Enhanced acetate utilization for value-added chemicals production in Yarrowia lipolytica by integration of metabolic engineering and microbial electrosynthesis
The limited supply of reducing power restricts the efficient utilization of acetate in Yarrowia lipolytica. Here, microbial electrosynthesis (MES) system, enabling direct conversion of inward electrons to NAD(P)H, was used to improve the production of fatty alcohols from acetate based on pathway eng...
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Veröffentlicht in: | Biotechnology and bioengineering 2023-10, Vol.120 (10), p.3013-3024 |
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creator | Huang, Congcong Chen, Yaru Cheng, Shuai Li, Mengxu Wang, Luxin Cheng, Meijie Li, Feng Cao, Yingxiu Song, Hao |
description | The limited supply of reducing power restricts the efficient utilization of acetate in Yarrowia lipolytica. Here, microbial electrosynthesis (MES) system, enabling direct conversion of inward electrons to NAD(P)H, was used to improve the production of fatty alcohols from acetate based on pathway engineering. First, the conversion efficiency of acetate to acetyl-CoA was reinforced by heterogenous expression of ackA-pta genes. Second, a small amount of glucose was used as cosubstrate to activate the pentose phosphate pathway and promote intracellular reducing cofactors synthesis. Third, through the employment of MES system, the final fatty alcohols production of the engineered strain YLFL-11 reached 83.8 mg/g dry cell weight (DCW), which was 6.17-fold higher than the initial production of YLFL-2 in shake flask. Furthermore, these strategies were also applied for the elevation of lupeol and betulinic acid synthesis from acetate in Y. lipolytica, demonstrating that our work provides a practical solution for cofactor supply and the assimilation of inferior carbon sources. |
doi_str_mv | 10.1002/bit.28465 |
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Here, microbial electrosynthesis (MES) system, enabling direct conversion of inward electrons to NAD(P)H, was used to improve the production of fatty alcohols from acetate based on pathway engineering. First, the conversion efficiency of acetate to acetyl-CoA was reinforced by heterogenous expression of ackA-pta genes. Second, a small amount of glucose was used as cosubstrate to activate the pentose phosphate pathway and promote intracellular reducing cofactors synthesis. Third, through the employment of MES system, the final fatty alcohols production of the engineered strain YLFL-11 reached 83.8 mg/g dry cell weight (DCW), which was 6.17-fold higher than the initial production of YLFL-2 in shake flask. Furthermore, these strategies were also applied for the elevation of lupeol and betulinic acid synthesis from acetate in Y. lipolytica, demonstrating that our work provides a practical solution for cofactor supply and the assimilation of inferior carbon sources.</description><identifier>ISSN: 0006-3592</identifier><identifier>ISSN: 1097-0290</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.28465</identifier><identifier>PMID: 37306471</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Acetic acid ; Alcohols ; Betulinic acid ; Carbon sources ; Direct conversion ; Dry cells ; Gene expression ; Metabolic engineering ; Microorganisms ; Pentose ; Pentose phosphate pathway ; Synthesis ; Yarrowia lipolytica</subject><ispartof>Biotechnology and bioengineering, 2023-10, Vol.120 (10), p.3013-3024</ispartof><rights>2023 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c313t-1fd397271ff8542fb4e8de438e3f293007d01f0dc92c24371a2d885352d951af3</citedby><cites>FETCH-LOGICAL-c313t-1fd397271ff8542fb4e8de438e3f293007d01f0dc92c24371a2d885352d951af3</cites><orcidid>0000-0002-8762-8356 ; 0000-0003-0447-3617</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37306471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Congcong</creatorcontrib><creatorcontrib>Chen, Yaru</creatorcontrib><creatorcontrib>Cheng, Shuai</creatorcontrib><creatorcontrib>Li, Mengxu</creatorcontrib><creatorcontrib>Wang, Luxin</creatorcontrib><creatorcontrib>Cheng, Meijie</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Cao, Yingxiu</creatorcontrib><creatorcontrib>Song, Hao</creatorcontrib><title>Enhanced acetate utilization for value-added chemicals production in Yarrowia lipolytica by integration of metabolic engineering and microbial electrosynthesis</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol Bioeng</addtitle><description>The limited supply of reducing power restricts the efficient utilization of acetate in Yarrowia lipolytica. 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Here, microbial electrosynthesis (MES) system, enabling direct conversion of inward electrons to NAD(P)H, was used to improve the production of fatty alcohols from acetate based on pathway engineering. First, the conversion efficiency of acetate to acetyl-CoA was reinforced by heterogenous expression of ackA-pta genes. Second, a small amount of glucose was used as cosubstrate to activate the pentose phosphate pathway and promote intracellular reducing cofactors synthesis. Third, through the employment of MES system, the final fatty alcohols production of the engineered strain YLFL-11 reached 83.8 mg/g dry cell weight (DCW), which was 6.17-fold higher than the initial production of YLFL-2 in shake flask. 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subjects | Acetic acid Alcohols Betulinic acid Carbon sources Direct conversion Dry cells Gene expression Metabolic engineering Microorganisms Pentose Pentose phosphate pathway Synthesis Yarrowia lipolytica |
title | Enhanced acetate utilization for value-added chemicals production in Yarrowia lipolytica by integration of metabolic engineering and microbial electrosynthesis |
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