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Monitoring bacterial spore metabolic activity using heavy water-induced Raman peak evolution
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.ORCID-id: 0000-0002-0168-0197
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik.ORCID-id: 0000-0002-0496-6692
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för fysik. Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR). (The Biophysics and Biophotonics group)ORCID-id: 0000-0002-9835-3263
2023 (engelsk)Inngår i: The Analyst, ISSN 0003-2654, E-ISSN 1364-5528, Vol. 148, nr 9, s. 2141-2148Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Endospore-forming bacteria are associated with food spoilage, food poisoning, and infection in hospitals. Therefore, methods to monitor spore metabolic activity and verify sterilization are of great interest. However, current methods for tracking metabolic activity are time-consuming and resource intensive. This work investigates isotope labeling and Raman microscopy as a low-cost rapid alternative. Specifically, we monitor the Raman spectrum of enterotoxic \textit{B. cereus} spores undergoing germination and cell division in D2O-infused broth. During germination and cell division, water is metabolized and deuterium from the broth is incorporated into proteins and lipids, resulting in the appearance of a Raman peak related to C-D bonds at 2190 cm-1. We find that a significant C-D peak appears after 2 h of incubation at 37◦C. Further, we found that the peak appearance coincides with the observed first cell division indicating little metabolic activity during germination. Lastly, the germination and cell growth rate of spores were not affected by adding 30 % heavy water to the broth. This shows the potential for real-time monitoring of metabolic activity from a bacterial spore to a dividing cell. In conclusion, our work proposes tracking the evolution of the C-D Raman peak in spores incubated with D2O-infused broth as an effective and time-, and cost-efficient method to monitor the outgrowth of a spore population, simultaneously allowing us to track for how long the bacteria have grown and divided.

sted, utgiver, år, opplag, sider
Royal Society of Chemistry, 2023. Vol. 148, nr 9, s. 2141-2148
Emneord [en]
Bacterial spores, Heavy water, D2O, Raman spectroscopy, Viability, Germination
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-206398DOI: 10.1039/D2AN02047EISI: 000968915700001PubMedID: 37040186Scopus ID: 2-s2.0-85153492235OAI: oai:DiVA.org:umu-206398DiVA, id: diva2:1748838
Forskningsfinansiär
Swedish Research Council, 2019-04016The Kempe Foundations, JCK1916.2Swedish Armed Forces, 470-A400821Tilgjengelig fra: 2023-04-04 Laget: 2023-04-04 Sist oppdatert: 2025-09-30bibliografisk kontrollert
Inngår i avhandling
1. Spotlight the killer: detecting harmful chemical and biological agents using optical spectroscopy
Åpne denne publikasjonen i ny fane eller vindu >>Spotlight the killer: detecting harmful chemical and biological agents using optical spectroscopy
2025 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Alternativ tittel[sv]
Lyset på mördaren : detektion av skadliga kemiska och biologiska ämnen med hjälp av optisk spektroskopi
Abstract [en]

Harmful chemical and biological agents are a significant threat to health and prosperity worldwide. Recent years have seen an increase in wars and conflicts around the globe, raising concerns about the potential deployment of chemical and biological warfare agents. On a less speculative level, harmful chemicals such as narcotic substances cause immense humanitarian and economic damage through overdoses and associated healthcare costs, while microbes such as pathogenic bacteria and parasites cause hospital-acquired infections and food spoilage at a cost of approximately 1 trillion euros every year. To combat the threat of these harmful agents, we must thus develop rapid and effective detection and diagnostic methods for harmful agents, allowing us to effectively deploy specific treatments and preventative measures.

Classically, while there exist numerous methods for the detection of both harmful chemical and biological agents, they often come with limitations that inhibit their effectiveness. These inhibitions often take the form of bulky equipment that is difficult to apply in the field or time-consuming preparation and measurement processes.

In this thesis we will explore an alternative category of assays for detecting and characterizing harmful materials – optical spectroscopy. Optical spectroscopy is a category of material characterization methods that use light to probe a material. While probing the material, we receive a signal characteristic of the molecules, chemical, and biological structure of our material. These optical spectroscopic methods, such as Raman spectroscopy and fluorescence spectroscopy, can be used to characterize a material within the span of minutes or even seconds, making them ideal for detection applications. Furthermore, they can often be made portable or even handheld, making them a great tool for initial field indication of harmful materials, ahead of thorough lab analysis.

I sincerely hope the studies presented herein can serve as a stepping stone to future technologies and detection assays, capable of saving both money and lives. 

sted, utgiver, år, opplag, sider
Umeå: Umeå University, 2025. s. 72
Emneord
Sensing, Raman spectroscopy, SERS, Fluorescence spectroscopy, CWA, nerve agents, bacterial spores, Cryptosporidium
HSV kategori
Identifikatorer
urn:nbn:se:umu:diva-244830 (URN)978-91-8070-780-0 (ISBN)978-91-8070-779-4 (ISBN)
Disputas
2025-10-24, Aula Anatomica, Biologihuset, 907 36, Umeå, Umeå, 13:00 (engelsk)
Opponent
Veileder
Merknad

This work was done in collaboration with, and with support from, the Swedish Defece Research Agency (FOI).

Tilgjengelig fra: 2025-10-03 Laget: 2025-09-30 Sist oppdatert: 2025-10-22bibliografisk kontrollert

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Öberg, RasmusDahlberg, TobiasMalyshev, DmitryAndersson, Magnus

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