Abstract
Evidence is presented indicating that free 70S ribosomes are real components of Bacillus stearothermophilus and Escherichia coli in exponential and stationary phases of growth.
After pulses of radioactive leucine or uracil were given, protein synthesis was instantaneously stopped by chloramphenicol, or polypeptide growth was allowed to proceed to completion in slowly cooled cells. Analysis of label distribution in sucrose gradients showed that 70S monomers, and not subunits, are final products of translation.
A ribosome cycle for protein synthesis in bacteria is proposed.
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Selected References
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- Dresden M. H., Hoagland M. B. Polyribosomes of Escherichia coli. Breakdown during glucose starvation. J Biol Chem. 1967 Mar 10;242(5):1065–1068. [PubMed] [Google Scholar]
- Dresden M. H., Hoagland M. B. Polyribosomes of Escherichia coli. Re-formation during recovery from glucose starvation. J Biol Chem. 1967 Mar 10;242(5):1069–1073. [PubMed] [Google Scholar]
- Eisenstadt J. M., Brawerman G. The role of the native subribosomal particles of Escherichia coli in polypeptide chain initiation. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1560–1565. doi: 10.1073/pnas.58.4.1560. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flessel C. P., Ralph P., Rich A. Polyribosomes of growing bacteria. Science. 1967 Nov 3;158(3801):658–660. doi: 10.1126/science.158.3801.658. [DOI] [PubMed] [Google Scholar]
- Ghosh H. P., Khorana H. G. Studies on polynucleotides, LXXXIV. On the role of ribosomal subunits in protein synthesis. Proc Natl Acad Sci U S A. 1967 Dec;58(6):2455–2461. doi: 10.1073/pnas.58.6.2455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Godson G. N., Sinsheimer R. L. Lysis of Escherichia coli with a neutral detergent. Biochim Biophys Acta. 1967 Dec 19;149(2):476–488. doi: 10.1016/0005-2787(67)90175-x. [DOI] [PubMed] [Google Scholar]
- Godson G. N., Sinsheimer R. L. The replication of bacteriophage MS2. VI. Interaction between bacteriophage RNA and cellular components in MS2-infected Escherichia coli. J Mol Biol. 1967 Feb 14;23(3):495–521. doi: 10.1016/s0022-2836(67)80121-9. [DOI] [PubMed] [Google Scholar]
- Gonzalez N. S., Goldemberg S. H., Algranati I. D. Protein synthesis and ribosomal distribution at different growth stages in Bacillus stearothermophilus. Biochim Biophys Acta. 1968 Oct 29;166(3):760–762. doi: 10.1016/0005-2787(68)90397-3. [DOI] [PubMed] [Google Scholar]
- Guthrie C., Nomura M. Initiation of protein synthesis: a critical test of the 30S subunit model. Nature. 1968 Jul 20;219(5151):232–235. doi: 10.1038/219232a0. [DOI] [PubMed] [Google Scholar]
- Joklik W. K., Becker Y. Studies on the genesis of polyribosomes. I. Origin and significance of the subribosomal particles. J Mol Biol. 1965 Sep;13(2):496–510. doi: 10.1016/s0022-2836(65)80112-7. [DOI] [PubMed] [Google Scholar]
- Kaempfer R. O., Meselson M., Raskas H. J. Cyclic dissociation into stable subunits and re-formation of ribosomes during bacterial growth. J Mol Biol. 1968 Jan 28;31(2):277–289. doi: 10.1016/0022-2836(68)90444-0. [DOI] [PubMed] [Google Scholar]
- Kaempfer R. Ribosomal subunit exchange during protein synthesis. Proc Natl Acad Sci U S A. 1968 Sep;61(1):106–113. doi: 10.1073/pnas.61.1.106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kohler R. E., Ron E. Z., Davis B. D. Significance of the free 70 s ribosomes in Escherichia coli extracts. J Mol Biol. 1968 Aug 28;36(1):71–82. doi: 10.1016/0022-2836(68)90220-9. [DOI] [PubMed] [Google Scholar]
- Mangiarotti G., Schlessinger D. Polyribosome metabolism in Escherichia coli. I. Extraction of polyribosomes and ribosomal subunits from fragile, growing Escherichia coli. J Mol Biol. 1966 Sep;20(1):123–143. doi: 10.1016/0022-2836(66)90122-7. [DOI] [PubMed] [Google Scholar]
- Nomura M., Lowry C. V., Guthrie C. The initiation of protein synthesis: joining of the 50S ribosomal subunit to the initiation complex. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1487–1493. doi: 10.1073/pnas.58.4.1487. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nomura M., Lowry C. V. PHAGE f2 RNA-DIRECTED BINDING OF FORMYLMETHIONYL-TRNA TO RIBOSOMES AND THE ROLE OF 30S RIBOSOMAL SUBUNITS IN INITIATION OF PROTEIN SYNTHESIS. Proc Natl Acad Sci U S A. 1967 Sep;58(3):946–953. doi: 10.1073/pnas.58.3.946. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oppenheim J., Scheinbuks J., Biava C., Marcus L. Polyribosomes in Azotobacter vinelandii. I. Isolation, characterization and distribution of ribosomes, polyribosomes and subunits in logarithmically growing azotobacter. Biochim Biophys Acta. 1968 Jul 23;161(2):386–401. [PubMed] [Google Scholar]
- Ron E. Z., Kohler R. E., Davis B. D. Polysomes extracted from Escherichia coli by freeze-thaw-lysozyme lysis. Science. 1966 Sep 2;153(3740):1119–1120. doi: 10.1126/science.153.3740.1119. [DOI] [PubMed] [Google Scholar]
- Schlessinger D., Mangiarotti G., Apirion D. The formation and stabilization of 30S and 50S ribosome couples in Escherichia coli. Proc Natl Acad Sci U S A. 1967 Oct;58(4):1782–1789. doi: 10.1073/pnas.58.4.1782. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAKANAMI M., ZUBAY G. AN ESTIMATE OF THE SIZE OF THE RIBOSOMAL SITE FOR MESSENGER RNA BINDING. Proc Natl Acad Sci U S A. 1964 May;51:834–839. doi: 10.1073/pnas.51.5.834. [DOI] [PMC free article] [PubMed] [Google Scholar]