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Novel optimization strategy for tannase production through a modified solid-state fermentation system

BACKGROUND: High amounts of insoluble substrates exist in the traditional solid-state fermentation (SSF) system. The presence of these substrates complicates the determination of microbial biomass. Thus, enzyme activity is used as the sole index for the optimization of the traditional SSF system, an...

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Autores principales: Wu, Changzheng, Zhang, Feng, Li, Lijun, Jiang, Zhedong, Ni, Hui, Xiao, Anfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879601/
https://www.ncbi.nlm.nih.gov/pubmed/29619088
http://dx.doi.org/10.1186/s13068-018-1093-0
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author Wu, Changzheng
Zhang, Feng
Li, Lijun
Jiang, Zhedong
Ni, Hui
Xiao, Anfeng
author_facet Wu, Changzheng
Zhang, Feng
Li, Lijun
Jiang, Zhedong
Ni, Hui
Xiao, Anfeng
author_sort Wu, Changzheng
collection PubMed
description BACKGROUND: High amounts of insoluble substrates exist in the traditional solid-state fermentation (SSF) system. The presence of these substrates complicates the determination of microbial biomass. Thus, enzyme activity is used as the sole index for the optimization of the traditional SSF system, and the relationship between microbial growth and enzyme synthesis is always ignored. This study was conducted to address this deficiency. All soluble nutrients from tea stalk were extracted using water. The aqueous extract was then mixed with polyurethane sponge to establish a modified SSF system, which was then used to conduct tannase production. With this system, biomass, enzyme activity, and enzyme productivity could be measured rationally and accurately. Thus, the association between biomass and enzyme activity could be easily identified, and the shortcomings of traditional SSF could be addressed. RESULTS: Different carbon and nitrogen sources exerted different effects on microbial growth and enzyme production. Single-factor experiments showed that glucose and yeast extract greatly improved microbial biomass accumulation and that tannin and (NH(4))(2)SO(4) efficiently promoted enzyme productivity. Then, these four factors were optimized through response surface methodology. Tannase activity reached 19.22 U/gds when the added amounts of tannin, glucose, (NH(4))(2)SO(4), and yeast extract were 7.49, 8.11, 9.26, and 2.25%, respectively. Tannase activity under the optimized process conditions was 6.36 times higher than that under the initial process conditions. The optimized parameters were directly applied to the traditional tea stalk SSF system. Tannase activity reached 245 U/gds, which is 2.9 times higher than our previously reported value. CONCLUSIONS: In this study, a modified SSF system was established to address the shortcomings of the traditional SSF system. Analysis revealed that enzymatic activity and microbial biomass are closely related, and different carbon and nitrogen sources have different effects on microbial growth and enzyme production. The maximal tannase activity was obtained under the optimal combination of nutrient sources that enhances cell growth and tannase accumulation. Moreover, tannase production through the traditional tea stalk SSF was markedly improved when the optimized parameters were applied. This work provides an innovative approach to bioproduction research through SSF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1093-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-58796012018-04-04 Novel optimization strategy for tannase production through a modified solid-state fermentation system Wu, Changzheng Zhang, Feng Li, Lijun Jiang, Zhedong Ni, Hui Xiao, Anfeng Biotechnol Biofuels Research BACKGROUND: High amounts of insoluble substrates exist in the traditional solid-state fermentation (SSF) system. The presence of these substrates complicates the determination of microbial biomass. Thus, enzyme activity is used as the sole index for the optimization of the traditional SSF system, and the relationship between microbial growth and enzyme synthesis is always ignored. This study was conducted to address this deficiency. All soluble nutrients from tea stalk were extracted using water. The aqueous extract was then mixed with polyurethane sponge to establish a modified SSF system, which was then used to conduct tannase production. With this system, biomass, enzyme activity, and enzyme productivity could be measured rationally and accurately. Thus, the association between biomass and enzyme activity could be easily identified, and the shortcomings of traditional SSF could be addressed. RESULTS: Different carbon and nitrogen sources exerted different effects on microbial growth and enzyme production. Single-factor experiments showed that glucose and yeast extract greatly improved microbial biomass accumulation and that tannin and (NH(4))(2)SO(4) efficiently promoted enzyme productivity. Then, these four factors were optimized through response surface methodology. Tannase activity reached 19.22 U/gds when the added amounts of tannin, glucose, (NH(4))(2)SO(4), and yeast extract were 7.49, 8.11, 9.26, and 2.25%, respectively. Tannase activity under the optimized process conditions was 6.36 times higher than that under the initial process conditions. The optimized parameters were directly applied to the traditional tea stalk SSF system. Tannase activity reached 245 U/gds, which is 2.9 times higher than our previously reported value. CONCLUSIONS: In this study, a modified SSF system was established to address the shortcomings of the traditional SSF system. Analysis revealed that enzymatic activity and microbial biomass are closely related, and different carbon and nitrogen sources have different effects on microbial growth and enzyme production. The maximal tannase activity was obtained under the optimal combination of nutrient sources that enhances cell growth and tannase accumulation. Moreover, tannase production through the traditional tea stalk SSF was markedly improved when the optimized parameters were applied. This work provides an innovative approach to bioproduction research through SSF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1093-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-02 /pmc/articles/PMC5879601/ /pubmed/29619088 http://dx.doi.org/10.1186/s13068-018-1093-0 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
Wu, Changzheng
Zhang, Feng
Li, Lijun
Jiang, Zhedong
Ni, Hui
Xiao, Anfeng
Novel optimization strategy for tannase production through a modified solid-state fermentation system
title Novel optimization strategy for tannase production through a modified solid-state fermentation system
title_full Novel optimization strategy for tannase production through a modified solid-state fermentation system
title_fullStr Novel optimization strategy for tannase production through a modified solid-state fermentation system
title_full_unstemmed Novel optimization strategy for tannase production through a modified solid-state fermentation system
title_short Novel optimization strategy for tannase production through a modified solid-state fermentation system
title_sort novel optimization strategy for tannase production through a modified solid-state fermentation system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879601/
https://www.ncbi.nlm.nih.gov/pubmed/29619088
http://dx.doi.org/10.1186/s13068-018-1093-0
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