Investigation into the Physiological State of Heat Stressed Escherichia coli Used in the Evaluation Testing of an Intrinsic Fluorescence-Based RMM.

Author:

IRIE KANAMI1,SCOTT ALLISON2,HASEGAWA NORIO1

Affiliation:

1. Azbil Corporation

2. Azbil North America Research and Development, Inc.

Publisher

The Society for Antibacterial and Antifungal Agents, Japan

Subject

Public Health, Environmental and Occupational Health,Applied Microbiology and Biotechnology

Reference61 articles.

1. Allwood, M. C., and Russell, A. D. (1970) Mechanisms of thermal injury in nonsporulating bacteria. Adv. Appl. Microbiol., 12, 89-119.

2. Bolivar, F., Rodriguez, R. L., Greene, P. J., Betlach, M. C., Heyneker, H. L., Boyer, H. W., Crosa, J. H., and Falkow, S. (1977) Construction and characterization of new cloning vehicle. II. A multipurpose cloning system. Gene, 2, 95-113.

3. Bukau, B., and Walker, G. C. (1989) Cellular defects caused by deletion of the Escherichia coli dnaK gene indicate roles for heat shock protein in normal metabolism. J. Bacteriol., 171, 2337-2346.

4. Calloni, G., Chen, T., Schermann, S. M., Chang, H., Genevaux, P., Agostini, F., Tartaglia, G. G., Hayer-Hartl, M., and Hartl, F. U. (2012) DnaK functions as a central hub in the E. coli chaperone network. Cell Rep., 1, 251-264.

5. Cha, H. J., Srivastava, R., Vakharia, V. N., Rao, G., and Bentley, W. (1999) Green fluorescent protein as a noninvasive stress probe in resting Escherichia coli cells. Appl. Environ. Microbiol., 65, 409-414.

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