Method for using recombinant candida parapsilosis strain to efficiently prepare (S)-phenyl glycol
A phenylethylene glycol, Candida technology, applied in microorganism-based methods, botanical equipment and methods, biochemical equipment and methods, etc., can solve the problem of unsatisfactory catalytic conversion efficiency of chiral compounds, lack of protein post-modification issues
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Embodiment 1
[0086] Candida parapsilosis ( C. parapsilosis ) CCTCC NO: M203011 (disclosed in the patent number: CN 03102140.2) cell culture, the composition of the growth medium YPD: glucose 2%, yeast extract 1%, peptone 2%. Candida parapsilosis was inoculated in a 5 mL test tube and cultured at 28°C and 200 r / min for 16-18 h with shaking.
Embodiment 2
[0088] Candida parapsilosis ( C. parapsilosis ) Genome extraction: The cells cultured in Example 1 were centrifuged at 12,000 r / min for 5 min, washed twice with saline, and the cells were collected to extract the genome using the Genomic DNA Mini Preparation Kit (Takara Company).
Embodiment 3
[0090] Extraction of target gene from Candida parapsilosis scr II, will scr Restriction site in II Kpn I sequence (GGTACC) synonymous mutation to GGCACA.
[0091] Synthetic primers at both ends
[0092] SCRII_ Sac I_F1: 5’-ttcgg gagct c atgcaccac caccaccacc acggcgaaat cgaatcttat t-3' ( Sac I),
[0093] SCRII_ Kpn I_R1:5'-cgg ggtacc c tatggacaag tgtaaccacc a-3', ( Kpn I),
[0094] Mutation Primer
[0095] Mut_ Kpn I_F2: 5'-atgtcgggca caattgttaa tgt-3',
[0096] Mut_ Kpn I_R2: 5'-acattaacaa ttgtgcccga cat-3',
[0097] contain Kpn I synonymous mutation site scr Acquisition of II genes:
[0098] PCR reaction system: ddH 2 O 24.5 μL, DNA polymerase 0.5 μL, Mut_ Kpn I_F2 primer 5 μL, Mut_ Kpn I_R2 primer 5 μL, 5×buffer 10 μL.
[0099] PCR reaction: thermal denaturation at 98°C for 10 s; 10 s at 98°C, 15 s at 52°C, and 1 min at 72°C. After 5-10 cycles, the PCR reaction solution was taken out, and 1 μL of primers SAT1_1 and URA3t_2 were added...
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