Loading…
A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis
The present study aims to investigate the numerous factors influencing Agrobacterium tumefaciens -mediated genetic transformation of Chinese cabbage ( Brassica rapa ssp. pekinensis ). Factors affecting transformation efficiency, such as age of explants, Agrobacterium concentration, and effect of ace...
Saved in:
Published in: | 3 Biotech 2016-03, Vol.6 (1) |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-p981-86baa7db6f39f354c50b59c9629b7751a5ddf711e9fd046fbcb7b4b07bed9fa03 |
container_end_page | |
container_issue | 1 |
container_start_page | |
container_title | 3 Biotech |
container_volume | 6 |
creator | Baskar, Venkidasamy Gangadhar, Baniekal H. Park, Se Won Nile, Shivraj Hariram |
description | The present study aims to investigate the numerous factors influencing
Agrobacterium tumefaciens
-mediated genetic transformation of Chinese cabbage (
Brassica rapa
ssp.
pekinensis
). Factors affecting transformation efficiency, such as age of explants,
Agrobacterium
concentration, and effect of acetosyringone, pre-cultivation, infection and co-cultivation time of
Agrobacterium
were examined. The pre-cultured hypocotyls from young seedlings prior to exposure to
Agrobacterium
showed higher shoot regeneration. The plant transformation with the modest
A. tumefaciens
concentrations (0.8 OD) and the 3 days co-cultivation periods increased transformation efficiency. Plant growth hormones [1-naphthyl acetic acid (NAA) and 6-benzyl amino purine (BAP)] were essential for callus and shoot formation. Root formation was effective in half strength MS medium without supplementation of root-inducing hormones. To maintain selection pressure, plant subculture was carried out every 2 weeks with selective antibiotics. The putative transgenic plants were acclimatized in the greenhouse. Polymerase chain reaction was performed to confirm the integration of T-DNA into the genome of transgenic plants. A transformation efficiency of 15 % was obtained. This protocol allows effective transformation and indirect regeneration of
Brassica rapa
. |
doi_str_mv | 10.1007/s13205-016-0402-1 |
format | article |
fullrecord | <record><control><sourceid>pubmedcentral_sprin</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4781812</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_4781812</sourcerecordid><originalsourceid>FETCH-LOGICAL-p981-86baa7db6f39f354c50b59c9629b7751a5ddf711e9fd046fbcb7b4b07bed9fa03</originalsourceid><addsrcrecordid>eNpVkE1qwzAQhUVpaUKaA3SnCzjV2JZlbQpp6B8EusmiOzGypVRpLBvJLvT2VUgpdDYz8GYebz5CboGtgDFxF6HIGc8YVBkrWZ7BBZnnIFnGRVFf_s35-4wsYzywVBy4BHZNZnldFAx4PSd-TaPrhqOh6FtqrHWNM36k633oNTajCW7qxqkzFk9CzDrTOhxNS4cjpr0xoI-2Dx2Orve0t_QhYIyuQRpwQBrjsKKD-XQ-Hbt4Q64sHqNZ_vYF2T097jYv2fbt-XWz3maDrCGrK40oWl3ZQtqClw1nmstGVrnUQnBA3rZWABhpW1ZWVjda6FIzoU0rLbJiQe7PtsOkU-AmfRTwqIbgOgzfqken_ivefah9_6VKUUMNeTLIzwYx3fi9CerQT8GnyAqYOvFXZ_4q8Vcn_gqKHzNPe3E</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis</title><source>Open Access: PubMed Central</source><source>Springer Nature</source><creator>Baskar, Venkidasamy ; Gangadhar, Baniekal H. ; Park, Se Won ; Nile, Shivraj Hariram</creator><creatorcontrib>Baskar, Venkidasamy ; Gangadhar, Baniekal H. ; Park, Se Won ; Nile, Shivraj Hariram</creatorcontrib><description>The present study aims to investigate the numerous factors influencing
Agrobacterium tumefaciens
-mediated genetic transformation of Chinese cabbage (
Brassica rapa
ssp.
pekinensis
). Factors affecting transformation efficiency, such as age of explants,
Agrobacterium
concentration, and effect of acetosyringone, pre-cultivation, infection and co-cultivation time of
Agrobacterium
were examined. The pre-cultured hypocotyls from young seedlings prior to exposure to
Agrobacterium
showed higher shoot regeneration. The plant transformation with the modest
A. tumefaciens
concentrations (0.8 OD) and the 3 days co-cultivation periods increased transformation efficiency. Plant growth hormones [1-naphthyl acetic acid (NAA) and 6-benzyl amino purine (BAP)] were essential for callus and shoot formation. Root formation was effective in half strength MS medium without supplementation of root-inducing hormones. To maintain selection pressure, plant subculture was carried out every 2 weeks with selective antibiotics. The putative transgenic plants were acclimatized in the greenhouse. Polymerase chain reaction was performed to confirm the integration of T-DNA into the genome of transgenic plants. A transformation efficiency of 15 % was obtained. This protocol allows effective transformation and indirect regeneration of
Brassica rapa
.</description><identifier>ISSN: 2190-572X</identifier><identifier>EISSN: 2190-5738</identifier><identifier>DOI: 10.1007/s13205-016-0402-1</identifier><identifier>PMID: 28330158</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agriculture ; Bioinformatics ; Biomaterials ; Biotechnology ; Cancer Research ; Chemistry ; Chemistry and Materials Science ; Original ; Original Article ; Stem Cells</subject><ispartof>3 Biotech, 2016-03, Vol.6 (1)</ispartof><rights>The Author(s) 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p981-86baa7db6f39f354c50b59c9629b7751a5ddf711e9fd046fbcb7b4b07bed9fa03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781812/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781812/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Baskar, Venkidasamy</creatorcontrib><creatorcontrib>Gangadhar, Baniekal H.</creatorcontrib><creatorcontrib>Park, Se Won</creatorcontrib><creatorcontrib>Nile, Shivraj Hariram</creatorcontrib><title>A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis</title><title>3 Biotech</title><addtitle>3 Biotech</addtitle><description>The present study aims to investigate the numerous factors influencing
Agrobacterium tumefaciens
-mediated genetic transformation of Chinese cabbage (
Brassica rapa
ssp.
pekinensis
). Factors affecting transformation efficiency, such as age of explants,
Agrobacterium
concentration, and effect of acetosyringone, pre-cultivation, infection and co-cultivation time of
Agrobacterium
were examined. The pre-cultured hypocotyls from young seedlings prior to exposure to
Agrobacterium
showed higher shoot regeneration. The plant transformation with the modest
A. tumefaciens
concentrations (0.8 OD) and the 3 days co-cultivation periods increased transformation efficiency. Plant growth hormones [1-naphthyl acetic acid (NAA) and 6-benzyl amino purine (BAP)] were essential for callus and shoot formation. Root formation was effective in half strength MS medium without supplementation of root-inducing hormones. To maintain selection pressure, plant subculture was carried out every 2 weeks with selective antibiotics. The putative transgenic plants were acclimatized in the greenhouse. Polymerase chain reaction was performed to confirm the integration of T-DNA into the genome of transgenic plants. A transformation efficiency of 15 % was obtained. This protocol allows effective transformation and indirect regeneration of
Brassica rapa
.</description><subject>Agriculture</subject><subject>Bioinformatics</subject><subject>Biomaterials</subject><subject>Biotechnology</subject><subject>Cancer Research</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Original</subject><subject>Original Article</subject><subject>Stem Cells</subject><issn>2190-572X</issn><issn>2190-5738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpVkE1qwzAQhUVpaUKaA3SnCzjV2JZlbQpp6B8EusmiOzGypVRpLBvJLvT2VUgpdDYz8GYebz5CboGtgDFxF6HIGc8YVBkrWZ7BBZnnIFnGRVFf_s35-4wsYzywVBy4BHZNZnldFAx4PSd-TaPrhqOh6FtqrHWNM36k633oNTajCW7qxqkzFk9CzDrTOhxNS4cjpr0xoI-2Dx2Orve0t_QhYIyuQRpwQBrjsKKD-XQ-Hbt4Q64sHqNZ_vYF2T097jYv2fbt-XWz3maDrCGrK40oWl3ZQtqClw1nmstGVrnUQnBA3rZWABhpW1ZWVjda6FIzoU0rLbJiQe7PtsOkU-AmfRTwqIbgOgzfqken_ivefah9_6VKUUMNeTLIzwYx3fi9CerQT8GnyAqYOvFXZ_4q8Vcn_gqKHzNPe3E</recordid><startdate>20160307</startdate><enddate>20160307</enddate><creator>Baskar, Venkidasamy</creator><creator>Gangadhar, Baniekal H.</creator><creator>Park, Se Won</creator><creator>Nile, Shivraj Hariram</creator><general>Springer Berlin Heidelberg</general><scope>C6C</scope><scope>5PM</scope></search><sort><creationdate>20160307</creationdate><title>A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis</title><author>Baskar, Venkidasamy ; Gangadhar, Baniekal H. ; Park, Se Won ; Nile, Shivraj Hariram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p981-86baa7db6f39f354c50b59c9629b7751a5ddf711e9fd046fbcb7b4b07bed9fa03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Agriculture</topic><topic>Bioinformatics</topic><topic>Biomaterials</topic><topic>Biotechnology</topic><topic>Cancer Research</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Original</topic><topic>Original Article</topic><topic>Stem Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baskar, Venkidasamy</creatorcontrib><creatorcontrib>Gangadhar, Baniekal H.</creatorcontrib><creatorcontrib>Park, Se Won</creatorcontrib><creatorcontrib>Nile, Shivraj Hariram</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>3 Biotech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baskar, Venkidasamy</au><au>Gangadhar, Baniekal H.</au><au>Park, Se Won</au><au>Nile, Shivraj Hariram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis</atitle><jtitle>3 Biotech</jtitle><stitle>3 Biotech</stitle><date>2016-03-07</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><issn>2190-572X</issn><eissn>2190-5738</eissn><abstract>The present study aims to investigate the numerous factors influencing
Agrobacterium tumefaciens
-mediated genetic transformation of Chinese cabbage (
Brassica rapa
ssp.
pekinensis
). Factors affecting transformation efficiency, such as age of explants,
Agrobacterium
concentration, and effect of acetosyringone, pre-cultivation, infection and co-cultivation time of
Agrobacterium
were examined. The pre-cultured hypocotyls from young seedlings prior to exposure to
Agrobacterium
showed higher shoot regeneration. The plant transformation with the modest
A. tumefaciens
concentrations (0.8 OD) and the 3 days co-cultivation periods increased transformation efficiency. Plant growth hormones [1-naphthyl acetic acid (NAA) and 6-benzyl amino purine (BAP)] were essential for callus and shoot formation. Root formation was effective in half strength MS medium without supplementation of root-inducing hormones. To maintain selection pressure, plant subculture was carried out every 2 weeks with selective antibiotics. The putative transgenic plants were acclimatized in the greenhouse. Polymerase chain reaction was performed to confirm the integration of T-DNA into the genome of transgenic plants. A transformation efficiency of 15 % was obtained. This protocol allows effective transformation and indirect regeneration of
Brassica rapa
.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28330158</pmid><doi>10.1007/s13205-016-0402-1</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2190-572X |
ispartof | 3 Biotech, 2016-03, Vol.6 (1) |
issn | 2190-572X 2190-5738 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4781812 |
source | Open Access: PubMed Central; Springer Nature |
subjects | Agriculture Bioinformatics Biomaterials Biotechnology Cancer Research Chemistry Chemistry and Materials Science Original Original Article Stem Cells |
title | A simple and efficient Agrobacteriumtumefaciens-mediated plant transformation of Brassica rapa ssp. pekinensis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T19%3A28%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral_sprin&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20simple%20and%20efficient%20Agrobacteriumtumefaciens-mediated%20plant%20transformation%20of%20Brassica%20rapa%20ssp.%20pekinensis&rft.jtitle=3%20Biotech&rft.au=Baskar,%20Venkidasamy&rft.date=2016-03-07&rft.volume=6&rft.issue=1&rft.issn=2190-572X&rft.eissn=2190-5738&rft_id=info:doi/10.1007/s13205-016-0402-1&rft_dat=%3Cpubmedcentral_sprin%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_4781812%3C/pubmedcentral_sprin%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p981-86baa7db6f39f354c50b59c9629b7751a5ddf711e9fd046fbcb7b4b07bed9fa03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/28330158&rfr_iscdi=true |