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首页> 外文期刊>Applied and Environmental Microbiology >Selection of a Highly Monensin-Resistant Prevotella bryantii Subpopulation with Altered Outer Membrane Characteristics
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Selection of a Highly Monensin-Resistant Prevotella bryantii Subpopulation with Altered Outer Membrane Characteristics

机译:具有改变的外膜特性的高度耐莫能菌素的丙酸小球藻亚群的选择

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Prevotella bryantii cultures treated with monensin grew more slowly than untreated cultures, but only if the monensin concentration was greater than 1 μM. Cultures that were repeatedly transferred (eight transfers or 25 doublings) with monensin always grew rapidly, even at a 10 μM concentration. The amount of monensin needed to facilitate half-maximal potassium depletion (Kd ) from monensin-selected cells was 16-fold greater than “unadapted” wild-type cultures (3,200 versus 200 nM). Cells taken from continuous culture had a Kd of 100 nM, and these inocula could not grow in batch culture when the monensin concentration was greater than 300 nM. Continuous cultures treated with monensin nearly washed out, but the surviving cells had aKd of 1,300 nM. When wild-type cells were transferred in batch culture with 10 μM monensin, theKd did not reach its maximum value (3,200 nM) until after eight transfers (25 doublings). Kd declined when monensin was removed, and it took eight transfers to reach the control value (200 nM). The most probable number of wild-type cells was 1,000-fold lower than of the monensin-selected cells, but calculations based on relative growth advantage andKd indicated that the wild-type culture had 1 to 10% highly monensin-resistant cells. Cell pellets of wild-type cultures were more difficult to disperse than were monensin-selected cells, and water-soluble phenol extracts of monensin-selected cells had 1.8-fold more anthrone-reactive material than did the wild type. Wild-type cultures that were washed in Tris buffer (pH 8.0) released little alkaline phosphatase and were agglutinated by lysozyme. Monensin-selected cultures leaked ninefold more alkaline phosphatase and were not agglutinated by lysozyme. Wild-type colonies taken from high-dilution agar roll tubes retained the lysozyme agglutination phenotype even if transferred with monensin, and monensin-selected colonies were never agglutinated. These observations indicated that wild-type P. bryantii cultures had a subpopulation with different outer membrane characteristics and increased monensin resistance.
机译:用莫能菌素处理的布氏丙酸杆菌培养物比未处理的培养物生长更慢,但前提是莫能菌素浓度大于1μM。用莫能菌素重复转移(八次转移或25倍加倍)的培养物始终快速生长,即使浓度为10μM。从莫能菌素选择的细胞中促进半数最大钾耗减(Kd)所需的莫能菌素的量比“未适应”的野生型培养物大16倍(3,200对200 nM)。连续培养的细胞Kd为100 nM,当莫能菌素浓度大于300 nM时,这些接种不能分批培养。用莫能菌素处理的连续培养物几乎被洗掉,但存活的细胞的ad为1300 nM。将野生型细胞与10μM莫能菌素分批培养时,Kd直到八次转移(25倍)后才达到最大值(3200 nM)。去除莫能菌素后,Kd下降,需要八次转移才能达到控制值(200 nM)。野生型细胞的最可能数量比莫能菌素选择的细胞低1,000倍,但是基于相对生长优势和Kd的计算表明,野生型培养物具有1%至10%的高度莫能菌素抗性细胞。野生型培养物的细胞团块比莫能菌素选择的细胞更难分散,莫能菌素选择的细胞的水溶性酚提取物的蒽醌反应性物质比野生型高1.8倍。在Tris缓冲液(pH 8.0)中洗涤过的野生型培养物几乎不释放碱性磷酸酶,并被溶菌酶凝集。莫能菌素选择的培养物泄漏的碱性磷酸酶多出九倍,并且不会被溶菌酶凝集。即使通过莫能菌素转移,从高稀释琼脂卷管中提取的野生型菌落也保留了溶菌酶凝集表型,并且莫能菌素选择的菌落从不凝集。这些观察结果表明,野生型布鲁氏假单胞菌培养物具有亚群,具有不同的外膜特性和莫能菌素抗性增加。

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