Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803
Schriek S, Rückert C, Staiger D, Pistorius EK, Michel K-P (2007)
BMC Genomics 8(1): 437.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
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Schriek, Sarah;
Rückert, ChristianUniBi ;
Staiger, DorotheeUniBi;
Pistorius, Elfriede K.;
Michel, Klaus-Peter
Einrichtung
Abstract / Bemerkung
BACKGROUND:So far very limited knowledge exists on L-arginine catabolism in cyanobacteria, although six major L-arginine-degrading pathways have been described for prokaryotes. Thus, we have performed a bioinformatic analysis of possible L-arginine-degrading pathways in cyanobacteria. Further, we chose Synechocystis sp. PCC 6803 for a more detailed bioinformatic analysis and for validation of the bioinformatic predictions on L-arginine catabolism with a transcript analysis.RESULTS:We have evaluated 24 cyanobacterial genomes of freshwater or marine strains for the presence of putative L-arginine-degrading enzymes. We identified an L-arginine decarboxylase pathway in all 24 strains. In addition, cyanobacteria have one or two further pathways representing either an arginase pathway or L-arginine deiminase pathway or an L-arginine oxidase/dehydrogenase pathway. An L-arginine amidinotransferase pathway as a major L-arginine-degrading pathway is not likely but can not be entirely excluded. A rather unusual finding was that the cyanobacterial L-arginine deiminases are substantially larger than the enzymes in non-photosynthetic bacteria and that they are membrane-bound. A more detailed bioinformatic analysis of Synechocystis sp. PCC 6803 revealed that three different L-arginine-degrading pathways may in principle be functional in this cyanobacterium. These are (i) an L-arginine decarboxylase pathway, (ii) an L-arginine deiminase pathway, and (iii) an L-arginine oxidase/dehydrogenase pathway. A transcript analysis of cells grown either with nitrate or L-arginine as sole N-source and with an illumination of 50 mumol photons m-2 s-1 showed that the transcripts for the first enzyme(s) of all three pathways were present, but that the transcript levels for the L-arginine deiminase and the L-arginine oxidase/dehydrogenase were substantially higher than that of the three isoenzymes of L-arginine decarboxylase.CONCLUSION:The evaluation of 24 cyanobacterial genomes revealed that five different L-arginine-degrading pathways are present in the investigated cyanobacterial species. In Synechocystis sp. PCC 6803 an L-arginine deiminase pathway and an L-arginine oxidase/dehydrogenase pathway represent the major pathways, while the L-arginine decarboxylase pathway most likely only functions in polyamine biosynthesis. The transcripts encoding the enzymes of the two major pathways were constitutively expressed with the exception of the transcript for the carbamate kinase, which was substantially up-regulated in cells grown with L-arginine.
Erscheinungsjahr
2007
Zeitschriftentitel
BMC Genomics
Band
8
Ausgabe
1
Art.-Nr.
437
ISSN
1471-2164
Page URI
https://pub.uni-bielefeld.de/record/2438963
Zitieren
Schriek S, Rückert C, Staiger D, Pistorius EK, Michel K-P. Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803. BMC Genomics. 2007;8(1): 437.
Schriek, S., Rückert, C., Staiger, D., Pistorius, E. K., & Michel, K. - P. (2007). Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803. BMC Genomics, 8(1), 437. https://doi.org/10.1186/1471-2164-8-437
Schriek, Sarah, Rückert, Christian, Staiger, Dorothee, Pistorius, Elfriede K., and Michel, Klaus-Peter. 2007. “Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803”. BMC Genomics 8 (1): 437.
Schriek, S., Rückert, C., Staiger, D., Pistorius, E. K., and Michel, K. - P. (2007). Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803. BMC Genomics 8:437.
Schriek, S., et al., 2007. Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803. BMC Genomics, 8(1): 437.
S. Schriek, et al., “Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803”, BMC Genomics, vol. 8, 2007, : 437.
Schriek, S., Rückert, C., Staiger, D., Pistorius, E.K., Michel, K.-P.: Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803. BMC Genomics. 8, : 437 (2007).
Schriek, Sarah, Rückert, Christian, Staiger, Dorothee, Pistorius, Elfriede K., and Michel, Klaus-Peter. “Bioinformatic evaluation of L-arginine catabolic pathways in 24 cyanobacteria and transcriptional analysis of genes encoding enzymes of L-arginine catabolism in the cyanobacterium Synechocystis sp. PCC 6803”. BMC Genomics 8.1 (2007): 437.
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INTERPRO
3 Einträge gefunden, die diesen Artikel zitieren
Arginine_N-succinylTrfase (INTERPRO: IPR017650)
Protein family/domain name: Arginine N-succinyltransferase
Protein family/domain name: Arginine N-succinyltransferase
Arg/Orn_succinylTfrase_asu (INTERPRO: IPR017651)
Protein family/domain name: Arginine/ornithine succinyltransferase, alpha subunit
Protein family/domain name: Arginine/ornithine succinyltransferase, alpha subunit
Arg_succinylTrfase_AstA/AruG (INTERPRO: IPR007041)
Protein family/domain name: Arginine N-succinyltransferase AstA/AruG
Protein family/domain name: Arginine N-succinyltransferase AstA/AruG
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