吸附树脂对吸湿链霉菌VKM Ac-2737D生物合成雷帕霉素的影响

V. Dzhavakhiya, E. Glagoleva, A. V. Matsyura
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摘要

雷帕霉素是吸湿链霉菌的代谢物,在医学上具有广泛的治疗应用。然而,其使用的可能性非常有限,因为这种微生物的现有天然菌株的生产率相当低,这对该物质的成本及其工业生产的可能数量产生了负面影响。与此同时,过量生产菌株的商业用途也很成问题,因为它们分泌大量代谢物,抑制微生物培养物的生长和目标产品的生物合成。解决该问题的一种可能方法包括在发酵培养基中添加吸附剂以结合过量代谢物。本研究对五种不同的选择性吸附树脂DIAION™HP20、DIAION™HP21、DIAION™hp20ss、Chromolite和LPS-500进行了测试,为早期开发的高活性吸湿链球菌VKM Ac-2737D生物合成雷帕霉素提供了最佳条件。实验在15l的生物反应器中进行,使用先前开发的优化发酵培养基并添加测试树脂。采用Chromolite 15AD2吸附树脂获得的雷帕霉素产率最高(1420±5 mg/L);这个结果比先前得到的产量高出11.4%。该树脂的吸附量为92%,可显著促进工业条件下雷帕霉素的分离和纯化过程。研究结果对进一步扩大雷帕霉素的工业化生产具有一定的参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of adsorbing resins on the rapamycin biosynthesis by Streptomyces hygroscopicus VKM Ac-2737D
Rapamycin, a metabolite of Streptomyces hygroscopicus, has a wide range of therapeutic applications in medicine. However, the possibility of its use is significantly limited, since the existing natural strains of this microorganism have rather low productivity that negatively influences the cost of the substance and the possible volumes of its industrial production. At the same time, the commercial use of overproducing strains is also very problematic, since they secrete a large number of metabolites suppressing both the growth of microbial culture and the biosynthesis of a target product. A possible way to solve the problem includes the addition of adsorbents to a fermentation medium for the binding of excess metabolites. In this study, five different selective adsorbing resins, DIAION™ HP20, DIAION™ HP21, DIAION™ HP 20SS, Chromolite, and LPS-500 were tested to provide optimal conditions for the rapamycin biosynthesis by the earlier developed highly-active S. hygroscopicus strain VKM Ac-2737D. The experiments were performed in a 15-L bioreactor using the optimized fermentation medium developed earlier and supplemented with the tested resins. The highest rapamycin yield (1420±5 mg/L) was obtained using a Chromolite 15AD2 adsorbing resin; this result exceeds the earlier obtained yield by 11.4%. The sorptive capacity of this resin was 92% that may significantly facilitate the processes of rapamycin isolation and purification under industrial conditions. The results of the study may be of certain interest for the further scaling-up of the industrial rapamycin production.
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