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The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei
is a biotechnologically important filamentous fungus with the remarkable ability to secrete large amounts of enzymes, whose production is strongly affected by both the carbon and nitrogen sources. While the carbon metabolism regulators are extensively studied, the regulation of enzyme production by...
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Published in: | International journal of molecular sciences 2019-08, Vol.20 (17), p.4100 |
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description | is a biotechnologically important filamentous fungus with the remarkable ability to secrete large amounts of enzymes, whose production is strongly affected by both the carbon and nitrogen sources. While the carbon metabolism regulators are extensively studied, the regulation of enzyme production by the nitrogen metabolism regulators is still poorly understood. In this study, the GATA transcription factor Are1, which is an orthologue of the
global nitrogen regulator AREA, was identified and characterized for its functions in regulation of both protease and cellulase production in
. Deletion of the
gene abolished the capability to secrete proteases, and complementation of the
gene rescued the ability to produce proteases. Quantitative RT-PCR analysis revealed that the transcripts of protease genes
and
were also significantly reduced in the Δ
strain when grown in the medium with peptone as the nitrogen source. In addition, deletion of
resulted in decreased cellulase production in the presence of (NH
)
SO
. Consistent with the reduction of cellulase production, the transcription levels of the major cellulase genes, including
,
,
, and
were dramatically decreased in Δ
. Sequence analysis showed that all promoter regions of the tested protease and cellulase genes contain the consensus GATA elements. However, the expression levels of the major cellulase transcription activator Xyr1 and the repressor Cre1 had no significant difference between Δ
and the parental strain QM9414, indicating that the regulatory mechanism deserves further investigation. Taken together, these results demonstrate the important role of Are1 in the regulation of protease and cellulase production in
, although these processes depend on the kind of nitrogen sources. The findings in this study contribute to the understanding of the regulation network of carbon and nitrogen sources in filamentous fungi. |
doi_str_mv | 10.3390/ijms20174100 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_e8cc6b899e354879a6a5aa6c5d09e0f0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_e8cc6b899e354879a6a5aa6c5d09e0f0</doaj_id><sourcerecordid>2332370480</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-5de4fcbeb890986edcc5b3ae7d817c420dfebc57b3091a5b6a4862e087eaf2603</originalsourceid><addsrcrecordid>eNpdkk1v1DAQhiMEoqVw44wsceFAwF-xkwvSatUvqQgO4WxNnEnXqyQOdoLolV-Ow7bVlpM9M4_fmfFMlr1l9JMQFf3s9kPklGnJKH2WnTLJeU6p0s-P7ifZqxj3lHLBi-pldiKYlEIW9DT7U--QXG7qTV7fTUjqAGO0wU2z8yP05ALs7APZBGTkq2-XHmaMZE5vzn9PAWNMGPFdsuYAFvs-EYF8D35GiImEsSXbg3s13ZgyOLvzLYYBSECM6F5nLzroI765P8-yHxfn9fYqv_l2eb3d3ORW6nLOixZlZxtsyopWpcLW2qIRgLotmbaS07bDxha6EbRiUDQKZKk40lIjdFxRcZZdH3RbD3szBTdAuDMenPnn8OHWQJid7dFgaa1KiSoUhSx1BQoKAGWLllZIu1Xry0FrWpohlYJj6r9_Ivo0MrqdufW_jNJSM6aTwId7geB_LhhnM7i4fiCM6JdoOK-qdXxSJfT9f-jeLyFNJ1FCcKGpLNeKPh4oG3yMAbvHYhg166KY40VJ-LvjBh7hh80QfwFXvbvY</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2332370480</pqid></control><display><type>article</type><title>The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central(OpenAccess)</source><creator>Qian, Yuanchao ; Sun, Yu ; Zhong, Lixia ; Sun, Ningning ; Sheng, Yifan ; Qu, Yinbo ; Zhong, Yaohua</creator><creatorcontrib>Qian, Yuanchao ; Sun, Yu ; Zhong, Lixia ; Sun, Ningning ; Sheng, Yifan ; Qu, Yinbo ; Zhong, Yaohua</creatorcontrib><description>is a biotechnologically important filamentous fungus with the remarkable ability to secrete large amounts of enzymes, whose production is strongly affected by both the carbon and nitrogen sources. While the carbon metabolism regulators are extensively studied, the regulation of enzyme production by the nitrogen metabolism regulators is still poorly understood. In this study, the GATA transcription factor Are1, which is an orthologue of the
global nitrogen regulator AREA, was identified and characterized for its functions in regulation of both protease and cellulase production in
. Deletion of the
gene abolished the capability to secrete proteases, and complementation of the
gene rescued the ability to produce proteases. Quantitative RT-PCR analysis revealed that the transcripts of protease genes
and
were also significantly reduced in the Δ
strain when grown in the medium with peptone as the nitrogen source. In addition, deletion of
resulted in decreased cellulase production in the presence of (NH
)
SO
. Consistent with the reduction of cellulase production, the transcription levels of the major cellulase genes, including
,
,
, and
were dramatically decreased in Δ
. Sequence analysis showed that all promoter regions of the tested protease and cellulase genes contain the consensus GATA elements. However, the expression levels of the major cellulase transcription activator Xyr1 and the repressor Cre1 had no significant difference between Δ
and the parental strain QM9414, indicating that the regulatory mechanism deserves further investigation. Taken together, these results demonstrate the important role of Are1 in the regulation of protease and cellulase production in
, although these processes depend on the kind of nitrogen sources. The findings in this study contribute to the understanding of the regulation network of carbon and nitrogen sources in filamentous fungi.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20174100</identifier><identifier>PMID: 31443450</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Amino acids ; Are1 ; Carbon ; Catabolism ; Cellulase ; Cellulases - genetics ; Cellulases - metabolism ; Enzymes ; Extracellular Space ; Fungi ; GATA factors ; Gene Deletion ; Gene expression ; Gene Expression Regulation, Fungal ; Genes ; Genomes ; Germination ; Investigations ; Milk ; Nitrogen ; Nitrogen metabolism ; Nitrogen sources ; Peptide Hydrolases - genetics ; Peptide Hydrolases - metabolism ; Peptones ; Phenotype ; Phenotypes ; Phylogenetics ; Phylogeny ; Protease ; Proteins ; Regulation ; Skim milk ; Sterol O-Acyltransferase - metabolism ; Transcription factors ; Transcription Factors - metabolism ; Trichoderma - classification ; Trichoderma - genetics ; Trichoderma - metabolism ; Trichoderma reesei</subject><ispartof>International journal of molecular sciences, 2019-08, Vol.20 (17), p.4100</ispartof><rights>2019. This work is licensed under https://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>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-5de4fcbeb890986edcc5b3ae7d817c420dfebc57b3091a5b6a4862e087eaf2603</citedby><cites>FETCH-LOGICAL-c478t-5de4fcbeb890986edcc5b3ae7d817c420dfebc57b3091a5b6a4862e087eaf2603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2332370480/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2332370480?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31443450$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qian, Yuanchao</creatorcontrib><creatorcontrib>Sun, Yu</creatorcontrib><creatorcontrib>Zhong, Lixia</creatorcontrib><creatorcontrib>Sun, Ningning</creatorcontrib><creatorcontrib>Sheng, Yifan</creatorcontrib><creatorcontrib>Qu, Yinbo</creatorcontrib><creatorcontrib>Zhong, Yaohua</creatorcontrib><title>The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>is a biotechnologically important filamentous fungus with the remarkable ability to secrete large amounts of enzymes, whose production is strongly affected by both the carbon and nitrogen sources. While the carbon metabolism regulators are extensively studied, the regulation of enzyme production by the nitrogen metabolism regulators is still poorly understood. In this study, the GATA transcription factor Are1, which is an orthologue of the
global nitrogen regulator AREA, was identified and characterized for its functions in regulation of both protease and cellulase production in
. Deletion of the
gene abolished the capability to secrete proteases, and complementation of the
gene rescued the ability to produce proteases. Quantitative RT-PCR analysis revealed that the transcripts of protease genes
and
were also significantly reduced in the Δ
strain when grown in the medium with peptone as the nitrogen source. In addition, deletion of
resulted in decreased cellulase production in the presence of (NH
)
SO
. Consistent with the reduction of cellulase production, the transcription levels of the major cellulase genes, including
,
,
, and
were dramatically decreased in Δ
. Sequence analysis showed that all promoter regions of the tested protease and cellulase genes contain the consensus GATA elements. However, the expression levels of the major cellulase transcription activator Xyr1 and the repressor Cre1 had no significant difference between Δ
and the parental strain QM9414, indicating that the regulatory mechanism deserves further investigation. Taken together, these results demonstrate the important role of Are1 in the regulation of protease and cellulase production in
, although these processes depend on the kind of nitrogen sources. The findings in this study contribute to the understanding of the regulation network of carbon and nitrogen sources in filamentous fungi.</description><subject>Amino acids</subject><subject>Are1</subject><subject>Carbon</subject><subject>Catabolism</subject><subject>Cellulase</subject><subject>Cellulases - genetics</subject><subject>Cellulases - metabolism</subject><subject>Enzymes</subject><subject>Extracellular Space</subject><subject>Fungi</subject><subject>GATA factors</subject><subject>Gene Deletion</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Genes</subject><subject>Genomes</subject><subject>Germination</subject><subject>Investigations</subject><subject>Milk</subject><subject>Nitrogen</subject><subject>Nitrogen metabolism</subject><subject>Nitrogen sources</subject><subject>Peptide Hydrolases - genetics</subject><subject>Peptide Hydrolases - metabolism</subject><subject>Peptones</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Protease</subject><subject>Proteins</subject><subject>Regulation</subject><subject>Skim milk</subject><subject>Sterol O-Acyltransferase - metabolism</subject><subject>Transcription factors</subject><subject>Transcription Factors - metabolism</subject><subject>Trichoderma - classification</subject><subject>Trichoderma - genetics</subject><subject>Trichoderma - metabolism</subject><subject>Trichoderma reesei</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhiMEoqVw44wsceFAwF-xkwvSatUvqQgO4WxNnEnXqyQOdoLolV-Ow7bVlpM9M4_fmfFMlr1l9JMQFf3s9kPklGnJKH2WnTLJeU6p0s-P7ifZqxj3lHLBi-pldiKYlEIW9DT7U--QXG7qTV7fTUjqAGO0wU2z8yP05ALs7APZBGTkq2-XHmaMZE5vzn9PAWNMGPFdsuYAFvs-EYF8D35GiImEsSXbg3s13ZgyOLvzLYYBSECM6F5nLzroI765P8-yHxfn9fYqv_l2eb3d3ORW6nLOixZlZxtsyopWpcLW2qIRgLotmbaS07bDxha6EbRiUDQKZKk40lIjdFxRcZZdH3RbD3szBTdAuDMenPnn8OHWQJid7dFgaa1KiSoUhSx1BQoKAGWLllZIu1Xry0FrWpohlYJj6r9_Ivo0MrqdufW_jNJSM6aTwId7geB_LhhnM7i4fiCM6JdoOK-qdXxSJfT9f-jeLyFNJ1FCcKGpLNeKPh4oG3yMAbvHYhg166KY40VJ-LvjBh7hh80QfwFXvbvY</recordid><startdate>20190822</startdate><enddate>20190822</enddate><creator>Qian, Yuanchao</creator><creator>Sun, Yu</creator><creator>Zhong, Lixia</creator><creator>Sun, Ningning</creator><creator>Sheng, Yifan</creator><creator>Qu, Yinbo</creator><creator>Zhong, Yaohua</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20190822</creationdate><title>The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei</title><author>Qian, Yuanchao ; Sun, Yu ; Zhong, Lixia ; Sun, Ningning ; Sheng, Yifan ; Qu, Yinbo ; Zhong, Yaohua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-5de4fcbeb890986edcc5b3ae7d817c420dfebc57b3091a5b6a4862e087eaf2603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amino acids</topic><topic>Are1</topic><topic>Carbon</topic><topic>Catabolism</topic><topic>Cellulase</topic><topic>Cellulases - genetics</topic><topic>Cellulases - metabolism</topic><topic>Enzymes</topic><topic>Extracellular Space</topic><topic>Fungi</topic><topic>GATA factors</topic><topic>Gene Deletion</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Fungal</topic><topic>Genes</topic><topic>Genomes</topic><topic>Germination</topic><topic>Investigations</topic><topic>Milk</topic><topic>Nitrogen</topic><topic>Nitrogen metabolism</topic><topic>Nitrogen sources</topic><topic>Peptide Hydrolases - genetics</topic><topic>Peptide Hydrolases - metabolism</topic><topic>Peptones</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Protease</topic><topic>Proteins</topic><topic>Regulation</topic><topic>Skim milk</topic><topic>Sterol O-Acyltransferase - metabolism</topic><topic>Transcription factors</topic><topic>Transcription Factors - metabolism</topic><topic>Trichoderma - classification</topic><topic>Trichoderma - genetics</topic><topic>Trichoderma - metabolism</topic><topic>Trichoderma reesei</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qian, Yuanchao</creatorcontrib><creatorcontrib>Sun, Yu</creatorcontrib><creatorcontrib>Zhong, Lixia</creatorcontrib><creatorcontrib>Sun, Ningning</creatorcontrib><creatorcontrib>Sheng, Yifan</creatorcontrib><creatorcontrib>Qu, Yinbo</creatorcontrib><creatorcontrib>Zhong, Yaohua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qian, Yuanchao</au><au>Sun, Yu</au><au>Zhong, Lixia</au><au>Sun, Ningning</au><au>Sheng, Yifan</au><au>Qu, Yinbo</au><au>Zhong, Yaohua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-08-22</date><risdate>2019</risdate><volume>20</volume><issue>17</issue><spage>4100</spage><pages>4100-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>is a biotechnologically important filamentous fungus with the remarkable ability to secrete large amounts of enzymes, whose production is strongly affected by both the carbon and nitrogen sources. While the carbon metabolism regulators are extensively studied, the regulation of enzyme production by the nitrogen metabolism regulators is still poorly understood. In this study, the GATA transcription factor Are1, which is an orthologue of the
global nitrogen regulator AREA, was identified and characterized for its functions in regulation of both protease and cellulase production in
. Deletion of the
gene abolished the capability to secrete proteases, and complementation of the
gene rescued the ability to produce proteases. Quantitative RT-PCR analysis revealed that the transcripts of protease genes
and
were also significantly reduced in the Δ
strain when grown in the medium with peptone as the nitrogen source. In addition, deletion of
resulted in decreased cellulase production in the presence of (NH
)
SO
. Consistent with the reduction of cellulase production, the transcription levels of the major cellulase genes, including
,
,
, and
were dramatically decreased in Δ
. Sequence analysis showed that all promoter regions of the tested protease and cellulase genes contain the consensus GATA elements. However, the expression levels of the major cellulase transcription activator Xyr1 and the repressor Cre1 had no significant difference between Δ
and the parental strain QM9414, indicating that the regulatory mechanism deserves further investigation. Taken together, these results demonstrate the important role of Are1 in the regulation of protease and cellulase production in
, although these processes depend on the kind of nitrogen sources. The findings in this study contribute to the understanding of the regulation network of carbon and nitrogen sources in filamentous fungi.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31443450</pmid><doi>10.3390/ijms20174100</doi><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Are1 Carbon Catabolism Cellulase Cellulases - genetics Cellulases - metabolism Enzymes Extracellular Space Fungi GATA factors Gene Deletion Gene expression Gene Expression Regulation, Fungal Genes Genomes Germination Investigations Milk Nitrogen Nitrogen metabolism Nitrogen sources Peptide Hydrolases - genetics Peptide Hydrolases - metabolism Peptones Phenotype Phenotypes Phylogenetics Phylogeny Protease Proteins Regulation Skim milk Sterol O-Acyltransferase - metabolism Transcription factors Transcription Factors - metabolism Trichoderma - classification Trichoderma - genetics Trichoderma - metabolism Trichoderma reesei |
title | The GATA-Type Transcriptional Factor Are1 Modulates the Expression of Extracellular Proteases and Cellulases in Trichoderma reesei |
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