Yeast engineering bacterium of high productive glycerin
A yeast engineering, yeast technology, applied in the fields of fermentation and biology, can solve the problem of unsatisfactory glycerol yield
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Embodiment 1
[0055] Cloning of 3-phosphate glycerol dehydrogenase gene from Dunaliella salina
[0056] 1. Collection of Dunaliella salina
[0057] Dunaliella salina (Dunaliella salina) was purchased from the algae bank of Wuhan Institute of Hydrobiology.
[0058] 2. Poly A + RNA isolation (Poly A + RNA isolation)
[0059] Total RNA of Dunaliella salina was extracted with Trizol reagent (Gibco, NY, USA). The quality of total RNA was identified by formaldehyde denaturing gel electrophoresis. Dunaliella salina mRNA was extracted using the kit instructions provided by Oligotex mRNA Kits (Qiagen).
[0060] 3. Construction of Dunaliella salina cDNA library (Cloning of Full-length cDNA)
[0061] The cDNA phage library of Dunaliella salina was constructed using the kit instructions provided by the Smart cDNA Library Construction Kit (Clon Tech) with λTriplEX2 as the vector.
[0062] 4. Cloning of Full-length cDNA
[0063] By comparing the 3-phosphate glycerol dehydrogenases of a large numb...
Embodiment 2
[0129] Isolation of Pichia powder pastoris strains
[0130]From the molasses of Leshan Qianwei Sugar Factory, the hypertonic medium was used as the selective medium (60% glucose YPD medium), and the hypertonic yeast was isolated, which was confirmed as powdery Pichia pastoris through microbial identification, and could be produced in 70% It grows in the above concentrations of glucose medium and has the ability to produce glycerol.
Embodiment 3
[0132] Construction of Powdery Pichia Genetic Engineering Strain Kaiya-0917
[0133] (1) Competent preparation of powdered Pichia pastoris
[0134] a. Use a sterile toothpick to pick a single colony of Pichia pastoris powder (Example 1) from the YEPD plate and place it in 2 mL of liquid YEPD medium, culture at 28° C. with shaking at 200 rpm overnight.
[0135] b. The next day, transfer to 200mLYEPD medium at 28°C and shake at 200rpm until OD 600 = Between 1.0 and 1.3.
[0136] c. Transfer the cells to a 50 mL centrifuge tube at 4000 rpm, centrifuge at 4°C for 10 min, and discard the supernatant.
[0137] d. Add an equal volume of deionized water into the centrifuge tube, resuspend the cells, and centrifuge at 4000rpm at 4°C for 10min. Discard the supernatant.
[0138] e. Add half the volume of deionized water into the centrifuge tube, resuspend the cells, and centrifuge at 4000rpm at 4°C for 10min. Discard the supernatant.
[0139] f. Add half volume of 1M sorbitol into ...
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