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PBP2b Mutations Improve the Growth of Phage-Resistant Lactococcus cremoris Lacking Polysaccharide Pellicle

机译:PBP2b突变改善缺乏多糖的噬菌体抗性乳球菌的生长

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Lactococcus lactis and Lactococcus cremoris are Gram-positive lactic acid bacteria widely used as starter in milk fermentations. Lactococcal cells are covered with a polysaccharide pellicle (PSP) that was previously shown to act as the receptor for numerous bacteriophages of the Caudoviricetes class. Thus, mutant strains lacking PSP are phage resistant. However, because PSP is a key cell wall component, PSP-negative mutants exhibit dramatic alterations of cell shape and severe growth defects, which limit their technological value. In the present study, we isolated spontaneous mutants with improved growth, from L. cremoris PSP-negative mutants. These mutants grow at rates similar to the wild-type strain, and based on transmission electron microscopy analysis, they exhibit improved cell morphology compared to their parental PSP-negative mutants. In addition, the selected mutants maintain their phage resistance. Whole-genome sequencing of several such mutants showed that they carried a mutation in pbp2b, a gene encoding a penicillin-binding protein involved in peptidoglycan biosynthesis. Our results indicate that lowering or turning off PBP2b activity suppresses the requirement for PSP and ameliorates substantially bacterial fitness and morphology.IMPORTANCE Lactococcus lactis and Lactococcus cremoris are widely used in the dairy industry as a starter culture. As such, they are consistently challenged by bacteriophage infections which may result in reduced or failed milk acidification with associated economic losses. Bacteriophage infection starts with the recognition of a receptor at the cell surface, which was shown to be a cell wall polysaccharide (the polysaccharide pellicle PSP) for the majority of lactococcal phages. Lactococcal mutants devoid of PSP exhibit phage resistance but also reduced fitness, since their morphology and division are severely impaired. Here, we isolated spontaneous, food-grade non-PSP-producing L. cremoris mutants resistant to bacteriophage infection with a restored fitness. This study provides an approach to isolate non-GMO phage-resistant L. cremoris and L. lactis strains, which can be applied to strains with technological functionalities. Also, our results highlight for the first time the link between peptidoglycan and cell wall polysaccharide biosynthesis. Lactococcus lactis and Lactococcus cremoris are widely used in the dairy industry as a starter culture. As such, they are consistently challenged by bacteriophage infections which may result in reduced or failed milk acidification with associated economic losses.
机译:乳酸乳球菌和克氏乳球菌是革兰氏阳性乳酸菌,广泛用作牛奶发酵的发酵剂。乳球菌细胞覆盖着多糖薄膜(PSP),该多糖薄膜先前已被证明是Caudoviricetes类许多噬菌体的受体。因此,缺乏PSP的突变菌株具有噬菌体抗性。然而,由于PSP是细胞壁的关键成分,PSP阴性突变体表现出细胞形状的急剧改变和严重的生长缺陷,这限制了其技术价值。在本研究中,我们从 L. cremoris PSP 阴性突变体中分离出生长改善的自发突变体。这些突变体以与野生型菌株相似的速度生长,并且基于透射电子显微镜分析,与亲本PSP阴性突变体相比,它们表现出改善的细胞形态。此外,选定的突变体保持其噬菌体抗性。对几个这样的突变体的全基因组测序表明,它们携带pbp2b的突变,pbp2b是一种编码参与肽聚糖生物合成的青霉素结合蛋白的基因。我们的结果表明,降低或关闭PBP2b活性可以抑制对PSP的需求,并显着改善细菌适应性和形态。重要性 乳酸乳球菌和克氏乳球菌在乳制品工业中被广泛用作发酵剂。因此,它们一直受到噬菌体感染的挑战,这可能导致牛奶酸化减少或失败,并造成相关的经济损失。噬菌体感染始于识别细胞表面的受体,该受体被证明是大多数乳球菌噬菌体的细胞壁多糖(薄膜多糖 [PSP])。缺乏 PSP 的乳球菌突变体表现出噬菌体抗性,但适应性也会降低,因为它们的形态和分裂严重受损。在这里,我们分离出自发的、食品级的、不产生 PSP 的 L. cremoris 突变体,这些突变体对噬菌体感染具有抗性,并恢复了健康。本研究提供了一种分离非转基因噬菌体抗性克氏乳杆菌和乳酸乳杆菌菌株的方法,该菌株可应用于具有技术功能的菌株。此外,我们的研究结果首次强调了肽聚糖与细胞壁多糖生物合成之间的联系。乳酸乳球菌和克氏乳球菌在乳制品工业中被广泛用作发酵剂。因此,它们一直受到噬菌体感染的挑战,这可能导致牛奶酸化减少或失败,并造成相关的经济损失。

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