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基于 CRISPR/Cas9 的丝状真菌里氏木霉基因组工程及其在 L-乳酸生产中的应用。

CRISPR/Cas9-based genome engineering in the filamentous fungus Rhizopus oryzae and its application to L-lactic acid production.

机构信息

Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, Anhui, P. R. China.

Science Island Branch of Graduate, University of Science and Technology of China, Hefei, Anhui, P. R. China.

出版信息

Biotechnol J. 2024 Sep;19(9):e2400309. doi: 10.1002/biot.202400309.

Abstract

The filamentous fungus Rhizopus oryzae is one of the main industrial strains for the production of a series of important chemicals such as ethanol, lactic acid, and fumaric acid. However, the lack of efficient gene editing tools suitable for R. oryzae makes it difficult to apply technical methods such as metabolic engineering regulation and synthetic biology modification. A CRISPR-Cas9 system suitable for efficient genome editing in R. oryzae was developed. Firstly, four endogenous U6 promoters of R. oryzae were identified and screened with the highest transcriptional activity for application to sgRNA transcription. It was then determined that the U6 promoter mediated CRISPR/Cas9 system has the ability to efficiently edit the genome of R. oryzae through NHEJ and HDR-mediated events. Furthermore, the newly constructed CRISPR-Cas9 dual sgRNAs system can simultaneously disrupt or insert different fragments of the R. oryzae genome. Finally, this CRISPR-Cas9 system was applied to the genome editing of R. oryzae by knocking out pyruvate carboxylase gene (PYC) and pyruvate decarboxylase gene (pdcA) and knocking in phosphofructokinase (pfkB) from Escherichia coli and L-lactate dehydrogenase (L-LDH) from Heyndrickxia coagulans, which resulted in a substantial increase in L-LA production. In summary, this study showed that the CRISPR/Cas9-based genome editing tool is efficient for manipulating genes in R. oryzae.

摘要

米根霉是生产一系列重要化学品(如乙醇、乳酸和富马酸)的主要工业菌株之一。然而,缺乏适合米根霉的高效基因编辑工具,使得代谢工程调控和合成生物学改造等技术方法难以应用。本研究开发了一种适合米根霉高效基因组编辑的 CRISPR-Cas9 系统。首先,鉴定并筛选了米根霉的四个内源性 U6 启动子,以获得最高的转录活性,用于 sgRNA 转录。结果表明,U6 启动子介导的 CRISPR/Cas9 系统通过 NHEJ 和 HDR 介导的事件具有高效编辑米根霉基因组的能力。此外,新构建的 CRISPR-Cas9 双 sgRNAs 系统可以同时敲除或插入米根霉基因组的不同片段。最后,该 CRISPR-Cas9 系统被用于敲除米根霉的丙酮酸羧化酶基因(PYC)和丙酮酸脱羧酶基因(pdcA),并敲入大肠杆菌的磷酸果糖激酶(pfkB)和 Heyndrickxia coagulans 的 L-乳酸脱氢酶(L-LDH),从而使 L-乳酸产量显著增加。综上所述,本研究表明基于 CRISPR/Cas9 的基因组编辑工具在米根霉基因操作中具有高效性。

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