Methid of regulating peach seedling-plant transition stage
A kind of seeding and stage technology, applied in the field of using physiological markers to assist in regulating the stage transition of peach seedling trees, to achieve the effects of eliminating sampling errors, reducing workload, and accurate results
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Embodiment 1
[0036] 1) Sampling
[0037] ①Changli Fruit Tree Research Institute took samples and monitored two year-old natural seed populations of Okubo and Yanhong in 2003. One sprouted tiller was selected from the root neck of peach seedling saplings in spring, sampled on September 15, and the selected sprouted tiller was cut. , starting from the base of the seedling tree, it rises with the node position, and every 5 nodes is a sampling unit. Take 30 seedling trees and mix them with the sampling units at the same node position. Repeat 1 time to select a total of 60 trees, and put them in the ice box. back;
[0038] ② After washing with tap water, remove the phloem, wrap it with gauze and put it into liquid nitrogen for testing;
[0039] 2) Determination:
[0040] The content of abscisic acid ABA, gibberellin GA, isopentenyl adenine iP, zeatin ZT contained in the endogenous hormone contained in the phloem sampling is determined by high performance liquid chromatography, and the conditi...
Embodiment 2
[0052] 1) Sampling: Sampling on August 20, 2003, the steps are the same as in Example 1;
[0053] 2) Determining the content of abscisic acid ABA, gibberellin GA, isopentenyl adenine iP, and zeatin ZT in endogenous hormones in the sampling, the steps are as follows:
[0054] ① Sampling was dried in a freeze dryer for 26 hours, ground into a fine powder, and passed through a 35-mesh sieve;
[0055] ②Take 0.7 g of freeze-dried sample powder, add 3 ml of 100% acetonitrile at 4°C containing 0.8 mmol of 2,6-di-tert-butyl-p-cresol (BHT), place in an ultrasonic bath at 35°C for 25 minutes, and extract in an ice bath 15 hours, centrifuge at 12,000 rpm for 8 minutes at 4°C;
[0056] ③ Take 2 ml of the supernatant obtained in ②, dry at 35°C, redissolve with 0.8 ml of 0.4 mol / L phosphate buffer solution with pH 8.0, add 0.6 ml of chloroform for extraction 5 times until the organic phase Colorless, adjust the pH of the aqueous phase to 8.0 with 25 μl of 1.5 mol / L NaOH, add 90 mg of inso...
Embodiment 3
[0064] 1) Sampling: Sampling on August 30, 2003, the steps are the same as in Example 1;
[0065] 2) Determining the content of abscisic acid ABA, gibberellin GA, isopentenyl adenine iP, and zeatin ZT in endogenous hormones in the sampling, the steps are as follows:
[0066] ① Sampling was dried by a freeze dryer for 22 hours, ground into a fine powder, and passed through a 38-mesh sieve;
[0067] ②Take 0.4 g of freeze-dried sample powder, add 2.5 ml of 100% acetonitrile at 4°C containing 0.9 mmol of 2,6-di-tert-butyl-p-cresol (BHT), place in an ultrasonic bath for 29 minutes at 28°C, and extract in an ice bath 11 hours, centrifuge at 11,000 rpm for 10 minutes at 4°C;
[0068] ③Take 1.4 ml of the supernatant obtained in ②, dry at 28°C, redissolve with 0.9 ml of 0.4 mol / L phosphate buffer solution with pH 8.0, add 0.5 ml of chloroform for extraction 3 times until the organic phase Colorless, adjust the pH of the aqueous phase to 8.0 with 18 μl of 1.8 mol / L NaOH, add 75 mg of ...
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