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Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions

The National Aeronautics and Space Administration (NASA) measures and validates the biological cleanliness of spacecraft surfaces by counting endospores using the NASA standard assay (NSA). NASA has also approved an adenosine-5′-triphosphate (ATP)-based detection methodology as a means to prescreen...

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Autores principales: Benardini, James N., Venkateswaran, Kasthuri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108744/
https://www.ncbi.nlm.nih.gov/pubmed/27844457
http://dx.doi.org/10.1186/s13568-016-0286-9
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author Benardini, James N.
Venkateswaran, Kasthuri
author_facet Benardini, James N.
Venkateswaran, Kasthuri
author_sort Benardini, James N.
collection PubMed
description The National Aeronautics and Space Administration (NASA) measures and validates the biological cleanliness of spacecraft surfaces by counting endospores using the NASA standard assay (NSA). NASA has also approved an adenosine-5′-triphosphate (ATP)-based detection methodology as a means to prescreen surfaces for the presence of microbial contamination, prior to the spore assay. During Mars Science Laboratory (MSL) spacecraft assembly, test, and launch operations, 4853 surface samples were collected to verify compliance with the bioburden requirement at launch. A subset of these samples was measured for microbial cleanliness using both the NSA (n = 272) and ATP assay (n = 249). NSA results revealed that ~8% (22/272) of the samples showed the presence of at least one spore, whereas ATP assay measurements indicated that ~15% (35/249) of samples exceeded the “threshold cleanliness limit” of 2.3 × 10(−11) mmol ATP per 25 cm(2) used by MSL. Of the 22 NSA samples with a spore, 18% (4/22) were considered above the level of acceptance by both techniques. Based on post launch data analysis presented here, it was determined that this threshold cleanliness limit of 2.3 × 10(−11) mmol ATP per 25 cm(2) could be adopted as a benchmark for assessing spacecraft surface cleanliness. This study clearly demonstrates the value of using alternative methods to rapidly assess spacecraft cleanliness, and provides useful information regarding the process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-016-0286-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-51087442016-12-07 Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions Benardini, James N. Venkateswaran, Kasthuri AMB Express Original Article The National Aeronautics and Space Administration (NASA) measures and validates the biological cleanliness of spacecraft surfaces by counting endospores using the NASA standard assay (NSA). NASA has also approved an adenosine-5′-triphosphate (ATP)-based detection methodology as a means to prescreen surfaces for the presence of microbial contamination, prior to the spore assay. During Mars Science Laboratory (MSL) spacecraft assembly, test, and launch operations, 4853 surface samples were collected to verify compliance with the bioburden requirement at launch. A subset of these samples was measured for microbial cleanliness using both the NSA (n = 272) and ATP assay (n = 249). NSA results revealed that ~8% (22/272) of the samples showed the presence of at least one spore, whereas ATP assay measurements indicated that ~15% (35/249) of samples exceeded the “threshold cleanliness limit” of 2.3 × 10(−11) mmol ATP per 25 cm(2) used by MSL. Of the 22 NSA samples with a spore, 18% (4/22) were considered above the level of acceptance by both techniques. Based on post launch data analysis presented here, it was determined that this threshold cleanliness limit of 2.3 × 10(−11) mmol ATP per 25 cm(2) could be adopted as a benchmark for assessing spacecraft surface cleanliness. This study clearly demonstrates the value of using alternative methods to rapidly assess spacecraft cleanliness, and provides useful information regarding the process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-016-0286-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-11-14 /pmc/articles/PMC5108744/ /pubmed/27844457 http://dx.doi.org/10.1186/s13568-016-0286-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Benardini, James N.
Venkateswaran, Kasthuri
Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title_full Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title_fullStr Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title_full_unstemmed Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title_short Application of the ATP assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
title_sort application of the atp assay to rapidly assess cleanliness of spacecraft surfaces: a path to set a standard for future missions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108744/
https://www.ncbi.nlm.nih.gov/pubmed/27844457
http://dx.doi.org/10.1186/s13568-016-0286-9
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