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清酒乳杆菌LTH 673产生的细菌素——片球菌素P的编码基因sakP的克隆与测序

Cloning and sequencing of sakP encoding sakacin P, the bacteriocin produced by Lactobacillus sake LTH 673.

作者信息

Tichaczek P S, Vogel R F, Hammes W P

机构信息

Institut für Lebensmitteltechnologie, Universität Hohenheim, Stuttgart, Germany.

出版信息

Microbiology (Reading). 1994 Feb;140 ( Pt 2):361-7. doi: 10.1099/13500872-140-2-361.

Abstract

Sakacin P is a heat-stable, unmodified peptide bacteriocin produced by Lactobacillus sake LTH 673. The strain was isolated from fermented dry sausages and is well adapted to this habitat. The bacteriocin inhibits the growth of the opportunistic food pathogens Enterococcus faecalis and Listeria monocytogenes and therefore, it may improve the hygienic status of fermented food, i.e. meat products. Oligonucleotide probes were designed from the N-terminal amino acid sequence of sakacin P and used to identify sakP, the structural gene of sakacin P, on the chromosome of L. sake LTH 673. SakP was cloned into Escherichia coli NM554 and the nucleotide sequence of the gene and its adjacent regions were determined. Sakacin P appears to be synthesized as a prepeptide of 61 amino acids which is proteolytically processed to the mature bacteriocin consisting of 43 amino acids. Sequencing of the cloned fragment also revealed the presence of two other open reading frames orfX and orfY, which are located upstream and downstream of sakP, respectively, putatively encoding proteins of 52 and 98 amino acids, respectively. The functions of both ORFs remain unknown. Primer extension analysis revealed a promoter upstream of sakP. Two transcripts of approximately 0.35 and 1.0 kb were detected by Northern hybridization encoding either only sakP, or both sakP and orfY, respectively.

摘要

片球菌素P是由清酒乳杆菌LTH 673产生的一种热稳定、未修饰的肽类细菌素。该菌株从发酵干香肠中分离得到,非常适应这种生境。这种细菌素可抑制兼性食品病原菌粪肠球菌和单核细胞增生李斯特菌的生长,因此,它可能改善发酵食品即肉类产品的卫生状况。根据片球菌素P的N端氨基酸序列设计了寡核苷酸探针,并用于鉴定清酒乳杆菌LTH 673染色体上片球菌素P的结构基因sakP。将sakP克隆到大肠杆菌NM554中,并测定了该基因及其相邻区域的核苷酸序列。片球菌素P似乎是以61个氨基酸的前肽形式合成的,该前肽经蛋白水解加工成由43个氨基酸组成的成熟细菌素。对克隆片段的测序还揭示了另外两个开放阅读框orfX和orfY的存在,它们分别位于sakP的上游和下游,推测分别编码52个和98个氨基酸的蛋白质。这两个开放阅读框的功能仍然未知。引物延伸分析揭示了sakP上游的一个启动子。通过Northern杂交检测到两个大小约为0.35和1.0 kb的转录本,分别仅编码sakP或同时编码sakP和orfY。

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