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A Microfluidic Platform for High-Throughput Screening of Small Mutant Libraries

机译:用于小突变图书馆的高通量筛选的微流体平台。

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摘要

The screening and isolation of target microorganisms from mutated recombinant libraries are crucial for the advancement of synthetic biology and metabolic engineering. However, conventional screening tools present several limitations in throughput, cost, and labor. Herein, we describe a novel microfluidic high-throughput screening (HTS) platform with several advantages. The platform utilizes a fluid array to compartmentalize bacterial cells in well-ordered separated microwells and allows long-term cell culture with high throughput. The platform enables the extraction of selected target cells from the fluid array for additional culture and postanalysis by using a capillary-driven sample relocation method. To confirm the feasibility of the platform, we demonstrated two different types of HTS methods based on the levels of reporter gene expression and cellular growth rate difference. For the reporter gene-based HTS, a spike recovery approach was taken to demonstrate that target cells are successfully screened out from a mixture containing nontarget cells by repeating the culture and extraction processes. Additionally, the same platform allowed us to screen and sort target cells according to their cellular growth rate difference, which seems hard in conventional screening methods. Hence, the platform could be used for various microbiological assays, including the detection of cell-excreted metabolites, microbial biosensors, and other HTS systems.
机译:从突变的重组文库中筛选和分离目标微生物对于合成生物学和代谢工程的发展至关重要。然而,常规的筛选工具在生产量,成本和人工上存在一些限制。在这里,我们描述了一种新颖的微流控高通量筛选(HTS)平台,具有多个优点。该平台利用流体阵列将细菌细胞分隔在秩序井然的分离微孔中,并允许以高通量进行长期细胞培养。该平台能够通过使用毛细管驱动的样品重定位方法从流体阵列中提取选定的靶细胞,以进行其他培养和后分析。为了证实该平台的可行性,我们基于报道基因表达水平和细胞生长速率差异展示了两种不同类型的HTS方法。对于基于报告基因的HTS,采用加标回收方法来证明通过重复培养和提取过程从含有非靶细胞的混合物中成功筛选出靶细胞。另外,同一平台使我们能够根据靶细胞的细胞生长率差异对其进行筛选和分类,这在常规筛选方法中似乎很难。因此,该平台可用于各种微生物测定,包括检测细胞分泌的代谢产物,微生物生物传感器和其他HTS系统。

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