UV-Induced Spectral and Morphological Changes in Bacterial Spores for Inactivation Assessment

被引:3
|
作者
Oberg, Rasmus [1 ,2 ]
Sil, Timir B. [2 ]
Johansson, Alexandra C. [1 ]
Malyshev, Dmitry [2 ]
Landstro''m, Lars [3 ]
Johansson, Susanne [1 ]
Andersson, Magnus [2 ,4 ]
Andersson, Per Ola [1 ]
机构
[1] Swedish Def Res Agcy FOI, S-90621 Umea, Sweden
[2] Umea Univ, Dept Phys, S-90187 Umea, Sweden
[3] Swedish Def Res Agcy FOI, S-13794 Norra Sorunda, Sweden
[4] Umea Ctr Microbial Res UCMR, S-90736 Umea, Sweden
基金
瑞典研究理事会;
关键词
BACILLUS-SUBTILIS SPORES; ABSORBING AMINO-ACIDS; RAMAN-SPECTROSCOPY; DIPICOLINIC ACID; FLUORESCENCE; GERMINATION; PHOTOCHEMISTRY; PHOTOPHYSICS; RADIATION; CONTRAST;
D O I
10.1021/acs.jpcb.3c07062
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ability to detect and inactivate spore-forming bacteria is of significance within, for example, industrial, healthcare, and defense sectors. Not only are stringent protocols necessary for the inactivation of spores but robust procedures are also required to detect viable spores after an inactivation assay to evaluate the procedure's success. UV radiation is a standard procedure to inactivate spores. However, there is limited understanding regarding its impact on spores' spectral and morphological characteristics. A further insight into these UV-induced changes can significantly improve the design of spore decontamination procedures and verification assays. This work investigates the spectral and morphological changes to Bacillus thuringiensis spores after UV exposure. Using absorbance and fluorescence spectroscopy, we observe an exponential decay in the spectral intensity of amino acids and protein structures, as well as a logistic increase in dimerized DPA with increased UV exposure on bulk spore suspensions. Additionally, using micro-Raman spectroscopy, we observe DPA release and protein degradation with increased UV exposure. More specifically, the protein backbone's 1600-1700 cm(-1) amide I band decays slower than other amino acid-based structures. Last, using electron microscopy and light scattering measurements, we observe shriveling of the spore bodies with increased UV radiation, alongside the leaking of core content and disruption of proteinaceous coat and exosporium layers. Overall, this work utilized spectroscopy and electron microscopy techniques to gain new understanding of UV-induced spore inactivation relating to spore degradation and CaDPA release. The study also identified spectroscopic indicators that can be used to determine spore viability after inactivation. These findings have practical applications in the development of new spore decontamination and inactivation validation methods.
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页码:1638 / 1646
页数:9
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