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Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis

BACKGROUND: Enzymatic conversion of lignocellulosic biomass into soluble sugars is a major bottleneck in the plant biomass utilization. Several anaerobic organisms cope these issues via multiple-enzyme complex system so called ‘cellulosome’. Hence, we proposed a “biomimic operon” concept for making...

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Autores principales: Chang, Jui-Jen, Anandharaj, Marimuthu, Ho, Cheng-Yu, Tsuge, Kenji, Tsai, Tsung-Yu, Ke, Huei-Mien, Lin, Yu-Ju, Ha Tran, Minh Dung, Li, Wen-Hsiung, Huang, Chieh-Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991470/
https://www.ncbi.nlm.nih.gov/pubmed/29930703
http://dx.doi.org/10.1186/s13068-018-1151-7
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author Chang, Jui-Jen
Anandharaj, Marimuthu
Ho, Cheng-Yu
Tsuge, Kenji
Tsai, Tsung-Yu
Ke, Huei-Mien
Lin, Yu-Ju
Ha Tran, Minh Dung
Li, Wen-Hsiung
Huang, Chieh-Chen
author_facet Chang, Jui-Jen
Anandharaj, Marimuthu
Ho, Cheng-Yu
Tsuge, Kenji
Tsai, Tsung-Yu
Ke, Huei-Mien
Lin, Yu-Ju
Ha Tran, Minh Dung
Li, Wen-Hsiung
Huang, Chieh-Chen
author_sort Chang, Jui-Jen
collection PubMed
description BACKGROUND: Enzymatic conversion of lignocellulosic biomass into soluble sugars is a major bottleneck in the plant biomass utilization. Several anaerobic organisms cope these issues via multiple-enzyme complex system so called ‘cellulosome’. Hence, we proposed a “biomimic operon” concept for making an artificial cellulosome which can be used as a promising tool for the expression of cellulosomal enzymes in Bacillus subtilis. RESULTS: According to the proteomic analysis of Clostridium thermocellum ATCC27405 induced by Avicel or cellobiose, we selected eight highly expressed cellulosomal genes including a scaffoldin protein gene (cipA), a cell-surface anchor gene (sdbA), two exoglucanase genes (celK and celS), two endoglucanase genes (celA and celR), and two xylanase genes (xynC and xynZ). Arranging these eight genes in two different orders, we constructed two different polycistronic operons using the ordered gene assembly in Bacillus method. This is the first study to express the whole CipA along with cellulolytic enzymes in B. subtilis. Each operon was successfully expressed in B. subtilis RM125, and the protein complex assembly, cellulose-binding ability, thermostability, and cellulolytic activity were demonstrated. The operon with a higher xylanase activity showed greater saccharification on complex cellulosic substrates such as Napier grass than the other operon. CONCLUSIONS: In this study, a strategy for constructing an efficient cellulosome system was developed and two different artificial cellulosomal operons were constructed. Both operons could efficiently express the cellulosomal enzymes and exhibited cellulose saccharification. This strategy can be applied to different industries with cellulose-containing materials, such as papermaking, biofuel, agricultural compost, mushroom cultivation, and waste processing industries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1151-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-59914702018-06-21 Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis Chang, Jui-Jen Anandharaj, Marimuthu Ho, Cheng-Yu Tsuge, Kenji Tsai, Tsung-Yu Ke, Huei-Mien Lin, Yu-Ju Ha Tran, Minh Dung Li, Wen-Hsiung Huang, Chieh-Chen Biotechnol Biofuels Research BACKGROUND: Enzymatic conversion of lignocellulosic biomass into soluble sugars is a major bottleneck in the plant biomass utilization. Several anaerobic organisms cope these issues via multiple-enzyme complex system so called ‘cellulosome’. Hence, we proposed a “biomimic operon” concept for making an artificial cellulosome which can be used as a promising tool for the expression of cellulosomal enzymes in Bacillus subtilis. RESULTS: According to the proteomic analysis of Clostridium thermocellum ATCC27405 induced by Avicel or cellobiose, we selected eight highly expressed cellulosomal genes including a scaffoldin protein gene (cipA), a cell-surface anchor gene (sdbA), two exoglucanase genes (celK and celS), two endoglucanase genes (celA and celR), and two xylanase genes (xynC and xynZ). Arranging these eight genes in two different orders, we constructed two different polycistronic operons using the ordered gene assembly in Bacillus method. This is the first study to express the whole CipA along with cellulolytic enzymes in B. subtilis. Each operon was successfully expressed in B. subtilis RM125, and the protein complex assembly, cellulose-binding ability, thermostability, and cellulolytic activity were demonstrated. The operon with a higher xylanase activity showed greater saccharification on complex cellulosic substrates such as Napier grass than the other operon. CONCLUSIONS: In this study, a strategy for constructing an efficient cellulosome system was developed and two different artificial cellulosomal operons were constructed. Both operons could efficiently express the cellulosomal enzymes and exhibited cellulose saccharification. This strategy can be applied to different industries with cellulose-containing materials, such as papermaking, biofuel, agricultural compost, mushroom cultivation, and waste processing industries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1151-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-07 /pmc/articles/PMC5991470/ /pubmed/29930703 http://dx.doi.org/10.1186/s13068-018-1151-7 Text en © The Author(s) 2018 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chang, Jui-Jen
Anandharaj, Marimuthu
Ho, Cheng-Yu
Tsuge, Kenji
Tsai, Tsung-Yu
Ke, Huei-Mien
Lin, Yu-Ju
Ha Tran, Minh Dung
Li, Wen-Hsiung
Huang, Chieh-Chen
Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title_full Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title_fullStr Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title_full_unstemmed Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title_short Biomimetic strategy for constructing Clostridium thermocellum cellulosomal operons in Bacillus subtilis
title_sort biomimetic strategy for constructing clostridium thermocellum cellulosomal operons in bacillus subtilis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991470/
https://www.ncbi.nlm.nih.gov/pubmed/29930703
http://dx.doi.org/10.1186/s13068-018-1151-7
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