Title : Marker assisted introgression of genes conferring resistance to bacterial blight and blast into hybrid rice parental line and evaluation of the gene introgressed lines

Type of Material: Thesis
Title: Marker assisted introgression of genes conferring resistance to bacterial blight and blast into hybrid rice parental line and evaluation of the gene introgressed lines
Researcher: Balachiranjeevi Ch
Guide: Hari Prasad A. S.
Department: Faculty of Biotechnology
Publisher: Jawaharlal Nehru Technological University, Hyderabad
Place: Hyderabad
Year: 2015
Language: English
Subject: Biotechnology and Applied Microbiology
Life Sciences
Microbiology
Rice diseases
Biotechnology
Engineering and Technology
Dissertation/Thesis Note: PhD; Faculty of Biotechnology, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad; 2015
Fulltext: Shodhganga

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040__|aJNTU_500028|dIN-AhILN
041__|aeng
100__|aBalachiranjeevi Ch|eResearcher
110__|aFaculty of Biotechnology|bJawaharlal Nehru Technological University, Hyderabad|dHyderabad|ein|0U-0017
245__|aMarker assisted introgression of genes conferring resistance to bacterial blight and blast into hybrid rice parental line and evaluation of the gene introgressed lines
260__|aHyderabad|bJawaharlal Nehru Technological University, Hyderabad|c2015
300__|a201p.|dDVD
502__|cFaculty of Biotechnology, Jawaharlal Nehru Technological University, Hyderabad, Hyderabad|d2015|bPhD
518__|dDecember 2015|oDate of Award
518__|oDate of Registration|d2010-01-01
520__|aDRR17A is a very fine-grain type wild-abortive cytoplasmic male sterile (WA-CMS) line of rice developed by the Indian Institute of Rice Research, Hyderabad. However, DRR17A and its maintainer line DRR17B are highly susceptible to two of the major rice diseases, bacterial blight (BB) and blast. To improve DRR17B for BB and blast resistance, we have introgressed two major dominant genes Xa21 + Xa33 each conferring resistance against BB and blast (Pi-54 + Pi2) into DRR17B through marker-assisted backcross breeding using Improved samba Mahsuri (for Xa21 gene), FBR1-15 (Xa33), Tetep (Pi54) and C101A51 (Pi2) as the donor parents. PCR-based molecular markers specific for Xa21, Xa33 Pi2 and Pi-54 were used for foreground selection, while parental polymorphic SSR markers were utilized for background selection for accelerating the recovery of the recurrent parent genome. In addition, at BC1F1 generation, molecular markers tightly linked to the fertility restorer genes, Rf3 and Rf4 were used for negative selection to
650__|aBiotechnology|2UGC
650__|aEngineering and Technology|2AIU
653__|aBiotechnology and Applied Microbiology
653__|aLife Sciences
653__|aMicrobiology
653__|aRice diseases
700__|eGuide|aHari Prasad A. S.
856__|uhttp://shodhganga.inflibnet.ac.in/handle/10603/292978|yShodhganga
905__|afromsg

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