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通过调节 Crp 介导的调控来优化土曲霉素链霉菌中 FK-506 的生产。

Optimization of FK-506 production in Streptomyces tsukubaensis by modulation of Crp-mediated regulation.

机构信息

Department of Microbiology and Biotechnology, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany.

Novartis AG, Stein, Switzerland.

出版信息

Appl Microbiol Biotechnol. 2023 May;107(9):2871-2886. doi: 10.1007/s00253-023-12473-9. Epub 2023 Mar 23.

Abstract

FK-506 is a potent immunosuppressive macrocyclic polyketide with growing pharmaceutical interest, produced by Streptomyces tsukubaensis. However, due to low levels synthesized by the wild-type strain, biotechnological production of FK-506 is rather limited. Optimization strategies to enhance the productivity of S. tsukubaensis by means of genetic engineering have been established. In this work primarily global regulatory aspects with respect to the FK-506 biosynthesis have been investigated with the focus on the global Crp (cAMP receptor protein) regulator. In expression analyses and protein-DNA interaction studies, the role of Crp during FK-506 biosynthesis was elucidated. Overexpression of Crp resulted in two-fold enhancement of FK-506 production in S. tsukubaensis under laboratory conditions. Further optimizations using fermentors proved that the strategy described in this study can be transferred to industrial scale, presenting a new approach for biotechnological FK-506 production. KEY POINTS: • The role of the global Crp (cAMP receptor protein) regulator for FK-506 biosynthesis in S. tsukubaensis was demonstrated • Crp overexpression in S. tsukubaensis was applied as an optimization strategy to enhance FK-506 and FK-520 production resulting in two-fold yield increase.

摘要

FK-506 是一种具有潜在免疫抑制作用的大环聚酮类化合物,具有越来越大的药物研发价值,由链霉菌(Streptomyces tsukubaensis)产生。然而,由于野生型菌株合成水平较低,FK-506 的生物技术生产受到限制。已经建立了通过遗传工程来优化链霉菌(Streptomyces tsukubaensis)生产能力的策略。在这项工作中,主要研究了 FK-506 生物合成的全局调控方面,重点关注全局 Crp(cAMP 受体蛋白)调节剂。在表达分析和蛋白-DNA 相互作用研究中,阐明了 Crp 在 FK-506 生物合成过程中的作用。在实验室条件下,Crp 的过表达导致 FK-506 的产量增加了两倍。在发酵罐中进一步优化证明,本研究中描述的策略可以转移到工业规模,为 FK-506 的生物技术生产提供了一种新方法。关键点:

  • 证明了全局 Crp(cAMP 受体蛋白)调节剂在链霉菌(Streptomyces tsukubaensis)中对 FK-506 生物合成的作用。

  • 将 Crp 在链霉菌(Streptomyces tsukubaensis)中的过表达应用于优化策略,以提高 FK-506 和 FK-520 的产量,使产量增加了两倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/10106351/0fdb645857fc/253_2023_12473_Fig1_HTML.jpg

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