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鼠李糖诱导的原儿茶酸生物合成基因的转录激活 QuiR,李斯特菌中的 LysR 型转录调节因子。

Shikimate Induced Transcriptional Activation of Protocatechuate Biosynthesis Genes by QuiR, a LysR-Type Transcriptional Regulator, in Listeria monocytogenes.

机构信息

Department of Cell and Systems Biology, University of Toronto, 25 Willcocks Street, Toronto, Ontario, Canada M5S 3B2.

Department of Molecular Genetics, University of Toronto, 1 King's College Cir, Toronto, Ontario, Canada M5S 1A8.

出版信息

J Mol Biol. 2018 Apr 27;430(9):1265-1283. doi: 10.1016/j.jmb.2018.03.003. Epub 2018 Mar 9.

Abstract

Listeria monocytogenes is a common foodborne bacterial pathogen that contaminates plant and animal consumable products. The persistent nature of L. monocytogenes is associated with millions of dollars in food recalls annually. Here, we describe the role of shikimate in directly modulating the expression of genes encoding enzymes for the conversion of quinate and shikimate metabolites to protocatechuate. In L. monocytogenes, these genes are found within two operons, named qui1 and qui2. In addition, a gene named quiR, encoding a LysR-Type Transcriptional Regulator (QuiR), is located immediately upstream of the qui1 operon. Transcriptional lacZ-promoter fusion experiments show that QuiR induces gene expression of both qui1 and qui2 operons in the presence of shikimate. Furthermore, co-crystallization of the QuiR effector binding domain in complex with shikimate provides insights into the mechanism of activation of this regulator. Together these data show that upon shikimate accumulation, QuiR activates the transcription of genes encoding enzymes involved in shikimate and quinate utilization for the production of protocatechuate. Furthermore, the accumulation of protocatechuate leads to the inhibition of Listeria growth. Since protocatechuate is not known to be utilized by Listeria, its role is distinct from those established in other bacteria.

摘要

李斯特菌是一种常见的食源性细菌病原体,会污染植物和动物可食用产品。李斯特菌具有持久性,每年会导致价值数百万美元的食品召回。在这里,我们描述了莽草酸在直接调节编码将莽草酸和奎尼酸代谢物转化为原儿茶酸的酶的基因表达中的作用。在李斯特菌中,这些基因位于两个操纵子中,分别命名为 qui1 和 qui2。此外,一个名为 quiR 的基因,编码一种 LysR 型转录调节因子(QuiR),位于 qui1 操纵子的上游。转录 lacZ-启动子融合实验表明,在存在莽草酸的情况下,QuiR 诱导 qui1 和 qui2 操纵子的基因表达。此外,QuiR 效应物结合域与莽草酸形成复合物的共结晶提供了对该调节剂激活机制的深入了解。这些数据表明,在莽草酸积累时,QuiR 激活编码参与莽草酸和奎尼酸利用以生产原儿茶酸的酶的基因的转录。此外,原儿茶酸的积累会抑制李斯特菌的生长。由于原儿茶酸未知被李斯特菌利用,其作用与其他细菌中的作用不同。

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