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In situ changes in native fluorescence from Bacillus subtilis during endospore formation

机译:原位植物枯草芽孢杆菌在腹腔形成期间的变化

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Native fluorescence emission and excitation spectra were used to monitor changes in Bacillus subtilis (Bs) and Staphylococcus aureus (Sa) subjected to starvation conditions. Initially, the fluorescence spectra from the Bs and Sa was dominated by tryptophan emission. After the second day, a fluorescence band with an emission peak at 410 nm and an excitation peak at 345 nm appeared in the Bs. This emission is from dipicolinic acid, a major constituent of bacterial endospores. The dipicolinic acid intensity increased steadily during the next 2 to 4 days as the number of Bs forming spores increased. No dipicolinic acid signal was observed in the (non-spore forming) Sa. The addition of β-hydroxybutyric acid to either the Bs or Sa resulted in the emergence of a third band with very strong fluorescence emission maximum at 460 nm and with excitation maxima at 250, 270 and 400 nm. This 460 nm emission was quenched with the addition of Fe~(2+), indicating that the source of this emission is a siderophore produced by the bacteria.
机译:使用本机荧光发射和激发光谱来监测枯草芽孢杆菌(BS)和金黄色葡萄球菌(SA)进行饥饿条件的变化。最初,来自BS和SA的荧光光谱由色氨酸发射主导。在第二天之后,BS中出现在410nm处的发射峰的荧光带出现在345nm处的激发峰值。这种发射来自丁二碱酸,细菌肠孢子的主要组成部分。随着形成孢子的BS的数量增加,在接下来的2至4天期间,二辛溶胶强度稳定地增加。在(非孢子成形)SA中没有观察到二辛溶胶信号。向BS或SA中加入β-羟基丁酸,导致在460nm处具有非常强烈的荧光发射的第三条带的出现,并且在250,270和400nm处具有激发最大值。通过添加Fe〜(2+)淬灭该460nm发射,表明该发射的来源是由细菌产生的侧的纵向。

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