Chandler D P, Brown J, Bruckner-Lea C J, Olson L, Posakony G J, Stults J R, Valentine N B, Bond L J
Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
Anal Chem. 2001 Aug 1;73(15):3784-9. doi: 10.1021/ac010264j.
We report on the development of a novel, continuous-flow, radially focused ultrasonic disruptor capable of lysing Bacillus spores in the absence of added chemical denaturants, enzymes, or microparticles. Greater than 99% disruption was achieved for Bacillus globigii spores and Escherichia coli and Bacillus subtilis vegetative cells with sample residence times of 62, 12, and 12 s, respectively. Microscopic and SEM images indicated that at equivalent power levels, the incidence of cell death or loss of viability typically exceeded the efficiency of (visible) cell lysis. However, semiquantitative PCR showed up to a 1,000-fold increase in intracellular DNA availability from ultrasonically disrupted spores, and liberated DNA was intact and available for subsequent detection.
我们报告了一种新型连续流径向聚焦超声破碎仪的研发情况,该仪器能够在不添加化学变性剂、酶或微粒的情况下裂解芽孢杆菌孢子。对于球状芽孢杆菌孢子以及大肠杆菌和枯草芽孢杆菌营养细胞,分别在62秒、12秒和12秒的样品停留时间下实现了大于99%的破碎率。显微镜和扫描电子显微镜图像表明,在同等功率水平下,细胞死亡或活力丧失的发生率通常超过(可见的)细胞裂解效率。然而,半定量聚合酶链反应显示,超声破碎的孢子细胞内DNA可利用性提高了多达1000倍,且释放出的DNA完整无损,可供后续检测。