Synergistic application of sugar metabolism and lipid metabolism to enhance the yield of fatty acid derivatives synthesized by Yarrowia lipolytica
A technology of Yarrowia lipolytica, fatty acid derivatives, applied in the field of synthetic biology
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Embodiment 1
[0059] Example 1: Construction of different alcohologenic lipolytic yeast strains, and use of transcriptome comparison to determine the main response pathways
[0060] Experimental Materials:
[0061] 1. Gene
[0062] 1) FAR: fatty acyl-CoA reductase, derived from Marinobacter aquaeolei VT8, codon optimized according to Yarrowia lipolytica, the optimized DNA encoding FAR has the nucleotides shown in SEQ ID No.1 Acid sequences were synthesized at GenScript Company.
[0063] 2. Gene expression vector information
[0064] The integration plasmid PUC57-IntF-HUM was synthesized from GenScript Company.
[0065] The integrated plasmid PUC57-RS8d-HUM was synthesized from GenScript Company.
[0066] 3. Reagents required for genetic manipulation
[0067] 1) Frozen EZ Yeast Transformation Kit II (Zymo Research Corporation) was purchased from Beijing Tianmo Technology Development Co., Ltd.;
[0068] 2) KOD FX DNA polymerase and dNTP (2.0mM each) were purchased from Toyobo Shanghai C...
Embodiment 2
[0118] Example 2: Using glycolytic promoters to synergistically enhance alcohol production in lipolytic yeast
[0119] Experimental Materials:
[0120] 1. Strain information: See Table 4 for the plasmid information used in this example, and Table 5 for the strain name, genotype information, and source.
[0121] 2. Other genetic information, reagents and culture medium are the same as in Example 1.
[0122] experimental method:
[0123] 1. Construction of recombinant plasmids related to glycolysis promoters
[0124] Use the primers shown in Table 5 to amplify the sequences of various glycolysis-related promoters using the genome of lipolytica ATCC201249 as a template, and perform amplification with the FAR fragment and the vector PUC57-K8Zero-HUM using BsaI, BsmbI or BbsI and T4 ligase respectively. The GoldenGate gene was assembled to obtain the recombinant plasmids PUC57-P1-K8Zero-FAR~PUC57-P11-K8Zero-FAR, and then digested with NotI and recovered the recombinant fragments...
Embodiment 3
[0162] Example 3: Increasing the carbon source concentration of the medium to further "push" the synergistic strains to produce alcohol
[0163] Experimental Materials:
[0164] The strain information, reagents, etc. are the same as those in Examples 1 and 2.
[0165]In addition to the YPD medium involved in Example 1 (in order to facilitate the distinction, the medium in Example 1 is marked as YPDx1 here), a glucose-doubled YPDx2 medium was also configured. The main components of YPDx2 medium are as follows: image 3 As shown in A.
[0166] experimental method:
[0167] 1. First, the JLFL-13 strain was image 3 A Each medium is fermented, and the optimal N source ratio of YPDx2 medium is determined.
[0168] 2. Comparatively ferment JLFL-1, JLFL-2 and JLFL-13 in the optimized YPDx2 and YPDx1 medium respectively, and the process is the same as in Example 1.
[0169] 3. the extraction of product, method process is with embodiment 1.
[0170] 4. The detection of product, ...
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