Application of protein and related biological materials thereof to regulation and control on mechanical strength of plants
A technology of mechanical strength and biological materials, applied in the fields of plant peptides, plant products, plant genetic improvement, etc., can solve the problems of difficult degradation of cell wall components, affecting crop rooting, low recycling efficiency, etc., to achieve high recycling efficiency.
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Embodiment 1
[0071] Embodiment 1 Discovery of rice brittle stalk and brittle leaf genes
[0072] 1. Acquisition of rice crisp stem and crisp leaf mutant bcl1
[0073] Rice brittle culm and leaf mutant brittle culm and leaf 1 (abbreviated as bcl1 or mutant bcl1) is a spontaneous mutation material in the tissue culture process of rice TP309.
[0074] 2. Phenotypic identification of rice brittle stem and brittle leaf mutant bcl1
[0075] Compared with rice TP309, mutant bcl1 mainly exhibits:
[0076] 1. Stems ( figure 1 shown): Compared with the stalks of rice TP309 (represented by "TP309" in the figure), the stalks of the mutant bcl1 (represented by "bcl1" in the figure) were brittle and the secondary cell walls of the sclerenchyma cells were Thin;
[0077] 2. Blades ( figure 2 Shown): Compared with the leaves of rice TP309 (represented by "TP309" in the figure), the leaves of the mutant bcl1 (represented by "bcl1" in the figure) became brittle and the secondary cell walls of the scle...
Embodiment 2
[0082] Example 2 Functional verification of BCL1 gene
[0083] 1. Acquisition of Complementary Vector Transgenic Plants
[0084] In order to verify the role of BCL1 in the regulation of rice stem and leaf fragility, functional verification was carried out by BCL1 genome complementation experiments in mutant bcl1.
[0085] 1) Construction of complementary vectors
[0086] 1. Genomic DNA of two-week-old seedlings of rice TP309 was extracted.
[0087] 2. Using the DNA in step 1 as a template, perform PCR amplification with a primer pair composed of BCL1-com1-F and BCL1-com1-R, and obtain a size of 5302 bp as shown in the 1-5302 position of sequence 1 in the sequence table The amplified product fragment a (SEQ forward direction).
[0088] BCL1-com1-F: 5′-CACTCCATACATTGCGGGGT-3′
[0089] BCL1-com1-R: 5′-ACATTCTTCCCGCTTTCGGT-3′
[0090] 3. Using fragment a in step 2 as a template, carry out PCR amplification with a primer pair composed of BCL1-com2-F and BCL1-com2-R (the underl...
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