Low-temperature culture medium for pichia pastoris
A culture medium and low-temperature technology, applied in the direction of microorganism-based methods, fungi, microorganisms, etc., to achieve the effect of increasing the overall yield, reducing the cost of industrial production, and reducing the difficulty of downstream purification treatment
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Embodiment 1
[0056] The preparation of embodiment 1 culture medium
[0057] In the following examples of the present invention, the culture medium used, by the total volume of the culture medium, the culture medium is composed of the following components:
[0058] Low temperature type modified medium:
[0059]
[0060] Low temperature type improved 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 respectively named as improved I, improved II and improved 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 to the final volume; after the prepared medium is sterilized at high temperature, add PTM1 solution to detect pH, adjusted to the requ...
Embodiment 228~32
[0066] Example 2 BSM+PTM at 28-32°C 1 Medium Fermentation Test
[0067] Adopt BSM medium as fermentation medium, carry out the cultivation and expression of recombinant insulin analogue precursor Pichia pastoris engineered bacterium in 1.5T fermentation scale, comprise the following steps:
[0068] Step 1: Take recombinant insulin analog precursor recombinant Pichia pastoris engineered bacteria, add 1000 μl of working strains to a 500ml Erlenmeyer flask containing 100ml YPG medium, and culture at 28-32°C and 220rpm / min for 52h; Add 750 μl of cultured bacterial solution for 52 hours to a 500-ml Erlenmeyer flask containing 150 ml of YPG medium, and culture at 28-32° C. with shaking at 220 rpm / min for 16 hours to obtain 6 L of secondary seed solution.
[0069] Step 2, prepare 54L fermentation medium (containing 60L medium component amount), add 6L secondary seed liquid in the above-mentioned fermentation medium by 10% inoculum size, carry out tertiary seed culture, control tempe...
Embodiment 2
[0075] In embodiment 2, the thalline wet weight growth situation in the BSM medium sees figure 1 , 108h recombinant protein detection chart see figure 2 , Induced to 108h bacterial wet weight and recombinant protein expression and heterogeneous impurity proportion results are shown in Table 2.
[0076] Table 2
[0077] Fermentation medium Cell wet weight recombinant protein expression Uneven ratio of N-terminal or C-terminal segments BSM 525g / L 5.06g / L 17.677%
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