Sea island cotton pollen tube passage method transgene technology
A pollen tube passage and transgenic technology, applied in the field of plant genetic engineering and agricultural biology, can solve the problems of difficult establishment of somatic cell regeneration system, prone to genotype variation, high transformation cost, etc., and achieve improved sea-island cotton varieties and high bell seat rate , The effect of high breeding efficiency
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Embodiment 1
[0036] Example 1. Transfer protein gene (GhABC1) into sea island cotton variety Xinhai No. 16 to cultivate a new sea island cotton variety with improved fiber quality
[0037] Xinhai No. 16 (provided by the Institute of Economic Crops, Xinjiang Academy of Agricultural Sciences) was planted to flowering, according to the "Guidelines for Molecular Cloning Experiments" (translated by Jin Dongyan, Li Mengfeng, etc., J. Sambrook, E.F. Fritsch, T. Maniartis) Science Press, 1992) Extraction of plasmid DNA containing transgene. Specifically, it is performed as follows.
[0038] The Escherichia coli strain containing the transgene gene was provided by the Institute of Plant Physiology and Biochemistry, Chinese Academy of Sciences. The strain was inoculated into 30ml of LB liquid medium (Luria-Bertani) containing the corresponding antibiotics, and each liter of medium was prepared in 950ml of distilled water. Add: 10 g tryptone, 5 g yeast extract, 10 g NaCl, shake the container until t...
Embodiment 2
[0071] Example 2. The Expansin gene (Expansin gene) was transferred into the sea-island cotton variety Xinhai No. 17, and the new sea-island cotton variety of improved fiber quality was cultivated
[0072] Xinhai No. 17 (provided by Alar Agricultural Science Institute, First Agricultural Division, Xinjiang) was planted until flowering, and the plasmid DNA containing the extensin gene was extracted according to the "Molecular Cloning Experiment Guide". details as follows.
[0073] Escherichia coli containing the extensin gene was provided by the Institute of Microbiology, Chinese Academy of Sciences, the strain was inoculated into 30ml of LB liquid medium (Luria-Bertani) containing the corresponding antibiotics, and each liter of medium was prepared, and should be added in 950ml of distilled water: pancreatic 10 g peptone, 5 g yeast extract, 10 g NaCl, shake the container until the solute is completely dissolved, adjust the pH to 7.0 with 5M NaOH, add distilled water to a total...
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