Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1997 Dec;179(24):7695–7704. doi: 10.1128/jb.179.24.7695-7704.1997

rpbA controls transcription of the constitutive phycocyanin gene set in Fremyella diplosiphon.

K Kahn 1, M R Schaefer 1
PMCID: PMC179731  PMID: 9401027

Abstract

Three gene sets encode alpha and beta subunits of the phycobiliprotein phycocyanin (PC) in the filamentous cyanobacterium Fremyella diplosiphon. The cpcB1A1 set (encodes PC1) is constitutively expressed, whereas the cpcB2A2 set (encodes PC2) is expressed only in red light and the cpcB3A3 set (encodes PC3) is expressed only during sulfur-limited growth. Primary pigment mutant strain FdBM1 is characterized by elevated levels of PC. DNA hybridization analysis showed that like many pigment mutants in our strain collection, strain FdBM1 harbors an extra genomic copy of endogenous transposon Tn5469. By direct cloning from FdBM1 genomic DNA, the extra copy of Tn5469 was localized to an open reading frame, which we have designated the rpbA gene. Complementation experiments correlated rpbA activity to the phenotype of strain FdBM1. The predicted RpbA protein contains two regions resembling the characterized helix-turn-helix motif which is involved in DNA recognition by many bacterial and phage transcription regulator proteins. RNA hybridization analysis showed that relative to the parental strain Fd33, the level of transcripts from cpcB1A1, but not cpcB2A2 or cpcB3A3, was significantly elevated in strain FdBM1. Introduction of the intact rpbA gene into strain FdBM1 restored the cpcB1A1 transcript level to that of strain Fd33. These results suggest that the rpbA gene product functions in controlling constitutive transcription from the cpcB1A1 gene set, possibly as a DNA-binding transcriptional repressor element.

Full Text

The Full Text of this article is available as a PDF (645.6 KB).

Selected References

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

  1. Aiba H., Fujimoto S., Ozaki N. Molecular cloning and nucleotide sequencing of the gene for E. coli cAMP receptor protein. Nucleic Acids Res. 1982 Feb 25;10(4):1345–1361. doi: 10.1093/nar/10.4.1345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  3. Bruns B. U., Briggs W. R., Grossman A. R. Molecular characterization of phycobilisome regulatory mutants of Fremyella diplosiphon. J Bacteriol. 1989 Feb;171(2):901–908. doi: 10.1128/jb.171.2.901-908.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Casey E. S., Kehoe D. M., Grossman A. R. Suppression of mutants aberrant in light intensity responses of complementary chromatic adaptation. J Bacteriol. 1997 Jul;179(14):4599–4606. doi: 10.1128/jb.179.14.4599-4606.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chiang G. G., Schaefer M. R., Grossman A. R. Complementation of a red-light-indifferent cyanobacterial mutant. Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9415–9419. doi: 10.1073/pnas.89.20.9415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cobley J. G., Zerweck E., Reyes R., Mody A., Seludo-Unson J. R., Jaeger H., Weerasuriya S., Navankasattusas S. Construction of shuttle plasmids which can be efficiently mobilized from Escherichia coli into the chromatically adapting cyanobacterium, Fremyella diplosiphon. Plasmid. 1993 Sep;30(2):90–105. doi: 10.1006/plas.1993.1037. [DOI] [PubMed] [Google Scholar]
  7. Conley P. B., Lemaux P. G., Grossman A. Molecular characterization and evolution of sequences encoding light-harvesting components in the chromatically adapting cyanobacterium Fremyella diplosiphon. J Mol Biol. 1988 Feb 5;199(3):447–465. doi: 10.1016/0022-2836(88)90617-1. [DOI] [PubMed] [Google Scholar]
  8. Dhaese P., Seurinck J., De Smet B., Van Montagu M. Nucleotide sequence and mutational analysis of an immunity repressor gene from Bacillus subtilis temperate phage phi 105. Nucleic Acids Res. 1985 Aug 12;13(15):5441–5455. doi: 10.1093/nar/13.15.5441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Duerring M., Schmidt G. B., Huber R. Isolation, crystallization, crystal structure analysis and refinement of constitutive C-phycocyanin from the chromatically adapting cyanobacterium Fremyella diplosiphon at 1.66 A resolution. J Mol Biol. 1991 Feb 5;217(3):577–592. doi: 10.1016/0022-2836(91)90759-y. [DOI] [PubMed] [Google Scholar]
  10. Farabaugh P. J. Sequence of the lacI gene. Nature. 1978 Aug 24;274(5673):765–769. doi: 10.1038/274765a0. [DOI] [PubMed] [Google Scholar]
  11. Grossman A. R., Schaefer M. R., Chiang G. G., Collier J. L. The phycobilisome, a light-harvesting complex responsive to environmental conditions. Microbiol Rev. 1993 Sep;57(3):725–749. doi: 10.1128/mr.57.3.725-749.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Harrison S. C., Aggarwal A. K. DNA recognition by proteins with the helix-turn-helix motif. Annu Rev Biochem. 1990;59:933–969. doi: 10.1146/annurev.bi.59.070190.004441. [DOI] [PubMed] [Google Scholar]
  13. Hsiang M. W., Cole R. D., Takeda Y., Echols H. Amino acid sequence of Cro regulatory protein of bacteriophage lambda. Nature. 1977 Nov 17;270(5634):275–277. doi: 10.1038/270275a0. [DOI] [PubMed] [Google Scholar]
  14. Kahn K., Mazel D., Houmard J., Tandeau de Marsac N., Schaefer M. R. A role for cpeYZ in cyanobacterial phycoerythrin biosynthesis. J Bacteriol. 1997 Feb;179(4):998–1006. doi: 10.1128/jb.179.4.998-1006.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kahn K., Schaefer M. R. Characterization of transposon Tn5469 from the cyanobacterium Fremyella diplosiphon. J Bacteriol. 1995 Dec;177(24):7026–7032. doi: 10.1128/jb.177.24.7026-7032.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kaneko T., Sato S., Kotani H., Tanaka A., Asamizu E., Nakamura Y., Miyajima N., Hirosawa M., Sugiura M., Sasamoto S. Sequence analysis of the genome of the unicellular cyanobacterium Synechocystis sp. strain PCC6803. II. Sequence determination of the entire genome and assignment of potential protein-coding regions. DNA Res. 1996 Jun 30;3(3):109–136. doi: 10.1093/dnares/3.3.109. [DOI] [PubMed] [Google Scholar]
  17. Kehoe D. M., Grossman A. R. New classes of mutants in complementary chromatic adaptation provide evidence for a novel four-step phosphorelay system. J Bacteriol. 1997 Jun;179(12):3914–3921. doi: 10.1128/jb.179.12.3914-3921.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kehoe D. M., Grossman A. R. Similarity of a chromatic adaptation sensor to phytochrome and ethylene receptors. Science. 1996 Sep 6;273(5280):1409–1412. doi: 10.1126/science.273.5280.1409. [DOI] [PubMed] [Google Scholar]
  19. Liu Y., Chatterjee A., Chatterjee A. K. Nucleotide sequence, organization and expression of rdgA and rdgB genes that regulate pectin lyase production in the plant pathogenic bacterium Erwinia carotovora subsp. carotovora in response to DNA-damaging agents. Mol Microbiol. 1994 Dec;14(5):999–1010. doi: 10.1111/j.1365-2958.1994.tb01334.x. [DOI] [PubMed] [Google Scholar]
  20. Mazel D., Marlière P. Adaptive eradication of methionine and cysteine from cyanobacterial light-harvesting proteins. Nature. 1989 Sep 21;341(6239):245–248. doi: 10.1038/341245a0. [DOI] [PubMed] [Google Scholar]
  21. Oelmüller R., Conley P. B., Federspiel N., Briggs W. R., Grossman A. R. Changes in Accumulation and Synthesis of Transcripts Encoding Phycobilisome Components during Acclimation of Fremyella diplosiphon to Different Light Qualities. Plant Physiol. 1988 Dec;88(4):1077–1083. doi: 10.1104/pp.88.4.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Reed K. C., Mann D. A. Rapid transfer of DNA from agarose gels to nylon membranes. Nucleic Acids Res. 1985 Oct 25;13(20):7207–7221. doi: 10.1093/nar/13.20.7207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sanger F., Coulson A. R., Hong G. F., Hill D. F., Petersen G. B. Nucleotide sequence of bacteriophage lambda DNA. J Mol Biol. 1982 Dec 25;162(4):729–773. doi: 10.1016/0022-2836(82)90546-0. [DOI] [PubMed] [Google Scholar]
  24. Schaefer M. R., Golden S. S. Differential expression of members of a cyanobacterial psbA gene family in response to light. J Bacteriol. 1989 Jul;171(7):3973–3981. doi: 10.1128/jb.171.7.3973-3981.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Van Kaer L., Gansemans Y., Van Montagu M., Dhaese P. Interaction of the Bacillus subtilis phage phi 105 repressor DNA: a genetic analysis. EMBO J. 1988 Mar;7(3):859–866. doi: 10.1002/j.1460-2075.1988.tb02885.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES