Design and Characterization of Myristoylated and Non-Myristoylated Peptides Effective against Candida spp. Clinical Isolates

The increasing resistance of fungi to antibiotics is a severe challenge in public health, and newly effective drugs are required. Promising potential medications are lipopeptides, linear antimicrobial peptides (AMPs) conjugated to a lipid tail, usually at the N-terminus. In this paper, we investigated the in vitro and in vivo antifungal activity of three short myristoylated and non-myristoylated peptides derived from a mutant of the AMP Chionodracine. We determined their interaction with anionic and zwitterionic membrane-mimicking vesicles and their structure during this interaction. We then investigated their cytotoxic and hemolytic activity against mammalian cells. Lipidated peptides showed a broad spectrum of activity against a relevant panel of pathogen fungi belonging to Candida spp., including the multidrug-resistant C. auris. The antifungal activity was also observed vs. biofilms of C. albicans, C. tropicalis, and C. auris. Finally, a pilot efficacy study was conducted on the in vivo model consisting of Galleria mellonella larvae. Treatment with the most-promising myristoylated peptide was effective in counteracting the infection from C. auris and C. albicans and the death of the larvae. Therefore, this myristoylated peptide is a potential candidate to develop antifungal agents against human fungal pathogens.     

Cathodic protection of carbon steel in natural seawater: Effect of sunlight radiation

Cathodic protection of metals in seawater is known to be influenced by chemical–physical parameters affecting cathodic processes (oxygen discharge, hydrogen evolution and calcareous deposit precipitation). In shallow seawater, these parameters are influenced by sunlight photoperiod and photosynthetic activity. The results presented here represent the first step in studies dedicated to cathodic protection in shallow photic seawater. This paper reports on carbon steel protected at −850 mV vs. Ag/AgCl (oxygen limiting current regime) in the presence of sunlight radiation but in the absence of biological and photosynthetic activity, the role of which deserves future research. Comparison of results obtained by exposing electrochemical cells to daylight cycles in both biologically inactivated natural seawater and in NaCl 3.5 wt.% solutions showed that sunlight affects current densities and that calcareous deposit interfere with light-currents effects. Sunlight radiation and induced heating of the solution have been separated, highlighting results not otherwise obvious: (1) observed current waves concomitant with sunlight radiation depend fundamentally on solar radiation, (2) solar radiation can determine current enhancements from early to late phases of aragonite crystal growth, (3) a three-day-old CaCO₃ layer reduces but does not eliminate the amplitude of the current waves. Theoretical calculations for oxygen limiting currents and additional field tests showed that sunlight, rather than bulk solution heating, is the main cause of daily current enhancements. This was confirmed by polarizations performed at −850 and −1000 mV vs. Ag/AgCl (constant bulk temperature), during which the electrode was irradiated with artificial lighting. This test also confirmed O₂ discharge to be the cathodic process involved. A mechanism of radiation conversion to heat in the oxygen diffusion layer region is proposed.     

Study of Some Experimental Parameters in the Synthesis of Triacylglycerols with CLA Isomers and Structural Analysis

The present research deals with the synthesis of structured triacylglycerols (TAG) by enzymatic treatment of sn-1,3-diacylglycerol (sn-1,3-DAG) with conjugated linoleic acid (CLA) isomers using the immobilized lipase from Rhizomucor miehei (Lipozyme^® IM) under different experimental conditions. In particular, the influence of reaction parameters, such as temperature, enzymatic load, reaction time and DAG/CLA ratio has been evaluated using an experimental design software with a screening objective. Two responses have been selected, they are the percentage of CLA isomers in total TAG and in the sn-2- position and a three-level-4-factor fractional factorial experimental design was used to screen the variables. The results showed that the selected experimental variables have an influence on the enzymatic reaction, in particular, the DAG/CLA substrate ratio and the temperature, both of which inversely correlated with CLA incorporation, but also the enzymatic load and the reaction time, both directly correlated with CLA incorporation. The best results for CLA isomer % content both in total TAG (46.3%) and in the sn-2- position (52.2%) were obtained at 40 °C for 96 h, with 20% enzymatic load and a 0.5 reactive ratio.     

Vicia faba–Lygus rugulipennis Interactions: Induced Plant Volatiles and Sex Pheromone Enhancement

The profiles of volatile chemicals emitted by Vicia faba plants damaged by Lygus rugulipennis feeding, and by feeding plus oviposition, were shown to be quantitatively different from those released by undamaged plants. Samples of volatile chemicals collected from healthy plants, plants damaged by males as a consequence of feeding, plants damaged by females as a consequence of feeding and oviposition, plants damaged by feeding with mated males still present, and plants damaged by feeding and oviposition with gravid females still present, showed significant differences in the emission of hexyl acetate, (Z)-β-ocimene, (E)-β-ocimene, (E)-β-caryophyllene, and methyl salicylate. In particular, treatments with mated females present on plants had a significant increase in emission levels of the above compounds, possibly due to eggs laid within plant tissues or active feeding, compared with undamaged plants and plants damaged by males feeding, with or without insects still present. Furthermore, the pheromonal blend released by mated L. rugulipennis females, mainly comprising hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-4-oxo-2-hexenal, was enhanced when females were active on broad bean plants, whereas such an increase was not observed in males. Both sexes gave electroantennogram responses to green leaf volatiles from undamaged plants and to methyl salicylate and (E)-β-caryophyllene emitted by Lygus-damaged plants, suggesting that these compounds may be involved in colonization of host plants by L. rugulipennis. In addition, mated males and females were responsive to hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-4-oxo-2-hexenal released by mated females on V. faba, indicating that these substances could have a dual function as a possible aggregation pheromone in female–female communication, and as a sex pheromone in female–male communication. An erratum to this article can be found at     

Alumina/Silicon Carbide Laminated Composites by Spark Plasma Sintering

Ceramic laminates composed of alumina/silicon carbide composite layers were produced by spark plasma sintering (SPS). Monolithic composite disks containing up to 30 vol% of silicon carbide were fabricated by stacking together and cosintering by SPS green layers prepared by tape casting water-based suspensions. An engineered laminate with a specific layer combination that is able to promote the stable growth of surface defects before final failure was also designed and produced. Fully dense materials with an optimum adhesion between the constituting layers and a homogeneous distribution of the two phases were obtained after SPS. Monolithic composites showed an increasing strength with SiC load, and biaxial strength values as high as 700 MPa were observed for a SiC content of 30 vol%. The engineered laminate showed a peculiar crack propagation that is responsible for the high strength value of about 600 MPa and for the evident insensitivity to surface defects.     

Phase separation kinetics of maya asphaltene emulsion and free-to-bound water transformation

Differential scanning calorimetry (DSC) and inelastic neutron scattering were applied to study the phase separation kinetics of Maya asphaltene water-in-oil emulsion by following the water separation from the upper phase. In addition, transformation of the separated water from the free state to the bound and/or restricted state was also investigated. Maya asphaltene in toluene with 0.1 M HCl forms emulsion following ultrasonic or high speed mechanical emulsification. Initially, water molecules in the emulsion are largely free water. The emulsion gradually separates into two phases and at the 7th day over 90% of water molecules have situated at the bottom phase. In the mean time water molecules at the free state initially slowly transform into bound state in a much slower pace (over 100 days) than the phase separation kinetics.     

Synthesis of novel DC-SIGN ligands with an alpha-fucosylamide anchor

The dendritic cell-specific intercellular adhesion molecule (ICAM) 3-grabbing nonintegrin (DC-SIGN) is a C-type lectin that appears to perform several different functions. Besides mediating adhesion between dendritic cells and T lymphocytes, DC-SIGN recognizes several pathogens some of which, including HIV, appear to exploit it to invade host organisms. The intriguing diversity of the roles attributed to DC-SIGN and their therapeutic implications have stimulated the search for new ligands that could be used as biological probes and possibly as lead compounds for drug development. The natural ligands of DC-SIGN consist of mannose oligosaccharides or fucose-containing Lewis-type determinants. Using the known 3D structure of the Lewis-x trisaccharide, we have identified some monovalent alpha-fucosylamides that bind to DC-SIGN with inhibitory constants 0.4-0.5 mM, as determined by SPR, and have characterized their interaction with the protein by STD NMR spectroscopy. This work establishes for the first time alpha-fucosylamides as functional mimics of chemically and enzymatically unstable alpha-fucosides and describes interesting candidates for the preparation of multivalent systems able to block the receptor DC-SIGN with high affinity and with potential biomedical applications.     

Electropolymerization of poly(3-methylthiophene) in pyrrolidinium-based ionic liquids for hybrid supercapacitors

The ionic liquids (ILs) N-butyl-N-methyl-pyrrolidinium trifluoromethanesulfonate (PYR₁₄Tf) and N-methyl-N-propyl-pyrrolidinium bis(fluorosulfonyl)imide (PYR₁₃FSI) are investigated as electropolymerization media for poly(3-methylthiophene) (pMeT) in view of their use in carbon/IL/pMeT hybrid supercapacitors. Data on the viscosity, solvent polarity, conductivity and electrochemical stability of PYR₁₄Tf and PYR₁₃FSI as well as the effect of their properties on the electropolymerization and electrochemical performance of pMeT, which features >200 Fg⁻¹ at 60 °C when prepared and tested in such ILs, are reported and discussed; the results of the electrochemical characterization in N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide of the so-obtained pMeT are also given, for comparison.     

Hydrotreating data interpretation by chemometrics

Hydrotreating in the presence of dispersed catalysts has been considered a promising route to obtain valuable fuels from heavy hydrocarbon cuts. A laboratory-scale study on the effect of operating conditions on heavy feedstock hydrotreating performances is reported. In order to maximise the effectiveness of the research activity, chemometrics was exploited both for experimental design and data interpretation.