Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)

This thesis report is submitted in partial fulfillment of the requirement for the degree of Masters of Science in Biotechnology, 2011

書誌詳細
第一著者: Razzaque, Samsad
その他の著者: Seraj, Dr. Zeba Islam
フォーマット: 学位論文
言語:English
出版事項: BRAC University 2012
主題:
オンライン・アクセス:http://hdl.handle.net/10361/1665
id 10361-1665
record_format dspace
spelling 10361-16652019-09-30T04:21:52Z Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S) Razzaque, Samsad Seraj, Dr. Zeba Islam Islam, Dr. Aparna Department of Mathematical and Natural Science, BRAC University Biotechnology This thesis report is submitted in partial fulfillment of the requirement for the degree of Masters of Science in Biotechnology, 2011 Cataloged from PDF version of thesis report. Includes bibliographical references (page 84-87). The costal belt of Bangladesh is under the threat of increasing salinity and thus reducing plant productivity. Consequently, salinity has become a major concern for ensuring food security. Salt tolerance is known to be a complex trait both genetically as well as physiologically and conferring this tolerance by introducing a single gene is therefore difficult. However, over expression of the vacuolar antiporter gene, NHX1 has been reported to provide salinity tolerance to a good extent. This work was carried out to clone the coding sequence of the rice antiporter gene (applying Gateway Technology) in a binary vector (pH7WG2.0) from where this can be easily introduced into a plant genome with a highly efficient constitutive promoter (CaMV35S). In this study, NHX 1 gene was first cloned into pENTR and confirmed the insertion through PCR, Restriction Digestion and Sequencing technique. Then the gene of interest was recombined from pENTR to the Destination vector (pH7WG2.0) and recombination was confirmed by PCR and Restriction Digestion respectively. Finally, recombinant vector was then transformed into Agrobacterium (the transformation was also confirmed by PCR and Restriction Digestion) to perform Agrobacterium mediated transformation into tomato plant. Samsad Razzaque M. Biotechnology 2012-03-14T05:38:43Z 2012-03-14T05:38:43Z 2011 2011-10 Thesis ID 10176007 http://hdl.handle.net/10361/1665 en BRAC University thesis are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. 87 pages application/pdf BRAC University
institution Brac University
collection Institutional Repository
language English
topic Biotechnology
spellingShingle Biotechnology
Razzaque, Samsad
Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
description This thesis report is submitted in partial fulfillment of the requirement for the degree of Masters of Science in Biotechnology, 2011
author2 Seraj, Dr. Zeba Islam
author_facet Seraj, Dr. Zeba Islam
Razzaque, Samsad
format Thesis
author Razzaque, Samsad
author_sort Razzaque, Samsad
title Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
title_short Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
title_full Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
title_fullStr Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
title_full_unstemmed Cloning of an antiporter gene (NHX1) from PCR amplicons into a recombination competent vector containing a constitutive promoter (caMV35S)
title_sort cloning of an antiporter gene (nhx1) from pcr amplicons into a recombination competent vector containing a constitutive promoter (camv35s)
publisher BRAC University
publishDate 2012
url http://hdl.handle.net/10361/1665
work_keys_str_mv AT razzaquesamsad cloningofanantiportergenenhx1frompcrampliconsintoarecombinationcompetentvectorcontainingaconstitutivepromotercamv35s
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