Biosynthesis of the Myxobacterial Antibiotic Corallopyronin A

Corallopyronin A is a myxobacterial compound with potent antibacterial activity. Feeding experiments with labelled precursors resulted in the deduction of all biosynthetic building blocks for corallopyronin A and revealed an unusual feature of this metabolite: its biosynthesis from two chains, one solely PKS‐derived and the other NRPS/PKS‐derived. The starter molecule is believed to be carbonic acid or its monomethyl ester. The putative corallopyronin A biosynthetic gene cluster is a trans‐AT‐type mixed PKS/NRPS gene cluster, containing a β‐branching cassette. Striking features of this gene cluster are a NRPS‐like adenylation domain that is part of a PKS‐type module and is believed to be responsible for glycine incorporation, as well as split modules with individual domains occurring on different genes. It is suggested that CorB is a trans‐acting ketosynthase and it is proposed that it catalyses the Claisen condensation responsible for the interconnection of the two chains. Additionally, the stereochemistry of corallopyronin A was deduced by a combination of a modified Mosher's method and ozonolysis with subsequent chiral GC analyses.     

Controlled synthesis of copper nano/microstructures using ascorbic acid in aqueous CTAB solution

This paper describes a low-temperature green chemical synthesis of various morphologies of copper nano/microstructures. These syntheses achieved high yields in aqueous solution using ascorbic acid as a reductant and the cationic surfactant cetyltrimethylammonium bromide (CTAB) as a capping agent. The resulting copper particles were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and UV-Vis. absorption spectroscopy techniques. From the SEM analysis, it was found that different morphologies of copper particles, including submicron polyhedrons, micrometer rods, spherical nanoparticles, and nanowires were obtained by varying factors such as the molar ratio of reactants (ascorbic acid and CuSO₄·5H₂O), pH, reaction time, and temperature. Increasing the molar ratio of ascorbic acid to precursor salt and increasing the pH led to a decrease in the size of copper particles formed. At short reaction times, spherical copper nanoparticles with an average diameter of 90 nm are obtained. When the reaction time was prolonged, the nanoparticles transformed into nanowires with diameters in the range of 100-250 nm, and lengths of up to 6-8 μm. When the reaction temperature was decreased, Cu mixed with Cu₂O particles were obtained instead of Cu particles. The resultant copper particles were confirmed by EDX and XRD to be pure Cu, with face-centred cubic (fcc) structures.     

Cathodic electrodeposition of Y(OH)3 and Y2O3 nanostructures from chloride bath. Part II: Effect of the bath temperature on the crystal structure,composition and morphology

Ultra-fine nanoparticles, mono-dispersed nanospheres and nanorods of Y(OH)₃ and Y₂O₃ were successfully prepared via electrodeposition from chloride bath at different temperatures of 10, 25, 40 and 80 °C followed by heat-treatments at 600 °C in dry air atmosphere. Thermal behavior of the hydroxide samples was investigated by differential scanning calorimetry (DSC) and thermogravimetric (TG) analysis. The structural and morphological characteristics of the products were determined by X-ray diffraction (XRD), FT-IR, scanning and transmission electron microscopy (SEM and TEM). Effects of bath temperature on the mechanism of base electrogeneration and deposit formation on the cathode surface were proposed and discussed. The results showed that the crystal structure, composition and morphology of the products are mainly affected by the temperature of electrodeposition bath.     

Fatty acids of the seeds of <Emphasis Type="Italic">Origanum onites</Emphasis> L. and <Emphasis Type="Italic">O. vulgare</Emphasis> L.

Seed oils of Origanum onites L. from the Antalya and Mugla regions and O. vulgare L. from the Kirklareli region of Turkey were extracted with hexane in a Soxhlet apparatus. The oil yields were 14.1–20.0 and 18.5%, respectively. FA compositions of the seed oils were determined by GC and GC/MS. Twenty FA were identified in both O. onites and O. vulgare seeds. The major FA of both species were linolenic (56.3–57.0%; 61.8%), linoleic (21.5–21.7%; 18.8%), oleic (8.7–8.9%; 5.9%), palmitic (5.9–6.5%; 5.5%), stearic (2.1–2.4%; 2.1%), and (Z)-11-octadecenoic (0.6–0.8%; 0.5%), respectively.     

Evaluation of damage to light structures erected on a fill material rich in expansive soil

The paper reports a study of the cause of defects in light structures and the toppling of a wall constructed on a fill material rich in Ankara clay. Laboratory tests were carried out on vertical and horizontal samples from boreholes and a trial pit was excavated near the damaged structures. The results showed that in the vicinity of the toppled wall, swelling pressures in the horizontal direction were greater than those measured in the vertical direction. The swelling properties of the fill material were higher than those of original Ankara clay as determined previously by other investigators, suggesting that breakdown of the cementing bonds and a change in the fabric are the main factors affecting the swelling pressure of disturbed and compacted expansive soils. The calculations to predict uplift showed a good agreement with the observations in the damaged structures. It is concluded that swelling was the main cause of the damage to the light structures at the study site and resulted from the highly expansive nature of the fill material, poor drainage, the semi-arid climate, poor construction methods and ineffective precautions. Some recommendations for minimizing the effects of swelling at the study site are briefly outlined.     

Hierarchical behavior categorization using correlation based adaptive resonance theory

This paper introduces a new model for robot behavior categorization. Correlation based adaptive resonance theory (CobART) networks are integrated hierarchically in order to develop an adequate categorization, and to elicit various behaviors performed by the robot. The proposed model is developed by adding a second layer CobART network which receives first layer CobART network categories as an input, and back-propagates the matching information to the first layer networks. The first layer CobART networks categorize self-behavior data of a robot or an object in the environment while the second layer CobART network categorizes the robot's behavior with respect to its effect on the object. Experiments show that the proposed model generates reasonable categorization of behaviors being tested. Moreover, it can learn different forms of the behaviors, and it can detect the relations between them. In essence, the model has an expandable architecture and it contains reusable parts. The first layer CobART networks can be integrated with other CobART networks for another categorization task. Hence, the model presents a way to reveal all behaviors performed by the robot at the same time.     

Dyeing properties of textiles by Turkish hazelnut (Corylus colurna): leaves,coat, shell and dice

Turkey has a great number of hazelnut trees that possess nutritious components. However, only the inside part of the hazelnut is used as a nutrient, while the rest of it is waste. This study suggests that the waste parts of the Turkish hazelnut could be used as a natural dye for dyeing textile fabrics. The dyeing properties of the leaves, coat, shell and dice of the hazelnut were studied on wool, cotton and viscose fabric by using three different mordants: copper sulphate, iron sulphate and aluminium sulphate. The selected dyed fibre sample surfaces were observed using a scanning electron microscope. The colour strength (K/S), light, washing, rubbing, and perspiration fastness levels of the dyed fabrics were investigated. The experimental natural dyeing results indicate that waste hazelnut‐based products can be used as a natural dye for textile coloration.     

Microstructure of Reaction Zone Formed During Diffusion Bonding of TiAl with Ni/Al Multilayer

In this article, the characterization of the interfacial structure of diffusion bonding a TiAl alloy is presented. The joining surfaces were modified by Ni/Al reactive multilayer deposition as an alternative approach to conventional diffusion bonding. TiAl substrates were coated with alternated Ni and Al nanolayers. The nanolayers were deposited by dc magnetron sputtering with 14 nm of period (bilayer thickness). Joining experiments were performed at 900 °C for 30 and 60 min with a pressure of 5 MPa. Cross sections of the joints were prepared for characterization of their interfaces by scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), high resolution TEM (HRTEM), energy dispersive x-ray spectroscopy (EDS), and electron backscatter diffraction (EBSD). Several intermetallic compounds form at the interface, assuring the bonding of the TiAl. The interface can be divided into three distinct zones: zone 1 exhibits elongated nanograins, very small equiaxed grains are observed in zone 2, while zone 3 has larger equiaxed grains. EBSD analysis reveals that zone 1 corresponds to the intermetallic Al₂NiTi and AlNiTi, and zones 2 and 3 to NiAl.     

Layered precursors for new zeolitic materials: Synthesis and characterization of B-RUB-39 and its condensation product B-RUB-41

Condensation of layered silicate precursors leads to new, all silica zeolite frameworks. In order to introduce catalytic functionality, boron has been substituted into the silicate layer of RUB-39 in a single step synthesis process. Condensation of the silicate layer to the zeolite framework of RUB-41, RRO framework structure type, preserved B as constituent of the material. Analysis of structural details obtained from Rietveld analysis of powder diffraction data, ¹¹B and ²⁹Si NMR experiments of the as synthesized precursor as well as of the zeolite condensation product, and crystal chemical reasoning indicates segregation of B on one specific T-site. This T-site is buried in the silicate anionic layer of the precursor shielding the additional negative charge introduced by the trivalent T-atom.