提高细胞游离代谢物产生的裂解物蛋白质组工程策略

IF 3.7 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
David C. Garcia , Jaime Lorenzo N. Dinglasan , Him Shrestha , Paul E. Abraham , Robert L. Hettich , Mitchel J. Doktycz
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引用次数: 6

摘要

无细胞系统为利用各种生物体的代谢潜力提供了一个重要的机会。去除细胞环境提供了在不需要维持细胞活力的情况下生产生物产品的能力,并使代谢工程师能够探索新的化学转化系统。粗提取物保留了细胞的大部分功能。然而,只有有限的工具可用于工程内容的提取物用于无细胞系统。因此,我们充分利用粗提取物的潜力进行无细胞代谢工程的能力受到限制。在这里,我们使用多重自动基因组工程(MAGE)来标记蛋白质,以便从粗提取物中选择性地去除,从而特异性地指导化学生产。在不显著影响细胞生长的情况下,对中枢代谢进行特异性编辑是可能的。丙酮酸降解酶的选择性去除导致工程粗裂解物的丙酮酸产量比非工程提取物增加了40倍。所描述的方法融合了系统和合成生物学的工具,以展示无细胞代谢工程在生物原型和生物生产等应用中的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A lysate proteome engineering strategy for enhancing cell-free metabolite production

A lysate proteome engineering strategy for enhancing cell-free metabolite production

A lysate proteome engineering strategy for enhancing cell-free metabolite production

A lysate proteome engineering strategy for enhancing cell-free metabolite production

Cell-free systems present a significant opportunity to harness the metabolic potential of diverse organisms. Removing the cellular context provides the ability to produce biological products without the need to maintain cell viability and enables metabolic engineers to explore novel chemical transformation systems. Crude extracts maintain much of a cell’s capabilities. However, only limited tools are available for engineering the contents of the extracts used for cell-free systems. Thus, our ability to take full advantage of the potential of crude extracts for cell-free metabolic engineering is constrained. Here, we employ Multiplex Automated Genomic Engineering (MAGE) to tag proteins for selective depletion from crude extracts so as to specifically direct chemical production. Specific edits to central metabolism are possible without significantly impacting cell growth. Selective removal of pyruvate degrading enzymes resulted in engineered crude lysates that are capable of up to 40-fold increases in pyruvate production when compared to the non-engineered extract. The described approach melds the tools of systems and synthetic biology to showcase the effectiveness of cell-free metabolic engineering for applications like bioprototyping and bioproduction.

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来源期刊
Metabolic Engineering Communications
Metabolic Engineering Communications Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
13.30
自引率
1.90%
发文量
22
审稿时长
18 weeks
期刊介绍: Metabolic Engineering Communications, a companion title to Metabolic Engineering (MBE), is devoted to publishing original research in the areas of metabolic engineering, synthetic biology, computational biology and systems biology for problems related to metabolism and the engineering of metabolism for the production of fuels, chemicals, and pharmaceuticals. The journal will carry articles on the design, construction, and analysis of biological systems ranging from pathway components to biological complexes and genomes (including genomic, analytical and bioinformatics methods) in suitable host cells to allow them to produce novel compounds of industrial and medical interest. Demonstrations of regulatory designs and synthetic circuits that alter the performance of biochemical pathways and cellular processes will also be presented. Metabolic Engineering Communications complements MBE by publishing articles that are either shorter than those published in the full journal, or which describe key elements of larger metabolic engineering efforts.
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