Bacterial strain for producing prodigiosin and method thereof
A technology for the production of prodigiosin and prodigiosin, applied in the direction of microorganism-based methods, biochemical equipment and methods, bacteria, etc., can solve the problems of low overall yield and large difference in prodigiosin synthesis ability, etc. Achieve high production efficiency, simple operation, and good genetic stability
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Embodiment 1
[0032] The preparation of embodiment 1 prodigiosin
[0033] Streak culture of Serratia marcescens strains (CGMCC 4074) on LB solid medium at 25-40°C for constant temperature, and then store at 2-4°C for a short period of time: the composition of the solid medium, In terms of weight and volume percentage, the unit is g / 100ml, including 1.0% peptone, 0.5% yeast powder, 1.0% NaCl, 2.0% agar powder, and a pH value of 6.5.
[0034] Insert the above-mentioned activated single bacterium colony into a 250ml Erlenmeyer flask equipped with a liquid medium, with a liquid volume of 50ml / 250ml shake flask, and cultivate it at a constant temperature at 37°C for 12h, and the rotation speed is 180rpm; the composition of the liquid medium is as follows: In terms of weight and volume percentage, the unit is g / 100ml, in which peptone is 1.0%, yeast powder is 0.5%, NaCl is 1.0%, and the pH value is 6.5.
[0035] Transfer the seed liquid into the sterilized liquid fermentation culture, the inocul...
Embodiment 2
[0039] The Plactet-Burman experiment optimization of embodiment 2 prodigiosin
[0040] According to experience and literature, 9 of the more important factors are selected for Plactet-Burman experiment. The factors and levels in the PLACKETT-BURMAN experiment are shown in Table 2, and the specific experimental design of the Plackett-Burman experiment is shown in Table 3.
[0041] Table 2 Factors and levels involved in the PLACKETT-BURMAN experiment
[0042]
[0043] Table 3 Design of PLACKETT-BURMAN experiment
[0044]
[0045] The seed solution was prepared according to Example 1, and the seed medium was inoculated into the above-mentioned fermentation medium according to the inoculum size of 5%, and incubated at a constant temperature of 28° C. for 48 hours with a rotation speed of 180 rpm. After fermentation, according to embodiment 1, the assay method of red pigment prodigiosin, detect the content of prodigiosin, the experimental data is calculated by Design-Expert...
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