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靶向16S rRNA mRNA结合位点的肽核酸对细菌生长的序列特异性抑制作用。

Sequence-specific bacterial growth inhibition by peptide nucleic acid targeted to the mRNA binding site of 16S rRNA.

作者信息

Hatamoto Masashi, Nakai Kazufumi, Ohashi Akiyoshi, Imachi Hiroyuki

机构信息

Department of Social and Environmental Engineering, Hiroshima University, Higashi-Hiroshima, Japan.

出版信息

Appl Microbiol Biotechnol. 2009 Oct;84(6):1161-8. doi: 10.1007/s00253-009-2099-0. Epub 2009 Jul 4.

Abstract

Peptide nucleic acid (PNA) targeted to the functional domains of 23S rRNA can inhibit translation and cell growth. However, effective inhibition of translation and cell growth using 16S rRNA-targeted PNA has still not been achieved. Here, we report that PNA targeted to the functional site of 16S rRNA could inhibit both gene expression in vitro and bacterial growth in pure culture with sequence specificity. We used 10-mer PNAs conjugated with a cell-penetrating peptide, which targeted the mRNA binding site at the 3' end of 16S rRNA. Using 0.6 microM of the peptide-PNAs, cell-free ss-galactosidase production decreased by 50%, whereas peptide-PNAs with one or two mismatches to the target sequence showed much weaker inhibition effects. To determine the growth inhibition and bactericidal effects of the peptide-PNA conjugate, we performed OD measurement and viable cell counting. We observed dose- and sequence-dependent inhibition of cell growth and bactericidal effects. These growth inhibitory effects are observed both in the Gram-negative bacterium of Escherichia coli and the Gram-positive bacteria Bacillus subtilis and Corynebacterium efficiens, although inhibitory concentrations were different for each bacterial species. These results present possibilities for 16S rRNA sequence-based specific bacterial growth inhibition using a peptide-PNA conjugate.

摘要

靶向23S rRNA功能域的肽核酸(PNA)可抑制翻译和细胞生长。然而,使用靶向16S rRNA的PNA有效抑制翻译和细胞生长仍未实现。在此,我们报告靶向16S rRNA功能位点的PNA可在体外抑制基因表达,并在纯培养中以序列特异性抑制细菌生长。我们使用与细胞穿透肽偶联的10聚体PNA,其靶向16S rRNA 3'端的mRNA结合位点。使用0.6微摩尔的肽-PNA,无细胞体系中β-半乳糖苷酶的产生减少了50%,而与靶序列有一个或两个错配的肽-PNA显示出弱得多的抑制作用。为了确定肽-PNA偶联物的生长抑制和杀菌作用,我们进行了光密度测量和活菌计数。我们观察到细胞生长抑制和杀菌作用具有剂量和序列依赖性。在革兰氏阴性菌大肠杆菌以及革兰氏阳性菌枯草芽孢杆菌和高效棒状杆菌中均观察到这些生长抑制作用,尽管每种细菌的抑制浓度不同。这些结果为使用肽-PNA偶联物基于16S rRNA序列特异性抑制细菌生长提供了可能性。

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