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通过对激酶Don3进行转录调控和化学抑制来控制非常规分泌以在[具体生物]中生产异源蛋白。

Controlling Unconventional Secretion for Production of Heterologous Proteins in through Transcriptional Regulation and Chemical Inhibition of the Kinase Don3.

作者信息

Hussnaetter Kai P, Philipp Magnus, Müntjes Kira, Feldbrügge Michael, Schipper Kerstin

机构信息

Institute for Microbiology, Heinrich Heine University Düsseldorf, Universitätsstraße 1, 40225 Düsseldorf, Germany.

出版信息

J Fungi (Basel). 2021 Mar 3;7(3):179. doi: 10.3390/jof7030179.

DOI:10.3390/jof7030179
PMID:33802393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7999842/
Abstract

Heterologous protein production is a highly demanded biotechnological process. Secretion of the product to the culture broth is advantageous because it drastically reduces downstream processing costs. We exploit unconventional secretion for heterologous protein expression in the fungal model microorganism . Proteins of interest are fused to carrier chitinase Cts1 for export via the fragmentation zone of dividing yeast cells in a lock-type mechanism. The kinase Don3 is essential for functional assembly of the fragmentation zone and hence, for release of Cts1-fusion proteins. Here, we are first to develop regulatory systems for unconventional protein secretion using Don3 as a gatekeeper to control when export occurs. This enables uncoupling the accumulation of biomass and protein synthesis of a product of choice from its export. Regulation was successfully established at two different levels using transcriptional and post-translational induction strategies. As a proof-of-principle, we applied autoinduction based on transcriptional regulation for the production and secretion of functional anti-Gfp nanobodies. The presented developments comprise tailored solutions for differentially prized products and thus constitute another important step towards a competitive protein production platform.

摘要

异源蛋白生产是一种需求旺盛的生物技术过程。将产物分泌到培养液中具有优势,因为这能大幅降低下游加工成本。我们利用非常规分泌方式在真菌模式微生物中进行异源蛋白表达。将感兴趣的蛋白与载体几丁质酶Cts1融合,通过分裂酵母细胞的裂解区以锁型机制输出。激酶Don3对于裂解区的功能组装至关重要,因此对于Cts1融合蛋白的释放也至关重要。在此,我们首次开发了用于非常规蛋白分泌的调控系统,使用Don3作为守门人来控制输出发生的时间。这使得生物质的积累和所选产物的蛋白合成与其输出得以解偶联。利用转录和翻译后诱导策略,成功在两个不同水平建立了调控。作为原理验证,我们应用基于转录调控的自诱导来生产和分泌功能性抗绿色荧光蛋白纳米抗体。所展示的进展包括针对不同价值产物的定制解决方案,因此朝着具有竞争力的蛋白生产平台又迈出了重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/8aa078550144/jof-07-00179-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/f55b7e4713e1/jof-07-00179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/a1604d0ec4f1/jof-07-00179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/cfcdfa0e5c61/jof-07-00179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/43192bc5b4f8/jof-07-00179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/7daf39f602fc/jof-07-00179-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/5625e19ea780/jof-07-00179-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/8aa078550144/jof-07-00179-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/f55b7e4713e1/jof-07-00179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/a1604d0ec4f1/jof-07-00179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/cfcdfa0e5c61/jof-07-00179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/43192bc5b4f8/jof-07-00179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/7daf39f602fc/jof-07-00179-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/5625e19ea780/jof-07-00179-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ada/7999842/8aa078550144/jof-07-00179-g007.jpg

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