Breeding method of japonica rice variety capable of controlling postprandial blood sugar of diabetes patient
A technology for postprandial blood sugar and diabetic patients, which is applied in the fields of botanical equipment and methods, applications, and plant genetic improvement, can solve the problems of waste of manpower and material resources, low efficiency, and inability to solve the difficulty of eating for diabetics, and achieves accelerated breeding process, Good reproducibility, accurate and consistent results with phenotypic measurements
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Embodiment 1
[0020] Example 1: The rice variety fibrin464 with high dietary fiber content excavated from immature immature embryos was treated with a chemical mutagen and the high-yield and high-quality rice line 007908 suitable for local ecological conditions was used as the male parent for hybridization, and the hybrid F1 generation was cultured for anthers. A genetically stable strain with high resistant starch content was obtained, and the field number was 08JD26. The japonica rice line 08JD26 with high resistant starch content was used as the female parent, and it was crossed with the indica rice variety Miyang 23. The offspring of the hybrids were self-crossed, and there was a significant correlation between the opaque grains of the F1 generation seeds and the content of resistant starch, and the offspring individuals with transparent grains No single plant with high resistant starch content appeared in the population, and the occurrence rate of high resistant starch content in the of...
Embodiment 2
[0026] Example 2: Screening using molecular markers closely linked to high resistant starch content;
[0027] DNA was extracted from the test samples using the CTAB method. Cut a small piece of leaf 4-5cm at the early stage of rice tillering, add 700μL 1.5×CTAB (containing 1.5%CTAB, 75mM Tris-HCl, 15mM EDTA, 1.05M NaCl), and grind thoroughly; 2) Transfer the homogenate into 1.5ml Centrifuge tube, cool to room temperature in a water bath at 56°C for 20 minutes; 3) Add an equal volume of chloroform:isoamyl alcohol (24:1) and shake well; 4) Centrifuge at the highest speed (13200rpm) for 10 minutes; 5) Transfer the supernatant to Create a new centrifuge tube, add twice the volume of pre-cooled 100% ethanol, and centrifuge to collect DNA after standing still for 20 minutes; 6) Remove the supernatant, air-dry the DNA, add 50-100 μL of double distilled water to dissolve, and detect in a UV spectrophotometer . Dilute the DNA to prepare a set of DNA working solution with a concentrat...
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