Effects of Egg Yolk Antibodies Produced in Response to Different Antigenic Fractions of E. coli O157:H7 on E. coli Suppression

Chae, H.S.,Singh, N.K.,Ahn, C.N.,Yoo, Y.M.,Jeong, S.G.,Ham, J.S.,Kim, D.W. Asian Australasian Association of Animal Productio 2006 Animal Bioscience Vol.19 No.11

The objective of this research was to provide the characterization and method for producing anti-E. coli O157:H7 antibodies in egg-laying hens and to determine if the antibody can restrain the proliferation of E. coli O157:H7 in-vitro. Selected antigenic fractions (whole cell, outer membrane protein and lipopolysaccharide (LPS)) from E. coli O157:H7 were injected to hens in order to produce anti-E. coli O157:H7 antibodies. The immune response and the egg yolk antibodies of laying hens against the whole cell, outer membrane protein and LPS antigens were monitored by ELISA. The level of antibodies against whole cell antigen monitored through ELISA sharply increased after the initial immunization, and it was found to be maximum on day 49 however, the level was maintained up to day 70. Antibodies (5 mg/ml) directed against the whole cell inhibited E. coli proliferation 10-13 times more than outer membrane protein or LPS. The antibody response against the whole cell antigens appeared to have higher activity in restraining the proliferation of E. coli O157:H7 than antibody against outer membrane protein or LPS. Results reflected that increasing the IgY's in the egg yolk could prevent greater economic losses due to human and animal health from pathogenic bacteria i.e. E. coli O157:H7.

A sensitive fluorescent probe for the polar solvation dynamics at protein-surfactant interfaces

Singh, P.,Choudhury, S.,Singha, S.,Jun, Y.,Chakraborty, S.,Sengupta, J.,Das, R.,Ahn, K. H.,Pal, S. Royal Society of Chemistry 2017 Physical chemistry chemical physics Vol.19 No.19

<P>Relaxation dynamics at the surface of biologically important macromolecules is important taking into account their functionality in molecular recognition. Over the years it has been shown that the solvation dynamics of a fluorescent probe at biomolecular surfaces and interfaces account for the relaxation dynamics of polar residues and associated water molecules. However, the sensitivity of the dynamics depends largely on the localization and exposure of the probe. For noncovalent fluorescent probes, localization at the region of interest in addition to surface exposure is an added challenge compared to the covalently attached probes at the biological interfaces. Here we have used a synthesized donor-acceptor type dipolar fluorophore, 6-acetyl-(2-((4-hydroxycyclohexyl)(methyl) amino) naphthalene) (ACYMAN), for the investigation of the solvation dynamics of a model protein-surfactant interface. A significant structural rearrangement of a model histone protein (H1) upon interaction with anionic surfactant sodium dodecyl sulphate (SDS) as revealed from the circular dichroism (CD) studies is nicely corroborated in the solvation dynamics of the probe at the interface. The polarization gated fluorescence anisotropy of the probe compared to that at the SDS micellar surface clearly reveals the localization of the probe at the protein-surfactant interface. We have also compared the sensitivity of ACYMAN with other solvation probes including coumarin 500 (C500) and 4-(dicyanomethylene)-2-methyl-6-(p-dimethylamino-styryl)-4H-pyran (DCM). In comparison to ACYMAN, both C500 and DCM fail to probe the interfacial solvation dynamics of a model protein-surfactant interface. While C500 is found to be delocalized from the protein-surfactant interface, DCM becomes destabilized upon the formation of the interface (protein-surfactant complex). The timescales obtained from this novel probe have also been compared with other femtosecond resolved studies and molecular dynamics simulations.</P>

Investigation of phase segregation in sol–gel derived ZnMgO thin films

Singh, Amanpal,Vij, Ankush,Kumar, Dinesh,Khanna, P K,Kumar, Mukesh,Gautam, Sanjeev,Chae, K H Institute of Physics 2013 Semiconductor science and technology Vol.28 No.2

<P>Highly c-axis-oriented Zn<SUB>1-x</SUB>Mg<SUB>x</SUB>O multilayered thin films have been deposited on p-type Si substrates with different concentration of Mg (x = 0.00−0.40) using a sol–gel spin-coating technique. The x-ray diffraction (XRD) shows that single-phase wurtzite thin films start showing phase segregation for a Mg content of x = 0.25 for the sol–gel-derived ZnMgO thin films. The element specific near edge x-ray fine structure (NEXAFS) collected at O K-edge also clearly evidence the phase segregation at x = 0.25. These results also show that films are deposited with wurtzite structure as dominant phase even after phase segregation. The NEXAFS spectra collected at Zn L<SUB>3</SUB>-edge rule out the presence of any Zn-related defect due to Mg doping. The atomic force microscopy (AFM) depicts the spherical shape of nanosized grains, and grain size varies slightly with Mg content. The single-phase ZnMgO thin films show a band gap tuning from 3.38 to 3.84 eV, which is also consistent with blue shifting of near-band edge PL emission. The electrical resistivity of thin films increases with Mg content before phase segregation. However, the optical band gap, photoluminescence and electrical resistivity show anomalous behavior at phase segregation limit which has been discussed and correlated with each other.</P>

Crystallite size induced crossover from paramagnetism to superparamagnetism in zinc ferrite nanoparticles

Singh, J.P.,Gautam, S.,Srivastava, R.C.,Asokan, K.,Kanjilal, D.,Chae, K.H. Academic Press 2015 Superlattices and microstructures Vol.86 No.-

Present work investigates the crossover from paramagnetism to superparamagnetism as a function of crystallite size in zinc ferrite nanoparticles using near edge X-ray absorption spectroscopy. Synthesized paramagnetic and superparamagnetic nanoparticles exhibit presence of Fe<SUP>2+</SUP> and Fe<SUP>3+</SUP> ions with dominant concentration of Fe<SUP>3+</SUP> ions. Fe L- and O K-edges spectra of paramagnetic nanoparticles consist of more intense spectral features compared to that of superparamagnetic nanoparticles. This reflects enhanced t<SUB>2g</SUB> and e<SUB>g</SUB> symmetry states of Fe-O hybridized states in paramagnetic nanoparticles induced by increased degree of crystallization.

Mechanistic insights into the interaction between energetic oxygen ions and nanosized ZnFe₂O₄: XAS-XMCD investigations

Singh, Jitendra Pal,Kaur, Baljeet,Sharma, Aditya,Kim, So Hee,Gautam, Sanjeev,Srivastava, Ramesh Chandra,Goyal, Navdeep,Lim, Weol Cheol,Lin, H.-J.,Chen, J. M.,Asokan, K.,Kanjilal, D.,Won, Sung Ok,Lee, The Royal Society of Chemistry 2018 Physical Chemistry Chemical Physics Vol.20 No.17

<P>The interactions of energetic ions with multi-cation compounds and their consequences in terms of changes in the local electronic structure, which may facilitate intriguing hybridization between O 2p and metal d orbitals and magnetic ordering, are the subject of debate and require a deep understanding of energy transfer processes and magnetic exchange mechanisms. In this study, nanocrystals of ZnFe2O4 were exposed to O<SUP>7+</SUP> ions with an energy of 100 MeV to understand, qualitatively and quantitatively, the metal-ligand field interactions, cation migration and magnetic exchange interactions by employing X-ray absorption fine structure measurements and X-ray magnetic circular dichroism to get deeper mechanistic insights. Nanosized zinc ferrite nanoparticles (NPs) with a size of ∼16 nm synthesized in the cubic spinel phase exhibited deterioration of the crystalline phase when 100 MeV O<SUP>7+</SUP> ions passed through them. However, the size of these NPs remained almost the same. The behaviour of crystal deterioration is associated with the confinement of heat in this interaction. The energy confined inside the nanoparticles promotes cation redistribution as well as the modification of the local electronic structure. Prior to this interaction, almost 42% of Zn<SUP>2+</SUP> ions occupied AO4 tetrahedra; however, this value increased to 63% after the interaction. An inverse effect was observed for metal ion occupancies in BO6 octahedra. The L-edge spectra of Fe and Zn reveal that the spin and valence states of the metal ions were not affected by this interaction. This effect is also supported by K-edge measurements for Fe and Zn. The t2g/eg intensity ratio in the O K-edge spectra decreased after this interaction, which is associated with detachment of Zn<SUP>2+</SUP> ions from the lattice. The extent of hybridization, as estimated from the ratio of the post-edge to the pre-edge region of the O K-edge spectra, decreased after this interaction. The metal-oxygen and metal-metal bond lengths were modified as a result of this interaction, as determined from extended X-ray absorption fine structure measurements. These measurements further support the observation of cation migration from AO4 tetrahedra to AO6 octahedra and <I>vice versa</I>. The Fe L-edge magnetic circular dichroism spectra indicate that Fe<SUP>3+</SUP> ions occupying sites in AO4 tetrahedra and BO6 octahedra exhibited antiferromagnetic-like ordering prior to this interaction. The NPs that interacted with energetic O ions displayed a different kind of magnetic ordering.</P>

Electronic structure studies of chemically synthesized MgFe₂O₄ nanoparticles

Singh, J.P.,Won, S.O.,Lim, W.C.,Lee, I.J.,Chae, K.H. Elsevier Scientific Pub. Co 2016 Journal of molecular structure Vol.1108 No.-

For present work, magnesium ferrite nanoparticles were synthesized using nitrates of metal ions and citric acid. Crystallite size of these nanoparticles varies from 2.1 +/- 0.1 to 62 +/- 10 nm as annealing temperatures increases from 300 to 1200 <SUP>o</SUP>C. Mg K-edge near-edge X-ray absorption fine-structure spectra reflect the presence of Mg<SUP>2+</SUP> ions in both tetrahedral (A-site) and octahedral (B-site) environment for nanoparticles synthesized at all temperatures. The integral area of spectral features of O K-edge spectra is associated with the change of unoccupied O p-projected density of states. Fe L-edge spectra envisage the presence of Fe<SUP>3+</SUP> state in these nanoparticles. Observed changes in the electronic structure of these nanoparticles are discussed on the basis of cation migration from A-site to B-site, degree of crystallization, and unsaturated bonds at crystallite surface. Fe-O distances at A-site and B-site changes with annealing temperature.

Influence of Nitric Oxide on Steroid Synthesis, Growth and Apoptosis of Buffalo (Bubalus bubalis) Granulosa Cells In vitro

Dubey, Pawan K.,Tripathi, Vrajesh,Singh, Ram Pratap,Sastry, K.V.H.,Sharma, G.Taru Asian Australasian Association of Animal Productio 2011 Animal Bioscience Vol.24 No.9

Objective of this study was to examine the effect of sodium nitroprusside (SNP), a nitric oxide (NO) donor on steroid synthesis, growth and apoptosis of buffalo granulosa cells (GCs) in vitro. Follicular fluid of antral follicles (3-5 mm diameter) was aspirated and GCs were cultured in 0 (control), $10^{-3}$, $10^{-5}$, $10^{-7}$, $10^{-9}\;M$ of SNP for 48 h. To evaluate whether this effect was reversible, GCs were cultured in presence of $10^{-5}\;M$ SNP+1.0 mM $N^{\omega}$-nitro-L-arginine methyl ester (L-NAME) a NO synthase (NOS) inhibitor or hemoglobin (Hb, $1.0{\mu}g$) as NO scavenger. Nitrate/nitrite concentration was evaluated by Griess method, progesterone and estradiol concentrations by RIA and apoptosis by TUNEL assay. SNP ($10^{-3}$, $10^{-5}$, $10^{-7}\;M$) significantly (p<0.05) inhibited estradiol and progesterone synthesis, growth, disorganized GCs aggregates and induced apoptosis in a dose dependent manner. However, $10^{-9}\;M$ SNP induced the progesterone synthesis and stimulated GCs to develop into a uniform monolayer. Combination of SNP $10^{-5}$ M+L-NAME strengthened the inhibitory effect while, SNP+Hb together reversed these inhibitory effects. In conclusion, SNP at greater concentrations ($10^{-3}$, $10^{-5}$ and $10^{-7}\;M$) has a cytotoxic effect and it may lead to cell death whereas, at a lower concentration ($10^{-9}\;M$) induced progesterone synthesis and growth of GCs. These findings have important implications that NOS derived NO are involved at physiological level during growth and development of buffalo GCs which regulates the steroidogenesis, growth and apoptosis.

Synthesis, magnetic and Mossbauer spectroscopic studies of Cr doped lithium ferrite nanoparticles

Srivastava, M.,Layek, S.,Singh, J.,Das, A.K.,Verma, H.C.,Ojha, A.K.,Kim, N.H.,Lee, J.H. Elsevier Sequoia 2014 JOURNAL OF ALLOYS AND COMPOUNDS Vol.591 No.-

Lithium-based ferrites are promising and potential magnetic materials for microwave applications. They possess a spinel (AB<SUB>2</SUB>O<SUB>4</SUB>) type crystal structure, where the distributions of metal cations over the tetrahedral (A) and octahedral (B) voids play a crucial role for exhibiting different physical properties. Among various parameter of synthesis, pH is an important factor that influences the cation distribution over A and B voids, overall growth of the nanoparticles and different physical properties. In the present work single phase Cr substituted lithium ferrite nanoparticles have been synthesized by the sol-gel method at different pH. The phase identification and crystallite size have been probed by X-ray diffraction studies. The crystallite size changes by 44.2-48.8nm upon varying the pH from 3.5 to 11.5. In order to investigate the cations distribution at A/B sites, Mossbauer spectroscopic measurements were done. The values of magnetic hyperfine field obtained from the Mossbauer data for the A and B sites are ~49.5T and 51T, respectively. Moreover, it is observed that the area ratio of B site to A site increases with increasing the pH. This observation further suggests that the B site is more preferable for Fe<SUP>3+</SUP> cations at higher pH than the A site. The magnetic parameter such as saturation magnetization (M<SUB>s</SUB>), remanent magnetization (M<SUB>r</SUB>), coercive field (H<SUB>C</SUB>) and squareness (S) are determined by vibrating sample magnetometer (VSM) measurements, which show a consistent increase with increasing pH. The reason for the variation in magnetic properties has been explained on the basis of increased Fe<SUP>3+</SUP> cation occupancies at the B site and size effect, which is well supported by Mossbauer spectroscopic and XRD studies.

Investigations on magnetic and electrical properties of Zn doped Fe₂O₃ nanoparticles and their correlation with local electronic structures

Kumar, Parmod,Sharma, Vikas,Singh, Jitendra P.,Kumar, Ashish,Chahal, Surjeet,Sachdev, K.,Chae, K.H.,Kumar, Ashok,Asokan, K.,Kanjilal, D. Elsevier 2019 Journal of magnetism and magnetic materials Vol.489 No.-

<P><B>Abstract</B></P> <P>Present work aims at investigating the structural, magnetic and dielectric properties of zinc doped Fe<SUB>2</SUB>O<SUB>3</SUB> nanoparticles (pure, 10%, 20% & 30%) and correlated with their local electronic structures using X-ray absorption near-edge structure (XANES) spectroscopy. X-ray diffraction and Raman measurements infer that doping of Zn cations lead to the formation of secondary phases corresponding to ZnFe<SUB>2</SUB>O<SUB>4</SUB> along with the hematite phase of Fe<SUB>2</SUB>O<SUB>3</SUB>. Magnetic measurements show that magnetization vs magnetic field curve for 10% Zn doping exhibit maximum saturation magnetization (~2.93 × 10<SUP>−3</SUP> emu/g) as well as the coercivity (~956 Oe). The values of these parameters decrease for higher content of Zn. The temperature dependence of dielectric behaviour follows the same trend as that of the lattice parameter and magnetic measurements. The XANES spectra at Fe L- and Fe K-edges indicate partial reduction of Fe<SUP>3+</SUP> ions into Fe<SUP>2+</SUP> upon Zn doping in the Fe<SUB>2</SUB>O<SUB>3</SUB> lattice. However, divalent state is favourable for Zn (i.e. Zn<SUP>2+</SUP>) within the doping range reported in this study.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Zn doped Fe<SUB>2</SUB>O<SUB>3</SUB> nanoparticles. </LI> <LI> Study of magnetic and electrical properties. </LI> <LI> Correlation of magnetic and electrical properties with local electronic structure. </LI> </UL> </P>

Role of low energy transition metal ions in interface formation in ZnO thin films and their effect on magnetic properties for spintronic applications

Bhardwaj, Richa,Kaur, Baljeet,Singh, Jitendra Pal,Kumar, Manish,Lee, H.H.,Kumar, Parmod,Meena, R.C.,Asokan, K.,Hwa Chae, Keun,Goyal, Navdeep,Gautam, Sanjeev Elsevier 2019 APPLIED SURFACE SCIENCE - Vol.479 No.-

<P><B>Abstract</B></P> <P>In this study, X-ZnO/ZnO/Si(100) (X = Co, Ni and Cu) bilayer structure is fabricated using low energy ion implantation technique. Five different fluences 1 × 10<SUP>15</SUP>, 5 × 10<SUP>15</SUP>, 1 × 10<SUP>16</SUP>, 2.5 × 10<SUP>16</SUP> and 5 × 10<SUP>16</SUP> ions/cm<SUP>2</SUP> with 100 keV ion-beam energy were selected in order to implant the ions up to the depth of ≈44 nm as calculated through Stopping Range of Ion in Matter and Transport Range of Ions in Matter software. Structural modification was investigated by high resolution X-ray diffraction measurements in ZnO bilayer system. An observed systematic 2<I>θ</I> shift in (002) peak with increasing fluence implies increased density of implanted metal ions in ZnO matrix revealing the substitution of implanted ion at Zn-site. The mechanism of bilayer formation by ion-beam implantation technique has been discussed for metal-ions by investigating their interface properties. Atomic force microscopy reveals the morphological modification after ion implantation. Near-edge X-ray absorption fine-structure (NEXAFS) measurements at metal <I>K</I>- and <I>L</I> <SUB>3,2</SUB>-edges have been used to investigate the nature of implanted ions in terms of their valance state and local electronic environment. Further, O <I>K</I>-edge NEXAFS measurement for Ni-ZnO/ZnO/Si bilayer is highly sensitive to incident beam angles whereas no spectral change is seen for Zn <I>L</I>-edge measurements. The magnetic measurements were performed via vibrating sample magnetometer that showed the films are ferromagnetic at room temperature. The origin of ferromagnetism has been understood through defect mediated bound magnetic polaron model. Further, perpendicular magnetic anisotropy is also observed for Ni-ZnO/ZnO/Si bilayer structure at room temperature, which is correlated with the angle dependent O K-edge NEXAFS measurements. Fabrication of ZnO bilayer via ion implantation and investigation of above properties may prove useful in spin related and optoelectronic applications.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Observance of RTFM in metal ion-implanted Ni-ZnO/ZnO/Si bilayer </LI> <LI> HRXRD and NEXAFS measurements confirms the wurtzite phase and Zn<SUP>2+</SUP> substitution in ZnO matrix. </LI> <LI> Angle dependent NEXAFS measurements provides the evidence of observed PMA. </LI> </UL> </P> <P><B>Graphical Abstract</B></P> <P>Mechanism of ion beam interaction X (X = Co, Ni and Cu) with ZnO lattice forming X-ZnO/ZnO/Si(100) bilayer structure. Films were implanted using a multi cathode source of negative-ions by cesium sputtering (MC-SNICS) and with the increasing ion flux, X can undergo one of two mechanisms of either substituting the Zn-site or occupy interstitial position in ZnO matrix. Angle dependent O K-edge NEXAFS measurements provides the evidence of perpendicular magnetic anisotropy in ZnO bilayer. </P> <P>[DISPLAY OMISSION]</P>