INTERACTION BETWEEN PHYTOCHROME AND THE BLUE LIGHT PHOTORECEPTOR SYSTEM IN Mougeotia*

Abstract— Face-to-profile chloroplast movement in Mougeotia was induced by sequences of strong blue and red short irradiations. This type of response occured only when blue light was applied prior to or simultaneously with red light, and far-red irradiation was necessary after the sequence to cancel the remaining gradient of the far-red absorbing form of phytochrome P_fr. The dependence of the response magnitude on blue and red light sequences was studied for a wide range of light durations and dark intervals. The relationship between the response and the dark interval points to the lack of direct coupling between phytochrome and blue-absorbing “cryptochrome”. It was postulated that a photoproduct having a life-time of2–3 min is formed by the blue-light-mediated reaction. This photoproduct interacts with phytochrome during its transformation or with its final P_fr form.     

Comparison of capillary electrophoretic techniques for analysis and characterization of metallothioneins

To explore and understand the significance of individual metallothionein isoforms, the methods of their identification are needed. Separation of these isoforms requires a high resolution technique which can exploit very small differences in mass, charge, and hydrophobicity. In this report, three different techniques of CE were analyzed and used for metallothionein separation: detection using capillary gel electrophoresis, capillary zone electrophoresis, and capillary isoelectric focusing. Also, three different metallothionein samples were used from horse kidney, rabbit liver, and human liver. We identified metallothionein isoforms based on the determination of their relative molecular masses, on the charge differences in different pH buffers, and based on the pI value. Methods used in this report allow metallothionein identification, permit to quantify the purity and content of its isoforms, and allow studying its polymerization. This report supports and endorses the increased application of CE methodology in proteomics.     

Simple Synthesis of 7‐Amino‐4,5‐dihydrobenzo[f][1,4]oxazepin‐3‐ones

A simple method for the synthesis of 7‐amino‐4,5‐dihydro‐benzo[f][1,4]oxazepin‐3‐ones from 5‐nitrobenzaldehydes and 2‐haloesters was described. The three‐step procedure involves the synthesis of methyl 2‐(2‐formyl‐4‐nitrophenoxy)alkanoates, followed by reaction with hydrazine hydrate and reductive cyclization of the formed aldazines. 2‐Hydroxyethyl derivatives of the title amines were prepared in good yields.     

Stimulation of Lignan Production in Schisandra rubriflora In Vitro Cultures by Elicitation

The study investigated the effect of elicitation with: chitosan (CH) (200 mg/L), yeast extract (YeE) (3000 mg/L), ethephon (ETH) (25 µM/L), and methyl jasmonate (MeJA) (50 µM/L), on lignan accumulation in agitated and bioreactor (Plantform temporary immersion systems) microshoot cultures of female (F) and male (M) Schisandra rubriflora Rehd. et Wils. (Schisandraceae) lines. The elicitors were supplemented on the 10th day of culture. Biomasses were collected at 24 h and 48 h, and 4, 6, and 8 days after the addition of each elicitor. The 24 compounds from the dibenzocyclooctadiene, aryltetralin, dibenzylbutane, and tetrahydrofuran lignans and neolignans were determined qualitatively and quantitatively in biomass extracts using the UHPLC–MS/MS method. The highest total contents [mg/100 g DW] of lignans were: for CH-95.00 (F, day 6) and 323.30 (M, 48 h); for YeE 104.30 (F, day 8) and 353.17 (M, day 4); for ETH 124.50 (F, 48 h) and 334.90 (M, day 4); and for MeJA 89.70 (F, 48 h) and 368.50 (M, 24 h). In the biomass extracts of M cultures grown in bioreactors, the highest total lignan content was obtained after MeJA elicitation (153.20 mg/100 g DW). The maximum total lignan contents in the biomass extracts from agitated and bioreactor cultures were 3.29 and 1.13 times higher, respectively, than in the extracts from the non-elicited cultures. The poor understanding of the chemical composition and the lack of studies in the field of plant biotechnology of S. rubriflora emphasize the innovativeness of the research.     

Energetic and geometric characteristics of the substituents. Part 1. The case of NO2 and NH2 groups in their mono-substituted derivatives of simple benzenoid hydrocarbons

Structural Chemistry - Simple polycyclic aromatic hydrocarbons, substituted by strongly electron-donating (NH2) and withdrawing (NO2) groups, are studied employing density functional theory (DFT)...     

Anodic polarization of nanocrystalline titanium

TiO₂ nanotubes are extensively investigated because of their unique properties and wide range of applications, e.g., in biomedicine. They are used as coatings on titanium implant materials accelerating osteoblast (bone cell) adhesion and improving osteointegration. Owing to its high mechanical properties, nanocrystalline titanium is likely to replace the widely used titanium alloys, which contains harmful ions such as V and Al. The performance properties of nanocrystalline titanium can be modified by subjecting it to various surface treatments tailored to the demands of a given application. The aim of this study is to determine whether the grain refinement of the titanium substrate has an influence on the formation of TiO₂ nanotubes. The TiO₂ nanotubes were fabricated by anodic polarization of micro- and nanotitanium at a constant voltage of 10, 15, and 20 V for 2 h in an electrolyte containing fluoride ions. The nanocrystalline bulk titanium (grade 2) with grain size of about 90 nm and high density of dislocations was obtained using hydrostatic extrusion. Commercially available coarse-grained titanium with grain size of 20 μm was used as a reference sample. The microstructure of the fabricated nanotubular layers was revealed using scanning electron microscopy and focus ion beam microscopy. Auger electron spectroscopy and X-ray photoelectron spectroscopy were used to determine the chemical composition of the fabricated layers. The results indicate that grain refinement influences the morphology of TiO₂ nanotubes while their chemistry remains unchanged.     

Determination of hafnium at the 10% level (relative to zirconium content) using neutron activation analysis,inductively coupled plasma mass spectrometry and inductively coupled plasma atomic emission spectrometry

Hafnium at the very low level of 1–8 ppm (in relation to zirconium) was determined in zirconium sulfate solutions (originating from investigations of the separation of ca. 44 ppm Hf from zirconium by means of the ion exchange method) by using three independent methods: inductively coupled plasma mass spectrometry (ICP MS), neutron activation analysis (NAA) and inductively coupled plasma atomic emission spectrometry (ICP-AES). The results of NAA and ICP MS determinations were consistent with each other across the entire investigated range (the RSD of both methods did not exceed 38%). The results of ICP-AES determination were more diverse, particularly at less than 5 ppm Hf (RSD was significantly higher: 29–253%). The ion exchange method exploiting Diphonix^® resin proved sufficient efficiency in Zr–Hf separation when the initial concentration ratio of the elements ([Zr]₀/[Hf]₀) ranged from 1200 to ca. 143,000.