Genome-Wide Identification and Characterization of PIN-FORMED (PIN) Gene Family Reveals Role in Developmental and Various Stress Conditions in Triticum aestivum L.

PIN-FORMED (PIN) genes play a crucial role in regulating polar auxin distribution in diverse developmental processes, including tropic responses, embryogenesis, tissue differentiation, and organogenesis. However, the role of PIN-mediated auxin transport in various plant species is poorly understood. Currently, no information is available about this gene family in wheat (Triticum aestivum L.). In the present investigation, we identified the PIN gene family in wheat to understand the evolution of PIN-mediated auxin transport and its role in various developmental processes and under different biotic and abiotic stress conditions. In this study, we performed genome-wide analysis of the PIN gene family in common wheat and identified 44 TaPIN genes through a homology search, further characterizing them to understand their structure, function, and distribution across various tissues. Phylogenetic analyses led to the classification of TaPIN genes into seven different groups, providing evidence of an evolutionary relationship with Arabidopsis thaliana and Oryza sativa. A gene exon/intron structure analysis showed a distinct evolutionary path and predicted the possible gene duplication events. Further, the physical and biochemical properties, conserved motifs, chromosomal, subcellular localization, transmembrane domains, and three-dimensional (3D) structure were also examined using various computational approaches. Cis-elements analysis of TaPIN genes showed that TaPIN promoters consist of phytohormone, plant growth and development, and stress-related cis-elements. In addition, expression profile analysis also revealed that the expression patterns of the TaPIN genes were different in different tissues and developmental stages. Several members of the TaPIN family were induced during biotic and abiotic stress. Moreover, the expression patterns of TaPIN genes were verified by qRT-PCR. The qRT-PCR results also show a similar expression with slight variation. Therefore, the outcome of this study provides basic genomic information on the expression of the TaPIN gene family and will pave the way for dissecting the precise role of TaPINs in plant developmental processes and different stress conditions.     

Statistical Analysis and Optimization of Process Parameters in Wire Cut Machining of Welded Nanostructured Hardfacing Material

Silicon - Wire electric discharge machining (WEDM) is a nontraditional machining technique to cut hard and conductive material with the assistance of a moving electrode. Nanostructured hardfacing...     

Synthesis and characterization of chemically stable sulfonated copoly(triazole imide)s with high proton conductivity

The synthesis and characterization of a series of new sulfonated copoly(triazole imide)s (PTPQSH‐XX) are reported in this work. The PTPQSH‐XX with different degree of sulfonation (DS) were prepared by click polymerization of equimolar amounts of a diimide‐based dialkyne monomer, namely bis‐N,N′‐(prop‐2‐ynyl)pyromellitic diimide (TP) and a mixture of two different diazide monomers (one sulfonated, 4,4‐bis[3′‐trifluoromethyl‐4′{4‐azidobenzoxy} benzyl] biphenyl, and another nonsulfonated, 4,4′‐diazido‐2,2′‐stilbene disulfonic acid disodium salt [SAZ]), in different molar ratios. The copolymers showed high inherent viscosity (1.12–1.28 dL/g) in n‐methyl pyrrolidone (NMP) indicating the formation of high molar masses. Freestanding membranes were prepared from these copolymers by solution casting method. DS of the copolymers was determined from ¹H NMR signal intensities, and the values were in good agreement with the quantity of SAZ monomer used in polymer feed, indicating the successful incorporation of the sulfonated monomer. The copolymers exhibited high thermal and mechanical stabilities. The PTPQSH‐80 membrane showed proton conductivity as high as 178 mS/cm at 90°C with good oxidative and hydrolytic stability. Cross‐sectional transmission electron microscope micrographs of the membranes indicated phase segregated morphology along with interconnected hydrophilic domains with dimension in the range 15–150 nm. POLYM. ENG. SCI., 59:2279–2289, 2019. © 2019 Society of Plastics Engineers     

Role of Flaxseed Meal Feeding for Different Durations in the Lipid Deposition and Meat Quality in Broiler Chickens

This study investigated the role of flaxseed meal (FSM), a rich terrestrial source of ω-3 fatty acids, in the alteration of the fatty acid profile and metabolism, health indices, physicochemical properties, and sensory quality of broiler chicken meat. The broiler chickens were fed 100 g FSM kg⁻¹ diet for different time periods (1, 2, 3, 4, and 5 weeks). The results revealed that 100 g FSM feeding in broiler chickens for at least 3 weeks increased (P < 0.01) the EPA, DHA, MUFA, PUFA, ω-3 PUFA, and ω-6 PUFA of broiler chicken meat with the corresponding decrease in palmitic acid, stearic acid, and SFA content. 100 g FSM feeding up to 3 weeks has increased the Δ⁹-desaturases (P < 0.05), thioesterase index (P < 0.01), and Δ⁵-desaturase + Δ⁶-desaturase activity (P < 0.01) along with an improvement in health indices (P < 0.01) of chicken meat. Similarly, a reduction in meat cholesterol and fat content of thigh meat (P < 0.01) was observed by feeding 100 g FSM for at least 3 weeks with no effect on the pH, color scores, and sensory evaluation of broiler chicken meat. The water-holding capacity (WHC) and extract release volume (ERV) decreased, whereas, drip loss of meat increased (P < 0.01) due to the feeding of 100 g FSM beyond 3 weeks. Thus, this study concluded that 100 g FSM feeding for 3 weeks in broiler chickens significantly improves the fatty acid profile, lipid metabolism, and health indices of meat, without compromising the physicochemical properties of broiler chicken meat.     

An Insight into molecular structure and properties of flexible amorphous polymers: A molecular dynamics simulation approach

Visualization of polymer molecules by molecular dynamics simulation remains a challenging area in molecular modeling, as it involves a number of factors like type of force field, simulation time, simulation steps, and so forth. In our present study, we have used the condensed-phase optimized molecular potentials for atomistic simulation studies (COMPASS) force field, which is specific for polymers and organic molecules, in order to visualize the macromolecular chains of various flexible amorphous polymers: natural rubber, polybutadiene rubber, styrene–butadiene rubber, nitrile rubber, polychloroprene rubber, and fluoroelastomer. The study covered a wide range from nonpolar rubbers to polar rubbers, and the COMPASS force field was promising to understand the local structure and the packing of the chains inside the simulation box. The distance between different adjacent pairs of carbon atoms within the polymer chains was discussed in detail from intramolecular radial distribution function and represented pictorially in the polymer chains. Various bond angles were also examined for further details. In addition, interchain contacts, glass-transition temperature, and solubility parameter were predicted and compared with the experimental values. The diffusive characteristic of the chains was assessed by mean square displacement which in turn described the polymer chain mobility. In essence, the present study is expected to aid in the vivid conceptualization of molecular orientation of various polymers and would help in predicting various physical properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47457     

Acetylation of hydroxytyrosol enhances its transport across differentiated Caco-2 cell monolayers

Hydroxytyrosol and hydroxytyrosyl acetate are two well-known phenolic compounds with antioxidant properties that are present in virgin olive oil. Since the in vivo biological activity of polyphenols is dependent on their intestinal absorption and metabolism, the absorption of hydroxytyrosol and hydroxytyrosyl acetate and the extent to which they are conjugated and metabolised during transfer across intestinal Caco-2/TC7 cell monolayers, was investigated. LC-DAD and LC-MS were used for the quantification and identification of metabolites. Further evidence was obtained by observing metabolite susceptibility to β-glucuronidase treatment and by comparison of products of in vitro conjugation reactions of authentic phenolics with those produced by the CaCo-2 cells. Homovanillyl alcohol was the only conjugate detected as a result of hydroxytyrosol metabolism, and accounted for 20% of the total metabolites detected in the basolateral compartment after 2 h of incubation. Hydroxytyrosyl acetate was largely converted into free hydroxytyrosol (38.4%) and subsequently metabolised into homovanillyl alcohol (6.7%). In addition, hydroxytyrosyl acetate glucuronide (17.4%) together with non-metabolised hydroxytyrosyl acetate (37.5%) were also detected. Both hydroxytyrosyl acetate and hydroxytyrosol were transferred across human Caco-2/TC7 cell monolayers, but the acetylated compound exhibited an apparent permeability (Papp_AP→BL/Papp _BL→AP) 2.1-fold higher than free hydroxytyrosol. For both compounds, all conjugates were preferentially transported to the basolateral side. These results show that the acetylation of hydroxytyrosol significantly increases its transport across the small intestinal epithelial cell barrier, and supports further research into hydroxytyrosyl acetate as a hydroxytyrosol prodrug offering enhanced bioavailability.     

Enhanced mechanical toughness of carbon nanofibrous-coated surface modified Kevlar reinforced polyurethane/epoxy matrix hybrid composites

High-performance Kevlar fiber had extensively been explored to upgraded mechanical properties of the advanced composites. Therefore, this study aimed a challenging work to grow carbon nanofibers onto the Kevlar fiber to improve its fiber-matrix interaction properties. It was successfully done through inexpensive flame deposition as well as modification of matrix with hybrid resin using polyurethane-epoxy mixture. A hand-layup method had been adopted to manufacture the composite laminates. The chemical and surface structures of the prepared laminae were examined by scanning electron microscopy, Raman spectroscopy, X-ray diffraction, and the composite's properties were evaluated tensile test, compact tension (CT) fracture test, fractography, and differential scanning calorimetry. The surface modified Kevlar laminae with CNF were used as reinforcing layer in the epoxy and PU/epoxy hybrid resin matrices. CNF-coated heated Kevlar reinforced laminated PU/epoxy hybrid composites (CNF-Kev/PU-Epoxy) showed highest elongation 47% and fracture toughness (11.7 MPa√m) along with good UTS 139 MPa. Therefore, these hybrid nanocomposites developed by simple inexpensive method would be the potential candidates for several advanced applications particularly in defense, automobile, aerospace, and spacecraft applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48802.     

Swelling and rheological study of calcium phosphate filled bacterial cellulose-based hydrogel scaffold

This work focuses mainly about swelling and rheological properties of calcium phosphate filled bacterial cellulose (BC)-based hydrogel scaffolds. Calcium phosphate is incorporated in the form of hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) in different ratios, that is, 00:00, 10:90, 20:80, 40:60, 50:50, and 60:40. These scaffolds are also comprised with polyvinylpyrrolidone (PVP), poly(ethylene glycol), agar, and glycerin; designated as “BC-PVP” and “BC-PVP-β-TCP/HA.” All the hydrogel scaffolds are showing the notable viscoelastic property at 28 and 37 °C temperatures. The degree of swelling is found significant in BC-PVP-β-TCP/HA_50:50 scaffold and it is notably elastic at 37 °C after 5 min of swelling. However, after 60 min of swelling and at equilibrium swelling state, the elastic property of BC-PVP-β-TCP/HA_20:80 is revealed the highest. Considering the degree of swelling and rheological properties, the BC-PVP-β-TCP/HA_50:50 and BC-PVP-β-TCP/HA_20:80 hydrogel scaffolds found suitable for their application in bone tissue engineering or bone tissue regeneration. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48522.     

Graphene oxide nanoflakes from various agrowastes

Nowadays, the synthesis of graphene/ graphene oxide from graphite precursor using oxidizing agents is the most common procedure, but the direct synthesis of graphene or graphene oxide from a non-graphitic carbonaceous material without using inert atmosphere is really a great challenge. Besides, the chemistry behind the development of graphitic structure from a non-graphitic material during the thermal heating is still not clearly understood. In this research work, three agrowaste materials viz. rice husk, sugarcane bagasse and newspaper were selected and subjected to pyrolysis in presence of trace amount of air. The continued heating at the optimum temperature has resulted in aromatization and condensation along with the oxidation within the cellulosic structure of the agrowaste, which finally resulted in the formation of graphene oxide nanoflakes directly. The mechanism of formation of graphene oxide from these agrowaste materials was studied, which suggested that any carbonaceous waste materials can be converted to graphene oxide by optimizing the thermal heating conditions.