Aqueous Agar Research Articles

Features of Bioluminescence Dynamics of Photobacterium phosphoreum IMV B-7071

The problem of the prolonged and stable intensity of bioluminescent signals is relevant in the development of any test systems that use biological objects. The aim of this work was to study the features of bioluminescence dynamics of Photobacterium phosphoreum IMV B-7071 in a liquid and on different stationary media. Methods. Bioluminescence studies were performed in liquid, agarose, and cellulose-cotton media. Bacterial suspensions were cultivated at 21°C in the mediums with standard composition. We studied both the background glow and its dynamics under conditions of mixing a liquid medium. Bioluminescence was recorded using digital photography with subsequent image processing of the samples. The measurements of luminescence were made by digital photo or video recording using Olympus digital camera SP560UZ, CANON 700D, and mobile device camera Samsung Galaxy 9 Note with specialized applications for mobile devices "Colorimeter (Lab Tools Apps)" and Camera Color Counter (Keuwsoft) at maximum light sensitivity in the automatic white balance mode at a fixed distance from the sample. Image processing was carried out using ImageJ and Origin Pro. Spectra of bacterial luminescence and its dynamics over time were measured using an LOMO MDR-23 spectrometer in the range of 200–750 nm. Results. The results of the study prove that in aqueous or solid agar and also on cellulose cotton medium, the intensity of bioluminescence of P. phosphoreum gradually increases, reaching a maximum within approximately 2 days, after which it slowly fades. It was established that the bioluminescence of photobacterium P. phosphoreum is a non-stationary process and has characteristic features of temporal dynamics associated with both the dynamics of the oxygen concentration in the environment of bacterial suspensions and the dynamics of the bacterial population density. Analysis of the luminescence spectra of bacteria shows that luminescence occurs mainly in the blue and green regions of the spectrum with luminescence maxima in the range of 460–520 nm, but the ultra-weak glow is also registered in the UV and red spectral ranges. The variability of photobacterial luminescence spectra over time in the spectral ranges of the main luminophores causes color fluctuations between the blue and green ranges. Conclusions. The key parameters of multi-day background and short-term induced bioluminescence dynamics of photobacteria in different environments were clarified, and the certain variability of the spectral characteristics of luminescent radiation over time was shown. The revealed features of the dynamics of the bioluminescence of P. phosphoreum must be taken into account in practical application to assess the toxicity of substances of various nature, as well as in environmental monitoring.

Biological attributes of Salibro™, a novel sulfonamide nematicide. Part 2: Impact on the fitness of various non-target nematodes

Summary Currently a renaissance in chemical nematicides is taking place with novel products like Nimitz® (a.s. fluensulfone), Velum Prime® (a.s. fluopyram) and Salibro™ (a.s. fluazaindolizine – Reklemel™ active) entering the marketplace. Although a considerable amount of published data is already available on their laboratory and field impact on plant-parasitic nematodes, little is understood of their compatibility with the beneficial or free-living nematodes that are part of the soil health network. In a range of laboratory studies, the effects of these nematicides on the vitality and reproduction of several species was tested, including both cosmopolitan free-living nematodes (Acrobeloides, Cruznema, Panagrobelus) as well as commercially applied entomopathogenic nematodes (Steinernema, Heterorhabditis). Within aqueous exposure and agar plate in vitro assays, species sensitivity to those nematicides differed significantly but their fitness (vitality and reproduction; infectivity to insect hosts) was generally not adversely impacted by concentrations of 5-50 ppm (a.s.) of Salibro. Even at 250 ppm (a.s.) of Salibro only some species of the bacterial-feeding species showed some negative impact. By contrast, both Nimitz at 50 ppm (a.s.) and Velum at 5 ppm (a.s.) consistently demonstrated stronger adverse impacts. In second level soil drenching assays, either no, or occasionally slight, adverse effects on the natural community of free-living nematodes were observed if soils were drenched with different volumes of Salibro at 5-50 ppm (a.s.), while relatively stronger reductions were measured within the plant-parasitic species (especially root-knot nematodes). Both Nimitz and Vydate (a.s. oxamyl) showed some degree of compatibility at 5 and 25 ppm (a.s.), respectively, which was generally higher than for Velum Prime at 5 ppm (a.s.). Overall, these data indicate that, when used at common field rates, Salibro will be one of the best options as part of integrated nematode management programmes where the use of chemical nematicides is required.

Silver nanoparticle stabilized by hydrolyzed collagen and natural polymers: Synthesis, characterization and antibacterial-antifungal evaluation

In synthesis of silver nanoparticles (AgNPs), the composition of the stabilizer used can be closely related to the effectiveness of the synthesis and to the shape of the final nanoparticles. Recently, the use of collagen as an effective nanoparticle stabilization agent was reported. In this work, synthesis of silver nanoparticles using mixed capping agents is reported. The capping agents used were cashew gum-hydrolyzed collagen; kappa carrageenan-hydrolyzed collagen, and agar-hydrolyzed collagen. We evaluated antibacterial action against Gram-positive and Gram-negative bacteria, as well as antifungal activity and cytotoxicity. Homogenized mixtures of collagen and aqueous cashew gum, carrageenan or agar respectively were used to produce the nanoparticles AgNPcolCashew, AgNPcolCarr and AgNPcolAgar. AgNP characterization was performed using Uv-vis, XRD, TEM and DLS and the biological activities were assayed using MIC and MBC analyses for both antibacterial and antifungal application. Results showed that the AgNPcollcar sample showed the strongest bacterial inhibition with MIC values of 62.5 and 31.25 μM/mL Ag against E. coli and P. aeruginosa respectively. Interestingly, AgNPcollAgar also presented the lowest cytotoxicity when compared with other AgNPs and AgNO3.

Abstract 1033: Cigarette smoke and bile acids induce metabolic reprogramming mediated by uncoupling protein-2 (UCP2) during esophageal carcinogenesis

Abstract Background: In cancer cells, glucose is processed not through mitochondrial respiration, but mainly through glycolysis to form lactate and minimal ATP (Warburg effect). Glutamine is an essential amino acid in cancer cells and the primary fuel for the mitochondria. Uncoupling protein 2 (UCP2) decreases mitochondrial proton membrane potential and reduces reactive oxygen species (ROS). Limited information is available regarding mechanisms that link environmental risk factors such as gastro-esophageal reflux and cigarette smoking to metabolomic alterations in esophageal adenocarcinoma (EAC). The present study was undertaken to examine the effects of cigarette smoke and bile acids on UCP2 expression, metabolic activity, and malignant phenotype of EAC cells. Methods: Ten EAC lines were screened for UCP2 expression using qRT-PCR and immunoblot techniques. Two EAC lines, Flo-1 and NCI-SB-ESC2 (Esc2), had low and high UCP2 expression, respectively. Flo-1 and Esc2 cells were exposed to normal media with or without cigarette smoke condensate (CSC) and/or the bile acid, deoxycholic acid (DCA) for 5 days. Cell growth, migration, invasion, and clonogenicity were examined using CellTiter 96® Aqueous Kit, scratch, and soft agar clonogenicity assays. Mitochondrial respiration and glycolytic capacity were analyzed using the Seahorse Extracellular Flux Analyzer, and ATP and Lactate Production Kits. Levels of ROS were quantitated using Cellular Reactive Oxygen Species Detection Kit. Results: Flo-1 cells had low UCP2 protein expression and large spare mitochondrial respiratory capacity, whereas Esc2 cells exhibited high UCP2 protein expression and no spare mitochondrial respiratory capacity. CSC and DCA mediated synergistic increases in lactate levels with decreases in ATP production (Warburg effect) without altering levels of UCP2 or ROS in Flo-1 cells. In contrast, similar treatment did not alter lactate or ATP production, but did synergistically deplete UCP2 and increase ROS levels in Esc2 cells. Whereas CSC and DCA exposure did not alter proliferation, migration, or invasion of Flo-1 cells, these treatments enhanced proliferation, migration, and invasion of Esc2 cells. Conclusions: Following exposure to CSC and DCA, EAC cells can shift toward glycolysis when spare mitochondrial respiration is present. In contrast, EAC cells with maximal utilization of glycolysis have no ability to increase glycolysis with CSC or DCA exposure. However, in these cells, CSC and DCA down-regulates UCP2 and increases ROS; these metabolic effects coincide with increased malignant phenotype of EAC cells. These differences suggest that low levels of UCP2 may function as a metabolic sensor whereas high levels may serve as a cellular redox trigger effecting ROS. These preliminary insights into mitochondrial function may help guide the development of novel therapeutic strategies for EAC. Citation Format: Yuan Xu, Kate Brown, Deborah R. Depew, Paul L. Feingold, Mahadev Rao, Jeremy Davis, David S. Schrump, R. Taylor Ripley. Cigarette smoke and bile acids induce metabolic reprogramming mediated by uncoupling protein-2 (UCP2) during esophageal carcinogenesis. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 1033.

Liquid culture production of microsclerotia of Purpureocillium lilacinum for use as bionematicide

The production of microsclerotia by Purpureocillium lilacinum in liquid culture for use as a biocontrol agent for management of root-knot nematode, Meloidogyne incognita, has not been described. To investigate the potential for microsclerotia production, P. lilacinum strain CQPL01 was cultured in liquid media containing various concentrations of ferrous sulphate. Under these conditions mycelia began to form microsclerotia. The maximum yield (11.8 × 104 microsclerotia ml−1) was obtained in medium containing 0.2 g l−1 ferrous sulphate and the greatest production of conidia (1.3 × 108 conidia g−1) was obtained by the culture of air-dried microsclerotia in aqueous agar medium. Subsequently, the viability of microsclerotia, including stress resistance, storage stability and pathogenicity against M. incognita, was investigated. The microsclerotia exhibited excellent nematophagous ability and greater thermotolerance and UV-B radiation tolerance compared to conidia. These results suggested that microsclerotia propagules might be superior to the use of conidia in P. lilacinum biocontrol products.

Toluene biodegradation in a solid/liquid system involving immobilized activated sludge and silicone oil as pollutant reservoir

A solid/liquid system involving activated sludge immobilized in an agar medium and a non-aqueous phase liquid containing the target pollutant has been considered to treat a model hydrophobic volatile organic compound, toluene. The positive impact of the use of a multiphase bioreactor is that the organic phase constitutes a pollutant reservoir and also helps to overcome possible pollutant toxicity. In addition and to overcome the drawbacks of the use of a solid organic phase (high pressure drop and low mass transfer) instead of a liquid organic phase, the considered solid phase was the aqueous. Consequently, silicone oil (polydimethylsiloxane) which showed its relevance for implementation in multiphase bioreactors was used. Promising results were observed from the analysis of toluene in the gaseous phase; for an initial amount of 2 g L−1 related to the organic phase, a v/v ratio of 0.5 of the organic phase to the aqueous agar phase, total toluene consumption was observed in about 9 days, leading to a global biodegradation rate of approximately 3.1 mg L−1 h−1, namely in the range of values previously observed in liquid/liquid systems.

Synthesis and characterization of high-surface-area millimeter-sized silica beads with hierarchical multi-modal pore structure by the addition of agar

Millimeter-sized spherical silica foams (SSFs) with hierarchical multi-modal pore structure featuring high specific surface area and ordered mesoporous frameworks were successfully prepared using aqueous agar addition, foaming and drop-in-oil processes. The pore-related properties of the prepared spherical silica (SSs) and SSFs were systematically characterized by field emission-scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), small-angle X-ray diffraction (SAXRD), Hg intrusion porosimetry, and N2 adsorption–desorption isotherm measurements. Improvements in the BET surface area and total pore volume were observed at 504m2g−1 and 5.45cm3g−1, respectively, after an agar addition and foaming process. Despite the increase in the BET surface area, the mesopore wall thickness and the pore size of the mesopores generated from the block copolymer with agar addition were unchanged based on the SAXRD, TEM, and BJH methods. The SSFs prepared in the present study were confirmed to have improved BET surface area and micropore volume through the agar loading, and to exhibit interconnected 3-dimensional network macropore structure leading to the enhancement of total porosity and BET surface area via the foaming process.

High internal phase agar hydrogel dispersions in cocoa butter and chocolate as a route towards reducing fat content

Reducing the fat content of chocolate formulations is a major challenge for the confectionery industry. We report the suspension of aqueous microgel agar particles of up to 80% v/v within sunflower oil, cocoa butter, and ultimately chocolate. The optimised emulsification process involves a shear-cooling step. We demonstrate the versatility of our method when applied to white, milk, and dark chocolate formulations, whilst preserving the desired polymorph V of the cocoa butter matrix. In addition, we show that this technology can be used as a strategy to disperse alcoholic beverages into chocolate confectionery.

Direct Geometric Observation of an Agar Gel Droplet on a Multipillar Surface

We successfully determined the three-dimensional structure of agar gel droplets on multipillared surfaces. The contact angle, length of penetration of the agar gel into the interspace between pillars, and curvature of the bottom surface of the droplets were changed with respect to changes in the volume and concentration of the aqueous agar solution and the distance between the surface-bound pillars.

Effect of static magnetic fields on the budding of yeast cells

The effect of static magnetic fields on the budding of single yeast cells was investigated using a magnetic circuit that was capable of generating a strong magnetic field (2.93 T) and gradient (6100 T² m⁻¹). Saccharomyces cerevisiae yeast cells were grown in an aqueous YPD agar in a silica capillary under either a homogeneous or inhomogeneous static magnetic field. Although the size of budding yeast cells was only slightly affected by the magnetic fields after 4 h, the budding angle was clearly affected by the direction of the homogeneous and inhomogeneous magnetic fields. In the homogeneous magnetic field, the budding direction of daughter yeast cells was mainly oriented in the direction of magnetic field B. However, when subjected to the inhomogeneous magnetic field, the daughter yeast cells tended to bud along the axis of capillary flow in regions where the magnetic gradient, estimated by B(dB/dx), were high. Based on the present experimental results, the possible mechanism for the magnetic effect on the budding direction of daughter yeast cells is theoretically discussed.

Combined Effect of Heat, Essential Oils and Salt on the Fungicidal Activity against Trichophyton mentagrophytes in Foot Bath

This work was originally undertaken to determine the effective conditions of essential oils against Trichophyton mentagrophytes in vitro for the treatment of tinea pedis in a foot bath. Agar blocks implanted with T. mentagrophytes were immersed in 0.1% aqueous agar containing two-fold dilutions of essential oils with or without sodium chloride at 27 degrees C, 37 degrees C and 42 degrees C for 10 and 20 min. The number of surviving mycelia on the agar blocks was determined from the standard curves of the colony diameter and original inocula of the conidia. At the same time, the thermal effect on the cellular morphology was examined using SEM. Most fungal mycelia (99.7%) were killed after treatment at 42 degrees C for 20 min without essential oil. The fungicidal activity of essential oils was markedly enhanced by treating at 42 degrees C for 20 min as compared with that at 27 degrees C, showing 1/4 - 1/32-fold reduction of minimum fungicidal concentration (MFC to kill 99.99%). The order of the fungicidal activity of 11 essential oils was oregano, thyme thymol, cinnamon bark > lemongrass > clove, palmarose, peppermint, lavender > geranium Bourbon, tea tree > thyme geraniol oils. MFCs were further reduced to 1/2 - 1/8 by the addition of 10% sodium chloride. The salt effect was explained, at least partly, by an increase in mycelial adsorption of antifungal constituents in the presence of sodium chloride. Considerable hyphal damage was done at 27 degrees C by the essential oils, but no further alteration in morphology of the hyphae treated at 42 degrees C with or without oil was observed by SEM. The inhibitory effect of heat and oils was also observed against mycelia of T. rubrum and conidia of T. mentagrophytes. Thermotherapy combined with essential oils and salt would be promising to treat tinea pedis in a foot bath.

Solidification by Convective Drying of Particle Layer Wetted with Dilute Agar Gel

: Solidified porous slab is formed through convective drying of glass particle layer wetted with aqueous dilute agar gel. Measured critical mean moisture content increases with increasing initial moisture or agar content. The agar gel moves in viscous flow caused by capillary pressure during drying. A new drying model based on the receding evaporation plane model is proposed. Drying period is divided into surface and internal evaporation periods. Wet slab consists of dried and wet zones during the internal evaporation period, while the wet slab consists of wet zone only during the surface evaporation period. In the new model, the evaporation rate from the wet zone in the internal drying period is estimated with the linear driving force (LDF) approximation in the field of adsorption engineering. Critical moisture content, that is, mean moisture content between the surface and internal periods, is estimated with a mass balance on the surface. Simulated results by the new drying model with reasonable fitting parameters agree very well with measured drying data.

A New Process to Make a Porous PTFE Structure from Aqueous PTFE Dispersion with the Help of Hydrogel

A novel method to make a porous material having relatively large cell diameter (200–300 μm), which consisted of mainly poly(tetrafluoroethylene) (PTFE), was developed from aqueous PTFE dispersion by using the characteristics of hydrogel with the addition of carbon nanofiber (CNF). The porous material was produced as follows: firstly, an aqueous agar gel containing PTFE and CNF was prepared; secondly, the gel was freeze-dried; thirdly, the dried gel was heat-treated at 400°C where the agar was almost decomposed and PTFE became molten. The porous material showed electric conductivity (about 50 Ω), high porosity (about 96 vol%), and relatively uniform cell structures without shrinkage during freeze drying and heat treatment. While the method without CNF resulted in large shrinkage during heat treatment, meaning that CNF prevented the shrinkage. It was explained by the idea that the existence of rigid CNF, which was dispersed in the cell wall, prohibited the shrinkage of PTFE during heat treatment. It was unexpectedly found by SEM analysis that the porous materials had another macro-porous structure inside the cell wall, suggesting that the developed materials had a double porous structure.

Cyanoethylation of alcohols catalyzed by a novel aqueous agar gel-entrapped NaOH catalyst

An aqueous solution of NaOH was entrapped in a gel matrix of agar agar to obtain a hard solid gel (composition 60% water:10% NaOH:30% agar agar), which was used to catalyze cyanoethylation of various primary aliphatic alcohols with acrylonitrile under very mild conditions in very good yields.

Phenylhydroxylamine: Role in Aniline-Associated Splenic Oxidative Stress and Induction of Subendocardial Necrosis

To elucidate the role of N-phenylhydroxylamine (PHA, N-hydroxylated metabolite of aniline) in the selective toxicity of aniline to the spleen, dose-dependent studies were conducted with PHA in rats. Male Sprague-Dawley rats were given four doses each (1 dose/day) of 0.025, 0.05, 0.1, or 0.2 mmol/kg PHA in 0.5 ml of aqueous agar (0.25%) by gavage. The control animals received an equal volume of vehicle only. The animals were euthanized 24 h following the last dose. PHA toxicity in the blood was evident from a dose-dependent increase of methemoglobin. The most affected organ was spleen, which appeared dark and enlarged (splenomegaly) and showed increased spleen-to-body weight ratios, which were 28, 40, 66, and 87% at PHA doses of 0.025, 0.05, 0.1, and 0.2 mmol/kg, respectively. Splenic lipid peroxidation (malondialdehyde content) was higher in all PHA-treated groups, whereas splenic protein oxidation (carbonyl content) increased in only the 0.05, 0.1, and 0.2 mmol/kg groups. The total iron content in the spleen also showed increases of 88, 135, 168, and 209% at PHA doses of 0.025, 0.05, 0.1, and 0.2 mmol/kg, respectively. These biochemical changes were accompanied by a dose-dependent vascular congestion in the spleen, a characteristic feature of aniline toxicity. Although the ratio of organ to body weight increased for both testes and heart at the highest dose, striking morphological changes were observed only in heart. The cardiac lesions consisted of a both acute and resolving multifocal subendocardial necrosis involving predominently the left ventricle. Our results suggest that PHA is a splenotoxin and thus contributes to the toxicity of aniline, while at a high dose, it is also cardiotoxic, perhaps due to anoxia associated with the marked methemoglobinemia. These results further support the involvement of oxidative stress in the splenotoxicity of aniline which may be caused by its reactive metabolite(s) such as PHA.

Effect of ebrotidine on the density of antral G‐cells in the gastric mucosa in the rat

Two groups of male rats were treated orally for 60 days with ebrotidine and cimetidine, used as reference standard, respectively. The dose used of both drugs was 500 mg/kg. A third group, used as control, received 10 ml/kg of an aqueous agar suspension. After receiving the last dose, the animals were killed by inhalation of CO2 in a sealed chamber and the stomachs were removed for histological preparation. The purpose of this study was to count antral G-cells throughout the gastric mucosa by light microscope. A PAP system-associated antigastrin immunohistochemical method was used for cell identification. Cell density, with respect to their location in the gastric mucosa and the treatments given, was calculated using image analysis techniques. The results showed that ebrotidine did not cause any significant differences in the density of the population of these cells compared with the control group, while cimetidine induced a significant proliferation of antral G-cells.

The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A.

We examined whether spectrally active phytochrome A (PhyA) and phytochrome B (PhyB) play specific roles in the induction of seed germination in Arabidopsis thaliana (L.) Heynh., using PhyA- and PhyB-null mutants, fre1-1 (A. Nagatani, J.W. Reed, J. Chory [1993] Plant Physiol 102: 269-277) and hy3-Bo64 (J. Reed, P.Nagpal, D.S. Poole, M. Furuya, J. Chory [1993] Plant Cell 5: 147-157). When dormant seeds of each genotype imbibed in the dark on aqueous agar plates, the hy3 (phyB) mutant did not germinate, whereas the fre1 (phyA) mutant germinated at a rate of 50 to 60%, and the wild type (WT) germinated at a rate of 60 to 70%. By contrast, seeds of all genotypes germinated to nearly 100% when plated in continuous irradiation with white or red light. When plated in continuous far-red light, however, frequencies of seed germination of the WT and the fre1 and hy3 mutants averaged 14, nearly 0, and 47%, respectively, suggesting that PhyB in the red-absorbing form prevents PhyA-dependent germination under continuous far-red light. When irradiated briefly with red or far-red light after imbibition for 1 h, a typical photoreversible effect on seed germination was observed in the fre1 mutant and the WT but not in the hy3 mutant. In contrast, when allowed to imbibe in the dark for 24 to 48 h and exposed to red light, the seed germination frequencies of the hy3 mutant were more than 40%. Immunoblot analyses of the mutant seeds showed that PhyB apoprotein accumulated in dormant seeds of the WT and the fre1 mutant as much as in the seeds that had imbibed. In contrast, PhyA apoprotein, although detected in etiolated seedlings grown in the dark for 5 d, was not detectable in the dormant seeds of the WT and the hy3 mutant. The above physiological and immunochemical evidence indicates that PhyB in the far-red-absorbing form was stored in the Arabidopsis seeds and resulted in germination in the dark. Hence, PhyA does not play any role in dark germination but induces germination under continuous irradiation with far-red light. Finally, we examined seeds from a signal transduction mutant, det1, and a det1/hy3 double mutant. The det1 seeds exhibited photoreversible responses of germination on aqueous agar plates, and the det1/hy3 double mutant seeds did not. Hence, DET1 is likely to act in a distinct pathway from PhyB in the photoregulation of seed germination.

Bacterial migration along solid surfaces.

An in vitro system was developed to study the migration of uropathogenic Escherichia coli strains. In this system an aqueous agar gel is placed against a solid surface, allowing the bacteria to migrate along the gel/solid surface interface. Bacterial strains as well as solid surfaces were characterized by means of water contact angle and zeta potential measurements. When glass was used as the solid surface, significantly different migration times for the strains investigated were observed. Relationships among the observed migration times of six strains, their contact angles, and their zeta potentials were found. Relatively hydrophobic strains exhibited migration times shorter than those of hydrophilic strains. For highly negatively charged strains shorter migration times were found than were found for less negatively charged strains. When the fastest-migrating strain with respect to glass was allowed to migrate along solid surfaces differing in hydrophobicity and charge, no differences in migration times were found. Our findings indicate that strategies to prevent catheter-associated bacteriuria should be based on inhibition of bacterial growth rather than on modifying the physicochemical character of the catheter surface.

The gas permeability coefficient of the cyanobacterial gas vesicle wall

Summary: The gas permeability coefficient of the cyanobacterial gas vesicle wall has been determined by comparing the concentration gradient of oxygen gas in a film of gas vesicles with the gradient in an underlying film of agar supported over an oxygen atmosphere. The gradients were determined with an oxygen microelectrode. The value of the gradient in aqueous agar was 0·81 of that in a suspension in which gas vesicles occupied 0·35 of the total volume. From this it was calculated that the notional diffusivity of oxygen through the gas vesicle was equivalent to 0·53 of the diffusivity in water. The permeability coefficient of the gas vesicle membrane is calculated to be k = 32 mm s -1, the rate coefficient for filling the gas vesicle by diffusion is a = 2·4 x 106 s -1 and the folding time for equilibration of gas into a gas vesicle is t e = 0·4 μs. The permeability coefficient is about 100-fold higher than the minimum value set by previous pressure rise experiments, and confirms that gas vesicles could not store gas. The measurements also show, however, that randomly oriented gas vesicles would not provide a diffusion channel with a diffusivity higher than that in water, although a layer of gas vesicles oriented with their long axes parallel to the diffusion gradient would provide a diffusivity 3·5-fold higher. The determination of the diffusivity was made with a theory, based on diffusion equations, which can be used in the determination of the diffusivity through other cell organelles.

Sonoluminescence in water and agar gels during irradiation with 0.75 mhz continuous-wave ultrasound

Free radicals, detected as light emissions (sonoluminescence), can be produced in both simple aqueous systems and agar gels by irradiation with 0.75 MHz continuous-wave (CW) ultrasound using acoustic pressures as low as 200 KPa. Although the acoustic pressures necessary for free radical formation in tap water gels (200 KPa), are considerably higher than those required for the formation of macroscopic visible bubbles (26 KPa), the sonoluminescence threshold (0.5 W/cm −2 SATA equivalent) falls at the lower end of the intensity range (0.5–3 W/cm −2) commonly used by ultrasonic physiotherapy equipment. In respect of the overall features of cavitation processes, agar gels appear to be suitable simple systems in which to model cavitation in vivo. However, cavitation processes leading to sonoluminescence are themselves complex as illustrated by the findings that small changes in ionic composition or pH have a significant effect on both the acoustic pressure threshold and the extent of sonoluminescence above this threshold.