Method for converting ustilaginoidea virens A by utilizing fungi and application of ustilaginoidea virens A
A rice aspergillus, biotransformation technology, applied in the biological field, can solve problems such as poisoning, internal organ lesions, and the decline of livestock and poultry growth and reproductive capacity.
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Embodiment 1
[0098] Example 1, Radecinium A transformed into rice germin I and J in phosphate buffer having a pH value of 7 via a rigidae chlamycosporin NitaF10 cell-free extract
[0099] First, experimental method
[0100] 1, the preparation method of the rigidae coridine Nitaf10 cell-free extract (pH is 7) is taken as follows: Take the activated rigid burgurous-agar medium (PDA) to activate a good rigidaeencore Nitaf10 inoculated to 100 ml of potato-glucose - In the 250ml triangular bottle of culture solution (PDB), the amount of fungus inoculated is 3-4 6mm sized, oscillated in the shaker for 3-5 days, and the shake good fermentation liquid (bacterial liquid) was loaded into 50ml. In the round bottom centrifuge tube, at 4 ° C, 12000 × g, centrifuged for 20 minutes, to the supernatant, and then add 0.5 M phosphate buffer (PBS) having a pH of about 30 ml of a pH of about 30 ml to the syride precipitate. In the ultrasonic cleaner (100% power) ice bath, ultrasonic oscillate 150 times, 2 seconds...
Embodiment 2
[0123] Example 2, Rice Rutin A is converted to rice gemmi Mikin M via a rigidae chlorofacial Nitaf10 cell-free extract in a carbonate buffer having a pH 9.
[0124] First, experimental method
[0125] 1, the preparation method of the brurry chrobus Nitaf10 cell-free extract (pH is 9) is as follows: Take the active Night Black Coridine Shell Nitaf10 in the potato-glucose-agar medium (PDA) inoculated to 100 ml of potato-glucose - In the 250ml triangular bottle of culture solution (PDB), the amount of fungus inoculated is 3-4 6mm sized, oscillated in the shaker for 3-5 days, and the shake good fermentation liquid (bacterial liquid) was loaded into 50ml. In the round bottom centrifuge tube, at 4 ° C, 12000 × g, centrifuge for 20 minutes, to the supernatant, and then add 0.5 M carbonate buffer (CBS) having a pH of about 30 ml of a pH of about 30 ml to the hyphae precipitate. In the ultrasonic cleaner (100% power), the ultrasonic oscillation is about 150 times, and each oscillates for 2...
Embodiment 3
[0135] Example 3 Dynamic changes in consumption and transformed product rice germin I and J production amount in the process of rice gemis A biological conversion time in Rice Coridin A biogenesis
[0136] First, experimental method
[0137] 1. 1 of the first step in the first step in Example 1.
[0138] 2. 2 of the second step in the first step in Example 1.
[0139] 3. The reaction is sampled at the first 0H, 6H, 12H, 24H, 36H, 48H, and 72H, and the reaction is stopped with an equal volume of methanol, and the HPLC analysis is carried out after 1 ml of ultrapure water.
[0140] Second, the experiment
[0141] The results are shown in Table 5, and the results showed that the transformed product was generated in the biological extract of rice germs A, and two transformed products occurred in the biological extract of the rigidaeen shell Nitaf10. The content of the prolongation of rice germs is gradually reduced, and the amount of rice germin I and J in the transformant product is ...
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