High-temperature detoxification method based on lily scales and leaf tips and application of high-temperature detoxification method
A lily and scale technology, applied in the field of high-temperature detoxification, can solve the problems of difficulty in obtaining stem tip materials, long heat treatment time, high cost, etc., and achieve the effects of high reproduction coefficient, increased detoxification rate, and low cost
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Embodiment 1
[0032] Embodiment 1 A kind of lily high temperature detoxification method based on scale leaf tip
[0033] 1) First-generation culture: take the virus-carrying 'Siberia' lily corm as material, wash it with washing powder, rinse it in running water for more than 30 minutes, and then put the bulbil in a sterile container on an ultra-clean workbench, wash it with 75% alcohol Soak for 40s, rinse with sterile water and then add 0.1% HgCl 2 Disinfect for 12 minutes, rinse with sterile water 6-8 times for use. Then the cleaned scales are placed on the primary culture medium with the inner side facing up to carry out induction culture for 2-3 weeks to obtain sterile buds.
[0034] 2) Subculture: use aseptic lily buds as explants, inoculate them in the subculture medium and culture them for 3 to 4 weeks to obtain normal-growing sterile bulblets.
[0035] 3) Thermal exercise treatment: place the lily tissue culture seedlings in a light incubator, treat them at a high temperature of 37...
Embodiment 2
[0047] The high temperature treatment temperature is 85° C., and other steps are the same as in Example 1.
[0048] After the high temperature treatment at 85℃, the growth of small scale leaf tip of 'Siberia' lily is shown in Table 3, and the growth of leaf tip of surviving 'Siberia' lily is as follows Figure 4 As shown, when the leaf tip was inserted into the medium, the leaf tip swelled and began to form adventitious buds in about 20 days; the adventitious buds grew leaves and developed roots in about 40 days, and developed into test-tube plantlets in 60 days.
[0049] Table 3 The growth of small scale leaf tips of 'Siberia' lily treated at 85℃
[0050]
[0051]
[0052] Survival rate = normal survival number / total number of inoculations
Embodiment 3 100
[0053] The detection of virus in the lily material of embodiment 3
[0054] Lily RNA extraction: In order to detect the detoxification effect, a certain number of seedlings were randomly selected from the lily test-tube seedlings prepared in Examples 1-2, and the total amount of leaf total was extracted using the Tiangen Plant RNA Small Extraction Kit (R4151). RNA was stored at -20°C for later use.
[0055] cDNA synthesis: The total volume of each cDNA synthesis reaction is 20 μl, and the first-strand cDNA is synthesized using the plant cDNA rapid reverse transcription kit (KR116) from TIANGEN Company. The reaction reagents include 2 μl of total RNA, 2 μl of 5×gDNA Buffer, and RNase-Free ddH 2 O 6μl, incubate at 42°C for 5min, place on ice; add 10×King RT Buffer 2, FastKing RTEnzyme Mix 1μl, FQ-RT Primer Mix 2μl, RNase-Free ddH 2 O 5 μl, the reaction program was incubated at 42°C for 30 minutes and inactivated at 70°C for 5 minutes.
[0056] PCR amplification: The PCR reacti...
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