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PMID: 2549050 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of the spoT gene of Escherichia coli.

The Journal of biological chemistry ·Vol. 264 ·No. 25 ·1989-09-05 ·Pages 15074-82

Sarubbi E, Rudd KE, Xiao H, Ikehara K, Kalman M, Cashel M

Abstract

The Escherichia coli spoT gene encodes a guanosine-3',5'-bispyrophosphate (ppGpp) 3'-pyrophosphohydrolase known to be responsible for cellular (ppGpp) degradation. The DNA sequence of the spoT region is presented. The spoT gene is deduced to be 702 codons long, with a probable UUG initiation codon, and a deduced mass of 79,342 daltons. Two spoT mutations (spoT202 and spoT203) have been localized to an open reading frame by complementation of function as well as by genetic marker rescue. The ability to overexpress the spoT gene is limited, but enough ppGppase activity can be made to reverse ppGpp accumulation during the stringent response to amino acid starvation. The spoT gene is located within a larger spo operon and is flanked by two smaller genes. The first gene in the operon encodes omega, a protein that copurifies with RNA polymerase (Gentry, D. R., and Burgess, R. R. (1986) Gene (Amst.) 48, 33-40). The spoT gene is the second gene in the operon; it is followed by a third open reading frame deduced to encode a protein with a mass of 25,343 daltons. Insertion of a kanamycin resistance gene in the omega gene reduces spoT gene expression as judged by lowered ppGppase activity, relA-dependent reduction of growth rate, and abolition of spoT mutant complementation activity. These effects are reversed by expression of the spoT gene, but not the omega gene, in trans. Transcription of the spo operon occurs in a clockwise direction on the E. coli chromosome and is probably directed by at least two promoters.

MeSH Terms
Alleles Amino Acid Sequence Bacterial Proteins/genetics,isolation & purification,metabolism Base Sequence Chromosome Deletion Chromosome Mapping DNA Transposable Elements DNA, Bacterial/isolation & purification Escherichia coli/enzymology,genetics GTP Phosphohydrolases/antagonists & inhibitors,genetics,isolation & purification Gene Expression Regulation Genes, Bacterial Genetic Complementation Test Genetic Markers Molecular Sequence Data Peptide Chain Initiation, Translational Phosphoric Monoester Hydrolases/genetics Plasmids Promoter Regions, Genetic Transcription, Genetic
Chemicals
Bacterial Proteins DNA Transposable Elements DNA, Bacterial Genetic Markers Phosphoric Monoester Hydrolases GTP Phosphohydrolases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sarubbi E
Section on Molecular Regulation, National Institute of Child Health and Human Development, Bethesda, Maryland 20892.
Rudd K E
Xiao H
Ikehara K
Kalman M
Cashel M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1989-09-05
Pages
15074-82
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
J04976
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