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单核细胞增生李斯特菌EGDe中IIa类细菌素新分子靶点的鉴定

Identification of a new molecular target of class IIa bacteriocins in Listeria monocytogenes EGDe.

作者信息

Calvez S, Prévost H, Drider D

机构信息

Laboratoire de Microbiologie, Ecole Nationale d'Ingénieurs des Techniques des Industries Agricoles et Alimentaires, 44322, Nantes Cedex 3, France.

出版信息

Folia Microbiol (Praha). 2008;53(5):417-22. doi: 10.1007/s12223-008-0063-5. Epub 2008 Dec 16.

DOI:10.1007/s12223-008-0063-5
PMID:19085076
Abstract

It was shown recently (Calvez et al. 2007) that glpQ and pde genes are involved in intermediate resistance of Enterococcus faecalis JH2-2 to DvnV41, a class IIa bacteriocin produced by Carnobacterium divergens V41. The listerial orthologs of lpQ and pde genes might be lmo0052 and lmo1292 genes, respectively. Here, the role of lmo0052 and lmo1292 genes in resistance of Listeria monocytogenes EGDe to DvnV41 and MesY105 was investigated. L. monocytogenes EGDe was inactivated in lmo0052 and/or lmo1292 by homologous recombination. Listerial mutant strain EGDSC02 (inactivated in the putative glpQ gene), was slightly resistant to DvnV41. The listerial mutant strain EGDSC01 (inactivated in the putative pde gene) remained, as the wild-type strain, sensitive to DvnV41, but was affected in growth parameters.

摘要

最近有研究表明(卡尔维兹等人,2007年),glpQ和pde基因参与粪肠球菌JH2-2对DvnV41的中度抗性,DvnV41是一种由分歧肉杆菌V41产生的IIa类细菌素。lpQ和pde基因在李斯特菌中的直系同源基因可能分别是lmo0052和lmo1292基因。在此,研究了lmo0052和lmo1292基因在单核细胞增生李斯特菌EGDe对DvnV41和MesY105抗性中的作用。通过同源重组使单核细胞增生李斯特菌EGDe的lmo0052和/或lmo1292基因失活。李斯特菌突变株EGDSC02(假定的glpQ基因失活)对DvnV41有轻微抗性。李斯特菌突变株EGDSC01(假定的pde基因失活)与野生型菌株一样,对DvnV41敏感,但生长参数受到影响。

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FEMS Microbiol Rev. 2007 Sep;31(5):592-613. doi: 10.1111/j.1574-6976.2007.00080.x.
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Microbiology (Reading). 2007 May;153(Pt 5):1609-1618. doi: 10.1099/mic.0.2006/004812-0.
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Improvement of enterocin P purification process.
肠球菌素P纯化工艺的改进。
Folia Microbiol (Praha). 2006;51(5):401-5. doi: 10.1007/BF02931583.
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Evidence on correlation between number of disulfide bridge and toxicity of class IIa bacteriocins.关于IIa类细菌素中二硫键数量与毒性之间相关性的证据。
Food Microbiol. 2006 Apr;23(2):175-83. doi: 10.1016/j.fm.2005.02.001.
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Microbiol Mol Biol Rev. 2006 Jun;70(2):564-82. doi: 10.1128/MMBR.00016-05.
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New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria.用于在天然不可转化、低GC含量的革兰氏阳性细菌中进行高效等位基因替换的新型载体。
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