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dc.creatorMuzaffar,Adnan
dc.creatorKiani,Sarfraz
dc.creatorKhan,Muhammad Azmat Ullah
dc.creatorRao,Abdul Qayyum
dc.creatorAli,Arfan
dc.creatorAwan,Mudassar Fareed
dc.creatorIqbal,Adnan
dc.creatorNasir,Idrees Ahmad
dc.creatorShahid,Ahmad Ali
dc.creatorHusnain,Tayyab
dc.date2015-01-01
dc.date.accessioned2019-05-02T21:22:25Z
dc.date.available2019-05-02T21:22:25Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100014
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/82497
dc.descriptionBACKGROUND: Insects have developed resistance against Bt-transgenic plants. A multi-barrier defense system to weaken their resistance development is now necessary. One such approach is to use fusion protein genes to increase resistance in plants by introducing more Bt genes in combination. The locating the target protein at the point of insect attack will be more effective. It will not mean that the non-green parts of the plants are free of toxic proteins, but it will inflict more damage on the insects because they are at maximum activity in the green parts of plants. RESULTS: Successful cloning was achieved by the amplification of Cry2A, Cry1Ac, and a transit peptide. The appropriate polymerase chain reaction amplification and digested products confirmed that Cry1Ac and Cry2A were successfully cloned in the correct orientation. The appearance of a blue color in sections of infiltrated leaves after 72 hours confirmed the successful expression of the construct in the plant expression system. The overall transformation efficiency was calculated to be 0.7%. The amplification of Cry1Ac-Cry2A and Tp2 showed the successful integration of target genes into the genome of cotton plants. A maximum of 0.673 μg/g tissue of Cry1Ac and 0.568 μg/g tissue of Cry2A was observed in transgenic plants. We obtained 100% mortality in the target insect after 72 hours of feeding the 2nd instar larvae with transgenic plants. The appearance of a yellow color in transgenic cross sections, while absent in the control, through phase contrast microscopy indicated chloroplast localization of the target protein. CONCLUSION: Locating the target protein at the point of insect attack increases insect mortality when compared with that of other transgenic plants. The results of this study will also be of great value from a biosafety point of view.
dc.formattext/html
dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.1186/s40659-015-0005-z
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.48 2015
dc.subjectChloroplast transient peptide
dc.subjectCry1Ac
dc.subjectCry2A
dc.subjectBt
dc.subjectcTP
dc.subjectCry genes
dc.subjectEndotoxins
dc.subjectGUS
dc.subjectTransgenic plants
dc.titleChloroplast localization of Cry1Ac and Cry2A protein- an alternative way of insect control in cotton


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