| Literature DB >> 29345939 |
Xiaohui Yan1, Huiming Ge1, Dong Yang1,2, Tingting Huang1, Ivana Crnovcic1, Chin-Yuan Chang1, Shi-Ming Fang1, Thibault Annaval1, Xiangcheng Zhu3,4, Yong Huang3, Li-Xing Zhao5, Yi Jiang5, Yanwen Duan3,4, Ben Shen1,2,6.
Abstract
The potent cytotoxicity and unique mode of action make the enediyne antitumor antibiotic C-1027 an exquisite drug candidate for anticancer chemotherapy. However, clinical development of C-1027 has been hampered by its low titer from the original producer Streptomyces globisporus C-1027. Here we report three new C-1027 alternative producers, Streptomyces sp. CB00657, CB02329, and CB03608, from The Scripps Research Institute actinomycetes strain collection. Together with the previously disclosed Streptomyces sp. CB02366 strain, four C-1027 alternative producers with C-1027 titers of up to 11-fold higher than the original producer have been discovered. The five C-1027 producers, isolated from distant geographic locations, are distinct Streptomyces strains based on morphology and taxonomy. Pulsed-field gel electrophoresis and Southern analysis of the five C-1027 producers reveal that their C-1027 biosynthetic gene clusters (BGCs) are all located on giant plasmids of varying sizes. The high nucleotide sequence similarity among the five C-1027 BGCs implies that they most likely have evolved from a common ancestor.Entities:
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Year: 2018 PMID: 29345939 PMCID: PMC6261254 DOI: 10.1021/acs.jnatprod.7b01013
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050