Antimicrobial Activity of Natural Agents against Saccharomyces cerevisiae

The antimicrobial (AM) activity of starch‐based films coated with linalool, carvacrol or thymol against Saccharomyces cerevisiae in vitro and/or inoculated on the surface of Cheddar cheese was investigated. In solid medium using the agar diffusion method and in experiments involving the inoculation of the microorganism on the surface of Cheddar cheese, all the films containing these AM agents in coatings demonstrated an inhibitory effect against S. cerevisiae. The results suggest that the overall inhibitory effect of linalool, carvacrol or thymol increased significantly (p ≤ 0.05) with the concentration of each of the AM agents in the film coating and that the response is linear in the concentration range of 1 to 5% (w/w) of the AM agent. Thymol had the highest AM efficacy followed by carvacrol, whereas linalool had the lowest efficacy amongst the three systems. The zones of inhibition in the agar diffusion test method at 25°C for S. cerevisiae were found to be 7.6, 7.1 and 6.1 mm for thymol, carvacrol and linalool at 1% (w/w) loading and 13.2, 12.2 and 11.2 mm at 5% (w/w) loading of the AM agents, respectively. The death rates of S. cerevisiae on Cheddar cheese wrapped in films coated with thymol, carvacrol and linalool and stored for up to 28 days at 15°C were found to be 0.044, 0.043 and 0.038 per day at 1% (w/w) loading and 0.077, 0.073 and 0.063 per day at 5% (w/w) loading of the AM agents, respectively. Copyright © 2011 John Wiley & Sons, Ltd.     

Differential regulation of angiotensinogen and AT1A receptor mRNA within the rat subfornical organ during dehydration

The present study describes the differential rostro-caudal patterning of angiotensinogen (AoGen) and AT1A receptor mRNAs in the rat SFO using specific and validated oligodeoxynucleotide probes for in situ hybridization. Highest levels of AoGen-specific gene expression were observed in the rostral region of the SFO with gradually decreasing intensity towards the caudal region of this sensory circumventricular organ lacking blood-brain barrier function. AoGen-related hybridization signals proved to be specifically prominent above cells in lateral aspects of the SFO, surrounding septal venules. Maximal expression of the AT1A receptor-specific gene, on the other hand, could be detected in the neuron-enriched, ventro-medial core region and dorsal annulus of the SFO, with low-intensity hybridization signals in its rostral and caudal parts. Water deprivation for 48 h, leading to extracellular hypertonic hypovolemia with elevated circulating AngII concentrations within the physiological range, caused a significant increase in AoGen-specific hybridization signals in the rostral and medial SFO regions. AT1A receptor gene expression and AngII receptor binding were markedly stimulated in the medial and caudal regions of the SFO (core and annulus) as compared to euhydrated animals. These data indicate, that mild dehydration differentially up-regulates AoGen- and AT1A receptor-specific mRNA formation as well as AT1 receptor binding in distinct regions of the SFO, and supports the involvement of different cellular subgroups in the expression of two major components of the central nervous renin-angiotensin system in this sensory circumventricular organ.     

Merocyanine 540 as a fluorescence indicator for molecular packing stress at the onset of lamellar-hexagonal transition of phosphatidylethanolamine bilayers

The fluorescence of Merocyanine 540 (MC 540) is sensitive to the molecular packing of membrane lipids. Therefore, the fluorescence of MC 540 is expected to be sensitive to the curvature-related packing stress at the onset of the lamellar-hexagonal phase transition. We measured the fluorescence intensity of MC 540 when the temperatures of lipid bilayers approached their lamellar-hexagonal phase transitions. The fluorescence of MC 540 in the presence of egg and dioleoylphosphatidylethanolamine bilayers increased at the respective lamellar-hexagonal phase transitions of these lipids. Furthermore, increases in fluorescence intensity were also observed at temperatures just below their phase transitions. The enhanced fluorescence was not due to the specific interaction of the dye with the ethanolamine headgroup, because no such increase was observed when the probe was exposed to phosphatidylethanolamines which do not form hexagonal phase within the range of applied temperature. In addition, when the temperature of the lamellar-hexagonal phase transition was shifted, by the addition of a small amount of phosphatidylcholine, the dependence of the fluorescence intensity on temperature was modified accordingly. We postulate that the change of MC 540 fluorescence intensity at temperatures approaching the lamellar-hexagonal phase transition reflects changes in the partition of MC 540 into the fluid lipid phase. The change in partition is influenced by the curvature stress in bilayers at temperatures just below the lamellar-hexagonal phase transition.     

The effects of pigments on the photostability of polyethylene

The affect of carbon black and various colourizing pigments on the ultraviolet (UV) stability of high and low density polyethylene (HDPE and LDPE) was determined using a novel method for the analysis of oxygen uptake profiles. Samples were exposed to 0.27 Wm⁻² (measured at 340 nm) UV irrdiation at 25.0±0.1° C in air at 1.0 atm. The usefulness of this method of assessment of UV stability is demonstrated. The method also enables the rapid collection of data that enable the comparison of the relative photostabilities of experimental and commercial formulations containing pigments and stabilizing additives. The results show that carbon black is an effective UV screening agent for HDPE when added at levels as low as 0.05% (wt/wt) and that increased photoprotection is achieved with increasing concentration of carbon black, up to 5% (wt/wt), above which there is no further significant increase in photostability. LDPE containing ultramarine blue pigment (Na₇Al₆Si₆O₂₄S₃) exhibits relatively poor photostability, whereas ferric oxide (Fe₂O₃) and chrome orange (PbCrO₄.PbO) pigments are better photostabilizers for this material. Cadmium sulphide (CdS) was found to photosensitize LDPE. A compound containing 0.10% (wt/wt) carbon black, 0.12% (wt/wt) titanium dioxide (TiO₂) and 1.78% (wt/wt) phthalocyanine green (C₃₃H₂N₈Cl₁₄Cu) is an effective formulation for the stabilization of LDPE. Formulations of LDPE containing ultramarine blue-TiO₂ or ferric oxidecarbon black combinations absorb heat on exposure and this may affect their photostability.