Immunosuppressive Activity of Elaiophylins

  • Lee, Sang-Yong (Department of Microbiology, Kyungpook National University) ;
  • Kim, Hang-Sub (Natural Products Biosynthesis R. U., Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Kim, Young-Ho (Natural Products Biosynthesis R. U., Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Han, Sang-Bae (Natural Products Biosynthesis R. U., Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Kim, Hwan-Mook (Natural Products Biosynthesis R. U., Korea Research Institute of Bioscience and Biotechnology (KRIBB)) ;
  • Hong, Soon-Duck (Department of Microbiology, Kyungpook National University) ;
  • Lee, Jung-Joon (Natural Products Biosynthesis R. U., Korea Research Institute of Bioscience and Biotechnology (KRIBB))
  • Published : 1997.08.01

Abstract

In the purification of elaiophylin from a culture of Streptomyces hygroscopicus MCY -846, mono- and di-methyl-elaiophylin were obtained through a O-methylation of the hemiketal hydroxy group of elaiophylin. All the three elaiophylins showed cytotoxicity against several human tumor cell lines and murine cell lines. Elaiophylin and monomethyl-elaiophylin also showed antimicrobial activities against gram-positive bacteria and potent inhibitory effects on the activation of B cells by lipopolysaccharide as well as on the proliferation of mouse splenic lymphocytes stimulated by mitogens but dimethyl-elaiophylin did not. This result indicates that elaiophylin and monomethyl-elaiophylin would be strong immunosuppressants. Furthermore this result revealed an interesting structure-activity relationship suggesting that the lack of symmetry and/or the free OH group at C-11 of elaiophylin might be important in conferring biological activities.

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