Bruno John G
Operational Technologies Corporation, 4100 NW Loop 410, Suite 230, San Antonio, TX, 78229, USA,
J Fluoresc. 2015 Jan;25(1):211-6. doi: 10.1007/s10895-014-1498-5. Epub 2014 Dec 28.
The metachromatic fluorophore acridine orange (AO) has demonstrated green fluorescent staining of dormant Bacillus spores and orange to red staining of transcriptionally active vegetative cells when used in the mid-micoMolar range. Despite the microscopic observation of numerous bright orange to red fluorescent vegetative cells following germination induction, no clear spectral emission peaks > 590 nm have ever been reported for spectrofluorometric analysis involving AO in conjunction with spore germination. This microscopy versus spectrofluorometry paradox is documented in the present report and hypotheses are put forth to explain the very weak spectral changes in the red region which do not appear to correlate with the abundant orange-red fluorescence of nascent vegetative cells seen through the fluorescence microscope.
当在中微摩尔范围内使用时,异染荧光团吖啶橙(AO)已显示出对休眠芽孢杆菌孢子的绿色荧光染色以及对转录活跃的营养细胞的橙色至红色染色。尽管在诱导萌发后通过显微镜观察到大量亮橙色至红色荧光的营养细胞,但从未有过关于在涉及AO与孢子萌发的荧光光谱分析中> 590 nm的清晰光谱发射峰的报道。本报告记录了这种显微镜观察与荧光光谱分析之间的矛盾,并提出了假设来解释红色区域非常微弱的光谱变化,这些变化似乎与通过荧光显微镜观察到的新生营养细胞丰富的橙红色荧光不相关。