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清酒乳杆菌的pepR基因在转录水平上受厌氧环境正调控。

The pepR gene of Lactobacillus sakei is positively regulated by anaerobiosis at the transcriptional level.

作者信息

Champomier-Vergès Marie-Christine, Marceau Anika, Méra Thérèse, Zagorec Monique

机构信息

Unité Flore Lactique et Environnement Carné, INRA, Domaine de Vilvert, 78 350 Jouy en Josas, France.

出版信息

Appl Environ Microbiol. 2002 Aug;68(8):3873-7. doi: 10.1128/AEM.68.8.3873-3877.2002.

Abstract

Lactobacillus sakei is a lactic acid bacterium belonging to the natural flora of meat products. It constitutes the main flora of vacuum-packed meat and is largely used in western Europe as a starter for the manufacturing of fermented sausages. This species is able to grow both under aerobiosis and anaerobiosis. In many technological processes involving it, oxygen is scarce. The aim of this study was to identify the major proteins affected by growth under anaerobiosis. Using two-dimensional electrophoresis, we showed that one spot was 10-fold overexpressed when cells were grown under anaerobiosis. By N-terminal sequencing it was identified as a peptidase (PepR), and the pepR gene was cloned. Northern analysis revealed that pepR was expressed as a single 1.27-kb transcript induced under anaerobiosis. A mutant was constructed by single crossover in the pepR gene, and its growth and survival were not affected by anaerobiosis.

摘要

清酒乳杆菌是一种属于肉制品天然菌群的乳酸菌。它是真空包装肉类的主要菌群,在西欧大量用作发酵香肠生产的起始菌。该菌种在需氧和厌氧条件下均能生长。在许多涉及它的工艺过程中,氧气稀缺。本研究的目的是鉴定受厌氧生长影响的主要蛋白质。使用二维电泳,我们发现当细胞在厌氧条件下生长时,有一个斑点的表达量增加了10倍。通过N端测序,它被鉴定为一种肽酶(PepR),并克隆了pepR基因。Northern分析表明,pepR以单一的1.27 kb转录本形式表达,在厌氧条件下被诱导。通过在pepR基因中进行单交换构建了一个突变体,其生长和存活不受厌氧条件的影响。

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本文引用的文献

1
Efficient transformation of Lactobacillus sake by electroporation.通过电穿孔法高效转化清酒乳杆菌
Microbiology (Reading). 1996 May;142(5):1273-1279. doi: 10.1099/13500872-142-5-1273.
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Carbohydrate Utilization in Lactobacillus sake.在清酒乳杆菌中碳水化合物的利用。
Appl Environ Microbiol. 1996 Jun;62(6):1922-7. doi: 10.1128/aem.62.6.1922-1927.1996.
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5
Protein expression under uracil privation in Lactobacillus sakei.清酒乳杆菌在尿嘧啶缺乏条件下的蛋白质表达
FEMS Microbiol Lett. 2001 Jun 12;200(1):49-52. doi: 10.1111/j.1574-6968.2001.tb10691.x.

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