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

被引:31
作者
Hatamoto, Masashi [1 ,2 ]
Nakai, Kazufumi [3 ]
Ohashi, Akiyoshi [2 ]
Imachi, Hiroyuki [1 ]
机构
[1] Japan Agcy Marine Earth Sci & Technol, Subsurface Geobiol Adv Res Team, Inst Biogeosci, Extremobiosphere Res Program, Yokosuka, Kanagawa 2370061, Japan
[2] Hiroshima Univ, Dept Social & Environm Engn, Higashihiroshima 7398527, Japan
[3] Nagaoka Univ Technol, Dept Environm Syst Engn, Niigata 9402188, Japan
基金
日本学术振兴会;
关键词
Peptide nucleic acid (PNA); 16S rRNA; mRNA binding site; Cell wall-permeablizing peptide; GENE-EXPRESSION; ESCHERICHIA-COLI; ANTISENSE INHIBITION; OLIGONUCLEOTIDES; OLIGOMER; TRANSLATION; PROTEIN;
D O I
10.1007/s00253-009-2099-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 A mu M of the peptide-PNAs, cell-free -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.
引用
收藏
页码:1161 / 1168
页数:8
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