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利用无细胞蛋白质合成技术直接从DNA进行非核糖体肽生物合成的体外重建。

In Vitro Reconstruction of Nonribosomal Peptide Biosynthesis Directly from DNA Using Cell-Free Protein Synthesis.

作者信息

Goering Anthony W, Li Jian, McClure Ryan A, Thomson Regan J, Jewett Michael C, Kelleher Neil L

机构信息

Department of Molecular Biosciences, and the Feinberg School of Medicine, ‡Department of Chemistry, and §Department of Chemical and Biological Engineering, Northwestern University , Evanston, Illinois 60208, United States.

出版信息

ACS Synth Biol. 2017 Jan 20;6(1):39-44. doi: 10.1021/acssynbio.6b00160. Epub 2016 Aug 9.

Abstract

Genome sequencing has revealed that a far greater number of natural product biosynthetic pathways exist than there are known natural products. To access these molecules directly and deterministically, a new generation of heterologous expression methods is needed. Cell-free protein synthesis has not previously been used to study nonribosomal peptide biosynthesis, and provides a tunable platform with advantages over conventional methods for protein expression. Here, we demonstrate the use of cell-free protein synthesis to biosynthesize a cyclic dipeptide with correct absolute stereochemistry. From a single-pot reaction, we measured the expression of two nonribosomal peptide synthetases larger than 100 kDa, and detected high-level production of a diketopiperazine. Using quantitative LC-MS and synthetically prepared standard, we observed production of this metabolite at levels higher than previously reported from cell-based recombinant expression, approximately 12 mg/L. Overall, this work represents a first step to apply cell-free protein synthesis to discover and characterize new natural products.

摘要

基因组测序表明,天然产物生物合成途径的数量远远超过已知天然产物的数量。为了直接且确定性地获取这些分子,需要新一代的异源表达方法。无细胞蛋白质合成此前尚未用于研究非核糖体肽的生物合成,它提供了一个可调节的平台,相较于传统的蛋白质表达方法具有优势。在此,我们展示了使用无细胞蛋白质合成来生物合成具有正确绝对立体化学结构的环二肽。从单锅反应中,我们测定了两种大于100 kDa的非核糖体肽合成酶的表达,并检测到二酮哌嗪的高水平产生。使用定量液相色谱 - 质谱联用仪和合成制备的标准品,我们观察到这种代谢物的产量高于此前基于细胞的重组表达所报道的水平,约为12 mg/L。总体而言,这项工作代表了将无细胞蛋白质合成应用于发现和表征新天然产物的第一步。

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