工具箱
合成生物学
工作流程
枯草芽孢杆菌
计算生物学
灵活性(工程)
质粒
穿梭机载体
计算机科学
生物
克隆(编程)
多克隆站点
载体(分子生物学)
遗传学
DNA
程序设计语言
数据库
基因
数学
重组DNA
统计
细菌
作者
Kristoffer Bach Falkenberg,Viviënne Mol,Arrate Sainz de la Maza Larrea,Ivan Pogrebnyakov,Morten H. H. Nørholm,Alex Toftgaard Nielsen,Sheila Ingemann Jensen
标识
DOI:10.1021/acssynbio.1c00130
摘要
Versatile DNA assembly standards and compatible, well-characterized part libraries are essential tools for creating effective designs in synthetic biology.However, to date, vector standards for Gram-positive hosts have limited flexibility.As a result, users often revert to PCR-based methods for building the desired genetic constructs.These methods are inherently prone to introducing mutations, which is problematic considering vector backbone parts are often left unsequenced in cloning workflows.To circumvent this, we present the ProUSER2.0toolbox: a standardized vector platform for building both integrative and replicative shuttle vectors forBacillus subtilis.The ProUSER2.0 vectors consist of a ProUSER cassette for easy and efficient insertion of cargo sequences and six exchangeable modules.Furthermore, the standard is semicompatible with several previously developed standards, allowing the user to utilize the parts developed for these.To provide parts for the toolbox, seven novel integration sites and six promoters were thoroughly characterized in B. subtilis.Finally, the capacity of the ProUSER2.0system was demonstrated through the construction of signal peptide libraries for two industrially relevant proteins.Altogether, the ProUSER2.0toolbox is a powerful and flexible framework for use in B. subtilis.
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