Analysis of the Raman spectra of Ca2+-dipicolinic acid alone and in the bacterial spore core in both aqueous and dehydrated environments

The Analyst ◽  
2012 ◽  
Vol 137 (16) ◽  
pp. 3683 ◽  
Author(s):  
Lingbo Kong ◽  
Peter Setlow ◽  
Yong-qing Li
2011 ◽  
Vol 65 (8) ◽  
pp. 866-875 ◽  
Author(s):  
Clint B. Smith ◽  
John E. Anderson ◽  
Jarrod D. Edwards ◽  
Kinson C. Kam

1992 ◽  
Vol 46 (2) ◽  
pp. 357-364 ◽  
Author(s):  
E. Ghiamati ◽  
R. Manoharan ◽  
W. H. Nelson ◽  
J. F. Sperry

UV resonance Raman spectra of Bacillus cereus, Bacillus megaterium, and Bacillus subtilis endospores have been excited at 222.7,230.7,242.5, and 251.1 nm, and spectra have been compared with those of vegetative cells. The resonance Raman spectra of aqueous solutions of dipicolinic acid and calcium dipicolinate have been measured at the same wavelengths. Spectra of endospores and their corresponding germinated spores show only modest differences when excited at 222, 231, and 251 nm. However, very substantial differences appear when excitation occurs at 242 nm. Difference spectra obtained at 242 nm by subtracting spectra of germinated spores of Bacillus cereus from spectra of their corresponding endospores are attributed almost entirely to dipicolinate. Vegetative cells and endospores show large spectral dissimilarities at all exciting wavelengths. These spectral differences, which vary strongly with exciting wavelength, appear to be the result of large differences in the amounts and composition of proteins and nucleic acids, especially ribosomal RNA. The very substantial resonance enhancement of Raman spectra has been obtained from aqueous solutions of pure dipicolinic acid and of sodium and calcium dipicolinate salts, as well as spores at the various exciting wavelengths. The strong enhancement of dipicolinate spectra in spores, however, was noted only with 242-nm excitation. Consequently, only with 242-nm light was it possible to selectively and sensitively excite and study calcium dipicolinate in spores. Resonance enhancement of the dipicolinate spectra with 242-nm excitation appears due primarily to resonance interactions with n-π* electronic transitions associated with the pyridine ring and/or the carboxylate group.


1967 ◽  
Vol 22 (9) ◽  
pp. 505-509
Author(s):  
Chikataro KAWASAKI ◽  
Masaomi KONDO ◽  
Jun SAKURAI

2021 ◽  
Vol 93 (6) ◽  
pp. 3146-3153
Author(s):  
Dmitry Malyshev ◽  
Tobias Dahlberg ◽  
Krister Wiklund ◽  
Per Ola Andersson ◽  
Sara Henriksson ◽  
...  

2003 ◽  
Vol 50 (15-17) ◽  
pp. 2369-2374
Author(s):  
Sergei N. Jerebtsov ◽  
Tomas Opatrny ◽  
Hans A. Schuessler ◽  
Marlan O. Scully ◽  
Alexandre A. Kolomenskii

2020 ◽  
Author(s):  
Xing Qiu ◽  
Wen Jie WU

Abstract In this work, the electro-mechanical stresses induced by pulsed electric fields (PEF) on bacterial spore germination was modeled and empirically tested using Bacillus atrophaeus spores. Specifically, a new model, termed as Qiu-Wu’s electro-mechanical (QW’s EM) spore model, was derived to analyze the effect of electro-mechanical stresses on spores subjected under electric fields. A non-linear inverse relationship was found between electric fields and thickness change of spore coat. SEM, pH, hydrophobicity and electrochemical measurements were implemented for verification of the model. PEF-treated spores germinated with a faster rate and a higher degree of homogeneity. The longer the treatment time, the better the homogeneity. The speed of dipicolinic acid (DPA) release was around 20% faster in PEF-treated samples, while the peak intensity of terbium-DPA from PEF-treated samples was up to 80% lower. Theoretical analysis and empirical results were consistent to show that PEF introduces electro-mechanical stresses to expedite spore germination. The significance and impact of this study is obvious: bacterial spore is implicated in food spoilage and foodborne diseases primarily via the process of germination, and PEF technology has been introduced to inactivate microorganisms in food. Understanding the mechanism of germination under PEF can provide deep understanding for inactivation of foodborne pathogens and better food preservation methods.


1967 ◽  
Vol 22 (8) ◽  
pp. 463-467 ◽  
Author(s):  
Chikataro KAWASAKI ◽  
Masaomi KONDO ◽  
Tsutomu NISHIHARA

1988 ◽  
Vol 43 (5) ◽  
pp. 927-930 ◽  
Author(s):  
Kazuhito WATABE ◽  
Kyoko MAEKAWA ◽  
Atsumi YAMADA ◽  
Tomihiko KOSHIKAWA ◽  
Setsuko OGAWA ◽  
...  

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