Lee You Jin, Lee Soojin, Kim Dong-Myung
Department of Chemical Engineering and Applied Chemistry, Daejeon, Korea.
Department of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Korea.
Front Bioeng Biotechnol. 2022 May 13;10:900162. doi: 10.3389/fbioe.2022.900162. eCollection 2022.
The information encoded in a single copy of DNA is processed into a plethora of protein molecules via the cascade of transcription and translation. Thus, the molecular process of gene expression can be considered an efficient biological amplifier from the viewpoint of synthetic biology. Cell-free protein synthesis (CFPS) enables the implementation of this amplification module for analysis of important biomolecules and avoids many of the problems associated with whole cell-based approaches. Here, we developed a method to analyze indole by using a combination of enzymatic conversion of indole and amino acid-dependent CFPS. In this method, indole molecules in the assay sample are used to generate tryptophan, which is incorporated into signal-generating proteins in the subsequent cell-free synthesis reaction. The activity of cell-free synthesized proteins was successfully used to estimate the indole concentration in the assay sample. In principle, the developed method could be extended to analyses of other important bioactive compounds.
DNA单拷贝中编码的信息通过转录和翻译的级联反应被加工成大量的蛋白质分子。因此,从合成生物学的角度来看,基因表达的分子过程可以被视为一种高效的生物放大器。无细胞蛋白质合成(CFPS)能够实现这个扩增模块,用于分析重要的生物分子,并且避免了许多与基于全细胞方法相关的问题。在这里,我们开发了一种方法,通过结合吲哚的酶促转化和氨基酸依赖性CFPS来分析吲哚。在这种方法中,测定样品中的吲哚分子被用于生成色氨酸,色氨酸在随后的无细胞合成反应中被掺入信号生成蛋白中。无细胞合成蛋白质的活性被成功用于估计测定样品中的吲哚浓度。原则上,所开发的方法可以扩展到对其他重要生物活性化合物的分析。