Abstract:Foster, John
W. (University of Georgia, Athens),
Robert M. Cowan, and Ted A. Maag
. Rupture of bacteria by explosive decompression. J. Bacteriol.
83:
330–334. 1962.—A device is described for instantaneously rupturing bacteria and other cells in a closed system under controlled conditions by explosive decompression. With this device, 31 to 59% of
Serratia marcescens
, ranging up to 20 mg (dry wt) of cells per ml, were ruptured a… Show more
“…Because of this sudden pressure release, the gas expands within the cells and part of the cell mechanically ruptures like a popped balloon. 30,[32][33][34][35] Solubilization of CO 2 in the lipid-rich microbial cells is the initial step of cell disruption. As a result, it is important to have a deep insight of CO 2 -cell interaction to design an efficient cell disruption process, which can be obtained through the knowledge of solubility of CO 2 in triglycerides.…”
“…Because of this sudden pressure release, the gas expands within the cells and part of the cell mechanically ruptures like a popped balloon. 30,[32][33][34][35] Solubilization of CO 2 in the lipid-rich microbial cells is the initial step of cell disruption. As a result, it is important to have a deep insight of CO 2 -cell interaction to design an efficient cell disruption process, which can be obtained through the knowledge of solubility of CO 2 in triglycerides.…”
“…To date, application of SCF in cell disruption (SC disruption) over a wide range of operating conditions has been confined to yeasts (26, 32 − 35 ) and a few bacteria (27, 36, 37). The process involves a sudden release of the applied SC‐CO 2 pressure that results in its penetration into the cells.…”
This research focuses on the disruption of the gram-negative bacterium Ralstonia eutropha cells by supercritical CO2 for poly(R-hydroxybutyrate) (PHB) recovery. The variables affecting cell disruption such as drying strategy, type of modifier, and cultivation time, as well as operating pressure, temperature, and repeated release of supercritical CO2 pressure, have been studied. Effect of this disruption technique on PHB molecular mass was also investigated. PHB recovery was examined using a combination of this method and chemical pretreatments. For salt pretreatment, the cells were exposed to 140 mM NaCl and heat (60 degrees C, 1 h). The cells were also exposed to 0.2-0.8% (w/w) NaOH to examine the effect of alkaline pretreatment. Bacterial cells treated in growth phase exhibited less resistance to disruption than nutrient-limited cells in the stationary phase. It was also found that the wet cells could be utilized to recover PHB, but purity of the product was lower than that obtained from freeze-dried cells. Pretreatment with a minimum of 0.4% (w/w) NaOH was necessary to enable complete disruption with two times pressure release. Salt pretreatment was less effective; however, disruption was improved by the application of alkaline shock. The proposed method is economic and comparable with other recovery methods in terms of the percentage of PHB recovery and energy consumption, while it is environmentally more benign.
“…filamentation) (ZoBell and Cobet 1964), and are increased in their susceptibility towards some antibiotics (Marquis 1973). Additionally, rapid compression and decompression (up to 500 bar) has been reported to reduce the viability of some microorganisms (Foster et al 1962). T h e pressures required in these studies to affect microbial physiologies were, however, significantly greater than those associated with centrifugation.…”
Sub-lethal injury of Escherichia coli has been detected following centrifugation at g-forces between 5 and 30 kg. The extent of injury was measured either as a reduction in colony forming ability when plated onto NaCl-containing plates (2% w/v), or as a reduction in transformation efficiency associated with plasmid pBR322 encoding ampicillin resistance. In both cases, the extent of sub-lethal injury was found to increase with increasing centrifugal force and probably reflects structural damage to the cell envelope.
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