KRISHI
ICAR RESEARCH DATA REPOSITORY FOR KNOWLEDGE MANAGEMENT
(An Institutional Publication and Data Inventory Repository)
"Not Available": Please do not remove the default option "Not Available" for the fields where metadata information is not available
"1001-01-01": Date not available or not applicable for filling metadata infromation
"1001-01-01": Date not available or not applicable for filling metadata infromation
Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/11606
Title: | Development of an efficient Agrobacterium mediated transformation system for chickpea (Cicer arietinum) |
Other Titles: | Not Available |
Authors: | Jaya Srivastava Subhojit Datta Sudhakar P Mishra |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR::Indian Institute of Pulses Research |
Published/ Complete Date: | 2017-02-01 |
Project Code: | ICAR NPTC |
Keywords: | Cicer arietinum chickpea Agrobacterium genetic transformation transformation |
Publisher: | De Gruyter |
Citation: | 2 |
Series/Report no.: | Not Available; |
Abstract/Description: | Morphologically normal and fertile transgenic chickpea plants have been regenerated through a standardized transformation protocols. This protocol is based on the infection of apical meristem explants (AME) with Agrobacterium strain EHA105. The stain, carrying pCAMBIA2301 vector contained β-glucuronidase (uidA) gene and neomycin phosphotransferase (nptII) genes. Different explants of chickpea and Agrobacterium specific conditions were standardized with the help of transient β-glucuronidase (uidA) gene expression to further optimize the transformation protocol. Pre-conditiong of the explants, vacuum infiltration and presence of acetosyringone significantly enhanced the frequency of gus expression. Positive transformants with nptII and gus genes were confirmed by PCR and histochemical gus analysis. An overall successful chickpea transformation frequency of 1.2 was achieved. This high efficiency and easy to use method may provide opportunities for the development of transgenic lines with different useful genes in chickpea in near future. |
Description: | Not Available |
ISSN: | (Online) 1336-9563, ISSN (Print) 0006-3088 |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Biologia |
NAAS Rating: | 6.81 |
Volume No.: | 72(2) |
Page Number: | 153-160 |
Name of the Division/Regional Station: | Biotechnology |
Source, DOI or any other URL: | DOI: https://doi.org/10.1515/biolog-2017-0015. https://www.degruyter.com/view/j/biolog.2017.72.issue-2/biolog-2017-0015/biolog-2017-0015.xml |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/11606 |
Appears in Collections: | CS-CRIJAF-Publication |
Files in This Item:
There are no files associated with this item.
Items in KRISHI are protected by copyright, with all rights reserved, unless otherwise indicated.