正反馈、比率计量生物传感器的表达提高了酵母的高通量代谢产物筛选效率。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2017-01-29 eCollection Date: 2017-01-01 DOI:10.1093/synbio/ysw002
Thomas C Williams, Xin Xu, Martin Ostrowski, Isak S Pretorius, Ian T Paulsen
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引用次数: 0

摘要

生物传感器是合成生物学中重要的多功能工具,可用于调节基因表达以应对各种刺激。配体反应转录因子是一类生物传感器,可用于将细胞内代谢物浓度与基因表达结合起来,从而实现动态调控和高通量代谢物生产者筛选。我们已将酿酒酵母 WAR1 转录调节因子和 PDR12 启动子确立为一种有机酸生物传感器,可用于检测莽草酸途径产生的不同水平的对羟基苯甲酸(PHBA),并输出绿色荧光蛋白(GFP)表达作为响应。通过对目标 PDR12 启动子中的 WAR1 转录调控因子进行正反馈表达,GFP 对 PHBA 的响应动态范围得到了显著提高。此外,通过将 GFP 荧光与每个细胞内组成型表达的 mCherry 荧光进行归一化,控制了群体级 GFP 表达的噪声。这些生物传感器的改良使工程化生产 PHBA 的酵母细胞的高通量筛选效率提高了 5000 倍,从而能够准确地用荧光激活细胞分拣技术分离出以万分之一的比例与非生产者混合的生产者细胞。正反馈、比率计量转录调控因子的表达可能适用于合成生物学和代谢工程中的许多其他转录因子/启动子对,可用于动态调控和高通量筛选应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Positive-feedback, ratiometric biosensor expression improves high-throughput metabolite-producer screening efficiency in yeast.

Positive-feedback, ratiometric biosensor expression improves high-throughput metabolite-producer screening efficiency in yeast.

Positive-feedback, ratiometric biosensor expression improves high-throughput metabolite-producer screening efficiency in yeast.

Positive-feedback, ratiometric biosensor expression improves high-throughput metabolite-producer screening efficiency in yeast.

Biosensors are valuable and versatile tools in synthetic biology that are used to modulate gene expression in response to a wide range of stimuli. Ligand responsive transcription factors are a class of biosensor that can be used to couple intracellular metabolite concentration with gene expression to enable dynamic regulation and high-throughput metabolite producer screening. We have established the Saccharomyces cerevisiae WAR1 transcriptional regulator and PDR12 promoter as an organic acid biosensor that can be used to detect varying levels of para-hydroxybenzoic acid (PHBA) production from the shikimate pathway and output green fluorescent protein (GFP) expression in response. The dynamic range of GFP expression in response to PHBA was dramatically increased by engineering positive-feedback expression of the WAR1 transcriptional regulator from its target PDR12 promoter. In addition, the noise in GFP expression at the population-level was controlled by normalising GFP fluorescence to constitutively expressed mCherry fluorescence within each cell. These biosensor modifications increased the high-throughput screening efficiency of yeast cells engineered to produce PHBA by 5,000-fold, enabling accurate fluorescence activated cell sorting isolation of producer cells that were mixed at a ratio of 1 in 10,000 with non-producers. Positive-feedback, ratiometric transcriptional regulator expression is likely applicable to many other transcription-factor/promoter pairs used in synthetic biology and metabolic engineering for both dynamic regulation and high-throughput screening applications.

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