Method for enhancing production of alpha-linolenic acid from rhodosporidium toruloides
A technology of Rhodosporidium toruloides and linolenic acid, which is applied in the field of strengthening the production of α-linolenic acid by Rhodosporidium toruloides, can solve the problems of low production of α-linolenic acid, achieve easy process control, increase utilization value, and simple operation Effect
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Embodiment 1
[0037] Rhodosporidium toruloides ACCC20341 was used as the fermentation strain.
[0038] Rhodosporidium toruloides strain R.toruloides was activated from the slant preservation medium, and the composition of the slant preservation medium was YEPD: glucose 20g / L, yeast powder 10g / L, peptone 10g / L, agar powder 15g / L, pH5.8~ 6.0, sterilized by saturated steam at 115°C for 20min. The Rhodosporidium toruloides strain preserved above was activated using YEPD medium, cultured in a 500mL Erlenmeyer flask with a liquid volume of 200mL, 30°C, 200rpm for 48h to OD 600 =12.
[0039] Then the yeast cells were centrifuged to collect the thallus, and inoculated into a 10L fermenter for fed-batch fermentation culture, with a liquid volume of 6L. The ingredients of fed-batch fermentation medium are: glucose 20g / L, xylose 30g / L, sodium glutamate 6.2g / L, inorganic salt KH 2 PO 4 :0.52%, K 2 HPO 4 :0.16%, MgCl 2 :0.48%. During the fermentation process, by feeding a mixed carbon source aqu...
Embodiment 2
[0041] The strain Rhodosporidium toruloides R. toruloides M18, which can grow and metabolize in non-detoxified cellulose hydrolyzate obtained by mutagenesis of Rhodosporidium toruloides ACCC20341 at normal temperature and pressure (Atmospheric and room temperature plasma) (references: FengQi, Yuki Kitahara, Zitian Wang, Xuebing Zhao, WeiDu, Dehua Li. Novel mutant strains of Rhodosporidium toruloides by plasmamutagenesis approach and their tolerance for inhibitors in lignocellulosic hydrolyzate. Journal of Chemical Technology and Biotechnology. 2014, 89(5): 735–742).
[0042] Use YEPD medium to activate the above-mentioned mutagenic R.toruloidesM18, culture in a 500mL Erlenmeyer flask with a liquid volume of 200mL, culture at 30°C, 200rpm for 48h to OD 600 =12. Then the yeast cells were centrifuged to collect the thallus, and inoculated into a 10L fermenter for fed-batch fermentation culture, with a liquid volume of 6L.
[0043] Use cellulose hydrolyzate as the main component ...
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