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恶臭假单胞菌中或非门的自动化设计与实现

Automated design and implementation of a NOR gate in Pseudomonas putida.

作者信息

Tas Huseyin, Grozinger Lewis, Goñi-Moreno Angel, de Lorenzo Victor

机构信息

Systems Biology Department, Centro Nacional de Biotecnología-CSIC, Madrid, Spain.

School of Computing, Newcastle University, Newcastle Upon Tyne, UK.

出版信息

Synth Biol (Oxf). 2021 Sep 1;6(1):ysab024. doi: 10.1093/synbio/ysab024. eCollection 2021.

Abstract

Boolean NOR gates have been widely implemented in as transcriptional regulatory devices for building complex genetic circuits. Yet, their portability to other bacterial hosts/chassis is generally hampered by frequent changes in the parameters of the INPUT/OUTPUT response functions brought about by new genetic and biochemical contexts. Here, we have used the circuit design tool CELLO for assembling a NOR gate in the soil bacterium and the metabolic engineering platform with components tailored for To this end, we capitalized on the functional parameters of 20 genetic inverters for each host and the resulting compatibility between NOT pairs. Moreover, we added to the gate library three inducible promoters that are specific to , thus expanding cross-platform assembly options. While the number of potential connectable inverters decreased drastically when moving the library from to , the CELLO software was still able to find an effective NOR gate in the new chassis. The automated generation of the corresponding DNA sequence and experimental verification accredited that some genetic modules initially optimized for can indeed be reused to deliver NOR logic in as well. Furthermore, the results highlight the value of creating host-specific collections of well-characterized regulatory inverters for the quick assembly of genetic circuits to meet complex specifications.

摘要

布尔或非门已被广泛用作构建复杂遗传电路的转录调控装置。然而,由于新的遗传和生化环境导致输入/输出响应函数参数频繁变化,它们在其他细菌宿主/底盘中的可移植性通常受到阻碍。在这里,我们使用电路设计工具CELLO在土壤细菌和代谢工程平台中组装或非门,其组件是为该平台量身定制的。为此,我们利用了每个宿主20个基因逆变器的功能参数以及由此产生的非门对之间的兼容性。此外,我们在门库中添加了三个特定于该平台的诱导型启动子,从而扩展了跨平台组装选项。当将库从一个平台转移到另一个平台时,潜在可连接逆变器的数量急剧减少,但CELLO软件仍能够在新底盘中找到有效的或非门。相应DNA序列的自动生成和实验验证证实,一些最初为一个平台优化的遗传模块确实也可以重新用于在另一个平台中实现或非逻辑。此外,结果突出了创建宿主特异性的、特征明确的调控逆变器集合对于快速组装遗传电路以满足复杂规格的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c1a/8546601/3cdf48423501/ysab024f5.jpg

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