Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, China.
School of Chemical Engineering and Technology, Tianjin University, Tianjin, China.
Appl Environ Microbiol. 2020 Sep 17;86(19). doi: 10.1128/AEM.01306-20.
NisI confers immunity against nisin, with high substrate specificity to prevent a suicidal effect in nisin-producing strains. However, the NisI maturation process as well as its influence on nisin resistance has not been characterized. Here, we report the roles of lipoprotein signal peptidase II (Lsp) and prolipoprotein diacylglyceryl transferase (Lgt) in NisI maturation and nisin resistance of F44. We found that the resistance of nisin of an Lsp-deficient mutant remarkably decreased, while no significant differences in growth were observed. We demonstrated that Lsp could cleave signal peptide of NisI precursor Moreover, diacylglyceryl modification of NisI catalyzed by Lgt played a decisive role in attachment of NisI on the cell envelope, while it exhibited no effects on cleavage of the signal peptides of NisI precursor. The dissociation constant ( ) for the interaction between nisin and NisI exhibited a 2.8-fold increase compared with that between nisin and pre-NisI with signal peptide by surface plasmon resonance (SPR) analysis, providing evidence that Lsp-catalyzed signal peptide cleavage was critical for the immune activity of NisI. Our study revealed the process of NisI maturation in and presented a potential strategy to enhance industrial nisin production. Nisin, a safe and natural antimicrobial peptide, has a long and impressive history as a food preservative and is also considered a novel candidate to alleviate the increasingly serious threat of antibiotic resistance. Nisin is produced by certain strains. The nisin immunity protein NisI, a membrane-bound lipoprotein, is expressed by nisin producers to avoid suicidal action. Here, we report the roles of Lsp and Lgt in NisI maturation and nisin resistance of F44. The results verified the importance of Lsp to NisI-conferred immunity and Lgt to localization. Our study revealed the process of NisI maturation in and presented a potential strategy to enhance industrial nisin production.
NisI 赋予对乳链菌肽的免疫性,具有高底物特异性,以防止在产生乳链菌肽的菌株中产生自杀效应。然而,NisI 的成熟过程及其对乳链菌肽抗性的影响尚未得到表征。在这里,我们报告了脂蛋白信号肽酶 II (Lsp) 和前乳链菌肽二酰基甘油转移酶 (Lgt) 在 NisI 成熟和 F44 乳链菌肽抗性中的作用。我们发现,Lsp 缺失突变体的乳链菌肽抗性显著降低,而生长没有明显差异。我们证明了 Lsp 可以切割 NisI 前体的信号肽。此外,Lgt 催化的 NisI 的二酰基甘油修饰在 NisI 附着在细胞包膜上起着决定性的作用,而它对 NisI 前体信号肽的切割没有影响。表面等离子体共振 (SPR) 分析表明,NisI 与 NisI 的相互作用的解离常数 ( ) 与 NisI 与带信号肽的前 NisI 相比增加了 2.8 倍,这表明 Lsp 催化的信号肽切割对于 NisI 的免疫活性至关重要。我们的研究揭示了 NisI 在 中的成熟过程,并提出了一种提高工业乳链菌肽生产的潜在策略。乳链菌肽是一种安全且天然的抗菌肽,作为食品防腐剂具有悠久而令人印象深刻的历史,也被认为是缓解日益严重的抗生素耐药性威胁的一种新型候选药物。乳链菌肽由某些 菌株产生。乳链菌肽免疫蛋白 NisI 是一种膜结合脂蛋白,由乳链菌肽产生菌表达,以避免自杀作用。在这里,我们报告了 Lsp 和 Lgt 在 NisI 成熟和 F44 乳链菌肽抗性中的作用。结果验证了 Lsp 对 NisI 赋予的免疫性和 Lgt 对定位的重要性。我们的研究揭示了 NisI 在 中的成熟过程,并提出了一种提高工业乳链菌肽生产的潜在策略。