Yeast for synthesizing 3-indole butyric acid and its application for preparing 3-indole butyric acid
A technology of indole butyric acid and yeast, applied in the direction of fermentation, fungi, microorganism-based methods, etc., to achieve the effect of solving complex process, mild conditions and environmental friendliness
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Embodiment 1
[0012] Saccharomyces sp. of the present invention, detailed separation and screening steps are as follows:
[0013] (1) Sample collection: Take the rhizosphere soil of plants with well-developed root system.
[0014] (2) Isolation of bacterial strains: Weigh 10g of the above soil sample and place it in a 250ml sterilized Erlenmeyer flask filled with 100ml of sterile water, place it in a shaker at 28°C for half an hour to obtain a suspension, and then gradually dilute the suspension with sterile water. diluted to 10 -3 , 10 -4 , 10 -5 The three dilutions are ready for use. Take 0.1ml of the above-mentioned diluted suspension and spread it on the solid PDA medium plate, spread 3 plates for each dilution, and culture it in a 28°C incubator for one week. After the grown strains are purified Do follow-up tests. The formula of the solid PDA medium is as follows: 200 grams of potatoes, 20 grams of glucose, 15-20 grams / liter of agar, 1000 milliliters of tap water, and natural pH. ...
Embodiment 2
[0021] The application of continuous culture of yeast with the function of synthesizing IBA to the synthesis of IBA.
[0022] (1) Inoculate a loop of yeast LY1 into 50 ml of liquid PDA medium from a slant storage tube, place it in a shaker at 28°C, shake at 150 rpm until the exponential phase, and use it as the primary seed liquid; the formula of the liquid PDA medium is as follows: Potato 200 grams, 20 grams of glucose, 1000 ml of tap water, natural pH,
[0023] (2) Take the seed solution obtained in step (1), inoculate it into the liquid PDA medium in a 20L fermenter with an inoculum volume of 5%, and culture it with aeration at 28°C until the exponential phase, as the secondary seed solution,
[0024] (3) Inoculate the secondary seed liquid into the YPDA medium of a 200L fermenter, cultivate to the stationary phase, and add 3-indoleacetic acid solution with a concentration of 0.8% by weight (3-indoleacetic acid is saturated with bicarbonate Dissolved in sodium solution or ...
Embodiment 3
[0027] The application of inoculating the bacterial strain with the function of synthesizing IBA into the fermented liquid of IAA-producing microorganisms to synthesize IBA.
[0028] (1) Microbial fermentation of IAA: Inoculate the IAA-producing strain Enterobacter LY6 (preservation number CGMCC NO 9539) into the medium (tryptone 0.8%, yeast extract 0.4%, NaCl 0.7%, glucose 2%, fructose 0.7%, L - 0.12% tryptophan, 0.02% sodium pyruvate, 0.01% copper sulfate, 1L water, pH 7.2), sterilized for 15 minutes after fermentation, and the sterilized fermentation broth was used for the synthesis of the yeast with the function of synthesizing IBA IBA.
[0029] (2) Preparation of yeast seed liquid: inoculate a ring of the yeast LY1 into 50 ml of liquid PDA medium from a slant preservation tube, place it in a shaker at 28°C, shake at 150 rpm until the exponential phase, and use it as the primary seed liquid; The primary seed solution was inoculated into the liquid PDA medium in a 20L ferm...
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