pBLAM1-x:用于高通量筛选的标准化转座子工具。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS Synthetic biology (Oxford, England) Pub Date : 2023-06-21 eCollection Date: 2023-01-01 DOI:10.1093/synbio/ysad012
Lorea Alejaldre, Ana-Mariya Anhel, Ángel Goñi-Moreno
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引用次数: 1

摘要

随着合成生物学的努力变得更加雄心勃勃,活细胞中预定义功能的工程需要越来越精确的工具。此外,遗传结构的表型表现的表征需要细致的测量和广泛的数据采集,以便在设计-构建-测试生命周期中提供数学模型和匹配预测。在这里,我们开发了一种易于高通量转座子插入测序(TnSeq)的遗传工具:携带Himar1 Mariner转座酶系统的pBLAM1-x质粒载体。这些质粒来源于mini-Tn5转座子载体pBAMD1-2,并按照欧洲标准载体架构(SEVA)格式的模块化标准构建。为了展示它们的功能,我们分析了60个土壤细菌Pseudomonas putida KT2440克隆的测序结果。新的pBLAM1-x工具已经包含在最新的SEVA数据库版本中,在这里我们描述它使用实验室自动化工作流的性能。图形抽象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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pBLAM1-x: standardized transposon tools for high-throughput screening.

The engineering of pre-defined functions in living cells requires increasingly accurate tools as synthetic biology efforts become more ambitious. Moreover, the characterization of the phenotypic performance of genetic constructs demands meticulous measurements and extensive data acquisition for the sake of feeding mathematical models and matching predictions along the design-build-test lifecycle. Here, we developed a genetic tool that eases high-throughput transposon insertion sequencing (TnSeq): the pBLAM1-x plasmid vectors carrying the Himar1 Mariner transposase system. These plasmids were derived from the mini-Tn5 transposon vector pBAMD1-2 and built following modular criteria of the Standard European Vector Architecture (SEVA) format. To showcase their function, we analyzed sequencing results of 60 clones of the soil bacterium Pseudomonas putida KT2440. The new pBLAM1-x tool has already been included in the latest SEVA database release, and here we describe its performance using laboratory automation workflows. Graphical Abstract.

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