植物乳杆菌WCFS1作为微生物工程平台的大范围穿梭载体构建及启动子评价

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2019-05-23 eCollection Date: 2019-01-01 DOI:10.1093/synbio/ysz012
Joseph R Spangler, Julie C Caruana, Daniel A Phillips, Scott A Walper
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引用次数: 15

摘要

随着合成生物学领域的发展,在非实验室细菌菌株中部署复杂遗传电路的努力将继续成为研究实验室的重点。乳杆菌属的成员是合成生物学研究的良好目标,因为一些物种已经在许多食品中用作益生菌。此外,乳酸菌为各种健康问题的微生物治疗提供了相对安全的载体,因为这些共生体通常是肠道微生物群落的次要组成部分,并维持异质行为。为了为工程研究奠定基础,我们在大肠杆菌中构建了穿梭载体进行亚克隆,并利用该载体对植物乳杆菌WCFS1原生启动子的转录和翻译活性进行了表征。此外,我们演示了该载体系统在多种乳酸菌物种中的应用,并提供了植物乳杆菌和大肠杆菌菌株识别非天然启动子的例子,这可能会使电路输出的快速评估成为可能。在整个生长过程中,各种启动子活性覆盖了一系列蛋白质表达水平在不同时间达到峰值,随后的定向突变被证明并建议进一步增加输出调节的程度。我们相信这些数据显示了L. plantarum WCFS1作为非传统合成生物学基础的潜力,并为我们的系统也可以过渡到其他益生菌乳酸菌物种提供证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Broad range shuttle vector construction and promoter evaluation for the use of <i>Lactobacillus plantarum</i> WCFS1 as a microbial engineering platform.

Broad range shuttle vector construction and promoter evaluation for the use of <i>Lactobacillus plantarum</i> WCFS1 as a microbial engineering platform.

Broad range shuttle vector construction and promoter evaluation for the use of <i>Lactobacillus plantarum</i> WCFS1 as a microbial engineering platform.

Broad range shuttle vector construction and promoter evaluation for the use of Lactobacillus plantarum WCFS1 as a microbial engineering platform.

As the field of synthetic biology grows, efforts to deploy complex genetic circuits in nonlaboratory strains of bacteria will continue to be a focus of research laboratories. Members of the Lactobacillus genus are good targets for synthetic biology research as several species are already used in many foods and as probiotics. Additionally, Lactobacilli offer a relatively safe vehicle for microbiological treatment of various health issues considering these commensals are often minor constituents of the gut microbial community and maintain allochthonous behavior. In order to generate a foundation for engineering, we developed a shuttle vector for subcloning in Escherichia coli and used it to characterize the transcriptional and translational activities of a number of promoters native to Lactobacillus plantarum WCFS1. Additionally, we demonstrated the use of this vector system in multiple Lactobacillus species, and provided examples of non-native promoter recognition by both L. plantarum and E. coli strains that might allow a shortcut assessment of circuit outputs. A variety of promoter activities were observed covering a range of protein expression levels peaking at various times throughout growth, and subsequent directed mutations were demonstrated and suggested to further increase the degree of output tuning. We believe these data show the potential for L. plantarum WCFS1 to be used as a nontraditional synthetic biology chassis and provide evidence that our system can be transitioned to other probiotic Lactobacillus species as well.

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