Streptomyces diastochromogenes, fermentation product and application thereof
A technology of Streptomyces chromogenes and amylase, applied in the field of microorganisms, can solve problems such as complex pest control, neglect of natural regulation, and environmental impact, and achieve good control effects, environmental friendliness, and low cost
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Embodiment 1
[0049] Example 1 , fermentation of strain 11339
[0050] Seed medium: glucose 2%, starch 5%, peanut cake powder 2%, soybean cake powder 1%, peptone 0.1%, yeast extract 0.4%, sodium chloride 0.2%, magnesium sulfate 0.5%, ammonium nitrate 0.2%, phosphoric acid Dipotassium hydrogen 0.05%, pH 7.2.
[0051] Fermentation medium: same as seed medium.
[0052] The seed medium was prepared according to the above formula, and then the bacterial strain 11399 growing on the Gaussian slant was inoculated in the prepared medium, and cultured at 28°C for 36-40 hours to obtain the seed liquid.
[0053] The seed liquid obtained above is taken, inoculated into the fermentation culture liquid composed of the above-mentioned culture medium at a ratio of 5-20%, and cultured with aeration and stirring at 28° C. for 90-96 hours to obtain a fermentation liquid.
Embodiment 2
[0054] Example 2 , Extraction of active ingredients
[0055] Get 10 kilograms of fermented culture liquid that embodiment 1 obtains, filter, obtain 8 kilograms of supernatants, process with membrane filtration after acidifying to PH4~5 with hydrochloric acid, obtain 10 kilograms of feed liquids, then use 1 kilogram of macroporous adsorption resin 1300 type Carry out adsorption, carry out eluting with 3 kilograms of ethanol water (alcohol: water=1: 1) (volume ratio), eluate is concentrated under reduced pressure, obtains 45 gram brown solids I, then with 400ml methanol water (methanol: water= 90:10) (volume ratio) was dissolved and left overnight in the refrigerator to obtain 10 g of white solid II.
Embodiment 3
[0056] Example 3 , The structure of the active ingredient is determined
[0057] 3.1. Determination of UV absorption spectrum
[0058] 0.5 mg of compound II obtained in Example 2 was dissolved in 50 ml of methanol, 3 ml was added to a colorimetric tank, and methanol was used as a blank control, and measured on an ultraviolet full-wavelength scanner (UV-2501PC, Shimadzu Corporation, Japan), Measure wavelength from 400nm to 200nm, obtain the ultraviolet absorption spectrum of this compound ( figure 2 ).
[0059] Depend on figure 2 It can be seen from the ultraviolet absorption spectrum that the compound II has absorption at the end.
[0060] 3.2. Determination of H NMR spectrum
[0061] Take 10 mg of compound II obtained in Example 2, dissolve it in 0.5 ml of deuterated chloroform, take tetramethylsilane TMS as the reference substance for measuring the chemical shift, and scan it on a VARIAN 500 MHz nuclear magnetic resonance instrument (VARIAN COMPANY) to obtain the com...
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