陆地曲霉培养中葡萄糖合成多衣康酸的串联转化工艺。

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bioprocess and Biosystems Engineering Pub Date : 2025-05-01 Epub Date: 2025-03-11 DOI:10.1007/s00449-025-03139-z
Ikumi Kinoshita, Tomonari Tanaka, Yuji Aso
{"title":"陆地曲霉培养中葡萄糖合成多衣康酸的串联转化工艺。","authors":"Ikumi Kinoshita, Tomonari Tanaka, Yuji Aso","doi":"10.1007/s00449-025-03139-z","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, a bio-based vinylidene monomer, itaconic acid (IA), produced by a fungus Aspergillus terreus NBRC 6123 was polymerized in the culture. The inhibition of IA polymerization by the culture components was eased by extraction with 4-methyltetrahydropyran (4mTHP). The extraction with 4mTHP for 4 days under aerobic condition resulted in IA production at 67.9 g/L (522 mM) in the organic phase from 180 g/L glucose. Interestingly, 4mTHP did not affect to the glucose consumption and respiration of A. terreus. IA polymerization in 4mTHP for 72 h using 400 mM IA and 1 mM 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile) as a radical initiator under anaerobic condition by N<sub>2</sub> gas purging resulted in that the IA conversion, and the weight-averaged molecular weight (Mw) and the molecular weight distribution (MWD) of the synthesized polyitaconic acid (polyIA) were 11.5%, 79.8 × 10<sup>3</sup> g/mol, and 1.26, respectively. The respiration by the IA producer itself was used to remove the residual oxygen in the flask by sealing after the IA production. Colorimetric evaluation with a redox indicator, resazurin, revealed that an anaerobic condition which is suitable for the IA polymerization can be accomplished by just incubation for 1 day after the sealing. The synthesis of polyIA from glucose in the same flask with 4mTHP was demonstrated, resulting in that the IA conversion, and Mw and MWD of the synthesized polyIA were 13.8%, 9.1 × 10<sup>3</sup> g/mol, and 1.24, respectively, when 47.1 g/L (362 mM) IA was produced by the extraction for 3 days. To our knowledge, this is the first demonstration of radical polymerization of vinylidene monomer in microbial cultures.</p>","PeriodicalId":9024,"journal":{"name":"Bioprocess and Biosystems Engineering","volume":" ","pages":"737-748"},"PeriodicalIF":3.5000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A tandem conversion process for the synthesis of polyitaconic acid from glucose in the Aspergillus terreus culture.\",\"authors\":\"Ikumi Kinoshita, Tomonari Tanaka, Yuji Aso\",\"doi\":\"10.1007/s00449-025-03139-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In this study, a bio-based vinylidene monomer, itaconic acid (IA), produced by a fungus Aspergillus terreus NBRC 6123 was polymerized in the culture. The inhibition of IA polymerization by the culture components was eased by extraction with 4-methyltetrahydropyran (4mTHP). The extraction with 4mTHP for 4 days under aerobic condition resulted in IA production at 67.9 g/L (522 mM) in the organic phase from 180 g/L glucose. Interestingly, 4mTHP did not affect to the glucose consumption and respiration of A. terreus. IA polymerization in 4mTHP for 72 h using 400 mM IA and 1 mM 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile) as a radical initiator under anaerobic condition by N<sub>2</sub> gas purging resulted in that the IA conversion, and the weight-averaged molecular weight (Mw) and the molecular weight distribution (MWD) of the synthesized polyitaconic acid (polyIA) were 11.5%, 79.8 × 10<sup>3</sup> g/mol, and 1.26, respectively. The respiration by the IA producer itself was used to remove the residual oxygen in the flask by sealing after the IA production. Colorimetric evaluation with a redox indicator, resazurin, revealed that an anaerobic condition which is suitable for the IA polymerization can be accomplished by just incubation for 1 day after the sealing. The synthesis of polyIA from glucose in the same flask with 4mTHP was demonstrated, resulting in that the IA conversion, and Mw and MWD of the synthesized polyIA were 13.8%, 9.1 × 10<sup>3</sup> g/mol, and 1.24, respectively, when 47.1 g/L (362 mM) IA was produced by the extraction for 3 days. To our knowledge, this is the first demonstration of radical polymerization of vinylidene monomer in microbial cultures.</p>\",\"PeriodicalId\":9024,\"journal\":{\"name\":\"Bioprocess and Biosystems Engineering\",\"volume\":\" \",\"pages\":\"737-748\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioprocess and Biosystems Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1007/s00449-025-03139-z\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/11 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioprocess and Biosystems Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s00449-025-03139-z","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/11 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在本研究中,对真菌土曲霉NBRC 6123产生的生物基乙烯单体衣康酸(IA)进行了培养聚合。用4-甲基四氢吡喃(4mTHP)萃取可以缓解培养组分对IA聚合的抑制作用。在有氧条件下,用4mTHP提取4天,从180 g/L葡萄糖中有机相产生67.9 g/L (522 mM)的IA。有趣的是,4mTHP对黄芪的葡萄糖消耗和呼吸没有影响。以400 mM的IA和1 mM的2,2′-偶氮唑(4-甲氧基-2,4-二甲基戊腈)为自由基引发剂,在厌氧条件下,N2气体净化,在4mTHP中聚合72 h,合成的聚衣通酸(polyIA)的IA转化率为11.5%,分子量(Mw)为79.8 × 103 g/mol,分子量分布(MWD)为1.26。在IA生产后,通过密封,利用IA生产者自身的呼吸作用除去烧瓶中的残余氧。用氧化还原指示剂resazurin进行比色评价,结果表明,密封后只需孵育1天即可达到适合IA聚合的厌氧条件。在相同的烧瓶中,用4mTHP从葡萄糖中合成polyIA,当提取47.1 g/L (362 mM) IA 3天后,合成的polyIA的IA转化率为13.8%,Mw和MWD分别为9.1 × 103 g/mol和1.24。据我们所知,这是第一次在微生物培养中证明偏乙烯单体的自由基聚合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A tandem conversion process for the synthesis of polyitaconic acid from glucose in the Aspergillus terreus culture.

In this study, a bio-based vinylidene monomer, itaconic acid (IA), produced by a fungus Aspergillus terreus NBRC 6123 was polymerized in the culture. The inhibition of IA polymerization by the culture components was eased by extraction with 4-methyltetrahydropyran (4mTHP). The extraction with 4mTHP for 4 days under aerobic condition resulted in IA production at 67.9 g/L (522 mM) in the organic phase from 180 g/L glucose. Interestingly, 4mTHP did not affect to the glucose consumption and respiration of A. terreus. IA polymerization in 4mTHP for 72 h using 400 mM IA and 1 mM 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile) as a radical initiator under anaerobic condition by N2 gas purging resulted in that the IA conversion, and the weight-averaged molecular weight (Mw) and the molecular weight distribution (MWD) of the synthesized polyitaconic acid (polyIA) were 11.5%, 79.8 × 103 g/mol, and 1.26, respectively. The respiration by the IA producer itself was used to remove the residual oxygen in the flask by sealing after the IA production. Colorimetric evaluation with a redox indicator, resazurin, revealed that an anaerobic condition which is suitable for the IA polymerization can be accomplished by just incubation for 1 day after the sealing. The synthesis of polyIA from glucose in the same flask with 4mTHP was demonstrated, resulting in that the IA conversion, and Mw and MWD of the synthesized polyIA were 13.8%, 9.1 × 103 g/mol, and 1.24, respectively, when 47.1 g/L (362 mM) IA was produced by the extraction for 3 days. To our knowledge, this is the first demonstration of radical polymerization of vinylidene monomer in microbial cultures.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Bioprocess and Biosystems Engineering
Bioprocess and Biosystems Engineering 工程技术-工程:化工
CiteScore
7.90
自引率
2.60%
发文量
147
审稿时长
2.6 months
期刊介绍: Bioprocess and Biosystems Engineering provides an international peer-reviewed forum to facilitate the discussion between engineering and biological science to find efficient solutions in the development and improvement of bioprocesses. The aim of the journal is to focus more attention on the multidisciplinary approaches for integrative bioprocess design. Of special interest are the rational manipulation of biosystems through metabolic engineering techniques to provide new biocatalysts as well as the model based design of bioprocesses (up-stream processing, bioreactor operation and downstream processing) that will lead to new and sustainable production processes. Contributions are targeted at new approaches for rational and evolutive design of cellular systems by taking into account the environment and constraints of technical production processes, integration of recombinant technology and process design, as well as new hybrid intersections such as bioinformatics and process systems engineering. Manuscripts concerning the design, simulation, experimental validation, control, and economic as well as ecological evaluation of novel processes using biosystems or parts thereof (e.g., enzymes, microorganisms, mammalian cells, plant cells, or tissue), their related products, or technical devices are also encouraged. The Editors will consider papers for publication based on novelty, their impact on biotechnological production and their contribution to the advancement of bioprocess and biosystems engineering science. Submission of papers dealing with routine aspects of bioprocess engineering (e.g., routine application of established methodologies, and description of established equipment) are discouraged.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信