CRAGE-mediated insertion of fluorescent chromosomal markers for accurate and scalable measurement of co-culture dynamics in Escherichia coli.

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2020-09-03 eCollection Date: 2020-01-01 DOI:10.1093/synbio/ysaa015
Avery J C Noonan, Yilin Qiu, Joe C H Ho, Jewel Ocampo, K A Vreugdenhil, R Alexander Marr, Zhiying Zhao, Yasuo Yoshikuni, Steven J Hallam
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引用次数: 3

Abstract

Monitoring population dynamics in co-culture is necessary in engineering microbial consortia involved in distributed metabolic processes or biosensing applications. However, it remains difficult to measure strain-specific growth dynamics in high-throughput formats. This is especially vexing in plate-based functional screens leveraging whole-cell biosensors to detect specific metabolic signals. Here, we develop an experimental high-throughput co-culture system to measure and model the relationship between fluorescence and cell abundance, combining chassis-independent recombinase-assisted genome engineering (CRAGE) and whole-cell biosensing with a PemrR-green fluorescent protein (GFP) monoaromatic reporter used in plate-based functional screening. CRAGE was used to construct Escherichia coli EPI300 strains constitutively expressing red fluorescent protein (RFP) and the relationship between RFP expression and optical density (OD600) was determined throughout the EPI300 growth cycle. A linear equation describing the increase of normalized RFP fluorescence during deceleration phase was derived and used to predict biosensor strain dynamics in co-culture. Measured and predicted values were compared using flow cytometric detection methods. Induction of the biosensor lead to increased GFP fluorescence normalized to biosensor cell abundance, as expected, but a significant decrease in relative abundance of the biosensor strain in co-culture and a decrease in bulk GFP fluorescence. Taken together, these results highlight sensitivity of population dynamics to variations in metabolic activity in co-culture and the potential effect of these dynamics on the performance of functional screens in plate-based formats. The engineered strains and model used to evaluate these dynamics provide a framework for optimizing growth of synthetic co-cultures used in screening, testing and pathway engineering applications.

crage介导的插入荧光染色体标记用于大肠杆菌共培养动力学的准确和可扩展测量。
监测群体动态在共培养是必要的工程微生物财团参与分布代谢过程或生物传感应用。然而,在高通量格式中测量菌株特异性生长动力学仍然很困难。这在利用全细胞生物传感器检测特定代谢信号的平板功能屏幕中尤其令人烦恼。在这里,我们开发了一个实验高通量共培养系统来测量和模拟荧光与细胞丰度之间的关系,结合了底盘独立重组酶辅助基因组工程(CRAGE)和全细胞生物传感,以及用于基于平板的功能筛选的pemmr -绿色荧光蛋白(GFP)单芳香报告基因。利用CRAGE构建表达红色荧光蛋白(RFP)的大肠杆菌EPI300菌株,并在EPI300生长周期内测定RFP表达与光密度(OD600)的关系。导出了描述归一化RFP荧光在减速阶段增加的线性方程,并用于预测共培养中的生物传感器菌株动态。用流式细胞术检测方法比较实测值和预测值。正如预期的那样,诱导生物传感器导致GFP荧光增加,归一化为生物传感器细胞丰度,但在共培养中,生物传感器菌株的相对丰度显著下降,总体GFP荧光下降。综上所述,这些结果突出了群体动态对共培养中代谢活动变化的敏感性,以及这些动态对基于平板格式的功能屏幕性能的潜在影响。用于评估这些动态的工程菌株和模型为优化用于筛选,测试和途径工程应用的合成共培养物的生长提供了框架。
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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