Trosine phenol lyase engineering bacteria as well as construction method thereof and application thereof
A tyrosine phenol and construction method technology, applied in the field of genetic engineering, can solve the problems of low L-DOPA yield, difficult to control reaction conditions, many by-products, etc., and achieve high yield, low cost, and less discharge of three wastes. Effect
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Embodiment 1
[0030] 1. Prepare BL21 (DE3) as competent cells
[0031] Use the TAKARA Competent Cell Preparation Kit and operate according to the instructions to prepare BL21 (DE3) competent cells.
[0032] 2. Whole gene synthesis of tyrosine phenol lyase gene fragment
[0033] According to the sequence provided by Gene ID: X66978.1, the whole gene fragment of tyrosine phenol lyase was synthesized.
[0034] 3. Construction of tyrosinase expression plasmid pFPL
[0035] The whole gene fragment of tyrosinase was subcloned into pET24a plasmid, restriction sites BamHI, XhoI.
[0036] 4. The expression plasmid pFPL is introduced into competent cells
[0037] 1) Immediately insert the competent state into an ice-water bath for 3 minutes after taking it out from -70°C;
[0038] 2) Add 1 microliter of plasmid pFPL to the competent state in the ultra-clean bench, flick and mix well, immediately insert into the ice water bath for 25 minutes, and let stand;
[0039] 3) Gently transfer the compete...
Embodiment 2
[0043] 1. Prepare BL21 (DE3) as competent cells
[0044] Use the TAKARA Competent Cell Preparation Kit and operate according to the instructions to prepare BL21 (DE3) competent cells.
[0045] 2. Whole gene synthesis of tyrosine phenol lyase gene fragment
[0046] According to the sequence provided by Gene ID: X66978.1, the whole gene fragment of tyrosine phenol lyase was synthesized.
[0047] 3. Construction of tyrosinase expression plasmid pFPL
[0048] The whole gene fragment of tyrosinase was subcloned into pET24a plasmid, and restriction sites BamHI and XhoI were cut.
[0049] 4. The expression plasmid pFPL is introduced into competent cells
[0050]6) Immediately insert the competent state into an ice-water bath for 3 minutes after taking it out from -70°C;
[0051] 7) Add 1 microliter of plasmid pFPL to the competent state in the ultra-clean bench, flick and mix well, immediately insert into the ice water bath for 25 minutes, and let stand;
[0052] 8) Gently trans...
Embodiment 3
[0064] The difference from Example 2 is that pKJE7 is selected as the chaperonin expression plasmid.
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