Bacterial strain with antiviral activity and application thereof
An antiviral activity, strain technology, applied in the application, disinfectant, fungi and other directions, can solve the problems of difficult artificial synthesis, many chiral carbons, high synthesis cost, etc., and achieves suitable promotion and application, good compatibility, and production And the effect of simple extraction process
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Embodiment 1
[0016] Embodiment 1: A kind of isolating and purifying antiviral active substance malformin A from Aspergillus tubingensis FJBJ11 fermented liquid 1 Methods
[0017] (1) Inoculate the pure strain of Aspergillus tubingensis FJBJll on the PDA plate medium and culture at 28°C for 3 days; (2) Use a sterilized puncher to punch out 5 pieces of bacteria with a diameter of 4 mm on the edge of the colony of the medium Put the fungus cake in a 250 mL Erlenmeyer flask filled with 100 mL of PDB medium, shake it at 28 °C and 120 r / min for 4 days as the seed liquid; (3) inoculate the seed liquid with 5 % The amount of access consists of 10 g of peptone, 30 g of glucose, and 15 g of yeast powder , CaC1 2 1.5 g and 1000 mL of distilled water in a liquid medium, cultured on a shaker at 28 °C and 120 r / min for 10 days. (4) 50L of the filtrate after the fermentation broth was filtered was adsorbed by D101 macroporous resin column chromatography, first eluted with 4 column volumes of water,...
Embodiment 2
[0020] Embodiment 2: teratin A 1 One of the antiviral activity assays
[0021] (1) Test method (half-leaf dead spot method) Select healthy and uniformly grown heart leaf tobacco at the 6-8 leaf stage, sprinkle a small amount of 500-mesh quartz sand evenly on the leaves to be inoculated, and inoculate the left half leaf with teratin A 1 Mixed solution with virus (final concentration of virus is 10 μg / mL), the right half leaf is inoculated with virus solution prepared with distilled water (final concentration of virus is 10 μg / mL) as a control, rinse the inoculated leaves with distilled water 10 minutes after inoculation . Inoculate 4 leaves for each treatment, repeat 3 times, count the number of dead spots after 3 days, and calculate the inhibition rate according to the following formula.
[0022] Inhibition rate (%)=[(control number of dead spots - treatment number of dead spots) / control number of dead spots]×100%
[0023] (2) Test results The half-leaf blotch method was us...
Embodiment 3
[0026] Embodiment 3: teratin A 1 Antiviral Activity Determination Test 2
[0027] (1) Test method (leaf disk method) Select healthy common tobacco K 326 8 hours after inoculation with TMV, a disk with a diameter of about 15 mm was taken from the inoculated leaf avoiding the veins with a puncher, and floated in a certain concentration of teratin A dissolved in a small amount of DMSO (final concentration: 1%). 1 In the aqueous solution, the leaf discs inoculated with the virus and the healthy tobacco leaf discs not inoculated with the virus were respectively set as positive controls and negative controls floating in distilled water containing 1% DMSO. The leaf disc inoculated with the virus in the middle was used as the standard drug control, and 3 leaf discs were treated for each treatment. After 48 hours of treatment, the leaf discs were weighed, coated with 1:20 (W / V) carbonate buffer, and ground. The OD of each assay well was measured by indirect ELISA method 405 value. ...
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