Abstract:Microcalorimetry is a useful tool for monitoring the growth behavior of microorganisms. In this study, microcalorimetry was used to investigate the effects of nitrogen, air, oxygen, nitrous oxide, argon, and krypton at high pressure on the growth of the yeast Saccharomyces cerevisiae. Growth thermograms (metabolic heat vs. incubation time) were generated to estimate metabolic activity under compressed gases and to determine the 50% inhibitory pressure (IP(50)) and minimum inhibitory pressure (MIP), which are r… Show more
“…While nitrogen and argon retard a growth in range of 20-35 MPa, oxygen, nitrous oxide and air inhibit growth at pressures of less than 1 MPa probably due to oxidative stress. 60) Exposure of yeast cells to temperatures higher than the optimum for growth (e.g., 42 C) enhances the synthesis of Hsps and the metabolism of trehalose. 61) Then the cells acquire the ability to survive under lethally high temperatures (e.g., 50 C) as well as under other stressful conditions.…”
Section: Recent Advanced Studies Of the Effects Of High Pressurementioning
“…While nitrogen and argon retard a growth in range of 20-35 MPa, oxygen, nitrous oxide and air inhibit growth at pressures of less than 1 MPa probably due to oxidative stress. 60) Exposure of yeast cells to temperatures higher than the optimum for growth (e.g., 42 C) enhances the synthesis of Hsps and the metabolism of trehalose. 61) Then the cells acquire the ability to survive under lethally high temperatures (e.g., 50 C) as well as under other stressful conditions.…”
Section: Recent Advanced Studies Of the Effects Of High Pressurementioning
“…The specific growth activities at various pressures were fitted after they were plotted against gas pressure. See other literatures for more details on the quantification of growth inhibition [3]. We determined both the 50% inhibitory pressure (IP 50 ), which reduces the growth of yeast by 50% and the minimum inhibitory pressure (MIP) at which yeast growth is completely inhibited.…”
Section: Ip 50 and Mip Values For Gaseous C2 Compoundsmentioning
confidence: 99%
“…Recently, we have proposed a new method to quantify the toxicity of various gases through observing the inhibition of yeast growth under high-pressure gases [3].Generally, at normal pressure, the solubilities of gases such as oxygen, nitrogen, hydrocarbon gases are low in aqueous systems. It is therefore difficult to evaluate the effects of gases on yeast growth in aqueous medium.…”
“…As cellular concentration of inert gas increases under pressure, physiological perturbations occur, leading to growth inhibition of various organisms (Arao et al, 2005). Mechanical damage in cells pressurized in the presence of inert gas and rapidly decompressed have also been described (Gottlieb and Adachi, 2000;Yandell and McCarthy, 1980).…”
Dried microorganisms are particularly resistant to high hydrostatic pressure effects. In this study, the survival of Saccharomyces cerevisiae was studied under pressure applied in different ways. Original processes and devices were purposely developed in our laboratory for long-term pressurization. Dried and wet yeast powders were submitted to high-pressure treatments (100-150 MPa for 24-144 h at 25 degrees C) through liquid media or inert gas. These powders were also pressurized after being vacuum-packed. In the case of wet yeasts, the pressurization procedure had little influence on the inactivation rate. In this case, inactivations were mainly due to hydrostatic pressure effects. Conversely, in the case of dried yeasts, inactivation was highly dependent on the treatment scheme. No mortality was observed when dried cells were pressurized in a non-aqueous liquid medium, but when nitrogen gas was used as the pressure-transmitting fluid, the inactivation rate was found to be between 1.5 and 2 log for the same pressure level and holding time. Several hypotheses were formulated to explain this phenomenon: the thermal effects induced by the pressure variations, the drying resulting from the gas pressure release and the sorption and desorption of the gas in cells. The highest inactivation rates were obtained with vacuum-packed dried yeasts. In this case, cell death occurred during the pressurization step and was induced by shear forces. Our results show that the mechanisms at the origin of cell death under pressure are strongly dependent on the nature of the pressure-transmitting medium and the hydration of microorganisms.
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