Electronic signals are electrogenetically relayed to control cell growth and co-culture composition

IF 3.7 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Metabolic Engineering Communications Pub Date : 2021-12-01 DOI:10.1016/j.mec.2021.e00176
Kristina Stephens , Fauziah Rahma Zakaria , Eric VanArsdale , Gregory F. Payne , William E. Bentley
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引用次数: 8

Abstract

There is much to be gained by enabling electronic interrogation and control of biological function. While the benefits of bioelectronics that rely on potential-driven ionic flows are well known (electrocardiograms, defibrillators, neural prostheses, etc) there are relatively few advances targeting nonionic molecular networks, including genetic circuits. Redox activities combine connectivity to electronics with the potential for specific genetic control in cells. Here, electrode-generated hydrogen peroxide is used to actuate an electrogenetic “relay” cell population, which interprets the redox cue and synthesizes a bacterial signaling molecule (quorum sensing autoinducer AI-1) that, in turn, signals increased growth rate in a second population. The dramatically increased growth rate of the second population is enabled by expression of a phosphotransferase system protein, HPr, which is important for glucose transport. The potential to electronically modulate cell growth via direct genetic control will enable new opportunities in the treatment of disease and manufacture of biological therapeutics and other molecules.

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电子信号通过电学传递来控制细胞生长和共培养成分
使电子审讯和控制生物功能成为可能将大有裨益。虽然依赖于电位驱动离子流的生物电子学的好处是众所周知的(心电图、除颤器、神经假体等),但针对非离子分子网络(包括遗传电路)的进展相对较少。氧化还原活动结合了与电子的连接以及细胞中特定遗传控制的潜力。在这里,电极产生的过氧化氢被用来驱动一个电遗传“中继”细胞群,它解释氧化还原信号并合成一种细菌信号分子(群体感应自诱导剂AI-1),反过来,在第二个群体中发出增长速度的信号。第二种群的生长速度急剧增加是由于磷酸转移酶系统蛋白HPr的表达,这对葡萄糖运输很重要。通过直接遗传控制电子调节细胞生长的潜力将为疾病治疗和生物疗法和其他分子的制造提供新的机会。
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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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