Loading…
Acetone production with metabolically engineered strains of Acetobacterium woodii
Expected depletion of oil and fossil resources urges the development of new alternative routes for the production of bulk chemicals and fuels beyond petroleum resources. In this study, the clostridial acetone pathway was used for the formation of acetone in the acetogenic bacterium Acetobacterium wo...
Saved in:
Published in: | Metabolic engineering 2016-07, Vol.36, p.37-47 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3 |
container_end_page | 47 |
container_issue | |
container_start_page | 37 |
container_title | Metabolic engineering |
container_volume | 36 |
creator | Hoffmeister, Sabrina Gerdom, Marzena Bengelsdorf, Frank R. Linder, Sonja Flüchter, Sebastian Öztürk, Hatice Blümke, Wilfried May, Antje Fischer, Ralf-Jörg Bahl, Hubert Dürre, Peter |
description | Expected depletion of oil and fossil resources urges the development of new alternative routes for the production of bulk chemicals and fuels beyond petroleum resources. In this study, the clostridial acetone pathway was used for the formation of acetone in the acetogenic bacterium Acetobacterium woodii. The acetone production operon (APO) containing the genes thlA (encoding thiolase A), ctfA/ctfB (encoding CoA transferase), and adc (encoding acetoacetate decarboxylase) from Clostridium acetobutylicum were cloned under the control of the thlA promoter into four vectors having different replicons for Gram-positives (pIP404, pBP1, pCB102, and pCD6). Stable replication was observed for all constructs. A. woodii [pJIR_actthlA] achieved the maximal acetone concentration under autotrophic conditions (15.2±3.4mM). Promoter sequences of the genes ackA from A. woodii and pta-ack from C. ljungdahlii were determined by primer extension (PEX) and cloned upstream of the APO. The highest acetone production in recombinant A. woodii cells was achieved using the promoters PthlA and Ppta-ack. Batch fermentations using A. woodii [pMTL84151_actthlA] in a bioreactor revealed that acetate concentration had an effect on the acetone production, due to the high Km value of the CoA transferase. In order to establish consistent acetate concentration within the bioreactor and to increase biomass, a continuous fermentation process for A. woodii was developed. Thus, acetone productivity of the strain A. woodii [pMTL84151_actthlA] was increased from 1.2mgL−1h−1 in bottle fermentation to 26.4mgL−1h−1 in continuous gas fermentation.
•Acetone production from CO2 is possible by recombinant Acetobacterium woodii.•6 different acetone producing recombinant A. woodii strains were constructed.•DNA sequence of 2 promoters from acetogens were determined using PEX analysis.•3 plasmid replicons were identified that are suitable for replication in A. woodii.•Continuous gas fermentation increased acetone productivity up to 26.4mgL−1h−1. |
doi_str_mv | 10.1016/j.ymben.2016.03.001 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1796246640</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1096717616300039</els_id><sourcerecordid>1796246640</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3</originalsourceid><addsrcrecordid>eNp9kMtOxCAUhonReH8CE9Olm1YYWigLF5OJt8TEmOiaUDgok7YoUCfz9qIzunTFIfn-c_kQOiO4Ipiwy2W1HjoYq1n-VJhWGJMddEiwYCUnbb37V3N2gI5iXGaANILso4MZE5wwJg7R01xD8iMU78GbSSfnx2Ll0lsxQFKd751Wfb8uYHx1I0AAU8QUlBtj4W3xk-2UThDcNBQr741zJ2jPqj7C6fY9Ri8318-Lu_Lh8fZ-MX8oNW1EKqHFRthaKMtbApQqpYRprAZja9OQpu4YbjlvOmDcdtpwTU2DlQFcY0uFpcfoYtM3b_4xQUxycFFD36sR_BQl4YLNasZqnFG6QXXwMQaw8j24QYW1JFh-u5RL-eNSfruUmMqsKqfOtwOmbgDzl_mVl4GrDQD5zE8HQUbtYMwnuAA6SePdvwO-AHDdiJU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1796246640</pqid></control><display><type>article</type><title>Acetone production with metabolically engineered strains of Acetobacterium woodii</title><source>ScienceDirect Journals</source><creator>Hoffmeister, Sabrina ; Gerdom, Marzena ; Bengelsdorf, Frank R. ; Linder, Sonja ; Flüchter, Sebastian ; Öztürk, Hatice ; Blümke, Wilfried ; May, Antje ; Fischer, Ralf-Jörg ; Bahl, Hubert ; Dürre, Peter</creator><creatorcontrib>Hoffmeister, Sabrina ; Gerdom, Marzena ; Bengelsdorf, Frank R. ; Linder, Sonja ; Flüchter, Sebastian ; Öztürk, Hatice ; Blümke, Wilfried ; May, Antje ; Fischer, Ralf-Jörg ; Bahl, Hubert ; Dürre, Peter</creatorcontrib><description>Expected depletion of oil and fossil resources urges the development of new alternative routes for the production of bulk chemicals and fuels beyond petroleum resources. In this study, the clostridial acetone pathway was used for the formation of acetone in the acetogenic bacterium Acetobacterium woodii. The acetone production operon (APO) containing the genes thlA (encoding thiolase A), ctfA/ctfB (encoding CoA transferase), and adc (encoding acetoacetate decarboxylase) from Clostridium acetobutylicum were cloned under the control of the thlA promoter into four vectors having different replicons for Gram-positives (pIP404, pBP1, pCB102, and pCD6). Stable replication was observed for all constructs. A. woodii [pJIR_actthlA] achieved the maximal acetone concentration under autotrophic conditions (15.2±3.4mM). Promoter sequences of the genes ackA from A. woodii and pta-ack from C. ljungdahlii were determined by primer extension (PEX) and cloned upstream of the APO. The highest acetone production in recombinant A. woodii cells was achieved using the promoters PthlA and Ppta-ack. Batch fermentations using A. woodii [pMTL84151_actthlA] in a bioreactor revealed that acetate concentration had an effect on the acetone production, due to the high Km value of the CoA transferase. In order to establish consistent acetate concentration within the bioreactor and to increase biomass, a continuous fermentation process for A. woodii was developed. Thus, acetone productivity of the strain A. woodii [pMTL84151_actthlA] was increased from 1.2mgL−1h−1 in bottle fermentation to 26.4mgL−1h−1 in continuous gas fermentation.
•Acetone production from CO2 is possible by recombinant Acetobacterium woodii.•6 different acetone producing recombinant A. woodii strains were constructed.•DNA sequence of 2 promoters from acetogens were determined using PEX analysis.•3 plasmid replicons were identified that are suitable for replication in A. woodii.•Continuous gas fermentation increased acetone productivity up to 26.4mgL−1h−1.</description><identifier>ISSN: 1096-7176</identifier><identifier>EISSN: 1096-7184</identifier><identifier>DOI: 10.1016/j.ymben.2016.03.001</identifier><identifier>PMID: 26971669</identifier><language>eng</language><publisher>Belgium: Elsevier Inc</publisher><subject>Acetates - metabolism ; Acetobacterium - physiology ; Acetobacterium woodii ; Acetone ; Acetone - isolation & purification ; Acetone - metabolism ; Biosynthetic Pathways - physiology ; Carbon dioxide ; Carbon Dioxide - metabolism ; CoA transferase ; Continuous gas fermentation ; Genetic Enhancement - methods ; Metabolic Engineering - methods ; Metabolic Networks and Pathways - physiology ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; Replicon for Gram-positives ; Syngas</subject><ispartof>Metabolic engineering, 2016-07, Vol.36, p.37-47</ispartof><rights>2016 International Metabolic Engineering Society</rights><rights>Copyright © 2016 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3</citedby><cites>FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26971669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoffmeister, Sabrina</creatorcontrib><creatorcontrib>Gerdom, Marzena</creatorcontrib><creatorcontrib>Bengelsdorf, Frank R.</creatorcontrib><creatorcontrib>Linder, Sonja</creatorcontrib><creatorcontrib>Flüchter, Sebastian</creatorcontrib><creatorcontrib>Öztürk, Hatice</creatorcontrib><creatorcontrib>Blümke, Wilfried</creatorcontrib><creatorcontrib>May, Antje</creatorcontrib><creatorcontrib>Fischer, Ralf-Jörg</creatorcontrib><creatorcontrib>Bahl, Hubert</creatorcontrib><creatorcontrib>Dürre, Peter</creatorcontrib><title>Acetone production with metabolically engineered strains of Acetobacterium woodii</title><title>Metabolic engineering</title><addtitle>Metab Eng</addtitle><description>Expected depletion of oil and fossil resources urges the development of new alternative routes for the production of bulk chemicals and fuels beyond petroleum resources. In this study, the clostridial acetone pathway was used for the formation of acetone in the acetogenic bacterium Acetobacterium woodii. The acetone production operon (APO) containing the genes thlA (encoding thiolase A), ctfA/ctfB (encoding CoA transferase), and adc (encoding acetoacetate decarboxylase) from Clostridium acetobutylicum were cloned under the control of the thlA promoter into four vectors having different replicons for Gram-positives (pIP404, pBP1, pCB102, and pCD6). Stable replication was observed for all constructs. A. woodii [pJIR_actthlA] achieved the maximal acetone concentration under autotrophic conditions (15.2±3.4mM). Promoter sequences of the genes ackA from A. woodii and pta-ack from C. ljungdahlii were determined by primer extension (PEX) and cloned upstream of the APO. The highest acetone production in recombinant A. woodii cells was achieved using the promoters PthlA and Ppta-ack. Batch fermentations using A. woodii [pMTL84151_actthlA] in a bioreactor revealed that acetate concentration had an effect on the acetone production, due to the high Km value of the CoA transferase. In order to establish consistent acetate concentration within the bioreactor and to increase biomass, a continuous fermentation process for A. woodii was developed. Thus, acetone productivity of the strain A. woodii [pMTL84151_actthlA] was increased from 1.2mgL−1h−1 in bottle fermentation to 26.4mgL−1h−1 in continuous gas fermentation.
•Acetone production from CO2 is possible by recombinant Acetobacterium woodii.•6 different acetone producing recombinant A. woodii strains were constructed.•DNA sequence of 2 promoters from acetogens were determined using PEX analysis.•3 plasmid replicons were identified that are suitable for replication in A. woodii.•Continuous gas fermentation increased acetone productivity up to 26.4mgL−1h−1.</description><subject>Acetates - metabolism</subject><subject>Acetobacterium - physiology</subject><subject>Acetobacterium woodii</subject><subject>Acetone</subject><subject>Acetone - isolation & purification</subject><subject>Acetone - metabolism</subject><subject>Biosynthetic Pathways - physiology</subject><subject>Carbon dioxide</subject><subject>Carbon Dioxide - metabolism</subject><subject>CoA transferase</subject><subject>Continuous gas fermentation</subject><subject>Genetic Enhancement - methods</subject><subject>Metabolic Engineering - methods</subject><subject>Metabolic Networks and Pathways - physiology</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>Replicon for Gram-positives</subject><subject>Syngas</subject><issn>1096-7176</issn><issn>1096-7184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOxCAUhonReH8CE9Olm1YYWigLF5OJt8TEmOiaUDgok7YoUCfz9qIzunTFIfn-c_kQOiO4Ipiwy2W1HjoYq1n-VJhWGJMddEiwYCUnbb37V3N2gI5iXGaANILso4MZE5wwJg7R01xD8iMU78GbSSfnx2Ll0lsxQFKd751Wfb8uYHx1I0AAU8QUlBtj4W3xk-2UThDcNBQr741zJ2jPqj7C6fY9Ri8318-Lu_Lh8fZ-MX8oNW1EKqHFRthaKMtbApQqpYRprAZja9OQpu4YbjlvOmDcdtpwTU2DlQFcY0uFpcfoYtM3b_4xQUxycFFD36sR_BQl4YLNasZqnFG6QXXwMQaw8j24QYW1JFh-u5RL-eNSfruUmMqsKqfOtwOmbgDzl_mVl4GrDQD5zE8HQUbtYMwnuAA6SePdvwO-AHDdiJU</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Hoffmeister, Sabrina</creator><creator>Gerdom, Marzena</creator><creator>Bengelsdorf, Frank R.</creator><creator>Linder, Sonja</creator><creator>Flüchter, Sebastian</creator><creator>Öztürk, Hatice</creator><creator>Blümke, Wilfried</creator><creator>May, Antje</creator><creator>Fischer, Ralf-Jörg</creator><creator>Bahl, Hubert</creator><creator>Dürre, Peter</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201607</creationdate><title>Acetone production with metabolically engineered strains of Acetobacterium woodii</title><author>Hoffmeister, Sabrina ; Gerdom, Marzena ; Bengelsdorf, Frank R. ; Linder, Sonja ; Flüchter, Sebastian ; Öztürk, Hatice ; Blümke, Wilfried ; May, Antje ; Fischer, Ralf-Jörg ; Bahl, Hubert ; Dürre, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetates - metabolism</topic><topic>Acetobacterium - physiology</topic><topic>Acetobacterium woodii</topic><topic>Acetone</topic><topic>Acetone - isolation & purification</topic><topic>Acetone - metabolism</topic><topic>Biosynthetic Pathways - physiology</topic><topic>Carbon dioxide</topic><topic>Carbon Dioxide - metabolism</topic><topic>CoA transferase</topic><topic>Continuous gas fermentation</topic><topic>Genetic Enhancement - methods</topic><topic>Metabolic Engineering - methods</topic><topic>Metabolic Networks and Pathways - physiology</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><topic>Replicon for Gram-positives</topic><topic>Syngas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffmeister, Sabrina</creatorcontrib><creatorcontrib>Gerdom, Marzena</creatorcontrib><creatorcontrib>Bengelsdorf, Frank R.</creatorcontrib><creatorcontrib>Linder, Sonja</creatorcontrib><creatorcontrib>Flüchter, Sebastian</creatorcontrib><creatorcontrib>Öztürk, Hatice</creatorcontrib><creatorcontrib>Blümke, Wilfried</creatorcontrib><creatorcontrib>May, Antje</creatorcontrib><creatorcontrib>Fischer, Ralf-Jörg</creatorcontrib><creatorcontrib>Bahl, Hubert</creatorcontrib><creatorcontrib>Dürre, Peter</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolic engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoffmeister, Sabrina</au><au>Gerdom, Marzena</au><au>Bengelsdorf, Frank R.</au><au>Linder, Sonja</au><au>Flüchter, Sebastian</au><au>Öztürk, Hatice</au><au>Blümke, Wilfried</au><au>May, Antje</au><au>Fischer, Ralf-Jörg</au><au>Bahl, Hubert</au><au>Dürre, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acetone production with metabolically engineered strains of Acetobacterium woodii</atitle><jtitle>Metabolic engineering</jtitle><addtitle>Metab Eng</addtitle><date>2016-07</date><risdate>2016</risdate><volume>36</volume><spage>37</spage><epage>47</epage><pages>37-47</pages><issn>1096-7176</issn><eissn>1096-7184</eissn><abstract>Expected depletion of oil and fossil resources urges the development of new alternative routes for the production of bulk chemicals and fuels beyond petroleum resources. In this study, the clostridial acetone pathway was used for the formation of acetone in the acetogenic bacterium Acetobacterium woodii. The acetone production operon (APO) containing the genes thlA (encoding thiolase A), ctfA/ctfB (encoding CoA transferase), and adc (encoding acetoacetate decarboxylase) from Clostridium acetobutylicum were cloned under the control of the thlA promoter into four vectors having different replicons for Gram-positives (pIP404, pBP1, pCB102, and pCD6). Stable replication was observed for all constructs. A. woodii [pJIR_actthlA] achieved the maximal acetone concentration under autotrophic conditions (15.2±3.4mM). Promoter sequences of the genes ackA from A. woodii and pta-ack from C. ljungdahlii were determined by primer extension (PEX) and cloned upstream of the APO. The highest acetone production in recombinant A. woodii cells was achieved using the promoters PthlA and Ppta-ack. Batch fermentations using A. woodii [pMTL84151_actthlA] in a bioreactor revealed that acetate concentration had an effect on the acetone production, due to the high Km value of the CoA transferase. In order to establish consistent acetate concentration within the bioreactor and to increase biomass, a continuous fermentation process for A. woodii was developed. Thus, acetone productivity of the strain A. woodii [pMTL84151_actthlA] was increased from 1.2mgL−1h−1 in bottle fermentation to 26.4mgL−1h−1 in continuous gas fermentation.
•Acetone production from CO2 is possible by recombinant Acetobacterium woodii.•6 different acetone producing recombinant A. woodii strains were constructed.•DNA sequence of 2 promoters from acetogens were determined using PEX analysis.•3 plasmid replicons were identified that are suitable for replication in A. woodii.•Continuous gas fermentation increased acetone productivity up to 26.4mgL−1h−1.</abstract><cop>Belgium</cop><pub>Elsevier Inc</pub><pmid>26971669</pmid><doi>10.1016/j.ymben.2016.03.001</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1096-7176 |
ispartof | Metabolic engineering, 2016-07, Vol.36, p.37-47 |
issn | 1096-7176 1096-7184 |
language | eng |
recordid | cdi_proquest_miscellaneous_1796246640 |
source | ScienceDirect Journals |
subjects | Acetates - metabolism Acetobacterium - physiology Acetobacterium woodii Acetone Acetone - isolation & purification Acetone - metabolism Biosynthetic Pathways - physiology Carbon dioxide Carbon Dioxide - metabolism CoA transferase Continuous gas fermentation Genetic Enhancement - methods Metabolic Engineering - methods Metabolic Networks and Pathways - physiology Recombinant Proteins - genetics Recombinant Proteins - metabolism Replicon for Gram-positives Syngas |
title | Acetone production with metabolically engineered strains of Acetobacterium woodii |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T14%3A09%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acetone%20production%20with%20metabolically%20engineered%20strains%20of%20Acetobacterium%20woodii&rft.jtitle=Metabolic%20engineering&rft.au=Hoffmeister,%20Sabrina&rft.date=2016-07&rft.volume=36&rft.spage=37&rft.epage=47&rft.pages=37-47&rft.issn=1096-7176&rft.eissn=1096-7184&rft_id=info:doi/10.1016/j.ymben.2016.03.001&rft_dat=%3Cproquest_cross%3E1796246640%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c359t-e80d9f49af781e33aaa9d5fcedf4d5154b608775be67fbcd7c3d50ade040f39f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1796246640&rft_id=info:pmid/26971669&rfr_iscdi=true |