首页> 外文期刊>Advances in Microbiology >Role of the Putative Polysaccharide Deacetylase BA1836 from &i&B. anthracis&/i& in Spore Development and Germination
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Role of the Putative Polysaccharide Deacetylase BA1836 from &i&B. anthracis&/i& in Spore Development and Germination

机译:推定的多糖脱乙酰酶Ba1836来自& i& b。炭疽病& / i&在孢子发育和发芽中

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Putative and known polysaccharide deacetylases (PDAs) from B. anthracis have key roles in resistance to host lysozyme, stabilization of the cell wall, biogenesis of peptidoglycan (PG) and for neutral polysaccharide modification and attachment to PG. Here we elucidated the physiological role of the putative PDA BA1836 from B. anthracis . The ba 1836 gene was expressed upon entrance into the stationary phase of growth and enhanced during the early stages of sporulation. The Δba 1836 knockout strain had normal growth rate, did not exhibit any significant alterations in PG pattern of stationary phase cells and was not sensitive to lysozyme, but showed a defect in cell separation. Strikingly, the Δba 1836 mutant strain exhibited a severe delay in spore development although mature spores were ultimately developed and had normal morphology. Additionally, digestion of Δba 1836 mutant spore PG with mutanolysin produced an almost identical muropeptide pattern compared to peptidoglycan from wild type spores, although the amount of all muropeptides was significantly reduced. Finally, knockout spores exhibited a lower germination rate. To our knowledge, BA1836 has a unique role, among the presently characterized PDAs from B. anthracis , in spore development and germination.
机译:来自B.炭疽的推定和已知的多糖脱乙酰酶(PDA)具有抗宿主溶菌酶抗性,细胞壁稳定,肽聚糖(PG)的生物发生和中性多糖改性和对PG附着的关键作用。在这里,我们阐明了推定的PDA Ba1836从 b的生理作用。炭疽病。在进入生长的静止阶段时表达 Ba 1836基因,并在孢子的早期阶段增强。 δ11836敲除菌株具有正常的生长速率,没有表现出固定相细胞的PG模式中的任何显着改变,并且对溶菌酶不敏感,但在细胞分离中表现出缺陷。令人惊讶的是,δ11836突变菌株在孢子发育中表现出严重的延迟,尽管最终发生了成熟的孢子并具有正常的形态。另外,与来自野生型孢子的肽聚糖相比,δ2的消化δ Ba 1836突变体孢子Pg与来自野生型孢子的肽聚糖相比,几乎相同的鼠肽图案,尽管所有Mur肽的量显着降低。最后,敲除孢子表现出较低的萌发率。据我们所知,BA1836具有独特的作用,目前表征来自 b的PDA。炭疽病,在孢子发育和萌发中。

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