Abstract
Phycoerythrin is a major pigmented component of the phycobilisome, a cyanobacterial light-harvesting complex. It contains bilin-type chromophores that absorb and transfer light energy to chlorophyll protein complexes of the photosynthetic membranes. In many cyanobacteria, phycoerythrin expression is regulated by light wavelength in a response known as chromatic adaptation. Green light-grown cells contain higher levels of this biliprotein than do cells grown in red light. The phycoerythrin gene set from the unicellular cyanobacterium Synechocystis sp. strain PCC 6701 was cloned and sequenced, and the 5' end of the phycoerythrin mRNA was localized. The amino acid sequences of the phycoerythrin subunits from Synechocystis strain 6701 and Fremyella diplosiphon were 90% identical. As observed in F. diplosiphon, the Synechocystis strain 6701 phycoerythrin transcript accumulated to high levels in green light-grown cells and low levels in red light-grown cells. Similar nucleotide sequences, which might control gene expression, occurred upstream of the transcription initiation sites of the phycoerythrin genes in both organisms. While the phycoerythrin structure and light-regulated transcript accumulation were similar in Synechocystis strain 6701 and F. diplosiphon, the steady-state levels of phycoerythrin subunits during growth in red light were quite different for the two organisms. This observation suggests that control of phycoerythrin levels in Synechocystis strain 6701 is complex and may involve posttranscriptional processes. We also characterized the phycoerythrin genes and mRNA levels in two phycobilisome assembly mutants, UV16-40 and UV16.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Anderson L. K., Grossman A. R. Structure and light-regulated expression of phycoerythrin genes in wild-type and phycobilisome assembly mutants of Synechocystis sp. strain PCC 6701. J Bacteriol. 1990 Mar;172(3):1297–1305. doi: 10.1128/jb.172.3.1297-1305.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson L. K., Rayner M. C., Eiserling F. A. Mutations that affect structure and assembly of light-harvesting proteins in the cyanobacterium Synechocystis sp. strain 6701. J Bacteriol. 1987 Jan;169(1):102–109. doi: 10.1128/jb.169.1.102-109.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bellemare G., Bartlett S. G., Chua N. H. Biosynthesis of chlorophyll a/b-binding polypeptides in wild type and the chlorina f2 mutant of barley. J Biol Chem. 1982 Jul 10;257(13):7762–7767. [PubMed] [Google Scholar]
- Bennett A., Bogorad L. Complementary chromatic adaptation in a filamentous blue-green alga. J Cell Biol. 1973 Aug;58(2):419–435. doi: 10.1083/jcb.58.2.419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Conley P. B., Lemaux P. G., Grossman A. R. Cyanobacterial light-harvesting complex subunits encoded in two red light-induced transcripts. Science. 1985 Nov 1;230(4725):550–553. doi: 10.1126/science.3931221. [DOI] [PubMed] [Google Scholar]
- 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]
- Curtis S. E. Genes encoding the beta and epsilon subunits of the proton-translocating ATPase from Anabaena sp. strain PCC 7120. J Bacteriol. 1987 Jan;169(1):80–86. doi: 10.1128/jb.169.1.80-86.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gantt E., Lipschultz C. A. Phycobilisomes of Porphyridium cruentum. I. Isolation. J Cell Biol. 1972 Aug;54(2):313–324. doi: 10.1083/jcb.54.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gingrich J. C., Blaha L. K., Glazer A. N. Rod substructure in cyanobacterial phycobilisomes: analysis of Synechocystis 6701 mutants low in phycoerythrin. J Cell Biol. 1982 Feb;92(2):261–268. doi: 10.1083/jcb.92.2.261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glazer A. N., Lundell D. J., Yamanaka G., Williams R. C. The structure of a "simple" phycobilisome. Ann Microbiol (Paris) 1983 Jul-Aug;134B(1):159–180. doi: 10.1016/s0769-2609(83)80103-3. [DOI] [PubMed] [Google Scholar]
- Houmard J., Capuano V., Coursin T., Tandeau de Marsac N. Genes encoding core components of the phycobilisome in the cyanobacterium Calothrix sp. strain PCC 7601: occurrence of a multigene family. J Bacteriol. 1988 Dec;170(12):5512–5521. doi: 10.1128/jb.170.12.5512-5521.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hunt T. P., Magasanik B. Transcription of glnA by purified Escherichia coli components: core RNA polymerase and the products of glnF, glnG, and glnL. Proc Natl Acad Sci U S A. 1985 Dec;82(24):8453–8457. doi: 10.1073/pnas.82.24.8453. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klotz A. V., Glazer A. N., Bishop J. E., Nagy J. O., Rapoport H. Phycobiliprotein-bilin linkage diversity. II. Structural studies on A- and D-ring-linked phycoerythrobilins. J Biol Chem. 1986 May 25;261(15):6797–6805. [PubMed] [Google Scholar]
- Lemaux P. G., Grossman A. R. Major light-harvesting polypeptides encoded in polycistronic transcripts in a eukaryotic alga. EMBO J. 1985 Aug;4(8):1911–1919. doi: 10.1002/j.1460-2075.1985.tb03870.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lindquist S. The heat-shock response. Annu Rev Biochem. 1986;55:1151–1191. doi: 10.1146/annurev.bi.55.070186.005443. [DOI] [PubMed] [Google Scholar]
- Lomax T. L., Conley P. B., Schilling J., Grossman A. R. Isolation and characterization of light-regulated phycobilisome linker polypeptide genes and their transcription as a polycistronic mRNA. J Bacteriol. 1987 Jun;169(6):2675–2684. doi: 10.1128/jb.169.6.2675-2684.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lundell D. J., Williams R. C., Glazer A. N. Molecular architecture of a light-harvesting antenna. In vitro assembly of the rod substructures of Synechococcus 6301 phycobilisomes. J Biol Chem. 1981 Apr 10;256(7):3580–3592. [PubMed] [Google Scholar]
- Mazel D., Guglielmi G., Houmard J., Sidler W., Bryant D. A., Tandeau de Marsac N. Green light induces transcription of the phycoerythrin operon in the cyanobacterium Calothrix 7601. Nucleic Acids Res. 1986 Nov 11;14(21):8279–8290. doi: 10.1093/nar/14.21.8279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Messing J. New M13 vectors for cloning. Methods Enzymol. 1983;101:20–78. doi: 10.1016/0076-6879(83)01005-8. [DOI] [PubMed] [Google Scholar]
- Norrander J., Kempe T., Messing J. Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis. Gene. 1983 Dec;26(1):101–106. doi: 10.1016/0378-1119(83)90040-9. [DOI] [PubMed] [Google Scholar]
- 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]
- Redlinger T., Gantt E. Phycobilisome Structure of Porphyridium cruentum: POLYPEPTIDE COMPOSITION. Plant Physiol. 1981 Dec;68(6):1375–1379. doi: 10.1104/pp.68.6.1375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schirmer T., Bode W., Huber R. Refined three-dimensional structures of two cyanobacterial C-phycocyanins at 2.1 and 2.5 A resolution. A common principle of phycobilin-protein interaction. J Mol Biol. 1987 Aug 5;196(3):677–695. doi: 10.1016/0022-2836(87)90040-4. [DOI] [PubMed] [Google Scholar]
- Schirmer T., Bode W., Huber R., Sidler W., Zuber H. X-ray crystallographic structure of the light-harvesting biliprotein C-phycocyanin from the thermophilic cyanobacterium Mastigocladus laminosus and its resemblance to globin structures. J Mol Biol. 1985 Jul 20;184(2):257–277. doi: 10.1016/0022-2836(85)90379-1. [DOI] [PubMed] [Google Scholar]
- Schirmer T., Huber R., Schneider M., Bode W., Miller M., Hackert M. L. Crystal structure analysis and refinement at 2.5 A of hexameric C-phycocyanin from the cyanobacterium Agmenellum quadruplicatum. The molecular model and its implications for light-harvesting. J Mol Biol. 1986 Apr 20;188(4):651–676. doi: 10.1016/s0022-2836(86)80013-4. [DOI] [PubMed] [Google Scholar]
- Schmidt G. W., Mishkind M. L. Rapid degradation of unassembled ribulose 1,5-bisphosphate carboxylase small subunits in chloroplasts. Proc Natl Acad Sci U S A. 1983 May;80(9):2632–2636. doi: 10.1073/pnas.80.9.2632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shine J., Dalgarno L. The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1342–1346. doi: 10.1073/pnas.71.4.1342. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sidler W., Kumpf B., Rüdiger W., Zuber H. The complete amino-acid sequence of C-phycoerythrin from the cyanobacterium Fremyella diplosiphon. Biol Chem Hoppe Seyler. 1986 Jul;367(7):627–642. doi: 10.1515/bchm3.1986.367.2.627. [DOI] [PubMed] [Google Scholar]
- Sidler W., Kumpf B., Suter F., Klotz A. V., Glazer A. N., Zuber H. The complete amino-acid sequence of the alpha and beta subunits of B-phycoerythrin from the rhodophytan alga Porphyridium cruentum. Biol Chem Hoppe Seyler. 1989 Feb;370(2):115–124. doi: 10.1515/bchm3.1989.370.1.115. [DOI] [PubMed] [Google Scholar]
- Tandeau de Marsac N. Occurrence and nature of chromatic adaptation in cyanobacteria. J Bacteriol. 1977 Apr;130(1):82–91. doi: 10.1128/jb.130.1.82-91.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vieira J., Messing J. Production of single-stranded plasmid DNA. Methods Enzymol. 1987;153:3–11. doi: 10.1016/0076-6879(87)53044-0. [DOI] [PubMed] [Google Scholar]
- Young R. A., Davis R. W. Efficient isolation of genes by using antibody probes. Proc Natl Acad Sci U S A. 1983 Mar;80(5):1194–1198. doi: 10.1073/pnas.80.5.1194. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu M. H., Glazer A. N. Cyanobacterial phycobilisomes. Role of the linker polypeptides in the assembly of phycocyanin. J Biol Chem. 1982 Apr 10;257(7):3429–3433. [PubMed] [Google Scholar]