A kind of oleaginous yeast lipid droplet protein and its coding gene and application
A yeast lipid and protein technology, applied in the application, genetic engineering, plant genetic improvement and other directions, can solve the problems of unpublished and unretrieved Rhodosporidium toruloides perilipin sequence information, etc., to improve the stability of lipid droplets, The effect of increasing oil content
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Embodiment 1
[0061] Example 1: Multi-omics study of Rhodosporidium toruloides
[0062] Whole-genome de novo sequencing of Rhodosporidium toruloides (R. toruloides): R. toruloidesATCC10788 was cultured in YEPD medium at a temperature of 30°C, a rotational speed of 200 rpm, and a culture time of 48 hours. Bacteria were collected, and genomic DNA was prepared according to the standard genomic DNA extraction method (refined Molecular Biology Experiment Guide (Fourth Edition), Osper et al., translated by Yan Ziying, etc., published by Science Press), and analyzed by a solexa sequencer. Finally, 94 scaffolds (genome framework) were obtained, and the genome length was 20.2Mb.
[0063]R. toruloides transcriptome sequencing: R. toruloides ATCC10788 was cultured in a 2L fermenter at a temperature of 30°C and a pH of 5.6. Stirring linkage), the YEPD medium flow acceleration rate is 0.828L / h (dilution rate is 0.53) (reactor working volume is 1.7L). After about 10 working volumes, samples were taken,...
Embodiment 2
[0065] Example 2: Discovery of Rhodosporidium toruloides perilipin
[0066] R.toruloidesCGMCC2.1389 was cultured in liquid YEPD medium at 30°C for 36h. The wet cells were collected by centrifugation, washed twice with distilled water, and stored in a -80°C refrigerator for RNA and protein extraction. The same cultured samples (parallel samples) were used to determine the dry cell weight and oil content. Sample named 'YEPD'.
[0067] R.toruloidesCGMCC2.1389 was fermented on nitrogen-limited medium to achieve oil accumulation. Carried out in a FUS-15L bioreactor with a liquid volume of 8L, an inoculum size of 10% (V / V), a temperature of 30°C, a ventilation rate of 0.8vvm, and dissolved oxygen controlled at 40-50% saturation value (dissolved oxygen and stirring linkage ). The pH was automatically controlled at 5.6 by adding 10.0M NaOH and 2M HCl dropwise. Take out 50mL of cell culture fluid cultured for 24h and 96h respectively, and the samples are named '24h' and '96h' resp...
Embodiment 3
[0093] Embodiment 3: Cloning of Rhodosporidium toruloides rldp1 gene
[0094] Gene-specific primers were designed according to the nucleotide sequence of rldp1 as follows:
[0095] rldp1-Fw:5'-atggccaccgtcaacgagaagc-3'
[0096] rldp1-Rv:5'-tcactgcttctccccctcgcc-3'
[0097] The total RNA of R.toruloidesCGMCC2.1389 was extracted by liquid nitrogen grinding plus RNAiso method [YangF, TanHD, ZhouYJ, LinXP, ZhangSF.Mol.Biotechnol.2010, 47(2):144-151]. The RNA was subjected to 1.5% agarose gel electrophoresis, observed and identified using a fluorescence-ultraviolet analyzer, and two clear bands could be seen. Analyze the total RNA sample with a UV / Vis spectrometer and measure the OD 260 / 280 =2.0, indicating good quality of total RNA. Total RNA samples were stored frozen at -80°C for later use.
[0098] cDNA first strand was synthesized using High Fidelity PrimeScript RT-PCRKit (purchased from Takara). 20 μl reaction system, first, add 2 μl total RNA (~1 μg), 100 nM each of...
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