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Tracking the cellulolytic activity of Clostridium thermocellum biofilms

BACKGROUND: Microbial cellulose conversion by Clostridium thermocellum 27405 occurs predominantly through the activity of substrate-adherent bacteria organized in thin, primarily single cell-layered biofilms. The importance of cellulosic surface exposure to microbial hydrolysis has received little a...

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Autores principales: Dumitrache, Alexandru, Wolfaardt, Gideon M, Allen, David Grant, Liss, Steven N, Lynd, Lee R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176736/
https://www.ncbi.nlm.nih.gov/pubmed/24286524
http://dx.doi.org/10.1186/1754-6834-6-175
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author Dumitrache, Alexandru
Wolfaardt, Gideon M
Allen, David Grant
Liss, Steven N
Lynd, Lee R
author_facet Dumitrache, Alexandru
Wolfaardt, Gideon M
Allen, David Grant
Liss, Steven N
Lynd, Lee R
author_sort Dumitrache, Alexandru
collection PubMed
description BACKGROUND: Microbial cellulose conversion by Clostridium thermocellum 27405 occurs predominantly through the activity of substrate-adherent bacteria organized in thin, primarily single cell-layered biofilms. The importance of cellulosic surface exposure to microbial hydrolysis has received little attention despite its implied impact on conversion kinetics. RESULTS: We showed the spatial heterogeneity of fiber distribution in pure cellulosic sheets, which made direct measurements of biofilm colonization and surface penetration impossible. Therefore, we utilized on-line measurements of carbon dioxide (CO(2)) production in continuous-flow reactors, in conjunction with confocal imaging, to observe patterns of biofilm invasion and to indirectly estimate microbial accessibility to the substrate’s surface and the resulting limitations on conversion kinetics. A strong positive correlation was found between cellulose consumption and CO(2) production (R(2) = 0.996) and between surface area and maximum biofilm activity (R(2) = 0.981). We observed an initial biofilm development rate (0.46 h(-1), 0.34 h(-1) and 0.33 h(-1)) on Whatman sheets (#1, #598 and #3, respectively) that stabilized when the accessible surface was maximally colonized. The results suggest that cellulose conversion kinetics is initially subject to a microbial limitation period where the substrate is in excess, followed by a substrate limitation period where cellular mass, in the form of biofilms, is not limiting. Accessible surface area acts as an important determinant of the respective lengths of these two distinct periods. At end-point fermentation, all sheets were digested predominantly under substrate accessibility limitations (e.g., up to 81% of total CO(2) production for Whatman #1). Integration of CO(2) production rates over time showed Whatman #3 underwent the fastest conversion efficiency under microbial limitation, suggestive of best biofilm penetration, while Whatman #1 exhibited the least recalcitrance and the faster degradation during the substrate limitation period. CONCLUSION: The results showed that the specific biofilm development rate of cellulolytic bacteria such as C. thermocellum has a notable effect on overall reactor kinetics during the period of microbial limitation, when ca. 20% of cellulose conversion occurs. The study further demonstrated the utility of on-line CO(2) measurements as a method to assess biofilm development and substrate digestibility pertaining to microbial solubilization of cellulose, which is relevant when considering feedstock pre-treatment options.
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spelling pubmed-41767362014-10-23 Tracking the cellulolytic activity of Clostridium thermocellum biofilms Dumitrache, Alexandru Wolfaardt, Gideon M Allen, David Grant Liss, Steven N Lynd, Lee R Biotechnol Biofuels Research BACKGROUND: Microbial cellulose conversion by Clostridium thermocellum 27405 occurs predominantly through the activity of substrate-adherent bacteria organized in thin, primarily single cell-layered biofilms. The importance of cellulosic surface exposure to microbial hydrolysis has received little attention despite its implied impact on conversion kinetics. RESULTS: We showed the spatial heterogeneity of fiber distribution in pure cellulosic sheets, which made direct measurements of biofilm colonization and surface penetration impossible. Therefore, we utilized on-line measurements of carbon dioxide (CO(2)) production in continuous-flow reactors, in conjunction with confocal imaging, to observe patterns of biofilm invasion and to indirectly estimate microbial accessibility to the substrate’s surface and the resulting limitations on conversion kinetics. A strong positive correlation was found between cellulose consumption and CO(2) production (R(2) = 0.996) and between surface area and maximum biofilm activity (R(2) = 0.981). We observed an initial biofilm development rate (0.46 h(-1), 0.34 h(-1) and 0.33 h(-1)) on Whatman sheets (#1, #598 and #3, respectively) that stabilized when the accessible surface was maximally colonized. The results suggest that cellulose conversion kinetics is initially subject to a microbial limitation period where the substrate is in excess, followed by a substrate limitation period where cellular mass, in the form of biofilms, is not limiting. Accessible surface area acts as an important determinant of the respective lengths of these two distinct periods. At end-point fermentation, all sheets were digested predominantly under substrate accessibility limitations (e.g., up to 81% of total CO(2) production for Whatman #1). Integration of CO(2) production rates over time showed Whatman #3 underwent the fastest conversion efficiency under microbial limitation, suggestive of best biofilm penetration, while Whatman #1 exhibited the least recalcitrance and the faster degradation during the substrate limitation period. CONCLUSION: The results showed that the specific biofilm development rate of cellulolytic bacteria such as C. thermocellum has a notable effect on overall reactor kinetics during the period of microbial limitation, when ca. 20% of cellulose conversion occurs. The study further demonstrated the utility of on-line CO(2) measurements as a method to assess biofilm development and substrate digestibility pertaining to microbial solubilization of cellulose, which is relevant when considering feedstock pre-treatment options. BioMed Central 2013-11-29 /pmc/articles/PMC4176736/ /pubmed/24286524 http://dx.doi.org/10.1186/1754-6834-6-175 Text en Copyright © 2013 Dumitrache et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dumitrache, Alexandru
Wolfaardt, Gideon M
Allen, David Grant
Liss, Steven N
Lynd, Lee R
Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title_full Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title_fullStr Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title_full_unstemmed Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title_short Tracking the cellulolytic activity of Clostridium thermocellum biofilms
title_sort tracking the cellulolytic activity of clostridium thermocellum biofilms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176736/
https://www.ncbi.nlm.nih.gov/pubmed/24286524
http://dx.doi.org/10.1186/1754-6834-6-175
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