex. However, the triad of Ser(999)-phosphorylated EPRS, Ser(77)-phosphorylated L13a, and GAPDH forms a functional GAIT complex that inhibits translation of GAIT target mRNAs. Thus, translational control by the heterotrimeric GAIT complex in mice exemplifies the distinctive species-specific responses of myeloid cells to inflammatory stimuli

Bioactive Silver Phosphate/Polyindole Nanocomposites

Materials capable of releasing reactive oxygen species (ROS) can display antibacterial and anticancer activity, and may also have anti-oxidant capacity if they suppress intracellular ROS (e.g. nitric oxide, NO) resulting in anti-inflammatory activity. Herein we report silver phosphate (Ag3PO4)/polyindole (Pln) nanocomposites which display antibacterial, anticancer and anti-inflammatory activity, and have therefore potential for a variety of biomedical applications

TLR3-Induced Placental miR-210 Down-Regulates the STAT6/Interleukin-4 Pathway

Several clinical studies have reported increased placental miR-210 expression in women with PE compared to normotensive women, but whether miR-210 plays a role in the etiology of PE is unknown. We reported that activation of TLR3 produces the PE-like symptoms of hypertension, endothelial dysfunction, and proteinuria in mice only when pregnant, but whether TLR3 activation in pregnant mice and human cytotrophoblasts (CTBs) increases miR-210 and modulates its targets related to inflammation are unknown. Placental miR-210 levels were increased significantly in pregnant mice treated with the TLR3 agonist poly I:C (P-PIC). Both HIF-1α and NF-κBp50, known to bind the miR-210 promoter and induce its expression, were also increased significantly in placentas of P-PIC mice. Target identification algorithms and gene ontology predicted STAT6 as an inflammation-related target of miR-210 and STAT6 was decreased significantly in placentas of P-PIC mice. IL-4, which is regulated by STAT6 and increases during normotensive pregnancy, failed to increase in serum of P-PIC mice. P-PIC TLR3 KO mice did not develop hypertension and placental HIF-1α, NF-κBp50, miR-210, STAT6, and IL-4 levels were unchanged. To determine the placental etiology, treatment of human CTBs with poly I:C significantly increased HIF-1α, NF-κBp50, and miR-210 levels and decreased STAT6 and IL-4 levels. Overexpression of miR-210 in CTBs decreased STAT6 and IL-4 while inhibition of miR-210 increased STAT6 and IL-4. These findings demonstrate that TLR3 activation induces placental miR-210 via HIF-1α and NF-κBp50 leading to decreased STAT6 and IL-4 levels and this may contribute to the development of PE

Dynamics of Logamediate and Intermediate Scenarios in the Dark Energy Filled Universe

We have considered a model of two component mixture i.e., mixture of Chaplygin gas and barotropic fluid with tachyonic field. In the case, when they have no interaction then both of them retain their own properties. Let us consider an energy flow between barotropic and tachyonic fluids. In both the cases we find the exact solutions for the tachyonic field and the tachyonic potential and show that the tachyonic potential follows the asymptotic behavior. We have considered an interaction between these two fluids by introducing a coupling term. Finally, we have considered a model of three component mixture i.e., mixture of tachyonic field, Chaplygin gas and barotropic fluid with or without interaction. The coupling functions decays with time indicating a strong energy flow at the initial period and weak stable interaction at later stage. To keep the observational support of recent acceleration we have considered two particular forms (i) Logamediate Scenario and (ii) Intermediate Scenario, of evolution of the Universe. We have examined the natures of the recent developed statefinder parameters and slow-roll parameters in both scenarios with and without interactions in whole evolution of the universe.Comment: 28 pages, 20 figure

EXACT2: the semantics of biomedical protocols

© 2014 Soldatova et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.This article has been made available through the Brunel Open Access Publishing Fund.Background: The reliability and reproducibility of experimental procedures is a cornerstone of scientific practice. There is a pressing technological need for the better representation of biomedical protocols to enable other agents (human or machine) to better reproduce results. A framework that ensures that all information required for the replication of experimental protocols is essential to achieve reproducibility. Methods: We have developed the ontology EXACT2 (EXperimental ACTions) that is designed to capture the full semantics of biomedical protocols required for their reproducibility. To construct EXACT2 we manually inspected hundreds of published and commercial biomedical protocols from several areas of biomedicine. After establishing a clear pattern for extracting the required information we utilized text-mining tools to translate the protocols into a machine amenable format. We have verified the utility of EXACT2 through the successful processing of previously ‘unseen’ (not used for the construction of EXACT2) protocols. Results: The paper reports on a fundamentally new version EXACT2 that supports the semantically-defined representation of biomedical protocols. The ability of EXACT2 to capture the semantics of biomedical procedures was verified through a text mining use case. In this EXACT2 is used as a reference model for text mining tools to identify terms pertinent to experimental actions, and their properties, in biomedical protocols expressed in natural language. An EXACT2-based framework for the translation of biomedical protocols to a machine amenable format is proposed. Conclusions: The EXACT2 ontology is sufficient to record, in a machine processable form, the essential information about biomedical protocols. EXACT2 defines explicit semantics of experimental actions, and can be used by various computer applications. It can serve as a reference model for for the translation of biomedical protocols in natural language into a semantically-defined format.This work has been partially funded by the Brunel University BRIEF award and a grant from Occams Resources