Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants
Maize is an important crop for billions of people globally. The existing immature embryo-based regeneration protocol of maize has major limitations due to the non-availability of explants throughout the year, limited durability for culturing, and its laborious nature. Mature embryos, especially in t...
Gespeichert in:
Veröffentlicht in: | Plant cell, tissue and organ culture tissue and organ culture, 2022-03, Vol.148 (3), p.557-571 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 571 |
---|---|
container_issue | 3 |
container_start_page | 557 |
container_title | Plant cell, tissue and organ culture |
container_volume | 148 |
creator | Kumar, Krishan Jha, Abhishek Kumar Kumar, Bhupender Karjagi, Chikkappa G. Abhishek, Alok Gambhir, Geetika Aggarwal, Chetana Tyagi, Akshita Sharma, Pooja Pandey, Pankaj Rakshit, Sujay |
description | Maize is an important crop for billions of people globally. The existing immature embryo-based regeneration protocol of maize has major limitations due to the non-availability of explants throughout the year, limited durability for culturing, and its laborious nature. Mature embryos, especially in tropical maize, are considered recalcitrant towards tissue culture. Therefore, standardization of a robust regeneration and transformation protocol in tropical maize using mature embryos or seeds as starting material is long envisaged. Considering this, in this study, 28 diverse tropical maize genotypes were evaluated for their embryogenic callus induction potential using two different explants (nodal explants and split embryo region) under two different callusing media. Out of 28 genotypes, better callus induction was achieved in four genotypes (BML 6, DHM 117, DMRH 1301, and DMRH 1308) from nodal explants. Further, in vitro regeneration was standardized using 22 different combinations of various auxins and cytokinins. Out of 28 genotypes, two recently commercialized and high-yielding cultivars (DMRH 1301 and DMRH 1308) demonstrated the best callusing and regeneration capability with an average regeneration percentage of 60.4% and 53.6%, respectively. Using the nodal explants-derived embryogenic calli, the genetic transformation was successfully carried out using the ‘Biolistic’ approach, and up to ~ 5% transformation efficiency was achieved. This efficient regeneration and transformation protocol can overcome the major limitations associated with the existing immature embryo-based protocol in tropical maize as mature seeds can be obtained easily in ample quantity round the year. Such a generalized and reproducible protocol has the potential to be a major tool for maize improvement using transgenic and genome-edited techniques.
Key message
The standardized protocol not only overcomes the major limitations associated with the existing and predominately used immature embryo-based protocol but it is easier, reproducible, and has either higher or comparable callusing, regeneration, and transformation efficiency. |
doi_str_mv | 10.1007/s11240-021-02207-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2628404312</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2628404312</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-ec327c519b5456b3d9b47467943b65bfaf0025aef2e95430723d7d993b0bfb3f3</originalsourceid><addsrcrecordid>eNp9kb1uFDEUhS0EEkvgBags0YRign_HmTLKD0RaiQYaGsseX68czdoT27PK8kQ8ZpxMJLoUln2Pz3evrg5Cnyk5o4Sob4VSJkhHGG2HEdUd36ANlYp3kgjxFm0I7VXXn0v1Hn0o5Y4Q0nNBN-jfFRxgSvMeYsXJYxMxeB_G8FSb6HCGOSe3jMFOgEPEh1BzauoOImRTQ4rPtppNLD7l_So1pqYxTbhJ7S_NYTQT3pvwF_DpHzDteSx4e_YVLyXEXSvrkgEXANc5yOEADsfkGgMP82RiLR_RO2-mAp9e7hP0--b61-WPbvvz--3lxbYbOR1qByNnapR0sFLI3nI3WKFErwbBbS-tN54QJg14BoMUnCjGnXLDwC2x3nLPT9CXtW9b4X6BUvVdWnJsIzXr2bkgglPWXGx1jTmVksHrOYe9yUdNiX5KRK-J6JaIfk5EHxvEV6g0c9xB_t_6FeoR8kaSXg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2628404312</pqid></control><display><type>article</type><title>Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants</title><source>Springer Nature - Complete Springer Journals</source><creator>Kumar, Krishan ; Jha, Abhishek Kumar ; Kumar, Bhupender ; Karjagi, Chikkappa G. ; Abhishek, Alok ; Gambhir, Geetika ; Aggarwal, Chetana ; Tyagi, Akshita ; Sharma, Pooja ; Pandey, Pankaj ; Rakshit, Sujay</creator><creatorcontrib>Kumar, Krishan ; Jha, Abhishek Kumar ; Kumar, Bhupender ; Karjagi, Chikkappa G. ; Abhishek, Alok ; Gambhir, Geetika ; Aggarwal, Chetana ; Tyagi, Akshita ; Sharma, Pooja ; Pandey, Pankaj ; Rakshit, Sujay</creatorcontrib><description>Maize is an important crop for billions of people globally. The existing immature embryo-based regeneration protocol of maize has major limitations due to the non-availability of explants throughout the year, limited durability for culturing, and its laborious nature. Mature embryos, especially in tropical maize, are considered recalcitrant towards tissue culture. Therefore, standardization of a robust regeneration and transformation protocol in tropical maize using mature embryos or seeds as starting material is long envisaged. Considering this, in this study, 28 diverse tropical maize genotypes were evaluated for their embryogenic callus induction potential using two different explants (nodal explants and split embryo region) under two different callusing media. Out of 28 genotypes, better callus induction was achieved in four genotypes (BML 6, DHM 117, DMRH 1301, and DMRH 1308) from nodal explants. Further, in vitro regeneration was standardized using 22 different combinations of various auxins and cytokinins. Out of 28 genotypes, two recently commercialized and high-yielding cultivars (DMRH 1301 and DMRH 1308) demonstrated the best callusing and regeneration capability with an average regeneration percentage of 60.4% and 53.6%, respectively. Using the nodal explants-derived embryogenic calli, the genetic transformation was successfully carried out using the ‘Biolistic’ approach, and up to ~ 5% transformation efficiency was achieved. This efficient regeneration and transformation protocol can overcome the major limitations associated with the existing immature embryo-based protocol in tropical maize as mature seeds can be obtained easily in ample quantity round the year. Such a generalized and reproducible protocol has the potential to be a major tool for maize improvement using transgenic and genome-edited techniques.
Key message
The standardized protocol not only overcomes the major limitations associated with the existing and predominately used immature embryo-based protocol but it is easier, reproducible, and has either higher or comparable callusing, regeneration, and transformation efficiency.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1007/s11240-021-02207-y</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Auxins ; Biomedical and Life Sciences ; Callus ; Commercialization ; Corn ; Cultivars ; Cytokinins ; Embryos ; Explants ; Genetic transformation ; Genomes ; Genotypes ; Life Sciences ; Original Article ; Plant Genetics and Genomics ; Plant Pathology ; Plant Physiology ; Plant Sciences ; Regeneration ; Seeds ; Standardization ; Tissue culture ; Transformations</subject><ispartof>Plant cell, tissue and organ culture, 2022-03, Vol.148 (3), p.557-571</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-ec327c519b5456b3d9b47467943b65bfaf0025aef2e95430723d7d993b0bfb3f3</citedby><cites>FETCH-LOGICAL-c319t-ec327c519b5456b3d9b47467943b65bfaf0025aef2e95430723d7d993b0bfb3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11240-021-02207-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11240-021-02207-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids></links><search><creatorcontrib>Kumar, Krishan</creatorcontrib><creatorcontrib>Jha, Abhishek Kumar</creatorcontrib><creatorcontrib>Kumar, Bhupender</creatorcontrib><creatorcontrib>Karjagi, Chikkappa G.</creatorcontrib><creatorcontrib>Abhishek, Alok</creatorcontrib><creatorcontrib>Gambhir, Geetika</creatorcontrib><creatorcontrib>Aggarwal, Chetana</creatorcontrib><creatorcontrib>Tyagi, Akshita</creatorcontrib><creatorcontrib>Sharma, Pooja</creatorcontrib><creatorcontrib>Pandey, Pankaj</creatorcontrib><creatorcontrib>Rakshit, Sujay</creatorcontrib><title>Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants</title><title>Plant cell, tissue and organ culture</title><addtitle>Plant Cell Tiss Organ Cult</addtitle><description>Maize is an important crop for billions of people globally. The existing immature embryo-based regeneration protocol of maize has major limitations due to the non-availability of explants throughout the year, limited durability for culturing, and its laborious nature. Mature embryos, especially in tropical maize, are considered recalcitrant towards tissue culture. Therefore, standardization of a robust regeneration and transformation protocol in tropical maize using mature embryos or seeds as starting material is long envisaged. Considering this, in this study, 28 diverse tropical maize genotypes were evaluated for their embryogenic callus induction potential using two different explants (nodal explants and split embryo region) under two different callusing media. Out of 28 genotypes, better callus induction was achieved in four genotypes (BML 6, DHM 117, DMRH 1301, and DMRH 1308) from nodal explants. Further, in vitro regeneration was standardized using 22 different combinations of various auxins and cytokinins. Out of 28 genotypes, two recently commercialized and high-yielding cultivars (DMRH 1301 and DMRH 1308) demonstrated the best callusing and regeneration capability with an average regeneration percentage of 60.4% and 53.6%, respectively. Using the nodal explants-derived embryogenic calli, the genetic transformation was successfully carried out using the ‘Biolistic’ approach, and up to ~ 5% transformation efficiency was achieved. This efficient regeneration and transformation protocol can overcome the major limitations associated with the existing immature embryo-based protocol in tropical maize as mature seeds can be obtained easily in ample quantity round the year. Such a generalized and reproducible protocol has the potential to be a major tool for maize improvement using transgenic and genome-edited techniques.
Key message
The standardized protocol not only overcomes the major limitations associated with the existing and predominately used immature embryo-based protocol but it is easier, reproducible, and has either higher or comparable callusing, regeneration, and transformation efficiency.</description><subject>Auxins</subject><subject>Biomedical and Life Sciences</subject><subject>Callus</subject><subject>Commercialization</subject><subject>Corn</subject><subject>Cultivars</subject><subject>Cytokinins</subject><subject>Embryos</subject><subject>Explants</subject><subject>Genetic transformation</subject><subject>Genomes</subject><subject>Genotypes</subject><subject>Life Sciences</subject><subject>Original Article</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Pathology</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Regeneration</subject><subject>Seeds</subject><subject>Standardization</subject><subject>Tissue culture</subject><subject>Transformations</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kb1uFDEUhS0EEkvgBags0YRign_HmTLKD0RaiQYaGsseX68czdoT27PK8kQ8ZpxMJLoUln2Pz3evrg5Cnyk5o4Sob4VSJkhHGG2HEdUd36ANlYp3kgjxFm0I7VXXn0v1Hn0o5Y4Q0nNBN-jfFRxgSvMeYsXJYxMxeB_G8FSb6HCGOSe3jMFOgEPEh1BzauoOImRTQ4rPtppNLD7l_So1pqYxTbhJ7S_NYTQT3pvwF_DpHzDteSx4e_YVLyXEXSvrkgEXANc5yOEADsfkGgMP82RiLR_RO2-mAp9e7hP0--b61-WPbvvz--3lxbYbOR1qByNnapR0sFLI3nI3WKFErwbBbS-tN54QJg14BoMUnCjGnXLDwC2x3nLPT9CXtW9b4X6BUvVdWnJsIzXr2bkgglPWXGx1jTmVksHrOYe9yUdNiX5KRK-J6JaIfk5EHxvEV6g0c9xB_t_6FeoR8kaSXg</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>Kumar, Krishan</creator><creator>Jha, Abhishek Kumar</creator><creator>Kumar, Bhupender</creator><creator>Karjagi, Chikkappa G.</creator><creator>Abhishek, Alok</creator><creator>Gambhir, Geetika</creator><creator>Aggarwal, Chetana</creator><creator>Tyagi, Akshita</creator><creator>Sharma, Pooja</creator><creator>Pandey, Pankaj</creator><creator>Rakshit, Sujay</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20220301</creationdate><title>Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants</title><author>Kumar, Krishan ; Jha, Abhishek Kumar ; Kumar, Bhupender ; Karjagi, Chikkappa G. ; Abhishek, Alok ; Gambhir, Geetika ; Aggarwal, Chetana ; Tyagi, Akshita ; Sharma, Pooja ; Pandey, Pankaj ; Rakshit, Sujay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-ec327c519b5456b3d9b47467943b65bfaf0025aef2e95430723d7d993b0bfb3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Auxins</topic><topic>Biomedical and Life Sciences</topic><topic>Callus</topic><topic>Commercialization</topic><topic>Corn</topic><topic>Cultivars</topic><topic>Cytokinins</topic><topic>Embryos</topic><topic>Explants</topic><topic>Genetic transformation</topic><topic>Genomes</topic><topic>Genotypes</topic><topic>Life Sciences</topic><topic>Original Article</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Pathology</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Regeneration</topic><topic>Seeds</topic><topic>Standardization</topic><topic>Tissue culture</topic><topic>Transformations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Krishan</creatorcontrib><creatorcontrib>Jha, Abhishek Kumar</creatorcontrib><creatorcontrib>Kumar, Bhupender</creatorcontrib><creatorcontrib>Karjagi, Chikkappa G.</creatorcontrib><creatorcontrib>Abhishek, Alok</creatorcontrib><creatorcontrib>Gambhir, Geetika</creatorcontrib><creatorcontrib>Aggarwal, Chetana</creatorcontrib><creatorcontrib>Tyagi, Akshita</creatorcontrib><creatorcontrib>Sharma, Pooja</creatorcontrib><creatorcontrib>Pandey, Pankaj</creatorcontrib><creatorcontrib>Rakshit, Sujay</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Plant cell, tissue and organ culture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Krishan</au><au>Jha, Abhishek Kumar</au><au>Kumar, Bhupender</au><au>Karjagi, Chikkappa G.</au><au>Abhishek, Alok</au><au>Gambhir, Geetika</au><au>Aggarwal, Chetana</au><au>Tyagi, Akshita</au><au>Sharma, Pooja</au><au>Pandey, Pankaj</au><au>Rakshit, Sujay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><stitle>Plant Cell Tiss Organ Cult</stitle><date>2022-03-01</date><risdate>2022</risdate><volume>148</volume><issue>3</issue><spage>557</spage><epage>571</epage><pages>557-571</pages><issn>0167-6857</issn><eissn>1573-5044</eissn><abstract>Maize is an important crop for billions of people globally. The existing immature embryo-based regeneration protocol of maize has major limitations due to the non-availability of explants throughout the year, limited durability for culturing, and its laborious nature. Mature embryos, especially in tropical maize, are considered recalcitrant towards tissue culture. Therefore, standardization of a robust regeneration and transformation protocol in tropical maize using mature embryos or seeds as starting material is long envisaged. Considering this, in this study, 28 diverse tropical maize genotypes were evaluated for their embryogenic callus induction potential using two different explants (nodal explants and split embryo region) under two different callusing media. Out of 28 genotypes, better callus induction was achieved in four genotypes (BML 6, DHM 117, DMRH 1301, and DMRH 1308) from nodal explants. Further, in vitro regeneration was standardized using 22 different combinations of various auxins and cytokinins. Out of 28 genotypes, two recently commercialized and high-yielding cultivars (DMRH 1301 and DMRH 1308) demonstrated the best callusing and regeneration capability with an average regeneration percentage of 60.4% and 53.6%, respectively. Using the nodal explants-derived embryogenic calli, the genetic transformation was successfully carried out using the ‘Biolistic’ approach, and up to ~ 5% transformation efficiency was achieved. This efficient regeneration and transformation protocol can overcome the major limitations associated with the existing immature embryo-based protocol in tropical maize as mature seeds can be obtained easily in ample quantity round the year. Such a generalized and reproducible protocol has the potential to be a major tool for maize improvement using transgenic and genome-edited techniques.
Key message
The standardized protocol not only overcomes the major limitations associated with the existing and predominately used immature embryo-based protocol but it is easier, reproducible, and has either higher or comparable callusing, regeneration, and transformation efficiency.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11240-021-02207-y</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-6857 |
ispartof | Plant cell, tissue and organ culture, 2022-03, Vol.148 (3), p.557-571 |
issn | 0167-6857 1573-5044 |
language | eng |
recordid | cdi_proquest_journals_2628404312 |
source | Springer Nature - Complete Springer Journals |
subjects | Auxins Biomedical and Life Sciences Callus Commercialization Corn Cultivars Cytokinins Embryos Explants Genetic transformation Genomes Genotypes Life Sciences Original Article Plant Genetics and Genomics Plant Pathology Plant Physiology Plant Sciences Regeneration Seeds Standardization Tissue culture Transformations |
title | Development of an efficient and reproducible in vitro regeneration and transformation protocol for tropical maize (Zea mays L.) using mature seed-derived nodal explants |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T11%3A17%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20an%20efficient%20and%20reproducible%20in%20vitro%20regeneration%20and%20transformation%20protocol%20for%20tropical%20maize%20(Zea%20mays%20L.)%20using%20mature%20seed-derived%20nodal%20explants&rft.jtitle=Plant%20cell,%20tissue%20and%20organ%20culture&rft.au=Kumar,%20Krishan&rft.date=2022-03-01&rft.volume=148&rft.issue=3&rft.spage=557&rft.epage=571&rft.pages=557-571&rft.issn=0167-6857&rft.eissn=1573-5044&rft_id=info:doi/10.1007/s11240-021-02207-y&rft_dat=%3Cproquest_cross%3E2628404312%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2628404312&rft_id=info:pmid/&rfr_iscdi=true |