Abstract
The era gene of Escherichia coli encodes a GTP-binding protein which has similarities to elongation factor Tu and the Saccharomyces cerevisiae RAS protein. To investigate its function, mutations affecting era were isolated. A mini-Tn10 insertion, which truncated 22 amino acids from the COOH end of Era, did not affect cell growth. By using this mini-Tn10 insert as a coselectable marker, a temperature-sensitive lethal era mutant was isolated by localized mutagenesis using P1 phage transduction. A single-base G to A change was found at position 23, causing a tyrosine residue to be substituted for the cysteine residue at position 8 (era-770), in addition to the COOH-terminal mini-Tn10 disruption. Both alterations were necessary for the temperature-sensitive phenotype. Purified Era-770 mutant protein exhibited reduced binding to GTP compared with that of the wild-type Era protein.
MeSH Terms
Amino Acid Sequence
Bacteriophage lambda/genetics
Base Sequence
Chromosomes, Bacterial
Escherichia coli/genetics
GTP-Binding Proteins/genetics
Genes
Genes, Bacterial
Genes, Lethal
Genetic Complementation Test
Genotype
Molecular Sequence Data
Mutation
Phenotype
Plasmids
Restriction Mapping
Temperature
Transduction, Genetic
Chemicals
GTP-Binding Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Inada T
Department of Tumor Biology, University of Tokyo, Japan.
Kawakami K
Chen S M
Takiff H E
Court D L
Nakamura Y
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