Diep Dzung B, Godager Linda, Brede Dag, Nes Ingolf F
Laboratory of Microbial Gene Technology, Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, N1432 Aas, Norway.
Microbiology (Reading). 2006 Jun;152(Pt 6):1649-1659. doi: 10.1099/mic.0.28794-0.
The genome of Pediococcus pentosaceus ATCC 25745 contains a gene cluster that resembles a regulated bacteriocin system. The gene cluster has an operon-like structure consisting of a putative pediocin-like bacteriocin gene (termed penA) and a potential immunity gene (termed peiA). Genetic determinants involved in bacteriocin transport and regulation are also found in proximity to penA and peiA but the so-called accessory gene involved in transport and the inducer gene involved in regulation are missing. Consequently, this bacterium is a poor bacteriocin producer. To analyse the potency of the putative bacteriocin operon, the two genes penA-peiA were heterologously expressed in a Lactobacillus sakei host that contains the complete apparatus for gene activation, maturation and externalization of bacteriocins. It was demonstrated that the heterologous host expressing penA and peiA produced a strong bacteriocin activity; in addition, the host became immune to its own bacteriocin, identifying the gene pair penA-peiA as a potent bacteriocin system. The novel pediocin-like bacteriocin, termed penocin A, has an isotopic mass [M+H]+ of 4684.6 Da as determined by mass spectrometry; this value corresponds well to the expected size of the mature 42 aa peptide containing a disulfide bridge. The bacteriocin is heat-stable but protease-sensitive and has a calculated pI of 9.45. Penocin A has a relatively broad inhibition spectrum, including pathogenic Listeria and Clostridium species. Immediately upstream of the regulatory genes reside some features that resemble remnants of a disrupted inducer gene. This degenerate gene was restored and shown to encode a double-glycine leader-containing peptide. Furthermore, expression of the restored gene triggered high bacteriocin production in P. pentosaceus ATCC 25745, thus confirming its role as an inducer in the pen regulon.
戊糖片球菌ATCC 25745的基因组包含一个类似于受调控的细菌素系统的基因簇。该基因簇具有操纵子样结构,由一个假定的类片球菌素细菌素基因(称为penA)和一个潜在的免疫基因(称为peiA)组成。在penA和peiA附近还发现了参与细菌素运输和调控的遗传决定因素,但缺少参与运输的所谓辅助基因和参与调控的诱导基因。因此,这种细菌是一种较差的细菌素生产者。为了分析假定的细菌素操纵子的效力,将penA-peiA这两个基因在含有细菌素基因激活、成熟和外排完整装置的清酒乳杆菌宿主中进行异源表达。结果表明,表达penA和peiA的异源宿主产生了很强的细菌素活性;此外,宿主对自身产生的细菌素具有免疫性,从而确定基因对penA-peiA是一个有效的细菌素系统。这种新型的类片球菌素细菌素称为penocin A,通过质谱测定其同位素质量[M+H]+为4684.6 Da;该值与预期的含有二硫键的42个氨基酸成熟肽的大小非常吻合。该细菌素对热稳定但对蛋白酶敏感,计算出的pI为9.45。Penocin A具有相对较广的抑制谱,包括致病性李斯特菌和梭菌属。在调控基因的紧邻上游存在一些类似于被破坏的诱导基因残余的特征。这个退化基因被修复并显示编码一种含双甘氨酸前导肽。此外,修复基因的表达触发了戊糖片球菌ATCC 25745中细菌素的高产量,从而证实了它在pen操纵子中作为诱导剂的作用。