posted on 2018-01-18, 21:13authored byXiaohui Yan, Hindra, Huiming Ge, Dong Yang, Tingting Huang, Ivana Crnovcic, Chin-Yuan Chang, Shi-Ming Fang, Thibault Annaval, Xiangcheng Zhu, Yong Huang, Li-Xing Zhao, Yi Jiang, Yanwen Duan, Ben Shen
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.