Influence of Pulsed Electric Field Protocols on the Reversible Permeabilization of Rucola Leaves

Reversible electropermeabilization of plant tissues with heterogeneous structure represents a technological challenge as the response of the different structures within the same specimen to the application of electric field may differ due to different cell sizes, extracellular space configurations, and electrical properties. The influence of five different pulsed electric field protocols with different pulse polarity, number of pulses (25, 50, 75, 100, 250, and 500), and intervals between pulses (no intervals and 1- and 2-ms intervals) on the reversible permeabilization of rucola (Eruca sativa) leaves was investigated. The electric field intensity was 600 V/cm. Electrical resistance of the bulk tissue was measured before and after electroporation, and propidium iodide was used to analyze the electroporation at the surface of the leaf. Leaf viability was assessed from survival in storage, and cell viability was investigated with fluorescein diacetate. Results indicate that the viability of the leaves could not be predicted by measurements of electrical resistance or permeabilization levels of the leaf surface. Higher survival rate was demonstrated when applying bipolar pulses compared with monopolar pulses, but the latter proved to be more effective than bipolar pulses for permeabilizing the surface of the leaves. Longer intervals between bipolar pulses resulted in increased viability preservation, while the number of electroporated cells on the leaf surface was comparable for all tested protocols.     

New Cyclams and Their Copper(II) and Iron(III) Complexes: Synthesis and Potential Application as Anticancer Agents

New cyclam derivatives (HOCH₂CH₂CH₂)₂(PhCH₂)₂Cyclam and (HOCH₂CH₂CH₂)₂( PhCH₂)₂Cyclam, as well as their Cu^II and Fe^III complexes, were synthesized and characterized and their stability in cellular media was assessed. The cytotoxic effect of all compounds was examined on human cervical cancer (HeLa) cells, revealing strong anticancer activity. After 24 h, only complexes with the (HOCH₂CH₂CH₂)₂( PhCH₂)₂Cyclam ligand are cytotoxic, whereas after incubation for 72 h all compounds show significant antiproliferative effects. Notably, compounds containing PhCH₂ pendant arms on the cyclam ring revealed the most activity, with cytotoxicity values up to 12 times higher than those of cisplatin. All metal complexes seem to induce cell death through the formation of reactive oxygen species.     

The effects of freezing and freeze-drying of Oenococcus oeni upon induction of malolactic fermentation in red wine

Summary The use of Oenococcus oeni starter cultures for the induction of malolactic fermentation (MLF) in wine permits control over the timing of the process and the quality of the wine. Successful inoculation of bacterial starter cultures into wine depends on the selection of suitable strains and on the preparation and conservation of those cultures. Medium for Leuconostoc oenos (MLO) is the best medium for easy and rapid growth of O. oeni cultures under laboratory controlled conditions for isolation and identification. However, this study showed that O. oeni cells inoculated in MLO failed to induce MLF in wine while cells grown in Medium of Preculture (MP) or wine, stored at −20 °C or freeze-dried retained the ability to induce MLF when inoculated in wine. Our results suggest that the use of freeze-dried cultures of O. oeni previously grown in MP is the best choice for industrial application.     

Understanding the Potential In Vitro Modes of Action of Bis(β-diketonato) Oxovanadium(IV) Complexes

To understand the potential in vitro modes of action of bis(β-diketonato) oxovanadium(IV) complexes, nine compounds of varying functionality have been screened using a range of biological techniques. The antiproliferative activity against a range of cancerous and normal cell lines has been determined, and show these complexes are particularly sensitive against the lung carcinoma cell line, A549. Annexin V (apoptosis) and Caspase-3/7 assays were studied to confirm these complexes induce programmed cell death. While gel electrophoresis was used to determine DNA cleavage activity and production of reactive oxygen species (ROS), the Comet assay was used to determine induced genomic DNA damage. Additionally, Förster resonance energy transfer (FRET)-based DNA melting and fluorescent intercalation displacement assays have been used to determine the interaction of the complexes with double strand (DS) DNA and to establish preferential DNA base-pair binding (AT versus GC).     

Fluorescence of 1,2-diaminoanthraquinone and its nitric oxide reaction product within macrophage cells

Nitric oxide (NO) is involved in many biological processes. Aromatic ortho-diamine derivatives are commonly used in the fluorescence imaging of NO in living cells. ortho-diamino (o-diamino) compounds are believed to react with NO in an oxygenated medium leading to the formation of a triazole derivative. One such o-diamino compound, 1,2-diaminoanthraquinone (DAA), is a nontoxic probe for the detection of NO in living tissues and cells. The formation of the DAA triazole derivative (DAA-TZ) upon reaction of DAA with NO/O(2) within cells has not been demonstrated previously. The aim of this study was to confirm that DAA-TZ is the species formed intracellularly when DAA reacts with NO in the presence of oxygen. The chemical synthesis and characterisation of DAA-TZ was performed together with intracellular studies of DAA and DAA-TZ. Raw 264.7 macrophages were loaded with the DAA or DAA-TZ under conditions of no-stimulation or stimulation with interferon-γ and lipopolysaccharide to produce NO. Confocal microscopy was used to image the DAA-loaded macrophage cells. Analysis of the emission spectra allowed precise discrimination of the fluorescence of each species in the macrophage cells, and confirmed the identity of DAA-TZ as the intracellular reaction product between DAA and NO in the presence of oxygen.     

Solid solutions of mixed metal Mn3−xMgxFe4(PO4)6 orthophosphates: Colouring performance within a double-firing ceramic glaze

Solid solutions of mixed metal Mn_3−xMg_xFe₄(PO₄)₆ orthophosphates (x = 0, 0.5, 1, 1.5, 2, 2.5, and 3) were prepared for the first time (from coprecipitate powders calcined up to 1000 °C) and characterized by thermal analysis, XRD, SEM/EDX, UV-vis-NIR spectroscopy and colour measurements (CIE-L*a*b*). Orthophosphate (Mn,Mg)_3−yFe_4+z(PO₄)₆ solid solutions isotypic to Fe₇(PO₄)₆ structure (triclinic P-1(2) spatial group) formed successfully as the major crystalline phase within the studied range of compositions, accompanied only by variable quantities of α- and/or β-Mg₂P₂O₇ diphosphates as secondary phases. Noteworthy, the obtained solid solutions were tested as potential ceramic dyes and exhibited an interesting interaction upon enamelling within a double-firing ceramic glaze: considerable amounts of Fe segregated from the solid solutions to be stabilized as hematite particles (α-Fe₂O₃) in the ceramic glaze and conferring the glaze an intense dark-brown colouration, which was almost independent of the amount of Mg doping. Thus, the obtained solid solutions with a minimized Mn content (especially Mg₃Fe₄(PO₄)₆ composition, without Mn) could serve as low-toxicity Fe reservoirs to stabilize hematite in double-firing glazes and produce an interesting dark-brown colouration, being an alternative to other brown ceramic pigments containing hazardous metals (i.e. Cr, Ni, Zn, or Sb).