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发现和描述可调控基因表达的天然启动子。

Discovery and Characterization of Native Promoters for Tunable Gene Expression.

机构信息

McKetta Department of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA.

Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, USA.

出版信息

Appl Environ Microbiol. 2019 Oct 16;85(21). doi: 10.1128/AEM.01356-19. Print 2019 Nov 1.

Abstract

The potential utilization of extremophiles as a robust chassis for metabolic engineering applications has prompted interest in the use of for bioremediation efforts, but current applications are limited by the lack of availability of genetic tools, such as promoters. In this study, we used a combined computational and experimental approach to identify and screen 30 predicted promoters for expression in using a fluorescent reporter assay. The top eight candidates were further characterized, compared to currently available promoters, and optimized for engineering through minimization for use in Of these top eight, two promoter regions, and , were stronger and more consistent than the most widely used promoter sequence in , Furthermore, half of the top eight promoters could be minimized by at least 20% (to obtain final sequences that are approximately 24 to 177 bp), and several of the putative promoters either showed activity in or were specific, broadening the use of the promoters for various applications. Overall, this work introduces a suite of novel, well-characterized promoters for protein production and metabolic engineering in The tolerance of the extremophile, , to numerous oxidative stresses makes it ideal for bioremediation applications, but many of the tools necessary for metabolic engineering are lacking in this organism compared to model bacteria. Although native and engineered promoters have been used to drive gene expression for protein production in , very few have been well characterized. Informed by bioinformatics, this study expands the repertoire of well-characterized promoters for via thorough characterization of eight putative promoters with various strengths. These results will help facilitate tunable gene expression, since these promoters demonstrate strong and consistent performance compared to the current standard, This study also provides a methodology for high-throughput promoter identification and characterization using fluorescence in The promoters identified in this study will facilitate metabolic engineering of and enable its use in biotechnological applications ranging from bioremediation to synthesis of commodity chemicals.

摘要

极端微生物作为代谢工程应用的强大底盘的潜在利用引起了人们对其在生物修复工作中应用的兴趣,但目前的应用受到缺乏遗传工具(如启动子)的限制。在这项研究中,我们使用了组合计算和实验方法,通过荧光报告测定筛选了 30 个预测的启动子,以在 中表达。对前 8 个候选者进行了进一步的特征描述,并与现有的启动子进行了比较,然后通过最小化工程进行了优化,以用于 。在这前 8 个中,两个启动子区域 和 比 中最广泛使用的启动子序列 更强、更一致。此外,前 8 个启动子中有一半可以至少减少 20%(获得最终序列约为 24 到 177bp),并且其中一些假定的启动子要么在 中具有活性,要么是 特异性的,拓宽了这些启动子在各种应用中的使用。总的来说,这项工作为 中的蛋白质生产和代谢工程引入了一系列新型、经过良好表征的启动子。由于极端微生物 对许多氧化应激的耐受性,使其非常适合生物修复应用,但与模型细菌相比,该生物缺乏进行代谢工程所需的许多工具。尽管已经使用天然和工程化的启动子来驱动 中的基因表达以生产蛋白质,但很少有得到很好的表征。本研究通过对具有不同强度的 8 个假定启动子进行全面表征,以生物信息学为指导,扩展了 中经过良好表征的启动子库。这些结果将有助于实现可调基因表达,因为与当前标准 相比,这些启动子表现出强大且一致的性能。本研究还提供了一种使用 中的荧光进行高通量启动子鉴定和表征的方法。本研究中鉴定的启动子将促进 的代谢工程,并使其能够在从生物修复到商品化学品合成的生物技术应用中得到应用。

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