Regulation of Phycocyanin Development by Phenolic Compounds in the Cyanobacterium Anabaena sp. PCC 7120

  • Published : 2006.12.30

Abstract

Phenolic compounds are manufacturing by-products commonly found in industrial wastewater. The toxicity of high level phenolic compounds in wastewater threatens not only the aquatic organisms, but also many components of the adjacent ecosystem. One of the major light harvesting pigments in cyanobacteria is phycocyanin which can be rapidly and specifically degraded by external stimuli such as nutritional depletion or environmental stress. We employed the cyanobacterium Anabaena sp. PCC 7120 as an indicator organism in estimating the pollution level by phenolic compounds. The phycocyanin content of the cyanobacterium decreased without significantly altering the total chlorophyll as the phenol concentration in a medium increased. We examined the phenol contamination level using the correlation of the phycocyanin content and the phenol concentration. Our results indicated that no significant pollution by phenolic compounds was found in several waterbodies in the vicinity of Daegu, South Korea.

Keywords

References

  1. Bryant, D.A. 1986. The cyanobacterial photosynthetic apparatus: comparisons to those of higher plants and photosynthetic bacteria. Canadian Bulleein of Fishers and Aquatic Sciences 214: 423-500
  2. Cronin, M.T., J.C. Dearden and A.J. Dobbs, 1991. QSAR studies of comparative toxicity in aquatic organisms. The Science of the Total Environment 109/110: 431-439 https://doi.org/10.1016/0048-9697(91)90198-N
  3. Chen, C-Y., J-N. Chen and S-D. Chen. 1999. Toxicity assessment of industrial wastewater by microbial testing method. Water Science and Technology 39: 139-143
  4. Collier, J.L. and A.R. Grossman. 1992. Chlorosis induced by nutrient deprivation in Synechococcus sp. strain PCC 7942: not all bleaching is the same. Journal of Bacteriology 174: 4718-4726 https://doi.org/10.1128/jb.174.14.4718-4726.1992
  5. Elmorjani, K., J.-C. Thomas and P. Sebban. 1986. Phycobilisomes of wild type and pigment mutants of the cyanobacterium Synechocystis PCC 6803. Archives of Microbiology 146: 186-191 https://doi.org/10.1007/BF00402349
  6. Glauser, M., D.A. Bryant, G. Frank, E. Wehrli, S.S. Rusconi, W. Sidler and H. Zuber. 1992. Phycobilisome structure in the cyanobacteria Mastigocladus laminosus and Anabaena sp. PCC 7120. European Journal of Biohemistry 205: 907-915 https://doi.org/10.1111/j.1432-1033.1992.tb16857.x
  7. Glazer, A.N. 1989. Light guides. Directional energy transfer in a photosynthetic antenna. Journal of Biological Chemistry 264: 1-4
  8. International Agency for Research on Cancer IARC, 1999. Summaries and evaluations. Phenol 71: 749
  9. Kirk-Othmer, 1978. Encyclopedia of chemical technology, 3rd ed. Wiley-Onterscience, New York
  10. Pardos, M., C. Benninghoff and R.L. Thomas. 1998. Photosynthetic and populations growth response of the test alga Selenastrum capricornutum Printz to zinc, cadmium, an dsuspended sediment elutriates. Journal of Applied Phycology 10: 145-151 https://doi.org/10.1023/A:1008043931094
  11. Richaud. C., G. Zabulon, A. Joder and J.-C. Thomas. 2001. Nitrogen or sulfur starvation differentially affects phycobilisome degradation and expression of nblA gene in Synechocystis strain PCC 6803. Journal of Bacteriology 183: 2989-2994 https://doi.org/10.1128/JB.183.10.2989-2994.2001
  12. Trevizo, C. and N. Nirmalakhandan. 1999. Prediction of microbial toxicity of industrial organic chemicals. Water Science and Technology 3910/3911: 63-69