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链霉菌的深层发酵为安丝菌素的生物合成、工程改造及生产提供了一个生物技术平台。

Submerged fermentation of Streptomyces uncialis providing a biotechnology platform for uncialamycin biosynthesis, engineering, and production.

作者信息

Yang Dong, Luo Jun, Huang Tingting, Yan Xiaohui, Adhikari Ajeeth, Teijaro Christiana N, Ge Huiming, Shen Ben

机构信息

Department of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.

Natural Products Discovery Center at Scripps Research, The Scripps Research Institute, Jupiter, FL 33458, USA.

出版信息

J Ind Microbiol Biotechnol. 2021 Jun 4;48(3-4). doi: 10.1093/jimb/kuab025.

Abstract

Uncialamycin (UCM) belongs to the anthraquinone-fused subfamily of 10-membered enediyne natural products that exhibits an extraordinary cytotoxicity against a wide spectrum of human cancer cell lines. Antibody-drug conjugates, utilizing synthetic analogues of UCM as payloads, are in preclinical development. UCM is exclusively produced by Streptomyces uncialis DCA2648 on solid agar medium with low titers (∼0.019 mg/l), limiting its supply by microbial fermentation and hampering its biosynthetic and engineering studies by in vivo pathway manipulation. Here, we report cultivation conditions that enable genetic manipulation of UCM biosynthesis in vivo and allow UCM production, with improved titers, by submerged fermentation of the engineered S. uncialis strains. Specifically, the titer of UCM was improved nearly 58-fold to ∼1.1 mg/l through the combination of deletion of biosynthetic gene clusters encoding unrelated metabolites from the S. uncialis wild-type, chemical mutagenesis and manipulation of pathway-specific regulators to generate the engineered S. uncialis strains, and finally medium optimization of the latter for UCM production. Genetic manipulation of UCM biosynthesis was demonstrated by inactivating selected genes in the engineered S. uncialis strains, one of which afforded a mutant strain accumulating tiancimycin B, a common biosynthetic intermediate known for the anthraquinone-fused subfamily of enediyne natural products. These findings highlight a biotechnology platform for UCM biosynthesis, engineering, and production that should facilitate both its fundamental studies and translational applications.

摘要

钩丝霉素(UCM)属于10元烯二炔天然产物的蒽醌稠合亚家族,对多种人类癌细胞系表现出非凡的细胞毒性。以UCM的合成类似物为有效载荷的抗体-药物偶联物正处于临床前开发阶段。UCM仅由钩丝链霉菌DCA2648在固体琼脂培养基上产生,效价较低(约0.019毫克/升),这限制了其通过微生物发酵的供应,并阻碍了通过体内途径操纵对其进行生物合成和工程研究。在此,我们报告了一些培养条件,这些条件能够在体内对UCM生物合成进行基因操作,并通过对工程化的钩丝链霉菌菌株进行深层发酵实现UCM的生产,且效价有所提高。具体而言,通过删除钩丝链霉菌野生型中编码不相关代谢产物的生物合成基因簇、化学诱变以及对途径特异性调节因子进行操纵以产生工程化的钩丝链霉菌菌株,最后对后者进行用于UCM生产的培养基优化,UCM的效价提高了近58倍,达到约1.1毫克/升。通过使工程化的钩丝链霉菌菌株中的选定基因失活,证明了对UCM生物合成的基因操作,其中一个基因产生了一个积累天丝霉素B的突变菌株,天丝霉素B是蒽醌稠合烯二炔天然产物亚家族中一种常见的生物合成中间体。这些发现突出了一个用于UCM生物合成、工程和生产的生物技术平台,该平台应有助于其基础研究和转化应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c7/9113176/ed89a1a9245d/kuab025fig1.jpg

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