A method for high-throughput screening of high-yielding strains of Monascus pigment
A monascus pigment, high-throughput technology, which is applied in the field of high-throughput screening of high-yielding monascus pigments, can solve the problems of cumbersome workload, low color price, and reduced screening effectiveness.
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Embodiment 1
[0043] Embodiment 1ARTP mutagenesis obtains the spore suspension of different lethality
[0044] Transfer Monascus from the slant of the test tube to the PDA plate, wash the Monascus plate with sterile water after cultivation and mature, and obtain a clean spore suspension after filtering with absorbent cotton. Then, wash with sterile deionized water for 2 to 3 times, remove the dissolved pigment, and suspend for future use. Get the prepared spore suspension, count on a hemocytometer to adjust the appropriate concentration (10 7 cells / mL, volume fraction 15% glycerol), 10 μL of spore suspension was evenly spread on the slide for mutagenesis. The mutagenesis conditions were set as follows: ventilation volume 10SLM, power 80W, control time were 0s, 10s, 20s, 30s, 40s, 50s, 60s, respectively, to obtain spore suspensions with different lethality.
[0045] The result is as figure 1 As shown, when the mutagenesis time is 40s, the positive mutation rate is 44.6%, and the lethal ra...
Embodiment 2
[0046] Embodiment 2FDA and PI dyeing agent are to the spore suspension staining after mutagenesis
[0047] After the mutagenesis is over, immerse the slide in 500 μL of PBS buffer with a pH of 7.2, shake for 2 minutes to elute, and adjust the concentration of the spore suspension to 10 by using a snowball counting board. 5 ~10 6 individual / mL. Add FDA dye to a certain volume of spore suspension, adjust the final concentration of FDA dye to 120 μg / mL, and stain at room temperature for 20 minutes; then add PI dye to a final concentration of 7 μg / mL, and stain at 4 °C for 10 minutes. Centrifuge to remove the supernatant, remove excess dye, and resuspend with the same volume of PBS buffer at pH 7.2. Repeat this step 2-3 times.
[0048] Example 3 Flow Cytometry Detection and Sorting
[0049] The unstained spore suspension was used as a negative control, representing the background fluorescence signal of the cells. The sample combined with no mutagenized spore suspension and FD...
Embodiment 4
[0050] Example 4 High-throughput screening of high-yield strains
[0051] Place the sorted orifice plate in a constant temperature incubator at 33.5°C for 5 days. After fermentation, add an equal volume of 70% alcohol to the orifice plate, shake and extract for 30 minutes, and centrifuge to take the supernatant , use a microplate reader to measure the absorbance value OD at 505nm at a suitable concentration, compare the relative level of monascus pigment accumulation, and select 2-3 high-yielding bacteria to inoculate the slant to protect the bacteria.
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