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Process engineering of pH tolerant Ustilago cynodontis for efficient itaconic acid production
Ustilago cynodontis ranks among the relatively unknown itaconate production organisms. In comparison to the well-known and established organisms like Aspergillus terreus and Ustilago maydis, genetic engineering and first optimizations for itaconate production were only recently developed for U. cyno...
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Published in: | Microbial cell factories 2019-12, Vol.18 (1), p.213-213, Article 213 |
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description | Ustilago cynodontis ranks among the relatively unknown itaconate production organisms. In comparison to the well-known and established organisms like Aspergillus terreus and Ustilago maydis, genetic engineering and first optimizations for itaconate production were only recently developed for U. cynodontis, enabling metabolic and morphological engineering of this acid-tolerant organism for efficient itaconate production. These engineered strains were so far mostly characterized in small scale shaken cultures.
In pH-controlled fed-batch experiments an optimum pH of 3.6 could be determined for itaconate production in the morphology-engineered U. cynodontis Δfuz7. With U. cynodontis ∆fuz7
∆cyp3
P
mttA P
ria1, optimized for itaconate production through the deletion of an itaconate oxidase and overexpression of rate-limiting production steps, titers up to 82.9 ± 0.8 g L
were reached in a high-density pulsed fed-batch fermentation at this pH. The use of a constant glucose feed controlled by in-line glucose analysis increased the yield in the production phase to 0.61 g
g
, which is 84% of the maximum theoretical pathway yield. Productivity could be improved to a maximum of 1.44 g L
h
and cell recycling was achieved by repeated-batch application.
Here, we characterize engineered U. cynodontis strains in controlled bioreactors and optimize the fermentation process for itaconate production. The results obtained are discussed in a biotechnological context and show the great potential of U. cynodontis as an itaconate producing host. |
doi_str_mv | 10.1186/s12934-019-1266-y |
format | article |
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In pH-controlled fed-batch experiments an optimum pH of 3.6 could be determined for itaconate production in the morphology-engineered U. cynodontis Δfuz7. With U. cynodontis ∆fuz7
∆cyp3
P
mttA P
ria1, optimized for itaconate production through the deletion of an itaconate oxidase and overexpression of rate-limiting production steps, titers up to 82.9 ± 0.8 g L
were reached in a high-density pulsed fed-batch fermentation at this pH. The use of a constant glucose feed controlled by in-line glucose analysis increased the yield in the production phase to 0.61 g
g
, which is 84% of the maximum theoretical pathway yield. Productivity could be improved to a maximum of 1.44 g L
h
and cell recycling was achieved by repeated-batch application.
Here, we characterize engineered U. cynodontis strains in controlled bioreactors and optimize the fermentation process for itaconate production. The results obtained are discussed in a biotechnological context and show the great potential of U. cynodontis as an itaconate producing host.</description><identifier>ISSN: 1475-2859</identifier><identifier>EISSN: 1475-2859</identifier><identifier>DOI: 10.1186/s12934-019-1266-y</identifier><identifier>PMID: 31830998</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acid production ; Acids ; Analysis ; Batch culture ; Bioreactors ; Clonal deletion ; Cytochrome P-450 ; Fermentation ; Genetic Engineering ; Genetically modified organisms ; Glucose ; Hydrogen-Ion Concentration ; Itaconic acid ; Metabolic engineering ; Morphology ; Optimization ; Organisms ; Oxidases ; pH control ; pH effects ; Process engineering ; Process optimization ; Product toxicity ; Production engineering ; Production management ; Productivity ; Strains (organisms) ; Succinates - chemistry ; Succinates - metabolism ; Toxicity ; Ustilago ; Ustilago - chemistry ; Ustilago - genetics ; Ustilago - metabolism ; Ustilago cynodontis</subject><ispartof>Microbial cell factories, 2019-12, Vol.18 (1), p.213-213, Article 213</ispartof><rights>COPYRIGHT 2019 BioMed Central Ltd.</rights><rights>2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-acdc4f024d37d75646c6bf63c5b45099f6a9729d94c4d7bcfb0c4c3deb6110ab3</citedby><cites>FETCH-LOGICAL-c594t-acdc4f024d37d75646c6bf63c5b45099f6a9729d94c4d7bcfb0c4c3deb6110ab3</cites><orcidid>0000-0002-2808-8652 ; 0000-0002-1590-1210</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909570/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2328957110?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31830998$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hosseinpour Tehrani, Hamed</creatorcontrib><creatorcontrib>Saur, Katharina</creatorcontrib><creatorcontrib>Tharmasothirajan, Apilaasha</creatorcontrib><creatorcontrib>Blank, Lars M</creatorcontrib><creatorcontrib>Wierckx, Nick</creatorcontrib><title>Process engineering of pH tolerant Ustilago cynodontis for efficient itaconic acid production</title><title>Microbial cell factories</title><addtitle>Microb Cell Fact</addtitle><description>Ustilago cynodontis ranks among the relatively unknown itaconate production organisms. In comparison to the well-known and established organisms like Aspergillus terreus and Ustilago maydis, genetic engineering and first optimizations for itaconate production were only recently developed for U. cynodontis, enabling metabolic and morphological engineering of this acid-tolerant organism for efficient itaconate production. These engineered strains were so far mostly characterized in small scale shaken cultures.
In pH-controlled fed-batch experiments an optimum pH of 3.6 could be determined for itaconate production in the morphology-engineered U. cynodontis Δfuz7. With U. cynodontis ∆fuz7
∆cyp3
P
mttA P
ria1, optimized for itaconate production through the deletion of an itaconate oxidase and overexpression of rate-limiting production steps, titers up to 82.9 ± 0.8 g L
were reached in a high-density pulsed fed-batch fermentation at this pH. The use of a constant glucose feed controlled by in-line glucose analysis increased the yield in the production phase to 0.61 g
g
, which is 84% of the maximum theoretical pathway yield. Productivity could be improved to a maximum of 1.44 g L
h
and cell recycling was achieved by repeated-batch application.
Here, we characterize engineered U. cynodontis strains in controlled bioreactors and optimize the fermentation process for itaconate production. The results obtained are discussed in a biotechnological context and show the great potential of U. cynodontis as an itaconate producing host.</description><subject>Acid production</subject><subject>Acids</subject><subject>Analysis</subject><subject>Batch culture</subject><subject>Bioreactors</subject><subject>Clonal deletion</subject><subject>Cytochrome P-450</subject><subject>Fermentation</subject><subject>Genetic Engineering</subject><subject>Genetically modified organisms</subject><subject>Glucose</subject><subject>Hydrogen-Ion Concentration</subject><subject>Itaconic acid</subject><subject>Metabolic engineering</subject><subject>Morphology</subject><subject>Optimization</subject><subject>Organisms</subject><subject>Oxidases</subject><subject>pH control</subject><subject>pH effects</subject><subject>Process engineering</subject><subject>Process optimization</subject><subject>Product toxicity</subject><subject>Production engineering</subject><subject>Production management</subject><subject>Productivity</subject><subject>Strains (organisms)</subject><subject>Succinates - chemistry</subject><subject>Succinates - metabolism</subject><subject>Toxicity</subject><subject>Ustilago</subject><subject>Ustilago - chemistry</subject><subject>Ustilago - genetics</subject><subject>Ustilago - metabolism</subject><subject>Ustilago cynodontis</subject><issn>1475-2859</issn><issn>1475-2859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhgdRbK3-AG9kwJt6MTVfk0xuhFLULhQUtZcSMsnJmDKbrElG3H9v1q21K5KLhJPnvCfn5G2a5xidYTzw1xkTSVmHsOww4bzbPmiOMRN9R4ZePrx3Pmqe5HyDEBaDoI-bI4oHiqQcjpuvH1M0kHMLYfIBIPkwtdG1m8u2xBmSDqW9zsXPeoqt2YZoYyg-ty6mFpzzxkMlfNEmBm9abbxtNynaxRQfw9PmkdNzhme3-0lz_e7tl4vL7urD-9XF-VVneslKp401zCHCLBVW9Jxxw0fHqelH1td3Oq6lINJKZpgVo3EjMsxQCyPHGOmRnjSrva6N-kZtkl_rtFVRe_U7ENOkdCrezKCA85E4IvWunpBUg2NEUARDD0wOtGq92WttlnEN1tT-kp4PRA9vgv-mpvhDcYlkL1AVOL0VSPH7Armotc8G5lkHiEtWhBIpGBtIX9GX_6A3cUmhjmpHDVWu9veXmnRtwAcXa12zE1XnvN4j2hNeqbP_UHVZWPv6O-B8jR8kvDpIqEyBn2XSS85q9fnTIYv3rEkx5wTubh4YqZ0X1d6LqnpR7byotjXnxf1B3mX8MR_9Ba4k2Xs</recordid><startdate>20191212</startdate><enddate>20191212</enddate><creator>Hosseinpour Tehrani, Hamed</creator><creator>Saur, Katharina</creator><creator>Tharmasothirajan, Apilaasha</creator><creator>Blank, Lars M</creator><creator>Wierckx, Nick</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2808-8652</orcidid><orcidid>https://orcid.org/0000-0002-1590-1210</orcidid></search><sort><creationdate>20191212</creationdate><title>Process engineering of pH tolerant Ustilago cynodontis for efficient itaconic acid production</title><author>Hosseinpour Tehrani, Hamed ; Saur, Katharina ; Tharmasothirajan, Apilaasha ; Blank, Lars M ; Wierckx, Nick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-acdc4f024d37d75646c6bf63c5b45099f6a9729d94c4d7bcfb0c4c3deb6110ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acid production</topic><topic>Acids</topic><topic>Analysis</topic><topic>Batch culture</topic><topic>Bioreactors</topic><topic>Clonal deletion</topic><topic>Cytochrome P-450</topic><topic>Fermentation</topic><topic>Genetic Engineering</topic><topic>Genetically modified organisms</topic><topic>Glucose</topic><topic>Hydrogen-Ion Concentration</topic><topic>Itaconic acid</topic><topic>Metabolic engineering</topic><topic>Morphology</topic><topic>Optimization</topic><topic>Organisms</topic><topic>Oxidases</topic><topic>pH control</topic><topic>pH effects</topic><topic>Process engineering</topic><topic>Process optimization</topic><topic>Product toxicity</topic><topic>Production engineering</topic><topic>Production management</topic><topic>Productivity</topic><topic>Strains (organisms)</topic><topic>Succinates - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Microbial cell factories</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hosseinpour Tehrani, Hamed</au><au>Saur, Katharina</au><au>Tharmasothirajan, Apilaasha</au><au>Blank, Lars M</au><au>Wierckx, Nick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Process engineering of pH tolerant Ustilago cynodontis for efficient itaconic acid production</atitle><jtitle>Microbial cell factories</jtitle><addtitle>Microb Cell Fact</addtitle><date>2019-12-12</date><risdate>2019</risdate><volume>18</volume><issue>1</issue><spage>213</spage><epage>213</epage><pages>213-213</pages><artnum>213</artnum><issn>1475-2859</issn><eissn>1475-2859</eissn><abstract>Ustilago cynodontis ranks among the relatively unknown itaconate production organisms. In comparison to the well-known and established organisms like Aspergillus terreus and Ustilago maydis, genetic engineering and first optimizations for itaconate production were only recently developed for U. cynodontis, enabling metabolic and morphological engineering of this acid-tolerant organism for efficient itaconate production. These engineered strains were so far mostly characterized in small scale shaken cultures.
In pH-controlled fed-batch experiments an optimum pH of 3.6 could be determined for itaconate production in the morphology-engineered U. cynodontis Δfuz7. With U. cynodontis ∆fuz7
∆cyp3
P
mttA P
ria1, optimized for itaconate production through the deletion of an itaconate oxidase and overexpression of rate-limiting production steps, titers up to 82.9 ± 0.8 g L
were reached in a high-density pulsed fed-batch fermentation at this pH. The use of a constant glucose feed controlled by in-line glucose analysis increased the yield in the production phase to 0.61 g
g
, which is 84% of the maximum theoretical pathway yield. Productivity could be improved to a maximum of 1.44 g L
h
and cell recycling was achieved by repeated-batch application.
Here, we characterize engineered U. cynodontis strains in controlled bioreactors and optimize the fermentation process for itaconate production. The results obtained are discussed in a biotechnological context and show the great potential of U. cynodontis as an itaconate producing host.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>31830998</pmid><doi>10.1186/s12934-019-1266-y</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-2808-8652</orcidid><orcidid>https://orcid.org/0000-0002-1590-1210</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acid production Acids Analysis Batch culture Bioreactors Clonal deletion Cytochrome P-450 Fermentation Genetic Engineering Genetically modified organisms Glucose Hydrogen-Ion Concentration Itaconic acid Metabolic engineering Morphology Optimization Organisms Oxidases pH control pH effects Process engineering Process optimization Product toxicity Production engineering Production management Productivity Strains (organisms) Succinates - chemistry Succinates - metabolism Toxicity Ustilago Ustilago - chemistry Ustilago - genetics Ustilago - metabolism Ustilago cynodontis |
title | Process engineering of pH tolerant Ustilago cynodontis for efficient itaconic acid production |
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