نمایش مختصر رکورد

dc.contributor.authorZamani, Akramen_US
dc.contributor.authorMotallebi, Mostafaen_US
dc.contributor.authorJonoubi, Parisaen_US
dc.contributor.authorGhafarian-Nia, Nayere Sadaten_US
dc.contributor.authorZamani, Mohammad Rezaen_US
dc.date.accessioned1399-07-08T20:19:51Zfa_IR
dc.date.accessioned2020-09-29T20:19:51Z
dc.date.available1399-07-08T20:19:51Zfa_IR
dc.date.available2020-09-29T20:19:51Z
dc.date.issued2012-04-01en_US
dc.date.issued1391-01-13fa_IR
dc.date.submitted2012-04-01en_US
dc.date.submitted1391-01-13fa_IR
dc.identifier.citationZamani, Akram, Motallebi, Mostafa, Jonoubi, Parisa, Ghafarian-Nia, Nayere Sadat, Zamani, Mohammad Reza. (2012). Heterologous expression of the Secale cereal thaumatinlike protein in transgenic canola plants enhances resistance to stem rot disease. Iranian Journal of Biotechnology, 10(2), 87-95.en_US
dc.identifier.issn1728-3043
dc.identifier.issn2322-2921
dc.identifier.urihttp://www.ijbiotech.com/article_7173.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/85987
dc.description.abstractCanola (Brassica napus L.) is an important oilseed crop. A serious problem in cultivation of this crop and<br />yield loss, are due to fungal disease stem rot caused by Sclerotinia sclerotiorum. The pathogenesis-related<br />(PR) proteins have the potential for enhancing resistance against fungal pathogen. Thaumatin-like proteins<br />(TLPs) have been shown to have antifungal activity on various fungal pathogens. In this study, the tlp gene<br />isolated from cereal rye (Secale cereal L.) was introduced into canola plants. The amplified DNA fragment<br />(about 500 bp) was analyzed and confirmed by restriction pattern and cloned into pUC19 and designated as<br />pUCNG1. Comparison of the cloned fragment with the DNA sequence indicated that this gene contains no<br />intron. The tlp gene was predicted to encode a protein of 173 amino acids with an estimated molecular mass<br />of 17.7 kDa. The deduced amino acid sequence of TLP showed a significant sequence identity with TLP<br />from S.cereal and other plants. We used a transgenic over-expression approach in order to investigate antifungal activity of expressed TLP on Sclerotinia sclerotiorum. TLP was overexpressed under the CaMV35S<br />constitutive promoter in (Brassica napus, R line Hyola 308). Transformation of cotyledonary petioles was<br />achieved via Agrobacterium tumefaciens LBA4404. The insertion of transgene was verified by the polymerase<br />chain reaction (PCR) and genomic DNA dot blotting. Antifungal activity was detected in transgenic<br />canola lines using detached leaf assay. The size of lesions induced by S. sclerotiorum in the leaves of<br />transgenic canola was significantly retarded when compared to that detected in non-transgenic plants.<br /><br />en_US
dc.format.extent1822
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherNational Institute of Genetic Engineering and Biotechnologyen_US
dc.relation.ispartofIranian Journal of Biotechnologyen_US
dc.subjectCanolaen_US
dc.subjectSclerotinia sclerotiorumen_US
dc.subjectSecale cerealen_US
dc.subjectThaumatin-like proteinsen_US
dc.subjectTransgenic planten_US
dc.titleHeterologous expression of the Secale cereal thaumatinlike protein in transgenic canola plants enhances resistance to stem rot diseaseen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentNational Institute of Genetic Engineering and Biotechnology, P.O. Box 14965/161, Tehran, I.R. Iranen_US
dc.contributor.departmentNational Institute of Genetic Engineering and Biotechnology, P.O. Box 14965/161, Tehran, I.R. Iran.en_US
dc.contributor.departmentDepartment of Biology, Kharazmi University, P.O. Box 31979-37551, Tehran, I.R. Iran.en_US
dc.contributor.departmentNational Institute of Genetic Engineering and Biotechnology, P.O. Box 14965/161, Tehran, I.R. Iran.en_US
dc.contributor.departmentNational Institute of Genetic Engineering and Biotechnology, P.O. Box 14965/161, Tehran, I.R. Iran.en_US
dc.citation.volume10
dc.citation.issue2
dc.citation.spage87
dc.citation.epage95


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