Development of a defined medium for heterologous expression in Leishmania tarentolae
A defined medium is essential for studying nutritional requirements of microorganisms and for selective supplementation of necessary substances. Hemin is an essential ingredient for growth of Leishmania tarentolae, but tends to precipitate in aqueous solutions without further stabilization. These ag...
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Veröffentlicht in: | Journal of basic microbiology 2008-12, Vol.48 (6), p.488-495 |
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creator | Fritsche, Claudia Sitz, Mandy Wolf, Marco Pohl, Hans-Dieter |
description | A defined medium is essential for studying nutritional requirements of microorganisms and for selective supplementation of necessary substances. Hemin is an essential ingredient for growth of Leishmania tarentolae, but tends to precipitate in aqueous solutions without further stabilization. These aggregates disturb the measurement of the optical density or the cell density and the following downstream processing. Therefore, we were looking for stabilizing substances and established a PEG-hemin-solution, which avoided flocculation and allowed the cultivation of L. tarentolae in a medium, which we termed SFP(II) medium. With addition of RNA from Saccharomyces cerevisiae to SFP(II) medium the SFP(III) medium was established. In this medium, the specific cell division rate was increased (0.103 h⁻¹) and stable for longer periods of time. The evaluation of the SFP(III) medium was done in shaker flasks by successful expression and segregation of the SAG2 protein, one of the main surface antigens of Toxoplasma gondii. With establishment and evaluation of this defined medium, the status of the Leishmania tarentolae expression system as an alternative to commonly used cell cultures is supported. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) |
doi_str_mv | 10.1002/jobm.200700389 |
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Hemin is an essential ingredient for growth of Leishmania tarentolae, but tends to precipitate in aqueous solutions without further stabilization. These aggregates disturb the measurement of the optical density or the cell density and the following downstream processing. Therefore, we were looking for stabilizing substances and established a PEG-hemin-solution, which avoided flocculation and allowed the cultivation of L. tarentolae in a medium, which we termed SFP(II) medium. With addition of RNA from Saccharomyces cerevisiae to SFP(II) medium the SFP(III) medium was established. In this medium, the specific cell division rate was increased (0.103 h⁻¹) and stable for longer periods of time. The evaluation of the SFP(III) medium was done in shaker flasks by successful expression and segregation of the SAG2 protein, one of the main surface antigens of Toxoplasma gondii. 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KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4059-4508a05da7a3ca7e8dd4f8641c969f0e11930c22e4861415864d38a919b96c263</citedby><cites>FETCH-LOGICAL-c4059-4508a05da7a3ca7e8dd4f8641c969f0e11930c22e4861415864d38a919b96c263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjobm.200700389$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjobm.200700389$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18759244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fritsche, Claudia</creatorcontrib><creatorcontrib>Sitz, Mandy</creatorcontrib><creatorcontrib>Wolf, Marco</creatorcontrib><creatorcontrib>Pohl, Hans-Dieter</creatorcontrib><title>Development of a defined medium for heterologous expression in Leishmania tarentolae</title><title>Journal of basic microbiology</title><addtitle>J. Basic Microbiol</addtitle><description>A defined medium is essential for studying nutritional requirements of microorganisms and for selective supplementation of necessary substances. Hemin is an essential ingredient for growth of Leishmania tarentolae, but tends to precipitate in aqueous solutions without further stabilization. These aggregates disturb the measurement of the optical density or the cell density and the following downstream processing. Therefore, we were looking for stabilizing substances and established a PEG-hemin-solution, which avoided flocculation and allowed the cultivation of L. tarentolae in a medium, which we termed SFP(II) medium. With addition of RNA from Saccharomyces cerevisiae to SFP(II) medium the SFP(III) medium was established. In this medium, the specific cell division rate was increased (0.103 h⁻¹) and stable for longer periods of time. The evaluation of the SFP(III) medium was done in shaker flasks by successful expression and segregation of the SAG2 protein, one of the main surface antigens of Toxoplasma gondii. With establishment and evaluation of this defined medium, the status of the Leishmania tarentolae expression system as an alternative to commonly used cell cultures is supported. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)</description><subject>Animals</subject><subject>Antigens, Protozoan - genetics</subject><subject>Antigens, Protozoan - metabolism</subject><subject>Culture Media - chemistry</subject><subject>Defined medium</subject><subject>Gene Expression Regulation</subject><subject>Hemin - metabolism</subject><subject>Hemin stabilization</subject><subject>L. tarentolae</subject><subject>Leishmania - growth & development</subject><subject>Leishmania - metabolism</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - metabolism</subject><subject>SAG2-expression</subject><issn>0233-111X</issn><issn>1521-4028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDtz1DAURjUMDNkEWkpQlc7LvXrYUgkJCY-FFCSETqO1rxMF21okLyT_Hme8E-ioVNzzndEcxl4gLBFAvL6J634pACoAaewjtkAtsFAgzGO2ACFlgYjf99h-zjcAYK2wT9kemkpbodSCnR_TL-ripqdh5LHlnjfUhoEa3lMTtj1vY-LXNFKKXbyK28zpdpMo5xAHHga-opCvez8Ez0efJknsPD1jT1rfZXq-ew_Yxcm786P3xers9MPRm1VRK9C2UBqMB934ysvaV2SaRrWmVFjb0rZAiFZCLQQpU6JCPZ0aabxFu7ZlLUp5wA5n7ybFn1vKo-tDrqnr_EDTV11pLQBWOIHLGaxTzDlR6zYp9D7dOQR339Hdd3QPHafBy515u55C_MV34SbAzsDv0NHdf3Tu49nbz__Ki3kb8ki3D1uffriykpV2l19OnS3Fpfn26diZiX81862Pzl-lkN3FVwEoAXUlSi3lHyaNl3Q</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Fritsche, Claudia</creator><creator>Sitz, Mandy</creator><creator>Wolf, Marco</creator><creator>Pohl, Hans-Dieter</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</scope><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>200812</creationdate><title>Development of a defined medium for heterologous expression in Leishmania tarentolae</title><author>Fritsche, Claudia ; Sitz, Mandy ; Wolf, Marco ; Pohl, Hans-Dieter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4059-4508a05da7a3ca7e8dd4f8641c969f0e11930c22e4861415864d38a919b96c263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antigens, Protozoan - genetics</topic><topic>Antigens, Protozoan - metabolism</topic><topic>Culture Media - chemistry</topic><topic>Defined medium</topic><topic>Gene Expression Regulation</topic><topic>Hemin - metabolism</topic><topic>Hemin stabilization</topic><topic>L. tarentolae</topic><topic>Leishmania - growth & development</topic><topic>Leishmania - metabolism</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - metabolism</topic><topic>SAG2-expression</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fritsche, Claudia</creatorcontrib><creatorcontrib>Sitz, Mandy</creatorcontrib><creatorcontrib>Wolf, Marco</creatorcontrib><creatorcontrib>Pohl, Hans-Dieter</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><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 basic microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fritsche, Claudia</au><au>Sitz, Mandy</au><au>Wolf, Marco</au><au>Pohl, Hans-Dieter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a defined medium for heterologous expression in Leishmania tarentolae</atitle><jtitle>Journal of basic microbiology</jtitle><addtitle>J. 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subjects | Animals Antigens, Protozoan - genetics Antigens, Protozoan - metabolism Culture Media - chemistry Defined medium Gene Expression Regulation Hemin - metabolism Hemin stabilization L. tarentolae Leishmania - growth & development Leishmania - metabolism Protozoan Proteins - genetics Protozoan Proteins - metabolism SAG2-expression |
title | Development of a defined medium for heterologous expression in Leishmania tarentolae |
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