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The Selective Inhibitory Activity of a Fusaricidin Derivative on a Bloom-Forming Cyanobacterium, Microcystis sp.

  • Ko, So-Ra (Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Lee, Young-Ki (IPst Company) ;
  • Srivastava, Ankita (Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Park, Seung-Hwan (Infections Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Ahn, Chi-Yong (Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Oh, Hee-Mock (Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB))
  • Received : 2018.04.14
  • Accepted : 2018.10.25
  • Published : 2019.01.28

Abstract

Fusaricidin analogs, produced by Paenibacillus polymyxa, were tested for selective control of a major bloom-forming cyanobacterium, Microcystis sp. Fusaricidin (A and B mixtures) and four analogs were isolated from P. polymyxa E681 and investigated for their inhibition of cyanobacterial cell growth. Among the four fusaricidin analogs, fraction 915 Da (designated as Fus901) showed growth inhibition activity for Microcystis aeruginosa but not for Anabaena variabilis and Scenedesmus acutus. Microcystin concentration decreased up to 70% and its content per cell also decreased over 50% after 3 days. Fusaricidin exhibited growth inhibition against Gram-positive bacteria but Fus901 did not. Molecular weights of fusaricidin A and B were 883 Da and 897 Da, whereas that of Fus901 was 915 Da. Structure analysis by a ring-opening method revealed a linear form for Fus901. Expression of the pod gene related to oxidative stress was increased 2.1-fold by Fus901 and that of mcyD decreased up to 40%. These results indicate that Fus901 exerts oxidative stress against M. aeruginosa. Thus, Fus901 can be used as a selective cyanobactericide without disturbing the ecological system and could help in decreasing the microcystin concentration.

Keywords

Acknowledgement

Supported by : National Research Foundation (NRF)

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