Planta Med 2019; 85(18): 1571-1572
DOI: 10.1055/s-0039-3400403
Main Congress Poster
Poster Session 2
© Georg Thieme Verlag KG Stuttgart · New York

Isolation of Lyngbyatoxin and other Teleocidin species from, Streptomyces Blastmyceticum” culture

S Bieringer
1   Organic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, TUM Campus Straubing,, Schulgasse 16, 94315 Straubing, Germany
,
C Urmann
1   Organic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, TUM Campus Straubing,, Schulgasse 16, 94315 Straubing, Germany
,
K Saurav
2   Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický mlýn,, Novohradská 237, 379 81 Třeboň, Czech Republic
,
P Hrouzek
2   Laboratory of Algal Biotechnology—Centre ALGATECH, Institute of Microbiology of the Czech Academy of Sciences, Opatovický mlýn,, Novohradská 237, 379 81 Třeboň, Czech Republic
,
H Riepl
1   Organic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, TUM Campus Straubing,, Schulgasse 16, 94315 Straubing, Germany
› Author Affiliations
Further Information

Publication History

Publication Date:
20 December 2019 (online)

 

Teleocidines originally found in japanese soil bacteria e. g. “Streptomyces mediocidicus” or “Streptomyces blastmyceticum” have aroused interest due to their ability of promoting tumor growth[1]. The structural feature which combines all these Teleocidin type substances is a 9-membered lactam ring linked to an indole nucleus[2]. It was reported that also Lyngbyatoxin, a secondary metabolite of the Hawaiian blue-green algae “Lyngbya Majuscula”, shows this structural feature[3]. Lyngbyatoxin is well-known for causing seaweed dermatitis to swimmers in Hawaii or Okinawa. Due to the structural similarity Lyngbyatoxin apparently was also proved to be a Tumor-promoter[1],[4]. We hereby report that “Streptomyces Blastmyceticum” can be induced to produce a slightly different spectrum of metabolites, by an altered cultivation scheme. Bacteria growth was performed in a very peptone rich medium for 4-5 days. LC / MS analysis of the culture solution showed presence of Lyngbyatoxin and other Teleocidin species. After centrifugation of the biomass, the supernatant solution was extracted with Amberlite XAD 1180N for 1 day. The crude extract was further purified by open normal phase and HPLC reversed phase chromatography. The LC / MS diagram of the purified compound can be seen in the figure below. The exact mass of Lyngbyatoxin was detected with less than 1 ppm error. Other Teleocidin compounds such as Olivoretin and Teleocidin B have been isolated in a similar manner. For further experiments other cultivation conditions will be tested on different strains of “Streptomyces” and the occurrence of Teleocidin compounds will be investigated.

Zoom Image
Fig. 1 Upper picture: Chromatogram of crude Amberlite extract, lower picture: Enrichment of purified compound Lyngbyatoxin
 
  • References

  • 1 Fujiki H, Mori M, Nakayasu M, Terada M, Sugimura T, Moore RE. Indole alkaloids: Dihydroteleocidin B, teleocidin, and lyngbyatoxin A as members of a new class of tumor promoters. Proc Natl Acad Sci USA 1981; 78: 3872-3876
  • 2 Sakai S, Aimi N, Yamaguchi K, Hitotsuyanagi Y, Watanabe C, Yokose K, Koyama Y, Shudo K, Itai A. Elucidation of the structure of olivoretin A and D (Teleocidin B). Chem Pharm Bull 1984; 32: 354-357
  • 3 Cardellina JH, Marner F, Moore RE. Seaweed Dermatitis: Structure of Lyngbyatoxin A. Sci 1979; 204: 193-195
  • 4 Fujiki H, Sugimura T, Moore RE. New Classes of Environmental Tumor Promoters: Indole Alkaloids and Polyacetates. Environ Health Perspect 1983; 50: 85-90.