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

At current, there's transforming into curiosity in excessive strain bioscience and biotechnology. The actions are approximately both disbursed among basic examine and purposes. With unique paintings on marine and terrestrial microbiology, biochemicstry, molecular biology, deep-sea diving, nutrition technological know-how and different commercial purposes, this publication covers the total diversity of present excessive strain bioscience. "Advances in excessive strain Bioscience and Biotechnology" could be welcomed by way of all commercial and educational researchers who're operating during this field.

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Additional info 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

Example text

59(3), 506-531. [8] Yamamori, T. , (1980); Temperature-induced synthesis of specific proteins in Escherichia coli: evidence for transcriptional control; 1. , 142,843-851. , Fujii, S. , 416, 1-5. Multiple Stress Resistance in Pressure Resistant Escherichia coli Mutants K. Hauben, T. Nystrom, A. Farewell and C. Michiels Laboratory of Food Microbiology, Katholieke Universiteit Leuven, Kard. be Abstract. The E. coli mutants LMMIOIO and LMM1030, which were previously isolated on the basis of their pressure resistance, are demonstrated here to show cross-resistance to acid, reactive oxygen and/or heat.

1). Whatever the conditions, yeast cells pressurized in low aw medium were more resistant to high-pressure treatment (about 3 log). 5 log). Although kinetics of aw variation was essential for cell survival at low aw [5], no significant differences were observed between osmotic shock and slope. The inactivation difference between low aw culture and cells recently stressed pointed out the importance of the proximity between the two treatments. A complete study using a variable delay has been carried out with binary medium (Fig.

Horikoshi samplers. The samples were carried to the sea-surface without temperature changes but with pressure changes. Most of the samples obtained were apportioned into 2 ml sterilized serum tubes and placed in a liquid nitrogen tank (-150 QC). S. YOKOSUKA. Total DNA was extracted from the sediment samples by a modification of the methods of Herrick et al. [1]. 16S rDNAs were PCR amplified and sequenced, and subsequently phylogenetic ally analyzed. Barophilic bacteria were isolated from the sediment according to the method described by Kato et al.

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