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https://hdl.handle.net/20.500.14094/0100502554
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2026-04-05
14:26 集計
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0100502554 (fulltext)
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2.92 MB
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メタデータID
0100502554
アクセス権
open access
出版タイプ
Version of Record
タイトル
Adaptive responses of genome-reduced Bacillus subtilis during enzyme secretion in a breathing vessel culture
著者
Öktem, Ayşegül ; Yokoyama, Kyosuke ; Wu, Yuzheng ; Grilli, Francesca ; Maaß, Sandra ; Ishikawa, Shu ; Yotsuya, Masato ; Sato, Ryosuke ; van Dijl, Jan Maarten ; Yoshida, Ken-ichi
著者名
Öktem, Ayşegül
著者名
Yokoyama, Kyosuke
著者名
Wu, Yuzheng
著者名
Grilli, Francesca
著者名
Maaß, Sandra
著者ID
A0019
研究者ID
1000030359872
ORCID
0000-0002-2239-1116
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=ff864c575b0045a5520e17560c007669
著者名
Ishikawa, Shu
石川, 周
イシカワ, シュウ
所属機関名
科学技術イノベーション研究科
著者名
Yotsuya, Masato
著者名
Sato, Ryosuke
著者名
van Dijl, Jan Maarten
著者ID
A1049
研究者ID
1000020230732
ORCID
0000-0002-3383-4664
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=81199c8c7ea4889b520e17560c007669
著者名
Yoshida, Ken-ichi
吉田, 健一
ヨシダ, ケンイチ
所属機関名
科学技術イノベーション研究科
言語
English (英語)
収録物名
Microbial Cell Factories
巻(号)
25(1)
ページ
53
出版者
BioMed Central
刊行日
2026-01-29
公開日
2026-03-16
抄録
Background: The utilisation of microbes for the production of enzymes and pharmaceutical proteins is an important step towards a sustainable future. However, the energy requirement for agitation, aeration and cooling during industrial fermentation processes is substantial. To address this challenge, we have previously developed a ‘breathing’ polytetrafluoroethylene fermenter vessel that allows effective gas exchange with ambient air and, thus, does not require sparger aeration. The present study aimed to explore the potential application of the breathing vessel for enzyme production by the Gram-positive bacterial cell factory Bacillus subtilis. Here, we compared production of the secreted α-amylase AmyQ by the genome-reduced multiple protease-deficient B. subtilis strain IIG-Bs-27-31 during parallel culturing in breathing vessels and shake flasks. Enzyme yields and the cellular and extracellular proteome compositions were assessed. Results: We observed comparable growth characteristics and AmyQ yields per liter in both culture systems. However, proteome analyses indicated statistically significant differences (p < 0.05, log₂fold change>|0.5|) in the utilization of carbon sources and stress responses between cells grown in the breathing vessels versus shake flasks. In particular, bacteria in the breathing vessel presented activation of the Sigma B-dependent general stress response, presumably to sustain bacterial growth and viability. In contrast, bacteria grown in shake flask presented activated cell envelope stress pathways and typical sheer stress symptoms. Conclusions: While the overall AmyQ yields per liter were similar in both fermentation systems, the total enzyme yields in the breathing fermenter were significantly higher due to the 15-fold increase in culture volume. Our findings imply that breathing fermentation vessels are suitable for B. subtilis enzyme production and, upon further scale-up, they may represent sustainable and cost-effective alternatives to traditional fermentation systems for microbial cell factories.
キーワード
Bacillus subtilis
‘breathing’ fermenter
Industrial enzyme production
Proteomics
Genome reduction
Stress response
カテゴリ
科学技術イノベーション研究科
学術雑誌論文
権利
© The Author(s) 2026
This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
関連情報
DOI
https://doi.org/10.1186/s12934-026-02942-x
PMID
41612395
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資源タイプ
journal article
eISSN
1475-2859
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助成情報
助成機関識別子
https://doi.org/10.13039/501100000781
助成機関名
European Research Council (ERC)
研究課題番号
101073056
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