Microbacterium and uses thereof
A microbacteria and application technology, applied in the field of microbacteria and its application, can solve the problems of low activity yield, influence on cultivation scale-up and industrialization, etc., and achieve the effect of increasing the content
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Embodiment 1
[0023] Embodiment 1, Microbacterium arborescens LG2 (CCTCC NO: M 2015083) isolation culture method is as follows:
[0024] 1. Collect wild Salvia miltiorrhiza plants in Zhongjiang, Sichuan, wash the roots and then ultrasonically treat them at 25KHz for 5 minutes;
[0025] 2. Under aseptic conditions, the material obtained in step 1 is rinsed 3 times with sterilized deionized water, and is surface-sterilized with 75% (v / v) alcohol and 3% (m / V) sodium hypochlorite solution respectively, thereby Kill microorganisms on the surface of the test material;
[0026] 3. In a sterile environment, rinse the test material obtained in step 2 with sterile water for 3 times, take 100 μl of the sterile water washing solution from the last rinse, spread it on the nutrient agar medium, and incubate at 30°C for 24 hours Afterwards, sterility verification is performed.
[0027] If no colonies are generated, continue to the subsequent step 4; if colonies are generated, return to step 2 to continu...
Embodiment 2
[0033] Embodiment 2, Microbacterium arborescens LG2 (CCTCC NO: M 2015083) elicitor preparation method, the following steps are carried out in sequence:
[0034] 1. Microbacterium arborescens LG2 (CCTCC NO: M 2015083) was transferred to the slant of nutrient agar and cultured at 30°C for 2 days;
[0035] The slant of nutrient agar is: peptone 10g, beef extract 3g, NaCl 5g, agar 18g and distilled water 1000mL, pH=7.2~7.4.
[0036] 2. Use an inoculation loop to pick up a loop of the slant strain obtained in step 1, inoculate it in a 250ml Erlenmeyer flask containing 50ml of nutrient broth medium, and culture it at 220rpm at 28°C for 72h to obtain the fermentation stock solution of Microbacterium arborescens LG2CCTCC M 2015083;
[0037] The nutrient broth medium is: peptone 10g, beef extract 3g, NaCl 5g and distilled water 1000mL, pH=7.2~7.4.
[0038] The above step 1 and step 2 are all cultured under natural light conditions.
[0039]3. Take the fermentation stock solution obta...
Embodiment 3
[0041] Embodiment 3, Microbacterium arborescens LG2 (CCTCC NO: M 2015083) promotes the accumulation of rosmarinic acid in Salvia miltiorrhiza root:
[0042] 1. Inoculate 0.3 g of the hairy root (mother root) of Salvia miltiorrhiza into a 250 ml Erlenmeyer flask containing 100 ml of 6.7-V medium, and culture it at 25°C and 100 rpm in the dark for 18 days; as a base;
[0043] Experimental group 1: Add 1.5ml of Microbacterium arborescens LG2 (CCTCC NO: M2015083) supernatant elicitor (gained in Example 2, bacterial liquid elicitor) to each bottle of base material, and continue the same conditions (at 25°C, 100rpm avoid light culture) for 6 days; as experimental group 1;
[0044] Experimental group 2: Add 1.5ml of Microbacterium arborescens LG2 (CCTCC NO: M2015083) cell elicitor (obtained in Example 2) to each bottle of base material, and continue to cultivate under the same conditions (25°C, 100rpm dark culture) for 6 days; as experimental group 2;
[0045] Negative control: add...
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