Abstract
We have identified the grpE gene product as the B25.3 heat shock protein of Escherichia coli on the following evidence: (i) a protein similar in size and isoelectric point to B25.3 was induced after infection of UV-irradiated bacteria by lambda grpE+ transducing phage, (ii) mutant phage lambda grpE40, isolated by its inability to propagate on grpE280 bacteria, failed to induce the synthesis of the B25.3 protein, and (iii) lambda grpE+ revertants, derived from phage grpE40 as able to propagate on grpE280 bacteria, simultaneously recovered the ability to induce synthesis of the B25.3 protein. In addition, we show that E. coli bacteria carrying the grpE280 mutation are temperature sensitive for bacterial growth at 43.5 degrees C. Through transductional analysis and temperature reversion experiments, it was demonstrated that the grpE280 mutation is responsible for both the inability of lambda to replicate at any temperature tested and the lack of colony formation at high temperature. At the nonpermissive temperature the rates of synthesis of DNA and RNA were reduced in grpE280 bacteria.
MeSH Terms
Bacterial Proteins/biosynthesis,genetics,physiology
Bacteriophage lambda/genetics,physiology
DNA Replication
DNA, Bacterial/biosynthesis
Escherichia coli/genetics,growth & development,metabolism
Genes, Bacterial
Heat-Shock Proteins/genetics,physiology
Mutation
RNA, Bacterial/biosynthesis
Temperature
Transduction, Genetic
Virus Replication
Chemicals
Bacterial Proteins
DNA, Bacterial
Heat-Shock Proteins
RNA, Bacterial
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ang D
Chandrasekhar G N
Zylicz M
Georgopoulos C
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