Two of the most common stresses in natural environments, as well as in bioreactors, that are of importance in biofuel or bioterrorism contexts are pH and temperature stresses. Superoxide generation has been suspected as a possible reason for the effects of the above stresses, and superoxide is suspected to play a role in cell signaling. But, no information is available on a direct relationship between environmental stress and intracellular superoxide levels. We hypothesize that the exposure of cells to pH stress induces superoxide radicals, which leads to oxidative cellular damage, and thus it affects cells in culture. We tested the hypothesis on a model organism, Bacillus subtilis, which is well studied, and has relevance in biofuel and bioterrorism contexts. Bacillus subtilis cells were exposed to different pH-stress conditions (pH 5, 6, 8, or 9) and temperature-stress conditions (42, 45, 48, and 55 °C). Specific superoxide levels at pH 8 and 9 were 22% and 160%, respectively, higher than that of normal growth pH (pH 7), which was 6.48 ( 0.37 mmol (10 12 live cells) À1 . Superoxide generation due to pH stress has not been reported thus far in the literature. Although detection of superoxide induced by temperature stress has been reported, it has not been quantified. When Bacillus subtilis cells were exposed to 42, 45, 48, and 55 °C for 1 h, the specific intracellular superoxide levels were 52%, 150%, 220%, and 314%, respectively, higher than the value at normal growth temperature, 37 °C. The extent of intracellular lipid peroxidation was higher under the stressed conditions. The mechanism for alkaline pH-stress-induced superoxide generation seems to be the continuation of metabolic activities even though the growth is arrested. The mode of temperature-stress-mediated cell death is necrosis, and the extent of cell death is correlated with the specific intracellular superoxide level.
Liquid phase oxygen supply strategy (LPOS), in which hydrogen peroxide (H(2)O(2)) is used to supply oxygen to the bioreactor, leads to low cell productivity despite high specific productivities of relevant metabolites. We hypothesized that high H(2)O(2) concentrations in the feed-zone led to local cell death, which in turn, lead to lower cell productivity. To test the hypothesis, a mathematical model was developed. Bacillus subtilis 168 was used as the model system in this study. The model simulations of cell concentrations in the bioreactor-zone were verified with the experimental results. The feed-zone H(2)O(2) concentrations remained 12-14 times higher than bulk bioreactor concentrations. The high local concentrations are expected to cause local cell killing, which explains the decrease in overall cell production by 50% at 300 rpm compared to conventional cultivation. Further, among the four different feed strategies studied using the model, dissolved oxygen (DO) controlled H(2)O(2) feed strategy caused least local cell killing and improved overall cell production by 34%.
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