Thousands of specialized, steroidal metabolites are found in a wide spectrum of plants. These include the steroidal glycoalkaloids (SGAs), produced primarily by most species of the genus , and metabolites belonging to the steroidal saponins class that are widespread throughout the plant kingdom. SGAs play a protective role in plants and have potent activity in mammals, including antinutritional effects in humans. The presence or absence of the double bond at the C-5,6 position (unsaturated and saturated, respectively) creates vast structural diversity within this metabolite class and determines the degree of SGA toxicity. For many years, the elimination of the double bond from unsaturated SGAs was presumed to occur through a single hydrogenation step. In contrast to this prior assumption, here, we show that the tomato GLYCOALKALOID METABOLISM25 (GAME25), a short-chain dehydrogenase/reductase, catalyzes the first of three prospective reactions required to reduce the C-5,6 double bond in dehydrotomatidine to form tomatidine. The recombinant GAME25 enzyme displayed 3β-hydroxysteroid dehydrogenase/Δ isomerase activity not only on diverse steroidal alkaloid aglycone substrates but also on steroidal saponin aglycones. Notably, down-regulation rerouted the entire tomato SGA repertoire toward the dehydro-SGAs branch rather than forming the typically abundant saturated α-tomatine derivatives. Overexpressing the tomato in the tomato plant resulted in significant accumulation of α-tomatine in ripe fruit, while heterologous expression in cultivated eggplant generated saturated SGAs and atypical saturated steroidal saponin glycosides. This study demonstrates how a single scaffold modification of steroidal metabolites in plants results in extensive structural diversity and modulation of product toxicity.

We report a facile two-furnace APCVD synthesis of 2H-WSe 2 . A systematic study of the process parameters is performed to show the formation of the phase-pure material. Extensive characterization of the bulk and exfoliated material confirm that 2H-WSe 2 is layered (i.e., 2D). X-ray diffraction (XRD) confirms the phase, while high-resolution scanning electron microscopy (HRSEM), high-resolution transmission electron microscopy (HRTEM), and atomic force microscopy (AFM) clarify the morphology of the material. Focused ion beam scanning electron microscopy (FIB-SEM) estimates the depth of the 2H-WSe 2 formed on W foil to be around 5–8 μm, and Raman/UV–vis measurements prove the quality of the exfoliated 2H-WSe 2 . Studies on the redox processes of lithium-ion batteries (LiBs) show an increase in capacity up to 500 cycles. On prolonged cycling, the discharge capacity up to the 50th cycle at 250 mA/g of the material shows a stable value of 550 mAh/g. These observations indicate that exfoliated 2H-WSe 2 has promising applications as an LiB electrode material.

Functional surface coatings were applied on high voltage spinel (LiNi0.5Mn1.5O4; LNMO) and Ni-rich (LiNi0.85Co0.1Mn0.05O2; NCM851005) NCM cathode materials using few-layered 2H tungsten diselenide (WSe2). Simple liquid-phase mixing with WSe2 in 2-propanol and low-temperature (130 °C) heat treatment in nitrogen flow dramatically improved electrochemical performance, including stable cycling, high-rate performance, and lower voltage hysteresis in Li coin cells at 30 and 55 °C. Significantly improved capacity retention at 30 °C [Q 401/Q 9 of 99% vs 38% for LNMO and Q 322/Q 23 of 64% vs 46% for NCM851005] indicated efficient functionality. TEM and XPS clarified the coating distribution and coordination with the cathode surface, while postcycling studies revealed its sustainability, enabling lower transition metal dissolution and minor morphological deformation/microcrack formation. A modified and stable SEI was apparently formed owing to W and Se deposition on the Li anode during cycling. The synergistic functionalization provided a significant dual benefit of cathodic and anodic stability.

A coating scheme was developed for enabling the operation of a GaAs-based Molecular Controlled Semiconductor Resistor (MOCSER) under biological conditions. Usually GaAs is susceptible to etching in an aqueous environment. Several methods of protecting the semiconductor based devices were suggested previously. However, even when protected, it is very difficult to ensure the operation of a GaAs-based electronic sensor in aqua solution for long periods. We developed a new depositing scheme of (3-mercaptopropyl)-trimethoxysilane (MPTMS) on GaAs substrate consisting of two separate steps. The first involves chemisorption of a dense primary MPTMS layer on the substrate, whereas in the second, a thin MPTMS polymer layer is deposited on the already adsorbed layer, resulting in a 15 -29 nm thick coating. We show that applying the new MPTMS deposition procedure to GaAs-based MOCSER devices allows up to 15 hours of continuous electrical measurements and stable performance of the sensing device in harsh biological environment. The new protection allows implementing GaAs technology in bioelectronics, particularly in biosensing.

Dense wavelength division multiplexers are key components of data communication networks. This paper presents a silicon-photonic eight-channel multiplexer device with a channel spacing of only 0.133 nm (17 GHz). Devices were fabricated in a commercial silicon foundry, in 8" silicon-on-insulator wafers. The device layout consists of seven unbalanced Mach-Zehnder interferometers in a cascaded tree topology, and each interferometer unit also includes a nested ring resonator element. The transfer function of each unit is that of a maximally flat, autoregressive, moving-average filter. The devices are characterized by uniform passbands, sharp spectral transitions between pass and stop bands, and strong out-of-band rejection. The worst-case optical power crosstalk is −22 dB. The proper function of the device requires careful control of optical phase delays over 14 distinct optical paths. Post-fabrication trimming of phase delays was performed through local illumination of a photo-sensitive upper cladding layer of chalcogenide glass. The de-multiplexing of three adjacent QAM-16, 40 Gbit/s wavelength-division channels was successfully demonstrated. The devices are applicable in data communication and in integrated-photonic processing of radio-over-fiber waveforms.

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The detection of covalent and noncovalent binding events between molecules and biomembranes is a fundamental goal of contemporary biochemistry and analytical chemistry. Currently, such studies are performed routinely using fluorescence methods, surface-plasmon resonance spectroscopy, and electrochemical methods. However, there is still a need for novel sensitive miniaturizable detection methods where the sample does not have to be transferred to the sensor, but the sensor can be brought into contact with the sample studied. We present a novel approach for detection and quantification of processes occurring on the surface of a lipid bilayer membrane, by monitoring the current change through the n-type GaAs-based molecularly controlled semiconductor resistor (MOCSER), on which the membrane is adsorbed. Since GaAs is susceptible to etching in an aqueous environment, a protective thin film of methoxysilane was deposited on the device. The system was found to be sensitive enough to allow monitoring changes in pH and in the concentration of amino acids in aqueous solution on top of the membrane. When biotinylated lipids were incorporated into the membrane, it was possible to monitor the binding of streptavidin or avidin. The device modified with biotin-streptavidin complex was capable of detecting the binding of streptavidin antibodies to immobilized streptavidin with high sensitivity and selectivity. The response depends on the charge on the analyte. These results open the way to facile electrical detection of protein-membrane interactions.

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