Advances in High Pressure Bioscience and Biotechnology: by A. A. Yayanos (auth.), Professor Dr. Horst Ludwig (eds.)

By A. A. Yayanos (auth.), Professor Dr. Horst Ludwig (eds.)

At current, there's starting to be curiosity in excessive strain bioscience and biotechnology. The actions are approximately both allotted among primary study and purposes. With unique paintings on marine and terrestrial microbiology, biochemicstry, molecular biology, deep-sea diving, nutrients technology and different business functions, this booklet covers the full variety of present excessive strain bioscience. "Advances in excessive strain Bioscience and Biotechnology" could be welcomed through all business and educational researchers who're operating during this field.

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Extra resources for Advances in High Pressure Bioscience and Biotechnology: Proceedings of the International Conference on High Pressure Bioscience and Biotechnology, Heidelberg, August 30 - September 3, 1998

Sample text

2-D analysis of protein synthesis was performed according to [2]. 32 K. Hauben et al. 1 Multiple Stress Resistance of Mutants Parent strain MGI655 and pressure resistant mutants LMMIOIO and LMMI030 were analysed for their resistance against heat, acid and reactive oxygen species. Decimal reduction values (D-values) for heat and acid inactivation are given in Table I. Oxidative stress was imposed by the superoxide generator plumbagin (Fig. I). Superoxide killing did not follow fIrst-order kinetics, which made calculation of D-values impossible.

As the amount of ribosome damage increased, proportionally more cells would have the ribosomes reduced to below the threshold. Eventually, when most cells had ribosome numbers below the threshold, further decreases in RAE could not result in further cell death. This model would be expected to result in a sigmoidal relationship between cell viability and RAE. The linear relationship observed suggests that cell death and ribosome damage is an "all-or-nothing" phenomenon. That is, the ribosomes in an individual cell remain relatively undamaged until they are all destroyed together in a single event.

This bacterium displays optimal growth at a temperature of 8 DC and at a pressure of 30 MPa [1]. Pressure-regulated operon and genes have been recognized and characterized in this bacterium [2, 3]. CspA has been identified as the major cold shock protein in E. coli. A family of cspAs sharing highly conserved sequences (>45% identity) has been recognized in a variety of Gram-positive and Gram-negative bacteria. CspA functions as a RNA chaperone and as a transcriptional regulator for itself and for other cold shock genes in E.

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