Improved cellulase production in recombinant Saccharomyces cerevisiae by disrupting the cell wall protein-encoding gene CWP2
Budding yeast Saccharomyces cerevisiae has been widely used for heterologous protein production. However, low protein production titer and secretion levels continue to challenge its practical applications. The yeast cell wall plays important roles in yeast cell growth and environmental responses. Ne...
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description | Budding yeast Saccharomyces cerevisiae has been widely used for heterologous protein production. However, low protein production titer and secretion levels continue to challenge its practical applications. The yeast cell wall plays important roles in yeast cell growth and environmental responses. Nevertheless, the effects of yeast cell wall proteins on heterologous protein production and secretion remain unclear. CWP2 encodes a mannoprotein that is the major component of the yeast cell wall. So far, studies on its function have been very limited. Here we show that CWP2 disruption improved extracellular cellobiohydrolase activity by 85.9%. A calcofluor white hypersensitivity assay revealed increased sensitivity of the mutant compared to the parental strain, indicating impaired cell wall integrity. However, no changes were observed in normal cell growth or growth stressed by tunicamycin and dithiothreitol, suggesting that the unfolded protein response pathway was not affected by the gene disruption. Comparative transcriptome analysis revealed changes in multiple genes involved in cell wall structure, biosynthesis, and cell wall integrity induced by CWP2 disruption, suggesting a pivotal role of Cwp2p in yeast cell wall organization. Notably, CWP2 disruption also led to elevated transcription of a large number of genes involved in ribosome biogenesis, which indicated that CWP2 is not only in yeast cell wall biosynthesis, but also in protein translation. This work reveals novel insights into the functions of CWP2 and also presents a new strategy to increase heterologous protein production in yeast strains by manipulating cell wall-related proteins.
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doi_str_mv | 10.1016/j.jbiosc.2019.08.012 |
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[Display omitted]</description><identifier>ISSN: 1389-1723</identifier><identifier>EISSN: 1347-4421</identifier><identifier>DOI: 10.1016/j.jbiosc.2019.08.012</identifier><identifier>PMID: 31537451</identifier><language>eng</language><publisher>Japan: Elsevier B.V</publisher><subject>Cell Wall - metabolism ; Cell Wall - ultrastructure ; Cell wall integrity ; Cell wall protein ; Cellulase ; Cellulase - biosynthesis ; CWP2 ; Heterologous protein expression ; Lignocellulosic biomass ; Membrane Glycoproteins - genetics ; Membrane Glycoproteins - metabolism ; Microscopy, Electron, Transmission ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae - ultrastructure ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism ; Stress tolerance ; Transcriptomic analysis</subject><ispartof>Journal of bioscience and bioengineering, 2020-02, Vol.129 (2), p.165-171</ispartof><rights>2019 The Society for Biotechnology, Japan</rights><rights>Copyright © 2019 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-a8e516fc0796313dbfc04ad61324f217e0e7f32ceff50a7207d4b43381e736953</citedby><cites>FETCH-LOGICAL-c455t-a8e516fc0796313dbfc04ad61324f217e0e7f32ceff50a7207d4b43381e736953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jbiosc.2019.08.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31537451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Jie</creatorcontrib><creatorcontrib>Zhang, Ming-Ming</creatorcontrib><creatorcontrib>Wan, Chun</creatorcontrib><creatorcontrib>Den Haan, Riaan</creatorcontrib><creatorcontrib>Bai, Feng-Wu</creatorcontrib><creatorcontrib>Zhao, Xin-Qing</creatorcontrib><title>Improved cellulase production in recombinant Saccharomyces cerevisiae by disrupting the cell wall protein-encoding gene CWP2</title><title>Journal of bioscience and bioengineering</title><addtitle>J Biosci Bioeng</addtitle><description>Budding yeast Saccharomyces cerevisiae has been widely used for heterologous protein production. However, low protein production titer and secretion levels continue to challenge its practical applications. The yeast cell wall plays important roles in yeast cell growth and environmental responses. Nevertheless, the effects of yeast cell wall proteins on heterologous protein production and secretion remain unclear. CWP2 encodes a mannoprotein that is the major component of the yeast cell wall. So far, studies on its function have been very limited. Here we show that CWP2 disruption improved extracellular cellobiohydrolase activity by 85.9%. A calcofluor white hypersensitivity assay revealed increased sensitivity of the mutant compared to the parental strain, indicating impaired cell wall integrity. However, no changes were observed in normal cell growth or growth stressed by tunicamycin and dithiothreitol, suggesting that the unfolded protein response pathway was not affected by the gene disruption. Comparative transcriptome analysis revealed changes in multiple genes involved in cell wall structure, biosynthesis, and cell wall integrity induced by CWP2 disruption, suggesting a pivotal role of Cwp2p in yeast cell wall organization. Notably, CWP2 disruption also led to elevated transcription of a large number of genes involved in ribosome biogenesis, which indicated that CWP2 is not only in yeast cell wall biosynthesis, but also in protein translation. This work reveals novel insights into the functions of CWP2 and also presents a new strategy to increase heterologous protein production in yeast strains by manipulating cell wall-related proteins.
[Display omitted]</description><subject>Cell Wall - metabolism</subject><subject>Cell Wall - ultrastructure</subject><subject>Cell wall integrity</subject><subject>Cell wall protein</subject><subject>Cellulase</subject><subject>Cellulase - biosynthesis</subject><subject>CWP2</subject><subject>Heterologous protein expression</subject><subject>Lignocellulosic biomass</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Microscopy, Electron, Transmission</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae - ultrastructure</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Stress tolerance</subject><subject>Transcriptomic analysis</subject><issn>1389-1723</issn><issn>1347-4421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv1DAQhS1ERUvhHyDkI5cEj-3EyQUJrQpUqgRSizhajj1pvdrYi50sWokfX4ctHLnYo_F7b8YfIW-A1cCgfb-tt4OP2dacQV-zrmbAn5ELEFJVUnJ4vtZdX4Hi4py8zHnLGCim4AU5F9AIJRu4IL-vp32KB3TU4m637ExGWhpusbOPgfpAE9o4DT6YMNNbY-2DSXE6WszFkfDgszdIhyN1PqdlP_twT-cH_BNHf5lylLgZfagw2OjW53sMSDc_vvFX5Gw0u4yvn-5L8v3T1d3mS3Xz9fP15uNNZWXTzJXpsIF2tEz1rQDhhlJK41oQXI4cFDJUo-AWx7FhRnGmnBykEB2gEm3fiEvy7pRbVvm5YJ715PO6oAkYl6w57xupGO_7IpUnqU0x54Sj3ic_mXTUwPTKXW_1ibteuWvW6cK92N4-TViGCd0_01_QRfDhJMDyz4PHpLP1hQg6XwDP2kX__wmPVSuXrA</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Li, Jie</creator><creator>Zhang, Ming-Ming</creator><creator>Wan, Chun</creator><creator>Den Haan, Riaan</creator><creator>Bai, Feng-Wu</creator><creator>Zhao, Xin-Qing</creator><general>Elsevier B.V</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>202002</creationdate><title>Improved cellulase production in recombinant Saccharomyces cerevisiae by disrupting the cell wall protein-encoding gene CWP2</title><author>Li, Jie ; Zhang, Ming-Ming ; Wan, Chun ; Den Haan, Riaan ; Bai, Feng-Wu ; Zhao, Xin-Qing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-a8e516fc0796313dbfc04ad61324f217e0e7f32ceff50a7207d4b43381e736953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cell Wall - metabolism</topic><topic>Cell Wall - ultrastructure</topic><topic>Cell wall integrity</topic><topic>Cell wall protein</topic><topic>Cellulase</topic><topic>Cellulase - biosynthesis</topic><topic>CWP2</topic><topic>Heterologous protein expression</topic><topic>Lignocellulosic biomass</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Microscopy, Electron, Transmission</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae - ultrastructure</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - metabolism</topic><topic>Stress tolerance</topic><topic>Transcriptomic analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Jie</creatorcontrib><creatorcontrib>Zhang, Ming-Ming</creatorcontrib><creatorcontrib>Wan, Chun</creatorcontrib><creatorcontrib>Den Haan, Riaan</creatorcontrib><creatorcontrib>Bai, Feng-Wu</creatorcontrib><creatorcontrib>Zhao, Xin-Qing</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>Journal of bioscience and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Jie</au><au>Zhang, Ming-Ming</au><au>Wan, Chun</au><au>Den Haan, Riaan</au><au>Bai, Feng-Wu</au><au>Zhao, Xin-Qing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved cellulase production in recombinant Saccharomyces cerevisiae by disrupting the cell wall protein-encoding gene CWP2</atitle><jtitle>Journal of bioscience and bioengineering</jtitle><addtitle>J Biosci Bioeng</addtitle><date>2020-02</date><risdate>2020</risdate><volume>129</volume><issue>2</issue><spage>165</spage><epage>171</epage><pages>165-171</pages><issn>1389-1723</issn><eissn>1347-4421</eissn><abstract>Budding yeast Saccharomyces cerevisiae has been widely used for heterologous protein production. However, low protein production titer and secretion levels continue to challenge its practical applications. The yeast cell wall plays important roles in yeast cell growth and environmental responses. Nevertheless, the effects of yeast cell wall proteins on heterologous protein production and secretion remain unclear. CWP2 encodes a mannoprotein that is the major component of the yeast cell wall. So far, studies on its function have been very limited. Here we show that CWP2 disruption improved extracellular cellobiohydrolase activity by 85.9%. A calcofluor white hypersensitivity assay revealed increased sensitivity of the mutant compared to the parental strain, indicating impaired cell wall integrity. However, no changes were observed in normal cell growth or growth stressed by tunicamycin and dithiothreitol, suggesting that the unfolded protein response pathway was not affected by the gene disruption. Comparative transcriptome analysis revealed changes in multiple genes involved in cell wall structure, biosynthesis, and cell wall integrity induced by CWP2 disruption, suggesting a pivotal role of Cwp2p in yeast cell wall organization. Notably, CWP2 disruption also led to elevated transcription of a large number of genes involved in ribosome biogenesis, which indicated that CWP2 is not only in yeast cell wall biosynthesis, but also in protein translation. This work reveals novel insights into the functions of CWP2 and also presents a new strategy to increase heterologous protein production in yeast strains by manipulating cell wall-related proteins.
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subjects | Cell Wall - metabolism Cell Wall - ultrastructure Cell wall integrity Cell wall protein Cellulase Cellulase - biosynthesis CWP2 Heterologous protein expression Lignocellulosic biomass Membrane Glycoproteins - genetics Membrane Glycoproteins - metabolism Microscopy, Electron, Transmission Recombinant Proteins - genetics Recombinant Proteins - metabolism Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae - ultrastructure Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - metabolism Stress tolerance Transcriptomic analysis |
title | Improved cellulase production in recombinant Saccharomyces cerevisiae by disrupting the cell wall protein-encoding gene CWP2 |
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