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无标记系统利用核糖体启动子增强红串酵母木糖/葡萄糖异构酶的生产。

Marker-Free System Using Ribosomal Promoters Enhanced Xylose/Glucose Isomerase Production in Streptomyces rubiginosus.

机构信息

State Key Laboratory of Microbial Metabolism, School of Life Science and Biotechnology, Shanghai Jiao Tong University, Shanghai, 200030, P. R. China.

Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education and School of Pharmaceutical Sciences, Wuhan University, Wuhan, 430071, P. R. China.

出版信息

Biotechnol J. 2019 Nov;14(11):e1900114. doi: 10.1002/biot.201900114. Epub 2019 Aug 22.

Abstract

Xylose/glucose isomerases are important industrial enzymes that are most widely used in food industries; however, their previously reported expression levels do not meet the requirements for industrial application. Here, an antibiotic resistance marker (ARM)-free system driven by ribosomal RNA (rRNA) promoters is developed to obtain high-level xylose/glucose isomerase (XI/GI) expression in Streptomyces rubiginosus (S. rubiginosus). The rRNA promoter rrnD yields the highest glucose isomerase production titer of XIs/GIs, which is eight times higher than that of ermEp* and 2.6 times higher than that of kasOp*. The integrated ARM gene is removed by further introduction of the Cre plasmid with a temperature-sensitive replicon. The production titer of XIs/GIs is further improved by replacing the xylR gene with an additional expression glucose isomerase cassette at the xylR locus. Ultimately, the glucose isomerase activity reaches up to 79.7 ± 7.5 U mL at 96 h. The results support the robustness and stability of XI/GI production with this ARM-free system using optimal ribosomal promoters in S. rubiginosus, demonstrating strong potential in large-scale industrial applications. Besides, the results imply that rRNA promoters are strong promoters that can be used for protein engineering or metabolic engineering.

摘要

木糖/葡萄糖异构酶是重要的工业酶,在食品工业中应用最为广泛;然而,它们以前报道的表达水平不符合工业应用的要求。在这里,开发了一种无抗生素抗性标记(ARM)系统,该系统由核糖体 RNA(rRNA)启动子驱动,用于在绛红链轮丝菌(S. rubiginosus)中获得高水平的木糖/葡萄糖异构酶(XI/GI)表达。rRNA 启动子 rrnD 产生的葡萄糖异构酶产量最高,是 ermEp的 8 倍,是 kasOp的 2.6 倍。通过进一步引入带有温度敏感复制子的 Cre 质粒,去除整合的 ARM 基因。通过在 xylR 基因座用额外的表达葡萄糖异构酶盒替换 xylR 基因,进一步提高了 XIs/GIs 的生产效价。最终,葡萄糖异构酶活性在 96 小时时达到 79.7±7.5 U/mL。这些结果表明,在绛红链轮丝菌中使用最优的核糖体启动子,该无 ARM 系统生产 XI/GI 具有稳健性和稳定性,在大规模工业应用中具有很强的潜力。此外,结果表明 rRNA 启动子是强启动子,可用于蛋白质工程或代谢工程。

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