Genetic Transformation and Green Fluorescent Protein Labeling in Ceratocystis paradoxa from Coconut
, the causal agent of stem-bleeding disease of the coconut palm, causes great losses to the global coconut industry. As the mechanism of pathogenicity of has not been determined, an exogenous gene marker was introduced into the fungus. In this study, pCT74-sGFP, which contains the green fluorescent...
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creator | Niu, Xiaoqing Pei, Mengtian Liang, Chenyu Lv, Yuexiao Wu, Xinyi Zhang, Ruina Lu, Guodong Yu, Fengyu Zhu, Hui Qin, Weiquan |
description | , the causal agent of stem-bleeding disease of the coconut palm, causes great losses to the global coconut industry. As the mechanism of pathogenicity of
has not been determined, an exogenous gene marker was introduced into the fungus. In this study, pCT74-sGFP, which contains the green fluorescent protein (GFP) gene, and the hygromycin B resistance gene as a selective marker, was used as an expression vector. Several protoplast release buffers were compared to optimize protoplast preparation. The plasmid pCT74-sGFP was successfully transformed into the genome of
, which was verified using polymerase chain reaction and green fluorescence detection. The transformants did not exhibit any obvious differences from the wild-type isolates in terms of growth and morphological characteristics. Pathogenicity tests showed that the transformation process did not alter the virulence of the X-3314
strain. This is the first report on the polyethylene glycol-mediated transformation of
carrying a 'reporter' gene GFP that was stably and efficiently expressed in the transformants. These findings provide a basis for future functional genomics studies of
and offer a novel opportunity to track the infection process of
. |
doi_str_mv | 10.3390/ijms20102387 |
format | Article |
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has not been determined, an exogenous gene marker was introduced into the fungus. In this study, pCT74-sGFP, which contains the green fluorescent protein (GFP) gene, and the hygromycin B resistance gene as a selective marker, was used as an expression vector. Several protoplast release buffers were compared to optimize protoplast preparation. The plasmid pCT74-sGFP was successfully transformed into the genome of
, which was verified using polymerase chain reaction and green fluorescence detection. The transformants did not exhibit any obvious differences from the wild-type isolates in terms of growth and morphological characteristics. Pathogenicity tests showed that the transformation process did not alter the virulence of the X-3314
strain. This is the first report on the polyethylene glycol-mediated transformation of
carrying a 'reporter' gene GFP that was stably and efficiently expressed in the transformants. These findings provide a basis for future functional genomics studies of
and offer a novel opportunity to track the infection process of
.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20102387</identifier><identifier>PMID: 31091742</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aroma ; Biological control ; Deoxyribonucleic acid ; Discoloration ; Disease ; Disease control ; DNA ; Fluorescence ; Fungi ; Genetic transformation ; Green fluorescent protein ; Infections ; Leaves ; Organic chemistry ; Pathogenesis ; Pathogens ; Polyethylene glycol ; Protoplasts ; Transformations</subject><ispartof>International journal of molecular sciences, 2019-05, Vol.20 (10), p.2387</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-c412t-3e1d51fdb41e0866b58d62eb83423fde165b12e45e6d414530ead64dcd32e2433</citedby><cites>FETCH-LOGICAL-c412t-3e1d51fdb41e0866b58d62eb83423fde165b12e45e6d414530ead64dcd32e2433</cites><orcidid>0000-0001-5348-8060 ; 0000-0001-6325-9165</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/PMC6566578/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566578/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31091742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niu, Xiaoqing</creatorcontrib><creatorcontrib>Pei, Mengtian</creatorcontrib><creatorcontrib>Liang, Chenyu</creatorcontrib><creatorcontrib>Lv, Yuexiao</creatorcontrib><creatorcontrib>Wu, Xinyi</creatorcontrib><creatorcontrib>Zhang, Ruina</creatorcontrib><creatorcontrib>Lu, Guodong</creatorcontrib><creatorcontrib>Yu, Fengyu</creatorcontrib><creatorcontrib>Zhu, Hui</creatorcontrib><creatorcontrib>Qin, Weiquan</creatorcontrib><title>Genetic Transformation and Green Fluorescent Protein Labeling in Ceratocystis paradoxa from Coconut</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>, the causal agent of stem-bleeding disease of the coconut palm, causes great losses to the global coconut industry. As the mechanism of pathogenicity of
has not been determined, an exogenous gene marker was introduced into the fungus. In this study, pCT74-sGFP, which contains the green fluorescent protein (GFP) gene, and the hygromycin B resistance gene as a selective marker, was used as an expression vector. Several protoplast release buffers were compared to optimize protoplast preparation. The plasmid pCT74-sGFP was successfully transformed into the genome of
, which was verified using polymerase chain reaction and green fluorescence detection. The transformants did not exhibit any obvious differences from the wild-type isolates in terms of growth and morphological characteristics. Pathogenicity tests showed that the transformation process did not alter the virulence of the X-3314
strain. This is the first report on the polyethylene glycol-mediated transformation of
carrying a 'reporter' gene GFP that was stably and efficiently expressed in the transformants. These findings provide a basis for future functional genomics studies of
and offer a novel opportunity to track the infection process of
.</description><subject>Aroma</subject><subject>Biological control</subject><subject>Deoxyribonucleic acid</subject><subject>Discoloration</subject><subject>Disease</subject><subject>Disease control</subject><subject>DNA</subject><subject>Fluorescence</subject><subject>Fungi</subject><subject>Genetic transformation</subject><subject>Green fluorescent protein</subject><subject>Infections</subject><subject>Leaves</subject><subject>Organic chemistry</subject><subject>Pathogenesis</subject><subject>Pathogens</subject><subject>Polyethylene glycol</subject><subject>Protoplasts</subject><subject>Transformations</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>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1rGzEQxUVpqB23t5yLoJcc4lTfu74EikmcgiE5pGehXc06MruSK2lL8t9XJk5wcpoH8-Mxbx5CZ5Rccr4gP912SIxQwnhdfUJTKhibE6Kqz0d6gk5T2pLCMLn4giackgWtBJuidgUesmvxQzQ-dSEOJrvgsfEWryKAxzf9GCKkFnzG9zFkcB6vTQO98xtc9BKiyaF9TtklvDPR2PBkcBfDgJehDX7MX9FJZ_oE3w5zhv7cXD8sb-fru9Xv5a_1vBWU5TkHaiXtbCMokFqpRtZWMWhqLhjvLFAlG8pASFBWUCE5AWOVsK3lDJjgfIauXnx3YzOA3V8cTa930Q0mPutgnH6_8e5Rb8I_raRSsqqLwfnBIIa_I6SsB1eC973xEMakWfkfYXUlSUF_fEC3YYy-xNOMF6qWrJKFunih2hhSitC9HUOJ3renj9sr-PfjAG_wa138P20mlz4</recordid><startdate>20190514</startdate><enddate>20190514</enddate><creator>Niu, Xiaoqing</creator><creator>Pei, Mengtian</creator><creator>Liang, Chenyu</creator><creator>Lv, Yuexiao</creator><creator>Wu, Xinyi</creator><creator>Zhang, Ruina</creator><creator>Lu, Guodong</creator><creator>Yu, Fengyu</creator><creator>Zhu, Hui</creator><creator>Qin, Weiquan</creator><general>MDPI AG</general><general>MDPI</general><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>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5348-8060</orcidid><orcidid>https://orcid.org/0000-0001-6325-9165</orcidid></search><sort><creationdate>20190514</creationdate><title>Genetic Transformation and Green Fluorescent Protein Labeling in Ceratocystis paradoxa from Coconut</title><author>Niu, Xiaoqing ; 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As the mechanism of pathogenicity of
has not been determined, an exogenous gene marker was introduced into the fungus. In this study, pCT74-sGFP, which contains the green fluorescent protein (GFP) gene, and the hygromycin B resistance gene as a selective marker, was used as an expression vector. Several protoplast release buffers were compared to optimize protoplast preparation. The plasmid pCT74-sGFP was successfully transformed into the genome of
, which was verified using polymerase chain reaction and green fluorescence detection. The transformants did not exhibit any obvious differences from the wild-type isolates in terms of growth and morphological characteristics. Pathogenicity tests showed that the transformation process did not alter the virulence of the X-3314
strain. This is the first report on the polyethylene glycol-mediated transformation of
carrying a 'reporter' gene GFP that was stably and efficiently expressed in the transformants. These findings provide a basis for future functional genomics studies of
and offer a novel opportunity to track the infection process of
.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31091742</pmid><doi>10.3390/ijms20102387</doi><orcidid>https://orcid.org/0000-0001-5348-8060</orcidid><orcidid>https://orcid.org/0000-0001-6325-9165</orcidid><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Aroma Biological control Deoxyribonucleic acid Discoloration Disease Disease control DNA Fluorescence Fungi Genetic transformation Green fluorescent protein Infections Leaves Organic chemistry Pathogenesis Pathogens Polyethylene glycol Protoplasts Transformations |
title | Genetic Transformation and Green Fluorescent Protein Labeling in Ceratocystis paradoxa from Coconut |
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