首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Characterization of Loosely Associated Material from the Cell Surface of Lactococcus lactis subsp. cremoris E8 and Its Phage-Resistant Variant Strain 398
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Characterization of Loosely Associated Material from the Cell Surface of Lactococcus lactis subsp. cremoris E8 and Its Phage-Resistant Variant Strain 398

机译:乳酸乳球菌亚种细胞表面松散结合物质的表征。 cremoris E8及其抗噬菌体变异株398

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摘要

Loosely associated material (LAM) was isolated by gentle extraction procedures from the cell surface of Lactococcus lactis subsp. cremoris E8 and its phage-resistant variant strain 398. LAM from both strains was chemically characterized, and its role in the adsorption of three small isometric bacteriophages, φ 618, φ 833, and φ 852, to the cell surface of the two strains was investigated. The phage-resistant strain (strain 398) produced LAM which differed significantly from the material produced by the parent strain. The total yield of LAM from strain 398 was two- to threefold higher than that from strain E8, and the material contained fivefold more rhamnose and twofold more galactose. Polyacrylamide gel electrophoretic analysis showed that LAM from strain 398 lacked a 21-kDa protein which was present in LAM from the parent strain. Inhibition studies of phage binding by using isolated LAM from two strains showed that although LAM from strain E8 reduced the titer of φ 618 and φ 852 by 53 and 82% respectively, LAM from strain 398 had no effect on the plaque-forming ability of any of the three phages tested. Treatment of LAM from strain E8 with sodium metaperiodate destroyed its ability to bind with φ 618 and φ 852. Phenotypically, strain 398 differed from its parent strain E8 in that it was more prone to cell lysis and required an osmotically adjusted buffer system for the extraction of LAM.
机译:通过温和的提取程序从乳酸乳球菌亚种的细胞表面分离出松散相关的物质(LAM)。 cremoris E8及其抗噬菌体变异菌株398.对两种菌株的LAM进行了化学表征,其在三种小等距噬菌体φ618,φ833和φ852到这两种菌株细胞表面的吸附作用为调查。噬菌体抗性菌株(菌株398)产生的LAM与亲本菌株产生的材料明显不同。来自菌株398的LAM的总产率比来自菌株E8的LAM的总产率高两倍至三倍,并且该材料含有更多的鼠李糖和两倍的半乳糖。聚丙烯酰胺凝胶电泳分析表明,来自菌株398的LAM缺乏来自亲本菌株的LAM中存在的21-kDa蛋白。使用来自两个菌株的分离的LAM抑制噬菌体结合的研究表明,尽管E8菌株的LAM分别降低φ618和φ852的效价53%和82%,但398菌株的LAM对任何菌株的噬菌斑形成能力没有影响测试的三个噬菌体中的一个。用偏高碘酸钠处理E8菌株的LAM破坏了其与φ618和φ852结合的能力。表型上,菌株398与其亲本菌株E8的不同之处在于,它更易于细胞裂解,需要通过渗透调节的缓冲液系统进行提取LAM。

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