Identification and in situ removal of an inhibitory intermediate to develop an efficient phytosterol bioconversion process using a cyclodextrin-resting cell system. Issue 40 (15th July 2021)
- Record Type:
- Journal Article
- Title:
- Identification and in situ removal of an inhibitory intermediate to develop an efficient phytosterol bioconversion process using a cyclodextrin-resting cell system. Issue 40 (15th July 2021)
- Main Title:
- Identification and in situ removal of an inhibitory intermediate to develop an efficient phytosterol bioconversion process using a cyclodextrin-resting cell system
- Authors:
- Wang, Da
Zhang, Jian
Cao, Dan-Dan
Wang, Xuedong
Wei, Dongzhi - Abstract:
- Abstract : We identified an inhibitory intermediate, 4-ene-3-keto steroids, that limits the bioconversion rate and provided a solution based on resin adsorption for improving 9α-OH-AD production efficiency in a commercial-scale process. Abstract : A classically versatile steroid intermediate, 9α-hydroxyandrost-4-ene-3, 17-dione (9α-OH-AD), can be obtained by phytosterol (PS) bioconversion using Mycobacterium . In this study, a cyclodextrin-resting cell reaction system with a high concentration of PS (50 g L −1 ) was used to produce 9α-OH-AD. However, the inhibitory effect of metabolic intermediates is a key factor limiting production efficiency. After the separation and identification of a series of metabolic intermediates, it was found that 4-ene-3-keto steroids, which are the first metabolites of sterol side-chain degradation, accumulated at the beginning of the bioprocess and had a remarkable inhibitory effect on bioconversion. The bioconversion rate was greatly improved when 5 g L −1 of macroporous adsorbent resin D101 was added to the reaction system in the initial phase. A certain amount of resin acted as a reservoir to remove the inhibitory intermediate in situ and facilitated the bioconversion process, and the 9α-OH-AD space–time yield increased to 8.51 g L −1 d −1, which was 23.15% higher than that without resin addition (6.91 g L −1 d −1 ) after 72 h bioconversion. In summary, we identified an inhibitory intermediate that limits the bioconversion rate and providedAbstract : We identified an inhibitory intermediate, 4-ene-3-keto steroids, that limits the bioconversion rate and provided a solution based on resin adsorption for improving 9α-OH-AD production efficiency in a commercial-scale process. Abstract : A classically versatile steroid intermediate, 9α-hydroxyandrost-4-ene-3, 17-dione (9α-OH-AD), can be obtained by phytosterol (PS) bioconversion using Mycobacterium . In this study, a cyclodextrin-resting cell reaction system with a high concentration of PS (50 g L −1 ) was used to produce 9α-OH-AD. However, the inhibitory effect of metabolic intermediates is a key factor limiting production efficiency. After the separation and identification of a series of metabolic intermediates, it was found that 4-ene-3-keto steroids, which are the first metabolites of sterol side-chain degradation, accumulated at the beginning of the bioprocess and had a remarkable inhibitory effect on bioconversion. The bioconversion rate was greatly improved when 5 g L −1 of macroporous adsorbent resin D101 was added to the reaction system in the initial phase. A certain amount of resin acted as a reservoir to remove the inhibitory intermediate in situ and facilitated the bioconversion process, and the 9α-OH-AD space–time yield increased to 8.51 g L −1 d −1, which was 23.15% higher than that without resin addition (6.91 g L −1 d −1 ) after 72 h bioconversion. In summary, we identified an inhibitory intermediate that limits the bioconversion rate and provided a solution based on resin adsorption for improving 9α-OH-AD production efficiency in a commercial-scale process. … (more)
- Is Part Of:
- RSC advances. Volume 11:Issue 40(2021)
- Journal:
- RSC advances
- Issue:
- Volume 11:Issue 40(2021)
- Issue Display:
- Volume 11, Issue 40 (2021)
- Year:
- 2021
- Volume:
- 11
- Issue:
- 40
- Issue Sort Value:
- 2021-0011-0040-0000
- Page Start:
- 24787
- Page End:
- 24793
- Publication Date:
- 2021-07-15
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1ra02774c ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 18319.xml