The gene encoding the elongation factor P protein is essential for viability and is required for protein synthesis - PubMed (original) (raw)
. 1997 Dec 19;272(51):32254-9.
doi: 10.1074/jbc.272.51.32254.
Affiliations
- PMID: 9405429
- DOI: 10.1074/jbc.272.51.32254
Free article
The gene encoding the elongation factor P protein is essential for viability and is required for protein synthesis
H Aoki et al. J Biol Chem. 1997.
Free article
Abstract
Elongation factor P (EFP) is a protein that stimulates the peptidyltransferase activity of fully assembled 70 S prokaryotic ribosomes and enhances the synthesis of certain dipeptides initiated by N-formylmethionine. This reaction appears conserved throughout species and is promoted in eukaryotic cells by a homologous protein, eIF5A. Here we ask whether the Escherichia coli gene encoding EFP is essential for cell viability. A kanamycin resistance (KanR) gene was inserted near the N-terminal end of the efp gene and was cloned into a plasmid, pMAK705, that has a temperature-sensitive origin of replication. After transformation into a recA+ E. coli strain, temperature-sensitive mutants were isolated, and their chromosomal DNA was sequenced. Mutants containing the efp-KanR gene in the chromosome grew at 33 degrees C only in the presence of the wild-type copy of the efp gene in the pMAK705 plasmid and were unable to grow at 44 degrees C. Incorporation of various isotopes in vivo suggests that translation is impaired in the efp mutant at 44 degrees C. At 44 degrees C, mutant cells are severely defective in peptide-bond formation. We conclude that the efp gene is essential for cell viability and is required for protein synthesis.
Similar articles
- The chvH locus of Agrobacterium encodes a homologue of an elongation factor involved in protein synthesis.
Peng WT, Banta LM, Charles TC, Nester EW. Peng WT, et al. J Bacteriol. 2001 Jan;183(1):36-45. doi: 10.1128/JB.183.1.36-45.2001. J Bacteriol. 2001. PMID: 11114898 Free PMC article. - In vivo selection of conditional-lethal mutations in the gene encoding elongation factor G of Escherichia coli.
Hou Y, Lin YP, Sharer JD, March PE. Hou Y, et al. J Bacteriol. 1994 Jan;176(1):123-9. doi: 10.1128/jb.176.1.123-129.1994. J Bacteriol. 1994. PMID: 8282687 Free PMC article. - Peptide bond synthesis: function of the efp gene product.
Ganoza MC, Aoki H. Ganoza MC, et al. Biol Chem. 2000 Jul;381(7):553-9. doi: 10.1515/BC.2000.071. Biol Chem. 2000. PMID: 10987361 - Divergent protein motifs direct elongation factor P-mediated translational regulation in Salmonella enterica and Escherichia coli.
Hersch SJ, Wang M, Zou SB, Moon KM, Foster LJ, Ibba M, Navarre WW. Hersch SJ, et al. mBio. 2013 Apr 23;4(2):e00180-13. doi: 10.1128/mBio.00180-13. mBio. 2013. PMID: 23611909 Free PMC article. - Prokaryotic gene expression in vitro: transcription-translation coupled systems.
Cenatiempo Y. Cenatiempo Y. Biochimie. 1986 Apr;68(4):505-15. doi: 10.1016/s0300-9084(86)80195-x. Biochimie. 1986. PMID: 3091086 Review.
Cited by
- Post-translational modification by β-lysylation is required for activity of Escherichia coli elongation factor P (EF-P).
Park JH, Johansson HE, Aoki H, Huang BX, Kim HY, Ganoza MC, Park MH. Park JH, et al. J Biol Chem. 2012 Jan 20;287(4):2579-90. doi: 10.1074/jbc.M111.309633. Epub 2011 Nov 29. J Biol Chem. 2012. PMID: 22128152 Free PMC article. - Suppression of Ribosomal Pausing by eIF5A Is Necessary to Maintain the Fidelity of Start Codon Selection.
Manjunath H, Zhang H, Rehfeld F, Han J, Chang TC, Mendell JT. Manjunath H, et al. Cell Rep. 2019 Dec 3;29(10):3134-3146.e6. doi: 10.1016/j.celrep.2019.10.129. Cell Rep. 2019. PMID: 31801078 Free PMC article. - Translation elongation factor P (EF-P).
Hummels KR, Kearns DB. Hummels KR, et al. FEMS Microbiol Rev. 2020 Mar 1;44(2):208-218. doi: 10.1093/femsre/fuaa003. FEMS Microbiol Rev. 2020. PMID: 32011712 Free PMC article. Review. - One-carbon metabolism, folate, zinc and translation.
Danchin A, Sekowska A, You C. Danchin A, et al. Microb Biotechnol. 2020 Jul;13(4):899-925. doi: 10.1111/1751-7915.13550. Epub 2020 Mar 9. Microb Biotechnol. 2020. PMID: 32153134 Free PMC article. - The roles of RNA in the synthesis of protein.
Moore PB, Steitz TA. Moore PB, et al. Cold Spring Harb Perspect Biol. 2011 Nov 1;3(11):a003780. doi: 10.1101/cshperspect.a003780. Cold Spring Harb Perspect Biol. 2011. PMID: 21068149 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases