Streptomyces setonii

Pometto AL, JB Sutherland, DL Crawford (1981) Streptomyces setonii catabolism of vanillic acid viaguaiacol and catechol. Can J Microbiol 27 636-638. 

Sutherland JB, DL Crawford, AL Pometto (1983) Metabolism of cinnamic, /7-coumaric, and ferulic acids by Streptomyces setonii. Can J Microbiol 29 1253-1257. 

Among the P-amino acid derivatives of cycloalkanes, one of the most exciting is (l/ ,25)-2-aminocyclopentanecarboxylic acid (cispentacin), an antifungal antibiotic, recently isolated independently by two Japanese groups from Bacillus cereus [2] and Streptomyces setonii [3]. 

Celastramycin B (22a) has been isolated together with celastramycin A (which is a halogenated acylpyrrole, and not an anthracycline) from endophytic Streptomyces setonii and S. sampsonii growing on wood of different Celastraceae plants [41]. It was the only halogen-containing anthracycline ... 

Larsen SH, Berry DM, Paschal JW, Gilliam JM. S-Hydroxymethylblasticidin S and blasti-cidin S from Streptomyces setonii culture A83094. ] Antibiot 1989 42 470-471. 

Ci8H28Ng06 452.469 From Streptomyces setonii. Phytotoxin. Herbicide. 

Several microorganisms have been discovered and/or engineered that are able to produce vanillin in high yields from ferulic acid. The most important strains for this purpose are ceitz n y Amycolatopsis sp. in particular, ATCC 39116 (formerly known as Streptomyces setonii) afforded a yield of 13.9 gl" [45,46]. 

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