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. 1970 Nov;67(3):1440–1447. doi: 10.1073/pnas.67.3.1440

Structure and Function of Bacterial Ribosomes, XI. Dependence of 50S Ribosomal Assembly on Simultaneous Assembly of 30S Subunits*

Hiroko Nashimoto 1,2, Masayasu Nomura 1,2
PMCID: PMC283371  PMID: 4922290

Abstract

Some spectinomycin-resistant mutants of Escherichia coli are cold-sensitive. They are unable to assemble both 30S and 50S ribosomal subunits at low temperatures. They accumulate two kinds of incomplete particles, related to 30S and 50S subunits respectively. A single mutation, causing an alteration in a 30S ribosomal component, is responsible for these phenotypes. These results show that assembly of 50S subunits in vivo is dependent on simultaneous assembly of 30S subunits. On the other hand, the assembly of 30S subunits appears to be independent of 50S assembly.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ADLER J., KAISER A. D. Mapping of the galactose genes of Escherichia coli by transduction with phage P1. Virology. 1963 Feb;19:117–126. doi: 10.1016/0042-6822(63)90001-1. [DOI] [PubMed] [Google Scholar]
  2. Adesnik M., Levinthal C. Synthesis and maturation of ribosomal RNA in Escherichia coli. J Mol Biol. 1969 Dec 14;46(2):281–303. doi: 10.1016/0022-2836(69)90422-7. [DOI] [PubMed] [Google Scholar]
  3. Anderson P., Davies J., Davis B. D. Effect of spectinomycin on polypeptide synthesis in extracts of Escherichia coli. J Mol Biol. 1967 Oct 14;29(1):203–215. doi: 10.1016/0022-2836(67)90191-x. [DOI] [PubMed] [Google Scholar]
  4. Anderson P. Sensitivity and Resistance to Spectinomycin in Escherichia coli. J Bacteriol. 1969 Nov;100(2):939–947. doi: 10.1128/jb.100.2.939-947.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Apirion D., Schlessinger D., Phillips S., Sypherd P. Escherichia coli: reversion from streptomycin dependence, a mutation in a specific 30 s ribosomal protein. J Mol Biol. 1969 Jul 28;43(2):327–329. doi: 10.1016/0022-2836(69)90271-x. [DOI] [PubMed] [Google Scholar]
  6. Birge E. A., Kurland C. G. Altered ribosomal protein in streptomycin-dependent Escherichia coli. Science. 1969 Dec 5;166(3910):1282–1284. doi: 10.1126/science.166.3910.1282. [DOI] [PubMed] [Google Scholar]
  7. Bollen A., Davies J., Ozaki M., Mizushima S. Ribosomal protein conferring sensitivity to the antibiotic spectinomycin in Escherichia coli. Science. 1968 Jul 4;165(3888):85–86. [PubMed] [Google Scholar]
  8. COX E. C., WHITE J. R., FLAKS J. G. STREPTOMYCIN ACTION AND THE RIBOSOME. Proc Natl Acad Sci U S A. 1964 Apr;51:703–709. doi: 10.1073/pnas.51.4.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dekio S., Takata R., Osawa S., Tanaka K., Tamaki M. Genetic studies of the ribosomal proteins in Escherichia coli. IV. Pattern of the alteration of ribosomal protein components in mutants resistant to spectinomycin or erythromycin in different strains of Escherichia coli. Mol Gen Genet. 1970;107(1):39–49. doi: 10.1007/BF00433222. [DOI] [PubMed] [Google Scholar]
  10. Guthrie C., Nashimoto H., Nomura M. Structure and function of E. coli ribosomes. 8. Cold-sensitive mutants defective in ribosome assembly. Proc Natl Acad Sci U S A. 1969 Jun;63(2):384–391. doi: 10.1073/pnas.63.2.384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Guthrie C., Nashimoto H., Nomura M. Studies on the assembly of ribosomes in vivo. Cold Spring Harb Symp Quant Biol. 1969;34:69–75. doi: 10.1101/sqb.1969.034.01.011. [DOI] [PubMed] [Google Scholar]
  12. Hecht N. B., Woese C. R. Separation of bacterial ribosomal ribonucleic acid from its macromolecular precursors by polyacrylamide gel electrophoresis. J Bacteriol. 1968 Mar;95(3):986–990. doi: 10.1128/jb.95.3.986-990.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Newcombe H. B., Hawirko R. SPONTANEOUS MUTATION TO STREPTOMYCIN RESISTANCE AND DEPENDENCE IN ESCHERICHIA COLI. J Bacteriol. 1949 May;57(5):565–572. doi: 10.1128/jb.57.5.565-572.1949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Nomura M., Traub P., Bechmann H. Hybrid 30S ribosomal particles reconstituted from components of different bacterial origins. Nature. 1968 Aug 24;219(5156):793–799. doi: 10.1038/219793b0. [DOI] [PubMed] [Google Scholar]
  15. Peacock A. C., Dingman C. W. Resolution of multiple ribonucleic acid species by polyacrylamide gel electrophoresis. Biochemistry. 1967 Jun;6(6):1818–1827. doi: 10.1021/bi00858a033. [DOI] [PubMed] [Google Scholar]
  16. Rosset R., Gorini L. A ribosomal ambiguity mutation. J Mol Biol. 1969 Jan 14;39(1):95–112. doi: 10.1016/0022-2836(69)90336-2. [DOI] [PubMed] [Google Scholar]
  17. Strnad B. C., Sypherd P. S. Unique protein moieties for 30S and 50S ribosomes of Escherichia coli. J Bacteriol. 1969 Jun;98(3):1080–1086. doi: 10.1128/jb.98.3.1080-1086.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Tai P. C., Kessler D. P., Ingraham J. Cold-sensitive mutations in Salmonella typhimurium which affect ribosome synthesis. J Bacteriol. 1969 Mar;97(3):1298–1304. doi: 10.1128/jb.97.3.1298-1304.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Traut R. R., Delius H., Ahmad-Zadeh C., Bickle T. A., Pearson P., Tissières A. Ribosomal proteins of E. Coli: stoichiometry and implications for ribosome structure. Cold Spring Harb Symp Quant Biol. 1969;34:25–38. doi: 10.1101/sqb.1969.034.01.007. [DOI] [PubMed] [Google Scholar]
  20. Weisblum B., Davies J. Antibiotic inhibitors of the bacterial ribosome. Bacteriol Rev. 1968 Dec;32(4 Pt 2):493–528. [PMC free article] [PubMed] [Google Scholar]

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