Real-Time Monitoring of H₂O₂ Sterilization on Individual <i>Bacillus atrophaeus</i> Spores by Optical Sensing with Trapping Raman Spectroscopy

Abstract

Hydrogen peroxide (H2O2), a strong oxidizer, is a commonly used sterilization agent employed during aseptic food processing and medical applications. To assess the sterilization efficiency with H2O2, bacterial spores are common microbial systems due to their remarkable robustness against a wide variety of decontamination strategies. Despite their widespread use, there is, however, only little information about the detailed time-resolved mechanism underlying the oxidative spore death by H2O2. In this work, we investigate chemical and morphological changes of individual Bacillus atrophaeus spores undergoing oxidative damage using optical sensing with trapping Raman microscopy in real-time. The time-resolved experiments reveal that spore death involves two distinct phases: (i) an initial phase dominated by the fast release of dipicolinic acid (DPA), a major spore biomarker, which indicates the rupture of the spore’s core; and (ii) the oxidation of the remaining spore material resulting in the subsequent fragmentation of the spores’ coat. Simultaneous observation of the spore morphology by optical microscopy corroborates these mechanisms. The dependence of the onset of DPA release and the time constant of spore fragmentation on H2O2 shows that the formation of reactive oxygen species from H2O2 is the rate-limiting factor of oxidative spore death.

Keywords

• optical sensor setup
• Raman spectroscopy
• optical trapping
• <i>Bacillus atrophaeus</i> spores
• sterilization
• DPA (dipicolinic acid)