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. 1982 Sep;151(3):1391–1396. doi: 10.1128/jb.151.3.1391-1396.1982

A gene coding for a periplasmic protein is located near the locus for termination of chromosome replication in Escherichia coli.

S Harayama, G L Hazelbauer
PMCID: PMC220419  PMID: 7050089

Abstract

Hybrid plasmids carrying trg, the genetic locus in closest proximity to terC, coded for several polypeptides in addition to the Trg protein. Polypeptides of 59,000 and 61,000 apparent molecular weight were the most prominent products synthesized in minicells containing the hybrid plasmids. Analysis of the effects of deletions generated by a restriction endonuclease identified a region of DNA immediately adjacent to trg as the putative gene coding for the two polypeptides. Studies with whole cells and minicells showed that the 59,000-dalton polypeptide is a periplasmic protein. Analysis by limited proteolysis indicated that the two polypeptides are related, and a number of observations support the notion that the 61,000-dalton protein is a precursor form of the 59,000-dalton mature exported protein. The identification and characterization of a protein, in addition to Trg, which is produced by a gene in close proximity to terC emphasizes the fact that the region does contain intact and active genes.

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Selected References

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  1. Anilionis A., Ostapchuk P., Riley M. Identification of a second cryptic lambdoid prophage locus in the E. coli K12 chromosome. Mol Gen Genet. 1980;180(2):479–481. doi: 10.1007/BF00425865. [DOI] [PubMed] [Google Scholar]
  2. Bachmann B. J., Low K. B. Linkage map of Escherichia coli K-12, edition 6. Microbiol Rev. 1980 Mar;44(1):1–56. doi: 10.1128/mr.44.1.1-56.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bachmann B. J., Low K. B., Taylor A. L. Recalibrated linkage map of Escherichia coli K-12. Bacteriol Rev. 1976 Mar;40(1):116–167. doi: 10.1128/br.40.1.116-167.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bitner R. M., Kuempel P. L. P1 transduction map spanning the replication terminus of Escherichia coli K12. Mol Gen Genet. 1981;184(2):208–212. doi: 10.1007/BF00272906. [DOI] [PubMed] [Google Scholar]
  5. Bitner R. M., Kuempel P. L. P1 transduction mapping of the trg locus in rac+ and rac strains of Escherichia coli K-12. J Bacteriol. 1982 Feb;149(2):529–533. doi: 10.1128/jb.149.2.529-533.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bouché J. P., Gélugne J. P., Louarn J., Louarn J. M., Kaiser K. Relationships between the physical and genetic maps of a 470 x 10(3) base-pair region around the terminus of Escherichia coli K12 DNA replication. J Mol Biol. 1982 Jan 5;154(1):21–32. doi: 10.1016/0022-2836(82)90414-4. [DOI] [PubMed] [Google Scholar]
  7. Clarke L., Carbon J. A colony bank containing synthetic Col El hybrid plasmids representative of the entire E. coli genome. Cell. 1976 Sep;9(1):91–99. doi: 10.1016/0092-8674(76)90055-6. [DOI] [PubMed] [Google Scholar]
  8. Daniels C. J., Bole D. G., Quay S. C., Oxender D. L. Role for membrane potential in the secretion of protein into the periplasm of Escherichia coli. Proc Natl Acad Sci U S A. 1981 Sep;78(9):5396–5400. doi: 10.1073/pnas.78.9.5396. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Date T., Goodman J. M., Wickner W. T. Procoat, the precursor of M13 coat protein, requires an electrochemical potential for membrane insertion. Proc Natl Acad Sci U S A. 1980 Aug;77(8):4669–4673. doi: 10.1073/pnas.77.8.4669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Enequist H. G., Hirst T. R., Harayama S., Hardy S. J., Randall L. L. Energy is required for maturation of exported proteins in Escherichia coli. Eur J Biochem. 1981 May 15;116(2):227–233. doi: 10.1111/j.1432-1033.1981.tb05323.x. [DOI] [PubMed] [Google Scholar]
  11. Engström P., Hazelbauer G. L. Multiple methylation of methyl-accepting chemotaxis proteins during adaptation of E. coli to chemical stimuli. Cell. 1980 May;20(1):165–171. doi: 10.1016/0092-8674(80)90244-5. [DOI] [PubMed] [Google Scholar]
  12. Fouts K. E., Barbour S. D. Insertion of transposons through the major cotransduction gap of Escherichia coli K-12. J Bacteriol. 1982 Jan;149(1):106–113. doi: 10.1128/jb.149.1.106-113.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Harayama S., Palva E. T., Hazelbauer G. L. Transposon-insertion mutants of Escherichia coli K12 defective in a component common to galactose and ribose chemotaxis. Mol Gen Genet. 1979 Mar 20;171(2):193–203. doi: 10.1007/BF00270005. [DOI] [PubMed] [Google Scholar]
  14. Hazelbauer G. L., Engström P., Harayama S. Methyl-accepting chemotaxis protein III and transducer gene trg. J Bacteriol. 1981 Jan;145(1):43–49. doi: 10.1128/jb.145.1.43-49.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hazelbauer G. L., Harayama S. Mutants in transmission of chemotactic signals from two independent receptors of E. coli. Cell. 1979 Mar;16(3):617–625. doi: 10.1016/0092-8674(79)90035-7. [DOI] [PubMed] [Google Scholar]
  16. Inouye M., Halegoua S. Secretion and membrane localization of proteins in Escherichia coli. CRC Crit Rev Biochem. 1980;7(4):339–371. doi: 10.3109/10409238009105465. [DOI] [PubMed] [Google Scholar]
  17. Josefsson L. G., Randall L. L. Processing in vivo of precursor maltose-binding protein in Escherichia coli occurs post-translationally as well as co-translationally. J Biol Chem. 1981 Mar 10;256(5):2504–2507. [PubMed] [Google Scholar]
  18. Kaiser K., Murray N. E. On the nature of sbcA mutations in E. coli K 12. Mol Gen Genet. 1980;179(3):555–563. doi: 10.1007/BF00271745. [DOI] [PubMed] [Google Scholar]
  19. Kaiser K. The origin of Q-independent derivatives of phage lambda. Mol Gen Genet. 1980;179(3):547–554. doi: 10.1007/BF00271744. [DOI] [PubMed] [Google Scholar]
  20. Koman A., Harayama S., Hazelbauer G. L. Relation of chemotactic response to the amount of receptor: evidence for different efficiencies of signal transduction. J Bacteriol. 1979 Jun;138(3):739–747. doi: 10.1128/jb.138.3.739-747.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kuempel P. L., Duerr S. A., Seeley N. R. Terminus region of the chromosome in Escherichia coli inhibits replication forks. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3927–3931. doi: 10.1073/pnas.74.9.3927. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Louarn J., Patte J., Louarn J. M. Map position of the replication terminus on the Escherichia coli chromosome. Mol Gen Genet. 1979 Apr 17;172(1):7–11. doi: 10.1007/BF00276208. [DOI] [PubMed] [Google Scholar]
  23. Palva E. T., Hirst T. R., Hardy S. J., Holmgren J., Randall L. Synthesis of a precursor to the B subunit of heat-labile enterotoxin in Escherichia coli. J Bacteriol. 1981 Apr;146(1):325–330. doi: 10.1128/jb.146.1.325-330.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Silverman M., Simon M. I. Bacterial flagella. Annu Rev Microbiol. 1977;31:397–419. doi: 10.1146/annurev.mi.31.100177.002145. [DOI] [PubMed] [Google Scholar]

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