Sahoo Susmita, Verma Rajesh K, Suresh A K, Rao K Krishnamurthy, Bellare Jayesh, Suraishkumar G K
Department of Chemical Engineering, Indian Institute of Technology, Bombay, Powai, Mumbai 400076 India.
Biotechnol Prog. 2003 Nov-Dec;19(6):1689-96. doi: 10.1021/bp034191w.
Responses of bacterial (Bacillus subtilis) cells under different shear levels, from both 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, sigma(B), in the bacterial responses to shear stress, which was unknown in the literature thus far; the sigma(B) expression correlated inversely with the siROS. Further, through experiments with ROS quenchers, we showed that ROS regulated sigma(B) expression under shear.
从宏观和基因层面呈现了不同剪切水平下细菌(枯草芽孢杆菌)细胞的反应。使用新型库埃特流生物反应器(CFB)对这些反应进行了研究,在该反应器中,整个培养过程可在规定的剪切条件下进行。通过使空气穿过固定在CFB内筒上的聚四氟乙烯(PTFE)膜,实现了氧气供应,而氧气供应是规定剪切条件下整个培养过程的正常限制因素。更重要的是,对氧气传递能力和剪切速率的分析表明,在该CFB中,可以在不受氧气供应影响干扰的情况下研究规定剪切的影响。此外,摇瓶可作为研究剪切效应的合适对照,主要是因为据估计,在190 rpm的正常摇床操作条件下,摇瓶中的剪切速率可忽略不计,为0.028 s⁻¹,而CFB中使用的最低转速下的剪切速率值为445 s⁻¹。在宏观层面,当剪切速率从0.028 s⁻¹增加到1482 s⁻¹时,细胞大小在1482 s⁻¹时比在0.028 s⁻¹时减小了近50%,生长速率增加了245%,最大细胞浓度增加了190%。与剪切速率为0.028 s⁻¹的对照培养物相比,在1482 s⁻¹时,细胞内过氧化氢酶的比活性增加了335%,蛋白酶增加了87%。此外,最高剪切速率下的细胞内活性氧比水平(siROS)是对照条件下的9.3倍。在基因层面,我们确定了转录因子sigma(B)参与细菌对剪切应力的反应,这在迄今为止的文献中尚属未知;sigma(B)的表达与siROS呈负相关。此外,通过使用活性氧淬灭剂的实验,我们表明活性氧在剪切作用下调节sigma(B)的表达。