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Mycelium differentiation and development of Streptomyces coelicolor in lab-scale bioreactors: Programmed cell death differentiation and lysis are closely linked to undecylprodigiosin and actinorhodin production

机译:在实验室规模的生物反应器中菌丝体的分化和天蓝色链霉菌的发展:程序性细胞死亡分化和裂解与十一碳黄酮素和放线菌素的产生紧密相关

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摘要

Streptomycetes are mycelium-forming bacteria that produce two thirds of clinically relevant secondary metabolites. Secondary metabolite production is activated at specific developmental stages of Streptomyces life cycle. Despite this, Streptomyces differentiation in industrial bioreactors tends to be underestimated and the most important parameters managed are only indirectly related to differentiation: modifications to the culture media, optimization of productive strains by random or directed mutagenesis, analysis of biophysical parameters, etc. In this work the relationship between differentiation and antibiotic production in lab-scale bioreactors was defined. Streptomyces coelicolor was used as a model strain. Morphological differentiation was comparable to that occurring during pre-sporulation stages in solid cultures: an initial compartmentalized mycelium suffers a programmed cell death, and remaining viable segments then differentiate to a second multinucleated antibiotic-producing mycelium. Differentiation was demonstrated to be one of the keys to interpreting biophysical fermentation parameters and to rationalizing the optimization of secondary metabolite production in bioreactors.
机译:链霉菌是形成菌丝体的细菌,可产生三分之二的临床相关次生代谢产物。次生代谢产物的产生在链霉菌生命周期的特定发育阶段被激活。尽管如此,趋向于低估了工业生物反应器中链霉菌的分化,所管理的最重要的参数仅与分化间接相关:对培养基的修改,通过随机或定向诱变优化生产菌株,分析生物物理参数等。这项工作定义了实验室规模的生物反应器中分化与抗生素生产之间的关系。天蓝色链霉菌被用作模型菌株。形态学分化可与固态培养中成孢前阶段的分化相媲美:最初的区室菌丝体经历了程序性的细胞死亡,剩余的存活片段随后分化为第二个产生多核抗生素的菌丝体。差异被证明是解释生物物理发酵参数和合理化生物反应器中次生代谢产物优化的关键之一。

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