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磷酸调节子的作用及亚磷酸盐依赖型大肠杆菌的基因重建

Role of the Pho regulon and genetic reconstruction of a phosphite-dependent Escherichia coli.

作者信息

Momokawa Naoki, Ikeda Takeshi, Ishida Takenori, Nimura-Matsune Kaori, Funabashi Hisakage, Watanabe Satoru, Kuroda Akio, Hirota Ryuichi

机构信息

Unit of Biotechnology, Division of Biological and Life Sciences, Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8530, Japan.

Department of Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan.

出版信息

J Biosci Bioeng. 2025 Sep;140(3):117-122. doi: 10.1016/j.jbiosc.2025.05.012. Epub 2025 Jun 16.

Abstract

A phosphite (Pt)-dependent biological containment strategy, achieved by introducing a Pt-metabolic pathway and disrupting endogenous phosphate transporters, renders Escherichia coli growth strictly dependent on Pt, a compound rarely detected in natural environments, thereby preventing unintended environmental spread. In this study, we demonstrated that expression of phosphate regulon (Pho regulon) genes was markedly upregulated in a Pt-dependent E. coli strain due to the elimination of phoU, a negative regulator of the Pho regulon, along with the high-affinity phosphate transporter pstSCAB. However, further genetic modification of this strain for detailed analysis was hindered by the presence of multiple antibiotic resistance markers. To overcome this limitation, we reconstructed a Pt-dependent E. coli strain using CRISPR-Cas12a-mediated genome editing, enabling the removal of the antibiotic resistance markers and facilitating subsequent genetic manipulation. Using this strain, we disrupted the PhoBR two-component regulatory genes and found that deletion of phoBR alleviated the constitutive overexpression of Pho regulon genes and partially restored growth of the Pt-dependent strain. These findings provide mechanistic insights and technical advances for the refinement and practical application of Pt-dependent biocontainment strategy.

摘要

一种依赖亚磷酸盐(Pt)的生物遏制策略,通过引入一条Pt代谢途径并破坏内源性磷酸盐转运体来实现,使得大肠杆菌的生长严格依赖于Pt,Pt是一种在自然环境中很少检测到的化合物,从而防止其意外扩散到环境中。在本研究中,我们证明,在一株依赖Pt的大肠杆菌菌株中,由于Pho调控子的负调节因子phoU以及高亲和力磷酸盐转运体pstSCAB的缺失,Pho调控子基因的表达显著上调。然而,由于存在多个抗生素抗性标记,对该菌株进行进一步的基因改造以进行详细分析受到了阻碍。为克服这一限制,我们利用CRISPR-Cas12a介导的基因组编辑技术重建了一株依赖Pt的大肠杆菌菌株,能够去除抗生素抗性标记并便于后续的基因操作。利用该菌株,我们破坏了PhoBR双组分调控基因,发现缺失phoBR可减轻Pho调控子基因的组成型过表达,并部分恢复依赖Pt菌株的生长。这些发现为依赖Pt的生物遏制策略的优化和实际应用提供了机制上的见解和技术进展。

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