Broadband forward scattering from dielectric cubic nanoantenna in lossless media

Dielectric photonics platform provides unique possibilities to control light scattering via utilizing high-index dielectric nanoantennas with peculiar optical signatures. Despite the intensively growing field of all-dielectric nanophotonics, it is still unclear how surrounding media affect scattering properties of a nanoantenna with complex multipole response. Here, we report on light scattering by a silicon cubic nanoparticle embedded in lossless media, supporting optical resonant response. We show that significant changes in the scattering process are governed by the electro-magnetic multipole resonances, which experience spectral red-shift and broadening over the whole visible and near-infrared spectra as the indices of media increase. Most interestingly, the considered nanoantenna exhibits the broadband forward scattering in the visible and near-infrared spectral ranges due to the Kerker-effect in high-index media. The revealed effect of broadband forward scattering is essential for highly demanding applications in which the influence of the media is crucial such as health-care, e.g., sensing, treatment efficiency monitoring, and diagnostics. In addition, the insights from this study are expected to pave the way toward engineering the nanophotonic systems including but not limited to Huygens-metasurfaces in media within a single framework

Evolution of multipole moments in silicon nanocylinder while varying the refractive index of surrounding medium

Here we use multipole decomposition approach to study optical properties of a silicon nanocylinder in different lossless media. We show that resonant peaks of multipole moments experience red shift, smoothing and broadening. Worth noting that electric multipoles experience bigger red shift than their magnetic counterparts. Our results can be applied to design optical devices within a single framework. © 2020 IOP Publishing Ltd

Cultured fish cells metabolize octadecapentaenoic acid (all-cis delta3,6,9,12,15–18∶5) to octadecatetraenoic acid (all-cis delta6,9,12,15–18∶4) via its 2-trans intermediate (trans delta2, all-cis delta6,9,12,15–18∶5)

Octadecapentaenoic acid (all-cis Δ3,6,9,12,15-18:5; 18:5n-3) is an unusual fatty acid found in marine dinophytes, haptophytes and prasinophytes. It is not present at higher trophic levels in the marine food web but its metabolism by animals ingesting algae is unknown. Here we studied the metabolism of 18:5n-3 in cell lines derived from turbot (Scophthalmus maximus), gilthead sea bream (Sparus aurata) and Atlantic salmon (Salmo salar). Cells were incubated in the presence of approximately 1 μM [U-14C] 18:5n-3 methyl ester or [U-14C] 18:4n-3 (octadecatetraenoic acid; all-cis Δ6,9,12,15-18:4) methyl ester, both derived from the alga Isochrysis galbana grown in H14CO3, and also with 25 μM unlabelled 18:5n-3 or 18:4n-3. Cells were also incubated with 25 μM trans Δ2, all-cis Δ6,9,12,15-18:5 (2-trans 18:5n-3) produced by alkaline isomerization of 18:5n-3 chemically synthesized from docosahexaenoic acid (all-cis Δ4,7,10,13,16,19-22:6; 22:6n-3). Radio- and mass analyses of total fatty acids extracted from cells incubated with 18:5n-3 were consistent with this fatty acid being rapidly metabolized to 18:4n-3 which was then elongated and further desaturated to eicosatetraenoic acid (all-cis Δ8,11,14,17,19-20:4; 20:4n-3) and eicosapentaenoic acid (all-cis Δ5,8,11,14,17-20:5; 20:5n-3). Similar mass increases of 18:4n-3 and its elongation and further desaturation products occurred in cells incubated with 18:5n-3 or 2-trans 18:5n-3. We conclude that 18:5n-3 is readily converted biochemically to 18:4n-3 via a 2-trans 18:5n-3 intermediate generated by a Δ3,Δ2-enoyl-CoA-isomerase acting on 18:5n-3. Thus, 2-trans 18:5n-3 is implicated as a common intermediate in the β-oxidation of both 18:5n-3 and 18:4n-3

Enhancement of circular dichroism in epsilon-near-zero chiral hyperbolic metamaterials

We are presenting a theoretical study of light transmission through a slab of hyperbolic metamaterial composed of gold rods, with chiral inclusions, thus possessing both hyperbolic and chiral properties. 4 × 4 transfer matrix formalism was used for solution of a wave transmission through a slab of a chiral hyperbolic material. We have shown that circular dichroism (CD) can be enhanced by several orders of magnitude in epsilon-near-zero (ENZ) mode when the diagonal component of the permittivity tensor corresponding to the normal to interface coordinate tends to zero. The necessary condition of the enhancement is a non-zero light incidence angle. This effect results from a considerable wavelength shortening in normal direction that increases the interaction between light and matter. We have shown that the increase of the incidence angle leads to the increase of dichroism in vicinity of ENZ wavelength range and the dichroism can change sign in this resonance area. The dichroism becomes huge at large incidence angles (θ > 30°) and for each incidence angle the maximal enhancement is observed within a certain wavelength range (in vicinity of-near-zero). In opposite to discussion of the enhancement of the pseudochirality reported previously in the literature, our study relates to the true chirality. We expect these results to be of interest to researchers engaged in chemical composition of organic substances by retrieval of effective parameters from measurements of the CD. © 2019 IOP Publishing Ltd

Dissection of Transient Oxidative Stress Response in Saccharomyces cerevisiae by Using DNA Microarrays

Yeast cells were grown in glucose-limited chemostat cultures and forced to switch to a new carbon source, the fatty acid oleate. Alterations in gene expression were monitored using DNA microarrays combined with bioinformatics tools, among which was included the recently developed algorithm REDUCE. Immediately after the switch to oleate, a transient and very specific stress response was observed, followed by the up-regulation of genes encoding peroxisomal enzymes required for fatty acid metabolism. The stress response included up-regulation of genes coding for enzymes to keep thioredoxin and glutathione reduced, as well as enzymes required for the detoxification of reactive oxygen species. Among the genes coding for various isoenzymes involved in these processes, only a specific subset was expressed. Not the general stress transcription factors Msn2 and Msn4, but rather the specific factor Yap1p seemed to be the main regulator of the stress response. We ascribe the initiation of the oxidative stress response to a combination of poor redox flux and fatty acid-induced uncoupling of the respiratory chain during the metabolic reprogramming phase