Nucleotide sequence of the secA gene and secA(Ts) mutations preventing protein export in Escherichia coli
- PMID: 2841285
- PMCID: PMC211308
- DOI: 10.1128/jb.170.8.3404-3414.1988
Nucleotide sequence of the secA gene and secA(Ts) mutations preventing protein export in Escherichia coli
Abstract
The DNA sequence of the secA gene, essential for protein export in Escherichia coli, was determined and found to encode a hydrophilic protein of 901 amino acid residues with a predicted molecular weight of 101,902, consistent with its previously determined size and subcellular location. Sequence analysis of 9 secA(Ts) mutations conferring general protein export and secA regulatory defects revealed that these mutations were clustered in three specific regions within the first 170 amino acid residues of the SecA protein and were the result of single amino acid changes predicted to be severely disruptive of protein structure and function. The DNA sequence immediately upstream of secA was shown to encode a previously inferred gene, gene X. Sequence analysis of a conditionally lethal amber mutation, am109, previously inferred to be located proximally in the secA gene, revealed that it was located distally in gene X and was conditionally lethal due to its polar effect on secA expression. This and additional evidence are presented indicating that gene X and secA are cotranscribed.
Similar articles
-
The sec and prl genes of Escherichia coli.J Bioenerg Biomembr. 1990 Jun;22(3):291-310. doi: 10.1007/BF00763169. J Bioenerg Biomembr. 1990. PMID: 2202721 Review.
-
Isolation and analysis of dominant secA mutations in Escherichia coli.J Bacteriol. 1991 Jan;173(2):860-8. doi: 10.1128/jb.173.2.860-868.1991. J Bacteriol. 1991. PMID: 1824769 Free PMC article.
-
Identification of a gene fragment which codes for the 364 amino-terminal amino acid residues of a SecA homologue from Bacillus subtilis: further evidence for the conservation of the protein export apparatus in gram-positive and gram-negative bacteria.Mol Gen Genet. 1991 Sep;228(3):417-23. doi: 10.1007/BF00260635. Mol Gen Genet. 1991. PMID: 1832735
-
Dual regulation of Escherichia coli secA translation by distinct upstream elements.J Mol Biol. 1997 Jan 17;265(2):128-41. doi: 10.1006/jmbi.1996.0723. J Mol Biol. 1997. PMID: 9020977
-
Genetic studies on protein export in bacteria.Curr Top Microbiol Immunol. 1986;125:5-27. doi: 10.1007/978-3-642-71251-7_2. Curr Top Microbiol Immunol. 1986. PMID: 3091324 Review. No abstract available.
Cited by
-
SecA: a potential antimicrobial target.Future Med Chem. 2015;7(8):989-1007. doi: 10.4155/fmc.15.42. Future Med Chem. 2015. PMID: 26062397 Free PMC article. Review.
-
The sec and prl genes of Escherichia coli.J Bioenerg Biomembr. 1990 Jun;22(3):291-310. doi: 10.1007/BF00763169. J Bioenerg Biomembr. 1990. PMID: 2202721 Review.
-
Sites of interaction between SecA and the chaperone SecB, two proteins involved in export.Protein Sci. 2004 Apr;13(4):1124-33. doi: 10.1110/ps.03410104. Epub 2004 Mar 9. Protein Sci. 2004. PMID: 15010547 Free PMC article.
-
The prediction of novel multiple lipid-binding regions in protein translocation motor proteins: a possible general feature.Cell Mol Biol Lett. 2011 Mar;16(1):40-54. doi: 10.2478/s11658-010-0036-y. Epub 2010 Oct 19. Cell Mol Biol Lett. 2011. PMID: 20957445 Free PMC article.
-
Comparative characterization of SecA from the alpha-subclass purple bacterium Rhodobacter capsulatus and Escherichia coli reveals differences in membrane and precursor specificity.J Bacteriol. 1997 Jun;179(12):4003-12. doi: 10.1128/jb.179.12.4003-4012.1997. J Bacteriol. 1997. PMID: 9190818 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases