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MeSH Review

Aphanizomenon

 
 
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Disease relevance of Aphanizomenon

  • In all methods, Anabaena strains that produced different toxic compounds (e.g. anatoxin-a, microcystin and an unknown neurotoxin) were clustered separately from each other but were grouped either with non-toxic Anabaena and/or Aphanizomenon strains [1].
 

High impact information on Aphanizomenon

  • The picked Aphanizomenon colonies did not contain nodularin and the dissolved nodularin concentrations were below detection limit [2].
  • Correspondence analysis of Anabaena, Aphanizomenon and Cylindrospermum showed that all hepatotoxic Anabaena strains grouped together, whereas the non-toxic and neurotoxic Anabaena strains grouped with the non-toxic Aphanizomenon strains [3].
  • The rate of CO2/Mg2+ activation was inhibited by RuBP in all enzymes, although the concentration of RuBP required to inhibit activation in the enzyme from the cyanobacterium Aphanizomenon flos-aquae was increased by an order of magnitude compared to other higher plant structural-type enzymes [4].
  • Antioxidant properties of a novel phycocyanin extract from the blue-green alga Aphanizomenon flos-aquae [5].
  • A new natural derivative of the sulfated guanidinium zwitterionic toxin cylindrospermopsin, 7-epi-cylindrospermopsin, was recently isolated from the cyanobacterium Aphanizomenon ovalisporum (Forti) [6].
 

Chemical compound and disease context of Aphanizomenon

  • A toxic strain of Aphanizomenon flos-aquae (NH-1), isolated from a toxic bloom in a pond in Durham, New Hampshire, has been mass cultured in the laboratory [7].
  • Mueggelone, a novel inhibitor of fish development from the fresh water cyanobacterium Aphanizomenon flos-aquae [8].
  • The mycosporine-like amino acid (MAA), porphyra-334 (lambda(max) = 334 nm; epsilon = 42 300 M(-1)cm(-1)), was isolated from the aquatic cyanobacterium Aphanizomenon flos-aquae (AFA) and its structure was verified by spectroscopic methods [9].
 

Gene context of Aphanizomenon

  • Anabaenopeptins I (1) and J (2), two new ureido bond-containing cyclic peptides, were isolated from the cultured cyanobacterium Aphanizomenon flos-aquae (NIES-81) as potent carboxypeptidase-A (CPA) inhibitors [10].
  • A novel C18 lipid, containing a 10-membered lactone, mueggelone (1), was isolated from a field-collected sample of Aphanizomenon flos-aquae, together with the known compound lupenyl acetate (3) [8].

References

  1. Phylogenetic comparison of the cyanobacterial genera Anabaena and Aphanizomenon. Gugger, M., Lyra, C., Henriksen, P., Couté, A., Humbert, J.F., Sivonen, K. Int. J. Syst. Evol. Microbiol. (2002) [Pubmed]
  2. Associations of cyanobacterial toxin, nodularin, with environmental factors and zooplankton in the Baltic Sea. Repka, S., Meyerhöfer, M., von Bröckel, K., Sivonen, K. Microb. Ecol. (2004) [Pubmed]
  3. Cellular fatty acids as chemotaxonomic markers of the genera Anabaena, Aphanizomenon, Microcystis, Nostoc and Planktothrix (cyanobacteria). Gugger, M., Lyra, C., Suominen, I., Tsitko, I., Humbert, J.F., Salkinoja-Salonen, M.S., Sivonen, K. Int. J. Syst. Evol. Microbiol. (2002) [Pubmed]
  4. Species variation in kinetic properties of ribulose 1,5-bisphosphate carboxylase/oxygenase. Jordan, D.B., Ogren, W.L. Arch. Biochem. Biophys. (1983) [Pubmed]
  5. Antioxidant properties of a novel phycocyanin extract from the blue-green alga Aphanizomenon flos-aquae. Benedetti, S., Benvenuti, F., Pagliarani, S., Francogli, S., Scoglio, S., Canestrari, F. Life Sci. (2004) [Pubmed]
  6. Uracil moiety is required for toxicity of the cyanobacterial hepatotoxin cylindrospermopsin. Banker, R., Carmeli, S., Werman, M., Teltsch, B., Porat, R., Sukenik, A. J. Toxicol. Environ. Health Part A (2001) [Pubmed]
  7. Comparison of the toxins of the blue-green alga Aphanizomenon flos-aquae with the Gonyaulax toxins. Ikawa, M., Wegener, K., Foxall, T.L., Sasner, J.J. Toxicon (1982) [Pubmed]
  8. Mueggelone, a novel inhibitor of fish development from the fresh water cyanobacterium Aphanizomenon flos-aquae. Papendorf, O., König, G.M., Wright, A.D., Chorus, I., Oberemm, A. J. Nat. Prod. (1997) [Pubmed]
  9. Porphyra-334, a potential natural source for UVA protective sunscreens. Torres, A., Enk, C.D., Hochberg, M., Srebnik, M. Photochem. Photobiol. Sci. (2006) [Pubmed]
  10. New anabaenopeptins, potent carboxypeptidase-A inhibitors from the cyanobacterium Aphanizomenon flos-aquae. Murakami, M., Suzuki, S., Itou, Y., Kodani, S., Ishida, K. J. Nat. Prod. (2000) [Pubmed]
 
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