| 第一作者： | Feng, XM (Feng, Xinming); Jin, MM (Jin, Miaomiao); Huang, W (Huang, Wei); Liu, W (Liu, Wei); Xian, M (Xian, Mo); |
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| 联系作者： | Feng, XM (Feng, Xinming); Jin, MM (Jin, Miaomiao); Huang, W (Huang, Wei); Liu, W (Liu, Wei); Xian, M (Xian, Mo); |
| 发表年度： | 2021 |
| 期： | 1 |
| 卷： | 20 |
| 页： | - |
| 摘要： | Background: Fluorinases play a unique role in the production of fluorine-containing organic molecules by biological methods. Whole-cell catalysis is a better choice in the large-scale fermentation processes, and over 60% of industrial biocatalysis uses this method. However, the in vivo catalytic efficiency of fluorinases is stuck with the mass transfer of the substrates. Results: A gene sequence encoding a protein with fluorinase function was fused to the N-terminal of ice nucleation protein, and the fused fluorinase was expressed in Escherichia coli BL21(DE3) cells. SDS-PAGE and immunofluorescence microscopy were used to demonstrate the surface localization of the fusion protein. The fluorinase displayed on the surface showed good stability while retaining the catalytic activity. The engineered E.coli with surface-displayed fluorinase could be cultured to obtain a larger cell density, which was beneficial for industrial application. And 55% yield of 5'-fluorodeoxyadenosine (5'-FDA) from S-adenosyl-L-methionine (SAM) was achieved by using the whole-cell catalyst. Conclusions: Here, we created the fluorinase-containing surface display system on E.coli cells for the first time. The fluorinase was successfully displayed on the surface of E.coli and maintained its catalytic activity. The surface display provides a new solution for the industrial application of biological fluorination. |
| 刊物名称： | MICROBIAL CELL FACTORIES |
| 影响因子： | 0 |
| 全文链接： | https://microbialcellfactories.biomedcentral.com/articles/10.1186/s12934-021-01697-x |
