A kind of Pichia pastoris low temperature medium
A culture medium and low-temperature technology, applied in the direction of microorganism-based methods, fungi, microorganisms, etc., to achieve the effect of expanding application conditions, reducing the difficulty of downstream purification treatment, and improving purity
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Embodiment 1
[0056] The preparation of embodiment 1 culture medium
[0057] In the following embodiments of the present invention, the culture medium used, according to the total volume of the culture medium, is composed of the following components:
[0058] Low temperature modified medium:
[0059]
[0060] Low temperature modified medium trace element solution formula:
[0061]
[0062] On the basis of the above-mentioned medium, the medium was prepared according to the formula in Table 1, and three different improved medium were obtained, which were named as Modified I, Modified II and Modified III.
[0063] Table 1
[0064]
[0065] The preparation process is as follows. Dissolve the ingredients in the table with 80% to 90% of the final volume of purified water. After fully stirring, use purified water to make up the volume to the final volume. After the prepared medium is sterilized by high temperature, add PTM1 solution to detect The pH was adjusted to the required pH wit...
Embodiment 228~32
[0066] Example 2 BSM+PTM at 28~32℃ 1 Fermentation test of culture medium
[0067] Adopt BSM substratum as fermentation substratum, in 1.5T fermentation scale, carry out the cultivation and expression of recombinant insulin analog precursor Pichia pastoris engineering bacteria, comprising the following steps:
[0068] Step 1, take the recombinant insulin analog precursor recombinant Pichia pastoris engineering bacteria, add 1000 μl working strains to a 500 ml Erlenmeyer flask containing 100 ml YPG medium, and shake at 28 to 32 ° C and 220 rpm / min for 52 hours; A 500ml conical flask containing 150ml of YPG medium was added with 750μl of bacterial liquid cultured for 52h, and incubated at 28 to 32°C with shaking at 220rpm / min for 16 hours to obtain 6L of secondary seed liquid.
[0069] Step 2, prepare 54L fermentation medium (containing 60L medium composition), add 6L secondary seed liquid to above-mentioned fermentation medium by 10% inoculation amount, carry out tertiary seed ...
Embodiment 2
[0075] In embodiment 2, in the BSM medium, the growth situation of thalline wet weight sees figure 1 , see the 108h recombinant protein detection chart figure 2 , after induction to 108h, the wet weight of bacteria, the expression of recombinant protein and the proportion of heterogeneous impurities are shown in Table 2.
[0076] Table 2
[0077] Fermentation medium Bacteria wet weight Recombinant protein expression Non-uniform proportion of N-terminal or C-terminal segment BSM 525g / L 5.06g / L 17.677%
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