Abstract

  Cotton is the chief fibre crop of global importance. It plays a significant role in the national economy. Cotton crop is vulnerable to a number of insect species, especially to the larvae of lepidopteron pests. 60% insecticides sprayed on cotton are meant to control the damage caused by bollworm complex. Transgenic technology has become a popular option for the development of bollworm resistant cotton.Spodoptera litura is one of the notorious emerging pests in cotton. Introduction ofcry1EC gene into commercial variety have very significant importance. This research work was carried out to transform chimeric δ-endotoxin Cry1EC into cotton. The tobacco cutworm (Spodoptera litura) is a polyphagous foliage insect which is susceptible to the chimeric δ-endotoxin Cry1EC. Six month-old highly friable embryogenic calli derived from cotyledonary explants of Coker 310 were used for transformation using Agrobacterium tumefaciens strain LBA4404 harboring plasmid pBI101.1 carrying the marker gene neomycin phosphotransferase II (npt II) and a synthetic cry 1EC gene under a constitutive 35 S promoter. Agrobacterium treatedcalli were selected on MS medium containing, 50 mg/L kanamycin, 500 mg/L cefotaxime, 30 g/L maltose and 0.4% phytagel. Embryos developed on kanamycin resistant calli were maintained on the same medium till somatic embryos matured. The cotyledonary stage embryos (3 to 5 mm size) were germinated on MS basal slat with 0.1 mg/L GA3 + 1.0 mg/L IAA, 30 g/L sucrose and solidified with 0.4% phytagel. The regenerated putative transgenic plants were hardened and transferred to the transgenic green house. Transgenic plants were confirmed by polymerase chain reaction (PCR) amplification of 800 bp npt II fragment, and 578 bp amplification ofcry1Ec gene. Transgenic plant with single copy insertion of cry1EC was selected in T0 by southern blot hybridization. Insect bioassay using Spodoptera litura larvae of first instar stages on T0 plants showed 70% mortality. Not much data has been published on the toxicity of the endotoxins to S. litura, which is a common pest in warm and humid climates. Efforts are aimed at recovering more efficient transgenic plants through efficient transformation system and developing high resistant transgenic cotton against S. litura and will paved a way for promising future in cotton production.                                                 Key words: Agrobacterium transformation, cry 1EC, molecular analysis, insect bioassay.

Highlights

  • Cotton (Gossypium spp.) is an important source of natural fibre, and plays a significant role in the Indian economy

  • Six month-old highly friable embryogenic calli derived from cotyledonary explants of Coker 310 were used for transformation using Agrobacterium tumefaciens strain LBA4404 harboring plasmid pBI101.1 carrying the marker gene neomycin phosphotransferase II and a synthetic cry 1EC gene under a constitutive 35 S promoter

  • Transgenic plants were confirmed by polymerase chain reaction (PCR) amplification of 800 bp neomycin phosphotransferase II (npt II) fragment, and 578 bp amplification of cry1Ec gene

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Summary

Full Length Research Paper

Genetic transformation of cry1EC gene into cotton (Gossypium hirsutum L.) for resistance against Spodoptera litura. Cotton is the chief fibre crop of global importance. It plays a significant role in the national economy. Transgenic technology has become a popular option for the development of bollworm resistant cotton. This research work was carried out to transform chimeric δ-endotoxin Cry1EC into cotton. The tobacco cutworm (Spodoptera litura) is a polyphagous foliage insect which is susceptible to the chimeric δ-endotoxin Cry1EC. Insect bioassay using Spodoptera litura larvae of first instar stages on T0 plants showed 70% mortality. Efforts are aimed at recovering more efficient transgenic plants through efficient transformation system and developing high resistant transgenic cotton against S. litura and will paved a way for promising future in cotton production

INTRODUCTION
Bacterial strain and vector
Plant material
Callus induction
Transformation and regeneration
Selection and regeneration
Insect bioassay
Total Number of larvae released
RESULTS AND DISCUSSION
Molecular confirmation and insect bioassay
Number of plants regenerated
Transgenic inheritance analysis
Full Text
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