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Effects of gene disruptions in the nisin gene cluster of Lactococcus lactis on nisin production and producer immunity

机译:乳酸乳球菌乳酸链球菌素基因簇中的基因破坏对乳酸链球菌素生产和生产者免疫力的影响

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摘要

The lantibiotic nisin is produced by several strains of Lactococcus lactis subsp. lactis. The chromosomally located gene cluster nisABTCIPRKFEG is required for biosynthesis, development of immunity, and regulation of gene expression. In-frame deletions in the nisB and nisT genes, and disruption of nisC by plasmid integration, eliminated nisin production and resulted in a strongly reduced level of immunity of the strains. The transcription of two nisin operons was inactivated in these mutant strains, but could be restored by addition of small amounts of nisin to growing cultures. The immunity levels of the mutants were also raised by adding nisin to growing cultures, albeit not to wild-type level. A strain with an in-frame deletion in the nisI gene was still able to produce active nisin, but the production and immunity levels were markedly lower. By measuring immunity levels of the knock-out strains and determining mRNA levels, it is concluded that NisI has an important function for nisin immunity and must cooperate with nisFEG-encoded proteins to provide a high level of immunity. Maximal immunity could not be obtained in the mutant strains, probably because the wild-type transcription levels from nisA and nisF promoters are not reached when essential nis genes are disrupted. Using Southern hybridization with a consensus promoter probe, no other DNA sequences similar to the nisA and nisF promoters could be detected, indicating that these two elements are probably the only ones in the chromosome regulated by nisin and are thus the only ones involved in the regulation of producer immunity.
机译:羊毛硫抗生素乳链菌肽是由乳酸乳球菌亚种的几种菌株产生的。乳酸菌。染色体定位的基因簇nisABTCIPRKFEG是生物合成,增强免疫力和调节基因表达所必需的。 nisB和nisT基因的框内缺失,以及质粒整合破坏nisC,消除了乳链菌肽的产生,并导致菌株的免疫力大大降低。在这些突变株中,两个乳链菌肽操纵子的转录被灭活,但是可以通过向生长的培养物中添加少量乳链菌肽来恢复。通过向生长的培养物中添加乳链菌肽,即使不是野生型也可以提高突变体的免疫水平。 nisI基因框内缺失的菌株仍能够产生活性乳链菌肽,但产量和免疫水平明显降低。通过测量敲除菌株的免疫水平并确定mRNA水平,可以得出以下结论:NisI对乳酸链球菌素具有重要的免疫功能,必须与nisFEG编码的蛋白质协同作用才能提供高水平的免疫力。在突变菌株中无法获得最大的免疫力,这可能是因为当必需的nis基因被破坏时,未达到nisA和nisF启动子的野生型转录水平。使用带有共有启动子探针的Southern杂交,无法检测到与nisA和nisF启动子相似的其他DNA序列,表明这两个元素可能是乳酸链球菌素调控的染色体中唯一的元素,因此是唯一参与调控的元素生产者免疫力。

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