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Macro-Level and Genetic-Level Responses of Bacillus subtilis to Shear Stress

机译:枯草芽孢杆菌对剪切应力的宏观和遗传水平响应

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Responses of bacterial (Bacillus subtilis)cells under different shear levels,from both 3,the macro and genetic viewpoints,have been presented.The responses were studied using a novel,couette flow bioreactor (CFB),in which the entire cultivation can be performed under defined shear conditions.Oxygen supply,the normal limiting factor for entire cultivations under defined shear conditions,has been achieved by passing air through a poly(tetrafluoroethylene)(PTFE)membrane fixed on the inner cylinder of the CFB.More importantly,analyses of the oxygen transfer capabilities as well as the shear rates show that in this CFB,the effects of defined shear can be studied:without interference from the effects of oxygen supply.Further,the shake flask can be used as a proper control for studying the shear effects,mainly because the shear rate in the shake flask under normal shaker operating conditions of 190 rpm has been estimated to be a negligible 0.028 s~(-1) compared to a value of 445 s~(-1) at the lowest rpm employed in the CFB.At the macro level the cell size decreased by almost 50% at 1482 s~(-1) compared to that at 0.028 s~(-1),the growth rate increased by 245%,and the maximum cell concentration increased by 190% when the shear rate was increased from 0.028 to 1482 s~(-1).The specific intracellular catalase level increased by 335% and protease by 87% at 1482 s~(-1) as compared to the control cultures at a shear rate 0.028 s~(-1).In addition,the specific intracellular reactive oxygen species level (siROS)at the highest shear rate was 9.3-fold compared to the control conditions.At the genetic level we have established the involvement of the transcription factor,GB,in the bacterial responses to shear stress,which was unknown in the literature thus far;the GB expression correlated inversely with the siROS.Further,through experiments with ROS quenchers,we showed that ROS regulated GB expression under shear.
机译:从宏观和遗传的角度,提出了三种不同剪切水平下细菌(枯草芽孢杆菌)细胞的响应。使用新型库埃特流式生物反应器(CFB)研究了该响应,可以进行整个培养供氧是在限定的剪切条件下整个栽培的正常限制因素,通过使空气流过固定在CFB内筒上的聚四氟乙烯(PTFE)膜可实现供氧。更重要的是,分析氧气的传递能力和剪切速率表明,在此CFB中,可以研究定义的剪切效果:不受氧气供应的影响。此外,摇瓶可作为研究剪切的合适控制方法这种影响主要是因为在190 rpm的正常摇床操作条件下,摇瓶中的剪切速率估计为0.028 s〜(-1),与之相比时的445 s〜(-1)可以忽略不计。 CFB的最低转速。在宏观水平上,1482 s〜(-1)的细胞大小比0.028 s〜(-1)的细胞大小减少了近50%,生长速率增加了245%,最大当剪切速率从0.028增加到1482 s〜(-1)时,细胞浓度增加了190%.1482 s〜(-1)时,细胞内过氧化氢酶的特异性水平增加了335%,蛋白酶增加了87%在0.028 s〜(-1)的剪切速率下进行培养。此外,在最高剪切速率下,细胞内活性氧的特定水平(siROS)是对照条件下的9.3倍。转录因子GB在细菌对剪应力的反应中的作用,至今尚未见文献报道; GB表达与siROS呈负相关。此外,通过ROS淬灭剂的实验,我们发现ROS在剪切条件下调节了GB的表达。

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