Microbial conversion of .EPSILON.-pyrromycinone and .EPSILON.-isorhodomycinone to 1-hydroxy-13-dihydrodaunomycin and n-formyl-1-hydroxy-13-dihydrodaunomycin and their bioactivities.
- 1 January 1980
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 33 (10) , 1150-1157
- https://doi.org/10.7164/antibiotics.33.1150
Abstract
New anthracycline antibiotics, I-hydroxy-13-dihydrodaunomycin and N-formyl-1-hydroxy-13-dihydrodaunomycin were biosynthesized by a blocked mutant of Streptomyces coeruleorubidus ME130-A4 from .epsilon.-pyrromycinone or .epsilon.-isorhodomycinine.This publication has 4 references indexed in Scilit:
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- The structure of baumycins A1, A2, B1, B2, C1 and C2.The Journal of Antibiotics, 1977
- Baumycins, new antitumor antibiotics related to daunomycin.The Journal of Antibiotics, 1977
- New anthracycline antibiotics, rhodirubins.The Journal of Antibiotics, 1977