This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chu, H.
Right arrow Articles by Walker, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chu, H.
Right arrow Articles by Walker, J. R.

 Previous Article  |  Next Article 

J Bacteriol. 1977 October; 132(1): 151-158
Copyright © 1977 American Society for Microbiology. All Rights Reserved.

Physiological Effects of Growth of an Escherichia coli Temperature-Sensitive dnaZ Mutant at Nonpermissive Temperatures

Herman Chu, Margaret M. Malone, William G. Haldenwang and James R. Walker

1 Department of Microbiology, The University of Texas at Austin, Austin, Texas 78712

ABSTRACT

The physiological effects of incubation at nonpermissive temperatures of Escherichia coli mutants that carry a temperature-sensitive dnaZ allele [dnaZ(Ts)2016] were examined. The temperature at which the dnaZ(Ts) protein becomes inactivated in vivo was investigated by measurements of deoxyribonucleic acid (DNA) synthesis at temperatures intermediate between permissive and nonpermissive. DNA synthesis inhibition was reversible by reducing the temperature of cultures from 42 to 30°C; DNA synthesis resumed immediately after temperature reduction and occurred even in the presence of chloramphenicol. Inasmuch as DNA synthesis could be resumed in the absence of protein synthesis, we concluded that the protein product of the dnaZ allele (Ts)2016 is renaturable. Cell division, also inhibited by 42°C incubation, resumed after temperature reduction, but the length of time required for resumption depended on the duration of the period at 42°C. Replicative synthesis of cellular DNA, examined in vitro in toluene-permeabilized cells, was temperature sensitive. Excision repair of ultraviolet light-induced DNA lesions was partially inhibited in dnaZ(Ts) cells at 42°C. The dnaZ+ product participated in the synthesis of both Okazaki piece (8–12S) and high-molecular-weight DNA. During incubation of dnaZ(Ts)({lambda}) lysogens at 42°C, prophage induction occurred, and progeny phage were produced during subsequent incubation at 30°C. The temperature sensitivity of both DNA synthesis and cell division in the dnaZ(Ts)2016 mutant was suppressed by high concentrations of sucrose, lactose, or NaCl. Incubation at 42°C was neither mutagenic nor antimutagenic for the dnaZ(Ts) mutant.


J Bacteriol. 1977 October; 132(1): 151-158
Copyright © 1977 American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Jarvis, T. C., Beaudry, A. A., Bullard, J. M., Ochsner, U., Dallmann, H. G., McHenry, C. S. (2005). Discovery and Characterization of the Cryptic {Psi} Subunit of the Pseudomonad DNA Replicase. J. Biol. Chem. 280: 40465-40473 [Abstract] [Full Text]  
  • Jarvis, T. C., Beaudry, A. A., Bullard, J. M., Janjic, N., McHenry, C. S. (2005). Reconstitution of a Minimal DNA Replicase from Pseudomonas aeruginosa and Stimulation by Non-cognate Auxiliary Factors. J. Biol. Chem. 280: 7890-7900 [Abstract] [Full Text]  
  • Skovgaard, O., Lobner-Olesen, A. (2005). Reduced initiation frequency from oriC restores viability of a temperature-sensitive Escherichia coli replisome mutant. Microbiology 151: 963-973 [Abstract] [Full Text]  
  • Walker, J. R., Hervas, C., Ross, J. D., Blinkova, A., Walbridge, M. J., Pumarega, E. J., Park, M.-O., Neely, H. R. (2000). Escherichia coli DNA Polymerase III tau - and gamma -Subunit Conserved Residues Required for Activity In Vivo and In Vitro. J. Bacteriol. 182: 6106-6113 [Abstract] [Full Text]