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利用融合到 dCas9(Cas9-Lag)的位置标签来操纵 DNA 表达盒的位置,以提高代谢途径效率。

Manipulating the position of DNA expression cassettes using location tags fused to dCas9 (Cas9-Lag) to improve metabolic pathway efficiency.

机构信息

College of Biotechnology, Tianjin University of Science and Technology, Tianjin, 300457, P. R. China.

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, P. R. China.

出版信息

Microb Cell Fact. 2020 Dec 14;19(1):229. doi: 10.1186/s12934-020-01496-w.

Abstract

BACKGROUND

Deactivated Cas9 (dCas9) led to significant improvement of CRISPR/Cas9-based techniques because it can be fused with a variety of functional groups to form diverse molecular devices, which can manipulate or modify target DNA cassettes. One important metabolic engineering strategy is to localize the enzymes in proximity of their substrates for improved catalytic efficiency. In this work, we developed a novel molecular device to manipulate the cellular location of specific DNA cassettes either on plasmids or on the chromosome, by fusing location tags to dCas9 (Cas9-Lag), and applied the technique for synthetic biology applications. Carotenoids like β-carotene serve as common intermediates for the synthesis of derivative compounds, which are hydrophobic and usually accumulate in the membrane compartment.

RESULTS

Carotenoids like β-carotene serve as common intermediates for the synthesis of derivative compounds, which are hydrophobic and usually accumulate in the membrane components. To improve the functional expression of membrane-bound enzymes and localize them in proximity to the substrates, Cas9-Lag was used to pull plasmids or chromosomal DNA expressing carotenoid enzymes onto the cell membrane. For this purpose, dCas9 was fused to the E. coli membrane docking tag GlpF, and gRNA was designed to direct this fusion protein to the DNA expression cassettes. With Cas9-Lag, the zeaxanthin and astaxanthin titer increased by 29.0% and 26.7% respectively. Due to experimental limitations, the electron microscopy images of cells expressing Cas9-Lag vaguely indicated that GlpF-Cas9 might have pulled the target DNA cassettes in close proximity to membrane. Similarly, protein mass spectrometry analysis of membrane proteins suggested an increased expression of carotenoid-converting enzymes in the membrane components.

CONCLUSION

This work therefore provides a novel molecular device, Cas9-Lag, which was proved to increase zeaxanthin and astaxanthin production and might be used to manipulate DNA cassette location.

摘要

背景

失活 Cas9(dCas9)显著提高了基于 CRISPR/Cas9 的技术,因为它可以与各种功能基团融合,形成多种分子设备,从而可以操作或修饰靶 DNA 盒。一种重要的代谢工程策略是将酶定位于其底物附近,以提高催化效率。在这项工作中,我们开发了一种新型分子设备,通过将定位标签与 dCas9(Cas9-Lag)融合,来操纵特定 DNA 盒在质粒或染色体上的细胞位置,并将该技术应用于合成生物学应用。类胡萝卜素如β-胡萝卜素作为合成衍生化合物的常见中间体,这些化合物具有疏水性,通常在膜组分中积累。

结果

类胡萝卜素如β-胡萝卜素作为合成衍生化合物的常见中间体,这些化合物具有疏水性,通常在膜组分中积累。为了提高膜结合酶的功能表达并将其定位于靠近底物的位置,Cas9-Lag 被用于将表达类胡萝卜素酶的质粒或染色体 DNA 拉到细胞膜上。为此,将 dCas9 融合到大肠杆菌膜停泊标签 GlpF 上,并设计了 gRNA 来指导该融合蛋白到 DNA 表达盒。使用 Cas9-Lag,叶黄素和虾青素的产量分别增加了 29.0%和 26.7%。由于实验限制,表达 Cas9-Lag 的细胞的电子显微镜图像模糊地表明,GlpF-Cas9 可能将靶 DNA 盒拉近了膜。同样,膜蛋白的蛋白质质谱分析表明,膜成分中类胡萝卜素转化酶的表达增加。

结论

因此,本工作提供了一种新型分子设备 Cas9-Lag,它被证明可以提高叶黄素和虾青素的产量,并可能用于操纵 DNA 盒的位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/730f/7737257/cd0a4b1db473/12934_2020_1496_Fig1_HTML.jpg

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