Synechococcus elongatus PCC 7942
   
   
 

Photo: L.A. Sherman and D.M. Sherman,
Purdue University

The freshwater cyanobacterium Synechococcus elongatus PCC 7942 holds a special place in the development of cyanobacterial molecular genetics. It was this isolate, previously known as Anacystis nidulans R2, that was the first cyanobacterium demonstrated to be reliably transformable by exogenously added DNA (32). Over the decades, many genetic tools have been developed for S. elongatus, and applied to other transformable cyanobacteria (1, 9, 16). Strain PCC 7942 is very closely related to, and considered the same species as, PCC 6301, which is the type strain for S. elongatus (13) and the first accession in the Pasteur Culture Collection (http://www.pasteur.fr/recherche/banques/PCC/). It is an obligate photoautotroph (13), with a genome of approximately 2.7 Mb (15). Two plasmids (approximately 8 and 46 kb) have been sequenced entirely (GenBank accessions S89470 and AF441790, respectively). S. elongatus has been extensively studied by a multi-national research community with respect to: acquisition of inorganic carbon (2, 8, 20, 22, 33), transport and regulation of nitrogen compounds (19, 23, 36), response to iron deprivation (3, 7, 21, 24, 37), acclimation to a variety of nutrient stresses (5, 6, 12, 27, 28, 31, 35), and adaptation to environmental variations in temperature (11, 14, 25, 26, 30) and light intensity (4, 17, 18, 29, 31, 34, 35). In recent years, S. elongatus PCC 7942 has again taken a pioneering position, as the only developed model system for exploring the mechanism of a prokaryotic circadian clock (10). A companion project to the JGI draft sequence is a functional genomics project (http://www.bio.tamu.edu/synecho/index.html) that aims to inactivate each gene in the genome and identify all loci that are important for circadian rhythms of gene expression in the organism.

1. Andersson CA, Tsinoremas NF, Shelton J, Lebedeva NV, Yarrow J, et al. 2000. Application of bioluminescence to the study of circadian rhythms in cyanobacteria. Methods Enzymol. 305: 527-42
2. Bonfil DJ, Ronen-Tarazi M, Sultemeyer D, Lieman-Hurwitz J, Schatz D, Kaplan A. 1998. A putative HCO3- transporter in the cyanobacterium Synechococcus sp. strain PCC 7942. FEBS Lett. 430: 236-40
3. Burnap RL, Troyan T, Sherman LA. 1993. The highly abundant chlorophyll-protein complex of iron-deficient Synechococcus sp. PCC7942 (CP43') is encoded by the isiA gene. Plant Physiol. 103: 893-902
4. Bustos SA, Golden SS. 1992. Light-regulated expression of the psbD gene family in Synechococcus sp. strain PCC 7942: evidence for the role of duplicated psbD genes in cyanobacteria. Mol. Gen. Genet. 232: 221-30
5. Collier JL, Grossman AR. 1992. Chlorosis induced by nutrient deprivation in Synechococcus sp. strain PCC 7942: not all bleaching is the same. J. Bacteriol. 174: 4718-26
6. Collier JL, Grossman AR. 1994. A small polypeptide triggers complete degradation of light-harvesting phycobiliproteins in nutrient-deprived cyanobacteria. Embo J. 13: 1039-47
7. Durham KA, Porta D, McKay RM, Bullerjahn GS. 2003. Expression of the iron-responsive irpA gene from the cyanobacterium Synechococcus sp strain PCC 7942. Arch. Microbiol. 179: 131-4
8. Gabay C, Lieman-Hurwitz J, Hassidim M, Ronen-Tarazi M, Kaplan A. 1998. Modification of topA in Synechococcus sp. PCC 7942 resulted in mutants capable of growing under low but not high concentration of CO2. FEMS Microbiol. Lett. 159: 343-7
9. Golden SS, Brusslan J, Haselkorn R. 1987. Genetic engineering of the cyanobacterial chromosome. Methods Enzymol. 153: 215-31
10. Golden SS, Johnson CH, Kondo T. 1998. The cyanobacterial circadian system: a clock apart. Curr. Opin. Microbiol. 1: 669-73
11. Gombos Z, Kanervo E, Tsvetkova N, Sakamoto T, Aro EM, Murata N. 1997. Genetic enhancement of the ability to tolerate photoinhibition by introduction of unsaturated bonds into membrane glycerolipids. Plant Physiol. 115: 551-9
12. Green LS, Laudenbach DE, Grossman AR. 1989. A region of a cyanobacterial genome required for sulfate transport. Proc. Natl. Acad. Sci. U S A 86: 1949-53
13. Herdman M, Castenholz RW, Iteman I, Waterbury JB, Rippka R. 2001. Subsection I: (Formerly Chroococcales Wettstein 1924, emend. Rippka, Deruelles, Waterbury, Herdman and Stanier 1979). In Bergey's Manual of Systematic Bacteriology, ed. DR Boone, RW Castenholz, GM Garrity, pp. 721. New York: Springler-Verlag
14. Hossain MM, Nakamoto H. 2002. HtpG plays a role in cold acclimation in cyanobacteria. Curr. Microbiol. 44: 291-6
15. Kaneko T, Matsubayashi T, Sugita M, Sugiura M. 1996. Physical and gene maps of the unicellular cyanobacterium Synechococcus sp. strain PCC6301 genome. Plant Mol. Biol. 31: 193-201
16. Kuhlemeier CJ, van Arkel GA. 1987. Host-vector systems for gene cloning in cyanobacteria. Methods Enzymol. 153: 199-215
17. Kulkarni RD, Golden SS. 1997. mRNA stability is regulated by a coding-region element and the unique 5' untranslated leader sequences of the three Synechococcus psbA transcripts. Mol Microbiol 24: 1131-42
18. Kulkarni RD, Schaefer MR, Golden SS. 1992. Transcriptional and posttranscriptional components of psbA response to high light intensity in Synechococcus sp. strain PCC 7942. J Bacteriol 174: 3775-81
19. Lee HM, Vazquez-Bermudez MF, de Marsac NT. 1999. The global nitrogen regulator NtcA regulates transcription of the signal transducer PII (GlnB) and influences its phosphorylation level in response to nitrogen and carbon supplies in the cyanobacterium Synechococcus sp. strain PCC 7942. J. Bacteriol. 181: 2697-702
20. Maeda S, Price GD, Badger MR, Enomoto C, Omata T. 2000. Bicarbonate binding activity of the CmpA protein of the cyanobacterium Synechococcus sp. strain PCC 7942 involved in active transport of bicarbonate. J. Biol. Chem. 275: 20551-5
21. Michel KP, Pistorius EK, Golden SS. 2001. Unusual regulatory elements for iron deficiency induction of the idiA gene of Synechococcus elongatus PCC 7942. J. Bacteriol. 183: 5015-24
22. Omata T, Gohta S, Takahashi Y, Harano Y, Maeda S. 2001. Involvement of a CbbR homolog in low CO2-induced activation of the bicarbonate transporter operon in cyanobacteria. J. Bacteriol. 183: 1891-8
23. Sakamoto T, Bryant DA. 1999. Nitrate transport and not photoinhibition limits growth of the freshwater cyanobacterium Synechococcus species PCC 6301 at low temperature. Plant Physiol. 119: 785-94
24. Sandstrom S, Ivanov AG, Park YI, Oquist G, Gustafsson P. 2002. Iron stress responses in the cyanobacterium Synechococcus sp. PCC7942. Physiol. Plant 116: 255-63
25. Sane PV, Ivanov AG, Sveshnikov D, Huner NP, Oquist G. 2002. A transient exchange of the photosystem II reaction center protein D1:1 with D1:2 during low temperature stress of Synechococcus sp. PCC 7942 in the light lowers the redox potential of QB. J. Biol. Chem. 277: 32739-45
26. Sarcina M, Tobin MJ, Mullineaux CW. 2001. Diffusion of phycobilisomes on the thylakoid membranes of the cyanobacterium Synechococcus 7942. Effects of phycobilisome size, temperature, and membrane lipid composition. J. Biol. Chem. 276: 46830-4
27. Sauer J, Gorl M, Forchhammer K. 1999. Nitrogen starvation in Synechococcus PCC 7942: involvement of glutamine synthetase and NtcA in phycobiliprotein degradation and survival. Arch. Microbiol. 172: 247-55
28. Sauer J, Schreiber U, Schmid R, Volker U, Forchhammer K. 2001. Nitrogen starvation-induced chlorosis in Synechococcus PCC 7942. Low-level photosynthesis as a mechanism of long-term survival. Plant Physiol. 126: 233-43
29. Schaefer MR, Golden SS. 1989. Light availability influences the ratio of two forms of D1 in cyanobacterial thylakoids. J. Biol. Chem. 264: 7412-7
30. Schelin J, Lindmark F, Clarke AK. 2002. The clpP multigene family for the ATP-dependent Clp protease in the cyanobacterium Synechococcus. Microbiology 148: 2255-65
31. Schwarz R, Grossman AR. 1998. A response regulator of cyanobacteria integrates diverse environmental signals and is critical for survival under extreme conditions. Proc. Natl. Acad. Sci. U S A 95: 11008-13
32. Shestakov SV, Khyen NT. 1970. Evidence for genetic transformation in blue-green alga Anacystis nidulans R2. Molec. Gen. Genet. 107: 372-5
33. Tchernov D, Helman Y, Keren N, Luz B, Ohad I, et al. 2001. Passive entry of CO2 and its energy-dependent intracellular conversion to HCO3- in cyanobacteria are driven by a photosystem I-generated deltamuH+. J. Biol. Chem. 276: 23450-5
34. Tsinoremas NF, Schaefer MR, Golden SS. 1994. Blue and red light reversibly control psbA expression in the cyanobacterium Synechococcus sp. strain PCC 7942. J. Biol. Chem. 269: 16143-7
35. van Waasbergen LG, Dolganov N, Grossman AR. 2002. nblS, a gene involved in controlling photosynthesis-related gene expression during high light and nutrient stress in Synechococcus elongatus PCC 7942. J. Bacteriol. 184: 2481-90
36. Vazquez-Bermudez MF, Paz-Yepes J, Herrero A, Flores E. 2002. The NtcA-activated amt1 gene encodes a permease required for uptake of low concentrations of ammonium in the cyanobacterium Synechococcus sp. PCC 7942. Microbiol. 148: 861-9
37. Webb R, Troyan T, Sherman D, Sherman LA. 1994. MapA, an iron-regulated, cytoplasmic membrane protein in the cyanobacterium Synechococcus sp. strain PCC7942. J. Bacteriol. 176: 4906-13