Composition for regulation of gametophytic self-incompatibility, control method of gametophytic self imcompatibility of a plant and the plant self-polli-nated by using said control method
A compound and gametophyte technology, which are applied to the compound regulating gametophyte self-incompatibility, regulating the gametophyte self-incompatibility of plants and using the above-mentioned regulation and self-pollination in the field of plants
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
example 1
[0064] Isolation and purification of column-specific RNase in Example 1, a regulatory protein of gametocyte self-incompatibility Isolation and purification of RNase from each organ of Fuji apple
[0065] Isolate RNase from the stem, root, leaf, handle, petal and calyx of Fuji apple, the experimental steps are as follows:
[0066] Add 10mM Na 2 PO 4 (pH 6.0), 10 mM EDTA, 1 mM PMSF and 1% polyvinylpyrrolidine buffer solution, mix them uniformly in a mortar, and extract the total protein. Utilize 40% Na 2 PO 4 Concentrate the proposed total protein, then dialyze the concentrated total protein to 5 mM Na using a semi-permeable membrane (molecular cutoff: 12,000 Dalton 2 PO 4 in the buffer solution. A fraction with high RNase activity was finally obtained, with a total RNase activity of 295,000 units.
[0067]Using a resin column (Bio-Rad, England) filled with Biogel P-60, the fraction with high RNase activity was subjected to gel filtration chromatography (Harris et al., P...
example 2
[0085] Inhibition of Pollen Tube Elongation in Self-Pollen by Stem-Specific RNase of Fuji Apple
[0086] In order to study the role of the purified, stele-specific RNases in Examples 1-4 on the elongation of pollen tubes of self-pollen, we conducted the following experiments. First, the self-pollen in the male stamens of the Fuji apple is isolated. The isolated pollen was cultured in a medium for pollen tube elongation, and 0, 2, 4 and 6 units (mg -1 min -1 ml), the S1 RNase purified in Example 1-4 was incubated in the dark for 24 hours. The medium for pollen tube elongation contained 20 mM Mes-KOH (pH 6.0), 0.07% Ca(NO 3 ) 2 4H 2 O, 0.02% MgSO 4 ·7H 2 O, 0.01% KNO 3 , 0.01%H 3 BO 3 And 2% sucrose, can artificially prolong the pollen tube.
[0087] For laboratory results of the pollen tube elongation pattern see image 3 . Such as image 3 As shown in , self-pollen pollen tube elongation was inhibited. From this result, it was confirmed that the decisive factor...
example 3
[0089] Study on Inhibitors of Stem Specific RNase
[0090] The difference in activity of the purified stem-specific S1 RNase and S2 RNase in Examples 1-4 can be studied by adding chemicals that act as inhibitors of proteolytic enzymes. By adding common RNase activity agonists, adding commercially available RNase activity inhibitors and adding the inhibitor of the column-specific RNase just invented at present, the activity of RNase can be detected (Singh A. et al., Plant Physiology , 96:61-68, 1991). Specifically, 1 mM EDTA, a representative inhibitor of proteolytic enzymes; 1 mM calcium chloride, an activator of RNase activity; 1 mM DEPC (Sigma), a commercially available lethal toxic Inhibitors of RNase activity; and 1mM ZnSO 4 and 1mM CuSO 4 , that is, the column-specific RNase inhibitor to detect RNase activity. See the experimental results Figure 4 .
[0091] The result is: compared with the control group with 100% RNase activity in phosphate buffer, when adding 1mM...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com