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脂质体中重组的基因编码酶催化的无细胞磷脂生物合成

Cell-Free Phospholipid Biosynthesis by Gene-Encoded Enzymes Reconstituted in Liposomes.

作者信息

Scott Andrew, Noga Marek J, de Graaf Paul, Westerlaken Ilja, Yildirim Esengul, Danelon Christophe

机构信息

Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Van der Maasweg 9, 2629 HZ, Delft, The Netherlands.

出版信息

PLoS One. 2016 Oct 6;11(10):e0163058. doi: 10.1371/journal.pone.0163058. eCollection 2016.

Abstract

The goal of bottom-up synthetic biology culminates in the assembly of an entire cell from separate biological building blocks. One major challenge resides in the in vitro production and implementation of complex genetic and metabolic pathways that can support essential cellular functions. Here, we show that phospholipid biosynthesis, a multiple-step process involved in cell membrane homeostasis, can be reconstituted starting from the genes encoding for all necessary proteins. A total of eight E. coli enzymes for acyl transfer and headgroup modifications were produced in a cell-free gene expression system and were co-translationally reconstituted in liposomes. Acyl-coenzyme A and glycerol-3-phosphate were used as canonical precursors to generate a variety of important bacterial lipids. Moreover, this study demonstrates that two-step acyl transfer can occur from enzymes synthesized inside vesicles. Besides clear implications for growth and potentially division of a synthetic cell, we postulate that gene-based lipid biosynthesis can become instrumental for ex vivo and protein purification-free production of natural and non-natural lipids.

摘要

自下而上的合成生物学的目标是最终从单独的生物构建模块组装出整个细胞。一个主要挑战在于体外构建和实现能够支持基本细胞功能的复杂遗传和代谢途径。在这里,我们表明,参与细胞膜稳态的多步骤磷脂生物合成过程,可以从编码所有必需蛋白质的基因开始进行重构。在无细胞基因表达系统中产生了总共八种用于酰基转移和头部基团修饰的大肠杆菌酶,并在脂质体中进行了共翻译重构。酰基辅酶A和3-磷酸甘油被用作标准前体来生成多种重要的细菌脂质。此外,这项研究表明,两步酰基转移可以发生在囊泡内合成的酶上。除了对合成细胞的生长和潜在分裂有明确影响外,我们推测基于基因的脂质生物合成对于天然和非天然脂质的离体和无蛋白质纯化生产可能会有帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d3/5053487/4a83e5949d29/pone.0163058.g001.jpg

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