Xu Peng, Vansiri Amerin, Bhan Namita, Koffas Mattheos A G
Center for Biotechnology and Interdisciplinary Studies and Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.
ACS Synth Biol. 2012 Jul 20;1(7):256-66. doi: 10.1021/sb300016b. Epub 2012 May 4.
Harnessing cell factories for producing biofuel and pharmaceutical molecules has stimulated efforts to develop novel synthetic biology tools customized for modular pathway engineering and optimization. Here we report the development of a set of vectors compatible with BioBrick standards and its application in metabolic engineering. The engineered ePathBrick vectors comprise four compatible restriction enzyme sites allocated on strategic positions so that different regulatory control signals can be reused and manipulation of expression cassette can be streamlined. Specifically, these vectors allow for fine-tuning gene expression by integrating multiple transcriptional activation or repression signals into the operator region. At the same time, ePathBrick vectors support the modular assembly of pathway components and combinatorial generation of pathway diversities with three distinct configurations. We also demonstrated the functionality of a seven-gene pathway (~9 Kb) assembled on one single ePathBrick vector. The ePathBrick vectors presented here provide a versatile platform for rapid design and optimization of metabolic pathways in E. coli.
利用细胞工厂生产生物燃料和药物分子激发了人们开发定制用于模块化途径工程和优化的新型合成生物学工具的努力。在此,我们报告了一组与BioBrick标准兼容的载体的开发及其在代谢工程中的应用。工程化的ePathBrick载体在关键位置包含四个兼容的限制性酶切位点,这样不同的调控控制信号可以重复使用,并且表达盒的操作可以简化。具体而言,这些载体通过将多个转录激活或抑制信号整合到操纵子区域来实现基因表达的微调。同时,ePathBrick载体支持途径组件的模块化组装以及通过三种不同配置进行途径多样性的组合生成。我们还展示了在单个ePathBrick载体上组装的七基因途径(约9 kb)的功能。本文介绍的ePathBrick载体为大肠杆菌中代谢途径的快速设计和优化提供了一个通用平台。