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Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii

Bacillus amyloliquefaciens is a generally recognized as safe (GRAS) microorganism that presents great potential for the production of heterologous proteins. In this study, we performed genomic and comparative transcriptome to investigate the critical modular in B. amyloliquefaciens on the production...

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Autores principales: Zhang, Jinfang, Zhu, Baoyue, Li, Xinyue, Xu, Xiaojian, Li, Dengke, Zeng, Fang, Zhou, Cuixia, Liu, Yihan, Li, Yu, Lu, Fuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046661/
https://www.ncbi.nlm.nih.gov/pubmed/35497355
http://dx.doi.org/10.3389/fbioe.2022.866066
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author Zhang, Jinfang
Zhu, Baoyue
Li, Xinyue
Xu, Xiaojian
Li, Dengke
Zeng, Fang
Zhou, Cuixia
Liu, Yihan
Li, Yu
Lu, Fuping
author_facet Zhang, Jinfang
Zhu, Baoyue
Li, Xinyue
Xu, Xiaojian
Li, Dengke
Zeng, Fang
Zhou, Cuixia
Liu, Yihan
Li, Yu
Lu, Fuping
author_sort Zhang, Jinfang
collection PubMed
description Bacillus amyloliquefaciens is a generally recognized as safe (GRAS) microorganism that presents great potential for the production of heterologous proteins. In this study, we performed genomic and comparative transcriptome to investigate the critical modular in B. amyloliquefaciens on the production of heterologous alkaline proteases (AprE). After investigation, it was concluded that the key modules affecting the production of alkaline protease were the sporulation germination module (Module I), extracellular protease synthesis module (Module II), and extracellular polysaccharide synthesis module (Module III) in B. amyloliquefaciens. In Module I, AprE yield for mutant BA ΔsigF was 25.3% greater than that of BA Δupp. Combining Module I synergistically with mutation of extracellular proteases in Module II significantly increased AprE production by 36.1% compared with production by BA Δupp. In Module III, the mutation of genes controlling extracellular polysaccharides reduced the viscosity and the accumulation of sediment, and increased the rate of dissolved oxygen in fermentation. Moreover, AprE production was 39.6% higher than in BA Δupp when Modules I, II and III were engineered in combination. This study provides modular engineering strategies for the modification of B. amyloliquefaciens for the production of alkaline proteases.
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spelling pubmed-90466612022-04-29 Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii Zhang, Jinfang Zhu, Baoyue Li, Xinyue Xu, Xiaojian Li, Dengke Zeng, Fang Zhou, Cuixia Liu, Yihan Li, Yu Lu, Fuping Front Bioeng Biotechnol Bioengineering and Biotechnology Bacillus amyloliquefaciens is a generally recognized as safe (GRAS) microorganism that presents great potential for the production of heterologous proteins. In this study, we performed genomic and comparative transcriptome to investigate the critical modular in B. amyloliquefaciens on the production of heterologous alkaline proteases (AprE). After investigation, it was concluded that the key modules affecting the production of alkaline protease were the sporulation germination module (Module I), extracellular protease synthesis module (Module II), and extracellular polysaccharide synthesis module (Module III) in B. amyloliquefaciens. In Module I, AprE yield for mutant BA ΔsigF was 25.3% greater than that of BA Δupp. Combining Module I synergistically with mutation of extracellular proteases in Module II significantly increased AprE production by 36.1% compared with production by BA Δupp. In Module III, the mutation of genes controlling extracellular polysaccharides reduced the viscosity and the accumulation of sediment, and increased the rate of dissolved oxygen in fermentation. Moreover, AprE production was 39.6% higher than in BA Δupp when Modules I, II and III were engineered in combination. This study provides modular engineering strategies for the modification of B. amyloliquefaciens for the production of alkaline proteases. Frontiers Media S.A. 2022-04-14 /pmc/articles/PMC9046661/ /pubmed/35497355 http://dx.doi.org/10.3389/fbioe.2022.866066 Text en Copyright © 2022 Zhang, Zhu, Li, Xu, Li, Zeng, Zhou, Liu, Li and Lu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Zhang, Jinfang
Zhu, Baoyue
Li, Xinyue
Xu, Xiaojian
Li, Dengke
Zeng, Fang
Zhou, Cuixia
Liu, Yihan
Li, Yu
Lu, Fuping
Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title_full Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title_fullStr Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title_full_unstemmed Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title_short Multiple Modular Engineering of Bacillus Amyloliquefaciens Cell Factories for Enhanced Production of Alkaline Proteases From B. Clausii
title_sort multiple modular engineering of bacillus amyloliquefaciens cell factories for enhanced production of alkaline proteases from b. clausii
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046661/
https://www.ncbi.nlm.nih.gov/pubmed/35497355
http://dx.doi.org/10.3389/fbioe.2022.866066
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