首页> 外文期刊>Journal of bacteriology >Biochemical and Genetic Evidence that Enterococcus faecium L50 Produces Enterocins L50A and L50B, thesec-Dependent Enterocin P, and a Novel Bacteriocin Secreted without an N-Terminal Extension Termed Enterocin Q
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Biochemical and Genetic Evidence that Enterococcus faecium L50 Produces Enterocins L50A and L50B, thesec-Dependent Enterocin P, and a Novel Bacteriocin Secreted without an N-Terminal Extension Termed Enterocin Q

机译:粪肠球菌L50产生肠球蛋白L50A和L50B,sec依赖性肠球蛋白P以及不经N末端延伸而分泌的新型细菌素称为肠球蛋白Q的生化和遗传证据。

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Enterococcus faecium L50 grown at 16 to 32°C produces enterocin L50 (EntL50), consisting of EntL50A and EntL50B, two unmodified non-pediocin-like peptides synthesized without an N-terminal leader sequence or signal peptide. However, the bacteriocin activity found in the cell-free culture supernatants following growth at higher temperatures (37 to 47°C) is not due to EntL50. A purification procedure including cation-exchange, hydrophobic interaction, and reverse-phase liquid chromatography has shown that the antimicrobial activity is due to two different bacteriocins. Amino acid sequences obtained by Edman degradation and DNA sequencing analyses revealed that one is identical to the sec-dependent pediocin-like enterocin P produced by E. faecium P13 (L. M. Cintas, P. Casaus, L. S. H?varstein, P. E. Hernández, and I. F. Nes, Appl. Environ. Microbiol. 63:4321–4330, 1997) and the other is a novel unmodified non-pediocin-like bacteriocin termed enterocin Q (EntQ), with a molecular mass of 3,980. DNA sequencing analysis of a 963-bp region of E. faecium L50 containing the enterocin P structural gene (entP) and the putative immunity protein gene (entiP) reveals a genetic organization identical to that previously found in E. faecium P13. DNA sequencing analysis of a 1,448-bp region identified two consecutive but diverging open reading frames (ORFs) of which one, termed entQ, encodes a 34-amino-acid protein whose deduced amino acid sequence was identical to that obtained for EntQ by amino acid sequencing, showing that EntQ, similarly to EntL50A and EntL50B, is synthesized without an N-terminal leader sequence or signal peptide. The second ORF, termed orf2, was located immediately upstream of and in opposite orientation toentQ and encodes a putative immunity protein composed of 221 amino acids. Bacteriocin production by E. faecium L50 showed that EntP and EntQ are produced in the temperature range from 16 to 47°C and maximally detected at 47 and 37 to 47°C, respectively, while EntL50A and EntL50B are maximally synthesized at 16 to 25°C and are not detected at 37°C or above.
机译:在16至32°C下生长的屎肠球菌 L50产生的肠球菌L50(EntL50),由EntL50A和EntL50B组成,这是两种未经修饰的非花椒素样肽,没有N末端前导序列或信号肽。但是,在较高温度(37至47°C)下生长后,无细胞培养上清液中发现的细菌素活性不是由于EntL50引起的。包括阳离子交换,疏水作用和反相液相色谱在内的纯化程序表明,抗菌活性是由于两种不同的细菌素引起的。通过Edman降解和DNA测序分析获得的氨基酸序列表明,该序列与 E产生的 sec 依赖的pediocin样肠球蛋白P相同。粪便 P13(LM Cintas,P。Casaus,LS H?varstein,PEHernández和IF Nes,Appl。Environ。Microbiol。63:4321–4330,1997),另一种是新型未修饰的非花椒素类细菌素称为肠球蛋白Q(EntQ),分子质量为3,980。对 E的963-bp区域的DNA测序分析。粪肠杆菌 L50包含肠毒素P结构基因( entP )和推定的免疫蛋白基因( entiP ),揭示了与以前在中发现的基因结构相同的基因结构> E。粪便 P13。对1448 bp区域的DNA测序分析确定了两个连续但不同的开放阅读框(ORF),其中一个称为 entQ ,编码一个34个氨基酸的蛋白质,其推导的氨基酸序列与通过氨基酸测序获得的EntQ结果表明EntQ与EntL50A和EntL50B类似,是在没有N末端前导序列或信号肽的情况下合成的。第二个ORF,称为 orf2 ,位于 entQ 的上游,且方向相反,并编码一个由221个氨基酸组成的推定免疫蛋白。 Eem生产细菌素。粪便L50表明EntP和EntQ在16至47°C的温度范围内产生,最高分别在47和37至47°C的温度下检测到,而EntL50A和EntL50B在16至25°C的温度下最大合成在37°C或更高温度下无法检测到。

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