Method for producing beta-amyrin with saccharomyces cerevisiae engineering bacterium
A technology of Saccharomyces cerevisiae and arysinol, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., which can solve the problems of low accumulation of β- arysinol and difficult synthesis by chemical methods, and achieve easy genetic manipulation , simplification of fermentation process, and efficient effect of gene assembly process
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Embodiment 1
[0016] Embodiment 1: Construction of Saccharomyces cerevisiae Genetic Engineering Bacteria
[0017] 1. The 2,3-oxidized squalene monooxygenase SQE gene fragment was cloned from Candida albicans CGMCC2.2086, which was consistent with the gene sequence of Candida albicans 2,3-oxidized squalene monooxygenase published by Genbank (Genbank registration sequence number AB037203) was compared by BLAST, and the homology analysis showed that the homology of the cloned SQE gene fragment and the Candida albicans 2,3-oxosqualene monooxygenase gene published in the Genbank gene bank was 100%.
[0018] The primer sequences are:
[0019] Primer 1: 5'> GATTAGCATCCATAACCGCATACTCTAATTGACGATAAC ATGAGTTCAGTTAAGTATGA<3' (as shown in SEQ ID No.1), the underlined sequence is the overlapping sequence with the promoter TYS1p.
[0020] Primer 2: 5'> GCCAAGTAGGCAATTTTTAGTACTGTCAGTATTGTTAT CTATCTTACAATCTCGTTCC<3' (as shown in SEQ ID No.2), the underlined sequence is the overlapping sequence with the...
Embodiment 2
[0049] Example 2: Verification of Saccharomyces cerevisiae Engineering Bacteria Fermentative Production of β-Arysinol
[0050] Select the Saccharomyces cerevisiae engineered bacterium screened out in Example 1, culture in shake flasks at 30°C in a medium containing 2% glucose, 2% peptone and 1% yeast powder, centrifuge at 5000rpm for 5min after 5 days, and use 10mL of 20% hydrogen for precipitation Resuspend in potassium oxide solution (containing 50% ethanol), boil in boiling water for 10 min, extract twice with n-hexane after cooling at room temperature, combine the extracts and concentrate to 1 mL, then add 100 μL pyridine and 50 μL N,O to the concentrated solution -Bis(trimethylsilyl)trifluoroacetamide, react at 37°C for 2h. Shimadzu Gas Chromatography-Mass Spectrometry GCMS-QP2010 equipped with Agilent Chromatographic Column DB-1 (30m*0.25mm*0.25um) was used to analyze the fermentation of Saccharomyces cerevisiae engineering bacteria to produce β-amyresinol. For component...
Embodiment 3
[0051] Example 3: Application of Saccharomyces cerevisiae Engineering Bacteria in the Fermentative Production of β-Arysinol
[0052] Seed liquid culture: Pick a single colony of Saccharomyces cerevisiae engineering bacteria screened in Examples 1 and 2 from the plate, inoculate in 40mL medium containing 2% glucose, 2% peptone and 1% yeast powder, 30°C, 170rpm Shake culture for 36h.
[0053] Fermentation test: transfer the inoculum solution to a 300mL shake flask containing 100mL fermentation medium (2% glucose, 2% peptone, 1% yeast powder, pH7.0) according to the inoculum size with an initial absorbance value of 0.10, at 30°C, 170rpm Shake culture for 120 hours, sample once every 24 hours, and measure the content of β-amyresinol in Saccharomyces cerevisiae cells. The results showed that the content of β-amyresinol reached 11.7 mg / L after fermentation of S. cerevisiae engineered bacteria.
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