Department of Physics, East Carolina University, Greenville, North Carolina, USA.
Department of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut, USA.
J Bacteriol. 2014 Jul;196(13):2443-54. doi: 10.1128/JB.01687-14. Epub 2014 Apr 25.
Short exposures of Bacillus spores to nutrient germinants can commit spores to germinate when germinants are removed or their binding to the spores' nutrient germinant receptors (GRs) is inhibited. Bacillus subtilis spores were exposed to germinants for various periods, followed by germinant removal to prevent further commitment. Release of spore dipicolinic acid (DPA) was then measured by differential interference contrast microscopy to monitor germination of multiple individual spores, and spores did not release DPA after 1 to 2 min of germinant exposure until ~7 min after germinant removal. With longer germinant exposures, percentages of committed spores with times for completion of DPA release (Trelease) greater than the time of germinant removal (Tb) increased, while the time Tlag - Tb, where Tlag represents the time when rapid DPA release began, was decreased but rapid DPA release times (ΔTrelease = Trelease - Tlag) were increased; Factors affecting average Trelease values and the percentages of committed spores were germinant exposure time, germinant concentration, sporulation conditions, and spore heat activation, as previously shown for commitment of spore populations. Surprisingly, germination of spores given a 2nd short germinant exposure 30 to 45 min after a 1st exposure of the same duration was significantly higher than after the 1st exposure, but the number of spores that germinated in the 2nd germinant exposure decreased as the interval between germinant exposures increased up to 12 h. The latter results indicate that spores have some memory, albeit transient, of their previous exposure to nutrient germinants.
芽孢短时间暴露于营养发芽剂中,当发芽剂被去除或其与芽孢营养发芽剂受体(GRs)的结合被抑制时,芽孢就会被诱导发芽。将枯草芽孢杆菌芽孢暴露于发芽剂中不同时间,然后去除发芽剂以防止进一步的诱导。然后通过相差显微镜测量芽孢释放出的二吡啶羧酸(DPA)来监测多个单个芽孢的发芽情况,在 1 到 2 分钟的发芽剂暴露后,芽孢不会释放 DPA,直到去除发芽剂后约 7 分钟。随着发芽剂暴露时间的延长,完成 DPA 释放的时间(Trelease)大于去除发芽剂时间(Tb)的有丝分裂孢子的比例增加,而时间 Tlag - Tb 减少,其中 Tlag 代表快速 DPA 释放开始的时间;快速 DPA 释放时间(ΔTrelease = Trelease - Tlag)增加;以前的研究表明,影响平均 Trelease 值和有丝分裂孢子比例的因素包括发芽剂暴露时间、发芽剂浓度、孢子形成条件和孢子热激活。令人惊讶的是,在第一次暴露相同持续时间的 30 至 45 分钟后,给予第二次短时间发芽剂暴露的芽孢的发芽率明显高于第一次暴露,但是在第二次发芽剂暴露中发芽的芽孢数量随着发芽剂暴露间隔的增加而减少,最高可达 12 小时。后一结果表明,尽管芽孢对营养发芽剂的先前暴露只有短暂的记忆,但它们确实有一些记忆。