Endosperm α 1,4—α 1,6 Glucopolysaccharides Utilization During Germination of Sweet Corn and Other Maize Genotypes

The quantity variations and the structural changes of the α 1,4 —α 1,6 glucopolysaccharides contained in the endosperm of sweet corn, waxy and amylose extender maize genotypes, were studied during early germination. The α 1,4 —α 1,6 glucopolysaccharides were fractionated according to their branching degree. The results obtained showed that: the degradation pattern of the α 1,4 —α 1,6 glucopolysaccharides was similar for the different corn genotypes studied. In addition, soluble dextrins or partial degradation products were not detected, but reducing sugars were accumulated. Furthermore, the structure of the remaining polysaccharides was similar to those present in the non germinating seed. These results led us to propose that once a polysaccharide molecule was used as the substrate by degradative enzymes during germination, that molecule was totally degraded.     

A satellite remote-sensing multi-index approach to discriminate pelagic Sargassum in the waters of the Yucatan Peninsula,Mexico

Recently, the need for quantitative information on the spatiotemporal distribution of floating macroalgae, particularly the two species of genus Sargassum, has grown because of blooms of these species in the Gulf of Mexico and Caribbean Sea. Remote sensing is one of the most frequently used tools to assess pelagic Sargassum distribution. The purpose of this study was to implement a methodological approach to detect floating algae in an efficient and replicable manner at a moderate cost. We analyzed Landsat 8 imagery, from which we calculated four vegetation indices and one floating-algae index to implement a supervised classification, together with the bands 2 and 5, using the Random Forest algorithm. The analysis was performed monthly from 2014 to 2015 for the northeastern Yucatan Peninsula, Mexico, with a total of 91 analyzed images. The quantitative performance metrics of the classifier (overall, Kappa and Tau) were greater than 80%, whereas bands 2 and 5 as well as the atmospherically resistant vegetation index made the greatest contributions to the classifications. During summer 2015, more than 4,000 ha of Sargassum coverage per image were observed, which was substantially greater than that over the rest of the period. This approach constitutes a transferable alternative for the systematic detection of Sargassum, which enables a quantitative semi-automated time series comparison.     

Mechanistic Investigation of ROS-Induced DNA Damage by Oestrogenic Compounds in Lymphocytes and Sperm Using the Comet Assay

Past research has demonstrated that oestrogenic compounds produce strand breaks in the DNA of sperm and lymphocytes via reactive oxygen species (ROS). In the current investigation, sperm and lymphocytes were treated in vitro with oestrogenic compounds (diethylstilboestrol, progesterone, 17β-oestradiol, noradrenaline and triiodotyronine) and several aspects of DNA damage were investigated. Firstly, mediation of DNA damage by lipid peroxidation was investigated in the presence of BHA (a lipid peroxidation blocker). BHA reduced the DNA damage generated by 17β-oestradiol and diethylstilboestrol in a statistically significant manner. No effects were observed for sperm. Secondly, the presence of oxidized bases employing FPG and EndoIII were detected for lymphocytes and sperm in the negative control and after 24 h recovery in lymphocytes but not immediately after treatment for both cell types. The successful detection of oxidized bases in the negative control (untreated) of sperm provides an opportunity for its application in biomonitoring studies. DNA repair at 24 h after exposure was also studied. A nearly complete recovery to negative control levels was shown in lymphocytes 24 h recovery after oestrogenic exposure and this was statistically significant in all cases. Rapid rejoining of DNA, in a matter of hours, is a characteristic of DNA damaged by ROS.     

Melt processing of ethylene–vinyl acetate/banana starch/Cloisite 20A organoclay nanocomposite films: structural,thermal and composting behavior

This work shows the preparation of ethylene vinyl acetate copolymer/banana starch/Cloisite 20A organoclay (EVA/starch/C20A) nanocomposites by melt processing. Wide angle X-ray diffraction (WAXD), field emission scanning electron microscopy (FE-SEM), differential scanning calorimetry and thermogravimetric analysis were used to characterize the obtained nanocomposites. Mechanical properties were also determined. In addition, the performance of the nanocomposite films under composting was preliminarily studied; it was conducted using the soil burial test method. Despite knowing that the starch is difficult to process by extrusion, nanocomposite films with high homogeneity were obtained. In this case, C20A organoclay acts as an effective surfactant to make the starch natural polymer compatible with the EVA synthetic polymer. The good compatibility between EVA, starch and C20A clay was also deduced by the formation of intercalated and intercalated-exfoliated structures determined by WAXD and FE-SEM. Physical evidence of the damage in EVA/starch/C20A nanocomposite films after the composting test was observed. It is worth noting that despite the absence of starch, the EVA/C20A nanocomposite film, used as a control, also showed surface damage. This behavior is related to the organic modifier linked to clay C20A, which contains molecules derived from fatty acids that can be used as a food source for microorganisms.

     

Comparison of rancimat evaluation modes to assess oxidative stability of fish oils

Two Rancimat evaluation modes, the induction period (IP), and the time needed to achieve a selected difference in conductivity (tΔK) were compared for assessing relative stability of anchovy, sardine, and hake liver oils. Mean coefficients of variation were 2.5 and 2.4% for IP and tΔK values, respectively, for oils oxidized in the range 55–90°C. Natural logarithms of IP and tΔK values varied linearly with temperature (P<0.001). A linear relationship (r=0.999) was established between the IP and tΔK values (P<0.001). Relative oxidative stability of fish oils was determined with the same degree of confidence by either IP or tΔK values.     

Supercritical Fluid Extraction of Eucalyptus globulus Bark-A Promising Approach for Triterpenoid Production

Eucalyptus bark contains significant amounts of triterpenoids with demonstrated bioactivity, namely triterpenic acids and their acetyl derivatives (ursolic, betulinic, oleanolic, betulonic, 3-acetylursolic, and 3-acetyloleanolic acids). In this work, the supercritical fluid extraction (SFE) of Eucalyptus globulus deciduous bark was carried out with pure and modified carbon dioxide to recover this fraction, and the results were compared with those obtained by Soxhlet extraction with dichloromethane. The effects of pressure (100-200 bar), co-solvent (ethanol) content (0, 5 and 8% wt), and multistep operation were studied in order to evaluate the applicability of SFE for their selective and efficient production. The individual extraction curves of the main families of compounds were measured, and the extracts analyzed by GC-MS. Results pointed out the influence of pressure and the important role played by the co-solvent. Ethanol can be used with advantage, since its effect is more important than increasing pressure by several tens of bar. At 160 bar and 40 °C, the introduction of 8% (wt) of ethanol greatly improves the yield of triterpenoids more than threefold.     

Use of a dispersed iron catalyst for upgrading extra-heavy crude oil using methane as source of hydrogen

The use of an iron dispersed catalyst, derived from Fe₃(CO)₁₂, for extra-heavy crude oil upgrading using methane as source of hydrogen was studied. The upgrading reactions were carried out batchwise in a stainless-steel 300 ml Parr reactor with 250 ppm of Fe at a temperature of 410-420 °C, a pressure of 11 MPa of CH₄, and a residence time of 1 h. In the presence of Fe₃(CO)₁₂, the reaction of Hamaca extra-heavy crude oil led to a reduction of two orders of magnitude in the viscosity (from 500 to 1.3 Pa s), 14% reduction in sulfur content, and 41% conversion of the >500 °C fraction in the upgraded product with respect to the original crude. The iron catalyst was isolated from the coke produced from the upgrading reaction and was analyzed by XPS, EDAX, and Mössbauer spectroscopy. The results indicated the presence of a Fe-V mixed sulfide species with a composition ca. (Fe_0.6V_0.4)_zS, where z is in the range 0.8-0.9.     

Investigation of the morphological changes promoted by heating of Si–C–O ceramics derived from a phenyl-rich hybrid polymer. Effect of Ni in the polymeric precursor

This study focuses on the structural and morphological changes promoted by heating of silicon oxycarbide ceramics obtained from hybrid polymeric precursors based on poly(methylsiloxane) and divinylbenzene, with or without nickel acetate, by pyrolysis under Ar at different temperatures. The increase of the temperature from 950 to 1500 °C promoted the densification and crystallization of SiC and graphite nanodomains in the ceramic bulk with or without Ni, as identified by HRTEM. Moreover, the Ni-containing precursor led to the formation of ultra-long amorphous nanowires on the surface and voids in the ceramic body obtained at 1500 °C. These nanowires presented different sizes and morphologies, but similar compositions, basically composed by silicon and oxygen, with the presence of carbon at their external layers. The growth mechanism and the nature of the nanowires are also proposed. The addition of nickel acetate in the polymeric precursor induced the formation of nanowires with different morphologies in the Si–O–C system.     

Lipase-catalyzed synthesis of poly-l-lactide using supercritical carbon dioxide

The present work shows that the enzyme mediated ring-opening polymerization of l-lactide at 65 °C can be achieved using supercritical carbon dioxide. It is reported a biphasic media system where the supercritical phase coexists with a liquid organic phase, which is mainly composed of melted monomer, wherein the growing poly-l-lactide chains are soluble. The immobilized lipase B from Candida antartica was used as the biocatalyst. The results indicated that semi-crystalline polymers with a molecular weight (M_w) up to 12,900 g mol⁻¹ can be attained and that the monomer conversion is related to the biocatalyst concentration and its initial water activity (a_wi). Experiments carried out with denatured enzyme gave no monomer conversion which confirms that the enzymatic mechanism is only involved in our system.