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Bauermeister, Anja ; Mahnert, Alexander ; Auerbach, Anna ; Böcker, Alexander ; Flier, Niwin ; Weber, Christina ; Probst, Alexander J. ; Haberer, Klaus ; Moissl-Eichinger, Christine

Quantification of encapsulated bioburden in spacecraft polymer materials by cultivation-dependent and molecular methods

Bauermeister, Anja, Mahnert, Alexander, Auerbach, Anna, Böcker, Alexander, Flier, Niwin, Weber, Christina, Probst, Alexander J., Haberer, Klaus und Moissl-Eichinger, Christine (2014) Quantification of encapsulated bioburden in spacecraft polymer materials by cultivation-dependent and molecular methods. PLOS ONE 9 (4), e4265.

Veröffentlichungsdatum dieses Volltextes: 30 Jul 2014 06:11
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.30499


Zusammenfassung

Bioburden encapsulated in spacecraft polymers (such as adhesives and coatings) poses a potential risk to jeopardize scientific exploration of other celestial bodies. This is particularly critical for spacecraft components intended for hard landing. So far, it remained unclear if polymers are indeed a source of microbial contamination. In addition, data with respect to survival of microbes during ...

Bioburden encapsulated in spacecraft polymers (such as adhesives and coatings) poses a potential risk to jeopardize scientific exploration of other celestial bodies. This is particularly critical for spacecraft components intended for hard landing. So far, it remained unclear if polymers are indeed a source of microbial contamination. In addition, data with respect to survival of microbes during the embedding/polymerization process are sparse. In this study we developed testing strategies to quantitatively examine encapsulated bioburden in five different polymers used frequently and in large quantities on spaceflight hardware. As quantitative extraction of the bioburden from polymerized (solid) materials did not prove feasible, contaminants were extracted from uncured precursors. Cultivation-based analyses revealed <0.1-2.5 colony forming units (cfu) per cm(3) polymer, whereas quantitative PCR-based detection of contaminants indicated considerably higher values, despite low DNA extraction efficiency. Results obtained from this approach reflect the most conservative proxy for encapsulated bioburden, as they give the maximum bioburden of the polymers irrespective of any additional physical and chemical stress occurring during polymerization. To address the latter issue, we deployed an embedding model to elucidate and monitor the physiological status of embedded Bacillus safensis spores in a cured polymer. Staining approaches using AlexaFluor succinimidyl ester 488 (AF488), propidium monoazide (PMA), CTC (5-cyano-2,3-diotolyl tetrazolium chloride) demonstrated that embedded spores retained integrity, germination and cultivation ability even after polymerization of the adhesive Scotch-Weld 2216 B/A. Using the methods presented here, we were able to estimate the worst case contribution of encapsulated bioburden in different polymers to the bioburden of spacecraft. We demonstrated that spores were not affected by polymerization processes. Besides Planetary Protection considerations, our results could prove useful for the manufacturing of food packaging, pharmacy industry and implant technology.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftPLOS ONE
Verlag:PUBLIC LIBRARY SCIENCE
Ort der Veröffentlichung:SAN FRANCISCO
Band:9
Nummer des Zeitschriftenheftes oder des Kapitels:4
Seitenbereich:e4265
Datum15 April 2014
InstitutionenBiologie und Vorklinische Medizin > Institut für Biochemie, Genetik und Mikrobiologie > Lehrstuhl für Mikrobiologie (Archaeenzentrum)
Identifikationsnummer
WertTyp
10.1371/journal.pone.0094265DOI
Stichwörter / KeywordsMICROBIAL DIVERSITY; ASSEMBLY-FACILITY; CLEAN ROOMS; MICROORGANISMS; BACTERIA; SPORES; MARS; SURFACES; CONTAMINATION; ENVIRONMENTS;
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-304998
Dokumenten-ID30499

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