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. 1986 Mar;165(3):942–950. doi: 10.1128/jb.165.3.942-950.1986

In vitro biosynthesis and membrane association of photosynthetic reaction center subunits from Rhodopseudomonas sphaeroides.

J H Hoger, J Chory, S Kaplan
PMCID: PMC214520  PMID: 3512531

Abstract

The reaction center of Rhodopseudomonas sphaeroides is an integral membrane protein complex responsible for primary photochemical charge separation in photosynthesis. We report the synthesis of two of the three subunits of the photosynthetic reaction center using a DNA-directed in vitro transcription-translation system prepared from R. sphaeroides. The in vitro-synthesized polypeptides, as resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, had apparent Mrs of 24,000 and 21,000 and were shown to be synthesized in equimolar amounts. This corresponds precisely to the in vivo reaction center subunits M and L, respectively. The in vitro-synthesized polypeptides were immunoprecipitated with antibody prepared against whole native reaction centers. In addition, the identity of the in vitro-synthesized polypeptides as L and M was verified by comparing the protease digestion products of in vivo- with in vitro-synthesized reaction center subunits. Both of the in vitro-synthesized polypeptides were also found to partition with the particulate material in the transcription-translation system and to associate with added membranes.

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Selected References

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  1. Bachmann R. C., Gillies K., Takemoto J. Y. Membrane topography of the photosynthetic reaction center polypeptides of Rhodopseudomonas sphaeroides. Biochemistry. 1981 Aug 4;20(16):4590–4596. doi: 10.1021/bi00519a012. [DOI] [PubMed] [Google Scholar]
  2. Baughman G., Nomura M. Localization of the target site for translational regulation of the L11 operon and direct evidence for translational coupling in Escherichia coli. Cell. 1983 Oct;34(3):979–988. doi: 10.1016/0092-8674(83)90555-x. [DOI] [PubMed] [Google Scholar]
  3. Brusilow W. S., Gunsalus R. P., Hardeman E. C., Decker K. P., Simoni R. D. In vitro synthesis of the F0 and F1 components of the proton translocating ATPase of Escherichia coli. J Biol Chem. 1981 Apr 10;256(7):3141–3144. [PubMed] [Google Scholar]
  4. Caulfield M. P., Horiuchi S., Tai P. C., Davis B. D. The 64-kilodalton membrane protein of Bacillus subtilis is also present as a multiprotein complex on membrane-free ribosomes. Proc Natl Acad Sci U S A. 1984 Dec;81(24):7772–7776. doi: 10.1073/pnas.81.24.7772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chory J., Donohue T. J., Varga A. R., Staehelin L. A., Kaplan S. Induction of the photosynthetic membranes of Rhodopseudomonas sphaeroides: biochemical and morphological studies. J Bacteriol. 1984 Aug;159(2):540–554. doi: 10.1128/jb.159.2.540-554.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chory J., Kaplan S. The in vitro transcription-translation of DNA and RNA templates by extracts of Rhodopseudomonas sphaeroides. Optimization and comparison of template specificity with Escherichia coli extracts and in vivo synthesis. J Biol Chem. 1982 Dec 25;257(24):15110–15121. [PubMed] [Google Scholar]
  7. Chory J., Muller E. D., Kaplan S. DNA-directed in vitro synthesis and assembly of the form II D-ribulose-1,5-bisphosphate carboxylase/oxygenase from Rhodopseudomonas sphaeroides. J Bacteriol. 1985 Jan;161(1):307–313. doi: 10.1128/jb.161.1.307-313.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cleveland D. W., Fischer S. G., Kirschner M. W., Laemmli U. K. Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis. J Biol Chem. 1977 Feb 10;252(3):1102–1106. [PubMed] [Google Scholar]
  9. Decker K. P., Brusilow W. S., Gunsalus R. P., Simoni R. D. In vitro membrane association of the F0 polypeptides of the Escherichia coli proton translocating ATPase. J Bacteriol. 1982 Nov;152(2):815–821. doi: 10.1128/jb.152.2.815-821.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dierstein R. Synthesis of pigment-binding protein in toluene-treated Rhodopseudomonas capsulata and in cell-free systems. Eur J Biochem. 1984 Feb 1;138(3):509–518. doi: 10.1111/j.1432-1033.1984.tb07945.x. [DOI] [PubMed] [Google Scholar]
  11. Ehring R., Beyreuther K., Wright J. K., Overath P. In vitro and in vivo products of E. coli lactose permease gene are identical. Nature. 1980 Feb 7;283(5747):537–540. doi: 10.1038/283537a0. [DOI] [PubMed] [Google Scholar]
  12. Fornari C. S., Kaplan S. Genetic transformation of Rhodopseudomonas sphaeroides by plasmid DNA. J Bacteriol. 1982 Oct;152(1):89–97. doi: 10.1128/jb.152.1.89-97.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fraker P. J., Kaplan S. Isolation and fractionation of the photosynthetic membranous organelles from Rhodopseudomonas spheroides. J Bacteriol. 1971 Oct;108(1):465–473. doi: 10.1128/jb.108.1.465-473.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hoger J. H., Kaplan S. Topology and neighbor analysis of the photosynthetic reaction center from Rhodopseudomonas sphaeroides. J Biol Chem. 1985 Jun 10;260(11):6932–6937. [PubMed] [Google Scholar]
  15. Laemmli U. K., Favre M. Maturation of the head of bacteriophage T4. I. DNA packaging events. J Mol Biol. 1973 Nov 15;80(4):575–599. doi: 10.1016/0022-2836(73)90198-8. [DOI] [PubMed] [Google Scholar]
  16. Lopatin D. E., Voss E. W., Jr Anti-lysergyl antibody: measurement of binding parameters in IgG fractions. Immunochemistry. 1974 Jun;11(6):285–293. doi: 10.1016/0019-2791(74)90364-4. [DOI] [PubMed] [Google Scholar]
  17. MUNKRES K. D., RICHARDS F. M. THE PURIFICATION AND PROPERTIES OF NEUROSPORA MALATE DEHYDROGENASE. Arch Biochem Biophys. 1965 Mar;109:466–479. doi: 10.1016/0003-9861(65)90391-7. [DOI] [PubMed] [Google Scholar]
  18. Müller M., Blobel G. Protein export in Escherichia coli requires a soluble activity. Proc Natl Acad Sci U S A. 1984 Dec;81(24):7737–7741. doi: 10.1073/pnas.81.24.7737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Normark S., Bergström S., Edlund T., Grundström T., Jaurin B., Lindberg F. P., Olsson O. Overlapping genes. Annu Rev Genet. 1983;17:499–525. doi: 10.1146/annurev.ge.17.120183.002435. [DOI] [PubMed] [Google Scholar]
  20. Oppenheim D. S., Yanofsky C. Translational coupling during expression of the tryptophan operon of Escherichia coli. Genetics. 1980 Aug;95(4):785–795. doi: 10.1093/genetics/95.4.785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Poulis M. I., Shaw D. C., Campbell H. D., Young I. G. In vitro synthesis of the respiratory NADH dehydrogenase of Escherichia coli. Role of UUG as initiation codon. Biochemistry. 1981 Jul 7;20(14):4178–4185. doi: 10.1021/bi00517a035. [DOI] [PubMed] [Google Scholar]
  22. Randall L. L., Hardy S. J. Export of protein in bacteria. Microbiol Rev. 1984 Dec;48(4):290–298. doi: 10.1128/mr.48.4.290-298.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Randall L. L., Josefsson L. G., Hardy S. J. Novel intermediates in the synthesis of maltose-binding protein in Escherichia coli. Eur J Biochem. 1980 Jun;107(2):375–379. doi: 10.1111/j.1432-1033.1980.tb06039.x. [DOI] [PubMed] [Google Scholar]
  24. Rhoads D. B., Tai P. C., Davis B. D. Energy-requiring translocation of the OmpA protein and alkaline phosphatase of Escherichia coli into inner membrane vesicles. J Bacteriol. 1984 Jul;159(1):63–70. doi: 10.1128/jb.159.1.63-70.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. SISTROM W. R. A requirement for sodium in the growth of Rhodopseudomonas spheroides. J Gen Microbiol. 1960 Jun;22:778–785. doi: 10.1099/00221287-22-3-778. [DOI] [PubMed] [Google Scholar]
  26. Santos E., Kung H., Young I. G., Kaback H. R. In vitro synthesis of the membrane-bound D-lactate dehydrogenase of Escherichia coli. Biochemistry. 1982 Apr 27;21(9):2085–2091. doi: 10.1021/bi00538a016. [DOI] [PubMed] [Google Scholar]
  27. Schmidt G. W., Bartlett S. G., Grossman A. R., Cashmore A. R., Chua N. H. Biosynthetic pathways of two polypeptide subunits of the light-harvesting chlorophyll a/b protein complex. J Cell Biol. 1981 Nov;91(2 Pt 1):468–478. doi: 10.1083/jcb.91.2.468. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Shepherd W. D., Kaplan S. A rapid method for the isolation of intracytoplasmic membranes from Rhodopseudomonas sphaeroides using an air-driven ultracentrifuge. Anal Biochem. 1978 Nov;91(1):194–198. doi: 10.1016/0003-2697(78)90831-x. [DOI] [PubMed] [Google Scholar]
  29. Shepherd W. D., Kaplan S. Effect of heat and 2-mercaptoethanol on intracytoplasmic membrane polypeptides of Rhodopseudomonas sphaeroides. J Bacteriol. 1978 Aug;135(2):656–667. doi: 10.1128/jb.135.2.656-667.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Silver P., Watts C., Wickner W. Membrane assembly from purified components. I. Isolated M13 procoat does not require ribosomes or soluble proteins for processing by membranes. Cell. 1981 Aug;25(2):341–345. doi: 10.1016/0092-8674(81)90052-0. [DOI] [PubMed] [Google Scholar]
  31. Walter P., Blobel G. Translocation of proteins across the endoplasmic reticulum III. Signal recognition protein (SRP) causes signal sequence-dependent and site-specific arrest of chain elongation that is released by microsomal membranes. J Cell Biol. 1981 Nov;91(2 Pt 1):557–561. doi: 10.1083/jcb.91.2.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wickner W. Assembly of proteins into membranes. Science. 1980 Nov 21;210(4472):861–868. doi: 10.1126/science.7001628. [DOI] [PubMed] [Google Scholar]
  33. Williams J. C., Steiner L. A., Feher G., Simon M. I. Primary structure of the L subunit of the reaction center from Rhodopseudomonas sphaeroides. Proc Natl Acad Sci U S A. 1984 Dec;81(23):7303–7307. doi: 10.1073/pnas.81.23.7303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Williams J. C., Steiner L. A., Ogden R. C., Simon M. I., Feher G. Primary structure of the M subunit of the reaction center from Rhodopseudomonas sphaeroides. Proc Natl Acad Sci U S A. 1983 Nov;80(21):6505–6509. doi: 10.1073/pnas.80.21.6505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wolfe P. B., Wickner W. Bacterial leader peptidase, a membrane protein without a leader peptide, uses the same export pathway as pre-secretory proteins. Cell. 1984 Apr;36(4):1067–1072. doi: 10.1016/0092-8674(84)90056-4. [DOI] [PubMed] [Google Scholar]
  36. Youvan D. C., Alberti M., Begusch H., Bylina E. J., Hearst J. E. Reaction center and light-harvesting I genes from Rhodopseudomonas capsulata. Proc Natl Acad Sci U S A. 1984 Jan;81(1):189–192. doi: 10.1073/pnas.81.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Zubay G. In vitro synthesis of protein in microbial systems. Annu Rev Genet. 1973;7:267–287. doi: 10.1146/annurev.ge.07.120173.001411. [DOI] [PubMed] [Google Scholar]

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