Tyrosol-producing recombinant <i>Escherichia coli </i>and construction method and application thereof

Abstract

The disclosure relates to a tyrosol-producing recombinant Escherichia coli and a construction method and application thereof and belongs to the technical field of bioengineering. The Escherichia coli undergoes heterologous expression of a codon-optimized Saccharomyces cerevisiae pyruvate decarboxylase gene ARO10*. According to the recombinant Escherichia coli, five sites of a lacI site, a trpE site, a pabB site, a pabA site and a pykF site of an Escherichia coli genome are deleted, and at the same time, the ARO10* gene is integrated at each site of the five sites to obtain a strain containing multiple copies of the ARO10* gene. On the basis of the above recombinant strain, the ARO10* gene is randomly integrated at multiple sites, and it is found that a strain with high-yield production of tyrosol can be obtained by inserting the ARO10* gene at a yccX site. Fermentation using this strain does not require inducers or antibiotics. After fermentation is carried out for 48 hours, the yield of tyrosol can reach 32.3 mM.

Claims

1. A recombinant Escherichia coli obtained by (i) introducing deletions in E. coli MG1655 at a lacI gene, a trpE gene, a pabB gene, a pabA gene, and a pykF gene, and (ii) integrating a Saccharomyces cerevisiae pyruvate decarboxylase ARO10* gene that comprises SEQ ID NO:1 in each of the lacI gene, trpE gene, pabB gene, pabA gene, and pykF gene having said deletions.

2. The recombinant Escherichia coli according to claim 1, wherein a yccX gene in said recombinant Escherichia coli is also deleted, and at the same time a Saccharomyces cerevisiae pyruvate decarboxylase ARO10* gene that comprises SEQ ID NO:1 is integrated in the yccX gene having said deletion.

3. The recombinant Escherichia coli according to claim 2, wherein deletion or gene integration is carried out by using CRISPR-Cas9 technology or Red homologous recombination.

4. A method for producing a tyrosol, wherein said method comprises fermenting the recombinant Escherichia coli according to claim 1.

5. The method according to claim 4, wherein an M9Y culture medium is used as a fermentation culture medium.

6. The method according to claim 4, wherein prior to fermenting, the method comprises (a) culturing the recombinant Escherichia coli on an LB plate, (b) selecting a single colony from said LB plate, (c) inoculating an LB liquid culture medium with said single colony, and (d) culturing said single colony for 8-10 hours to produce a seed solution.

7. The method according to claim 6, wherein said method further comprises inoculating an LB liquid solution with the seed solution at an inoculation volume percentage of 1%-5%, culturing said inoculated LB liquid solution in a shaker at 200-220 rpm for 8-12 hours at 35° C.-39° C., collecting all cells after culturing, removing the culture medium from the cells, cleaning the cells after removing the cell culture medium, transferring the clean cells into an M9Y medium, and culturing the cells in the M9Y medium in a shaker at 200-220 rpm for 40-60 hours at 28° C.-30° C.

8. The method according to claim 6, wherein said method further comprises inoculating an LB liquid solution with the seed solution at an inoculation volume percentage of 1%-5% to obtain an initial OD.sub.600 of 0.05-0.06, culturing said inoculated LB liquid solution in a shaker at 200-220 rpm at 35° C.-39° C. until the OD.sub.600 reaches 0.25-0.30 to obtain a fermentation seed solution, inoculating a fermenter that comprises a M9Y medium with the fermentation seed solution, and fermenting for 40-60 hours.

9. The method according to claim 8, wherein the M9Y medium comprises 17.1 g/L Na.sub.2HPO.sub.4.12H.sub.2O, 3 g/L KH.sub.2PO.sub.4, 0.5 g/L NaCl, 1 g/L NH.sub.4Cl, 20 g/L glucose, 0.25 g/L yeast powder and 5 mM MgSO.sub.4, wherein MgSO.sub.4 is added after sterilization.

10. The method according to claim 4, wherein the tyrosol produced is used to prepare food or medicine.

11. A method for constructing a recombinant Escherichia coli, wherein said method comprises (i) introducing deletions in an E. coli MG1655 cell at a lacI gene, a trpE gene, a pabB gene, a pabA gene, and a pykF gene, and (ii) integrating a Saccharomyces cerevisiae pyruvate decarboxylase ARO10* gene that comprises SEQ ID NO:1 in each of the lacI gene, trpE gene, pabB gene, pabA gene, and pykF gene having said deletions.

12. The method according to claim 11, wherein said method further comprises introducing a deletion in said E. coli MG1655 cell at a yccX gene, and at the same time integrating a Saccharomyces cerevisiae pyruvate decarboxylase ARO10* gene that comprises SEQ ID NO:1 in the yccX gene having said deletion.

13. The method according to claim 11, wherein deletion or gene integration is carried out by using CRISPR-Cas9 technology or Red homologous recombination.

Description

BRIEF DESCRIPTION OF FIGURES

(1) FIG. 1: The yield result of fermented tyrosol of 9 strains (YMGRA; YMGEA, YMGR2A; YMGB2A, YMGR3A; YMGA3A, YMGR4A; YMGF4A, YMGR5A) constructed in the disclosure.

(2) FIG. 2: The yield result of fermented tyrosol of YMGR5A constructed in the disclosure in a fermenter.

(3) FIG. 3: The yield result of fermented tyrosol of YMGR6A constructed in the disclosure in a fermenter.

DETAILED DESCRIPTION

(4) I. High Performance Liquid Chromatography (HPLC) is Used for Detecting the Yield of Tyrosol

(5) Specific chromatographic detection conditions are as follows: An Agela Innoval C18 chromatographic column (4.6*250 mm, pore size 5 μm); a mobile phase comprising 0.1% formic acid (80%) and methanol (20%); flow rate: 1 mL.Math.min.sup.−1; sample injection volume: 10 μL; a UV detector, detection wavelength: 276 nm; and column temperature: 30° C.

(6) II. Culture Mediums

(7) An M9Y culture medium: 17.1 g/L Na.sub.2HPO.sub.4.12H.sub.2O, 3 g/L KH.sub.2PO.sub.4, 0.5 g/L NaCl, 1 g/L NH.sub.4Cl, 20 g/L glucose and 0.25 g/L yeast powder; and MgSO.sub.4 is added at a final concentration of 5 mM after sterilization.

(8) An LB culture medium: 10 g/L tryptone, 5 g/L yeast extract, and 10 g/L NaCl.

Example 1 Heterologous Expression of a Saccharomyces cerevisiae Pyruvate Decarboxylase Gene in Escherichia coli MG1655 to Produce Tyrosol

(9) I. Construction of a Plasmid pKK223-3-ARO10*

(10) A codon-optimized ARO10* gene sequence is chemically synthesized by Suzhou Hongxun Biotechnologies CO., LTD. The synthesized gene sequence is inserted into the EcoR I and Hind III sites of a plasmid pKK223-3 to obtain a recombinant plasmid pKK223-3-ARO10*.

(11) II. Construction of a lacI::ARO10* Deletion Expression Cassette

(12) The plasmid pKK223-3 is used as a template, designed primers ARO10-L and LacIR (Table 1) are used for amplification to obtain an expression fragment of tac-ARO10*-rrnB with a promoter and a terminator, and the expression fragment is inserted into a pMD19-T simple plasmid to obtain a recombinant plasmid 19Ts-tac-ARO10*-rrnB. Primers LacIL and PKDR are designed, and pKD13 is used as a template for amplification to obtain a Kana resistant fragment. The plasmid 19Ts-tac-ARO10*-rrnB and the Kana resistant fragment are subjected to enzyme digestion and ligation with Xho I to obtain a recombinant plasmid 19Ts-Kana-tac-ARO10*-rrnB. The constructed plasmid 19Ts-Kana-tac-ARO10*-rrnB is used as a template, and lacIL and lacIR are used as primers for PCR amplification to obtain a lacI::ARO10* deletion expression cassette.

(13) TABLE-US-00001 TABLE 1 Primers Primer name Sequence (5′-3′) Sequence ARO10-L GGCTCGAGATGGCTGTGCAGGTCGTAAAT SEQ ID NO: 2 IacIR GGGGTACCGTGAAACCAGTAACGTTATACGATG SEQ ID NO: 3 TCGCAGAGTTCA TCACTGCCCGCTTTCCAGTCGGGAAACCTGTCG TGCCAGCTGCATTAATGAATCGGCCAACGCGCG GGGAGAAGAGTTTGTAGAAACGC LacIL CCCTCGAGGTGAAACCAGTAACGTTATACGATG SEQ ID NO: 4 TCGCAGAGTATGCCGGTGTCTCTTATCAGACCG TTTGTGTAGGCTGGAGCTGCTTC PKDR CCCTCGAGattccggggatccgtcgacc SEQ ID NO: 5 YLACIL GAAGCGGCATGCATTTACGT SEQ ID NO: 6 YLACIR ACAACATACGAGCCGGAAGC SEQ ID NO: 7 pTarget-R CGGACTAGTATTATACCTAGGACTGAGC SEQ ID NO: 8 sg-trpE CGGACTAGTCCTGTTCTCTTATGACCTTGGTTTT SEQ ID NO: 9 AGAGCTAGAAATAGC sg-trpE-test CCTGTTCTCTTATGACCTTG SEQ ID NO: 10 700trpE-U-L gagtcggtgctttttttgaattctctagaCCAGGT SEQ ID NO: 11 ATTTGCGCTTTTTCAAGTC 700trpE-U-R ATTTACGACCTGCACAGCCA SEQ ID NO: 12 TCGGGCTGGGTATCTGATTGCTT trpE-ARO10-L AAGCAATCAGATACCCAGCCCGatggctgtgcaggt SEQ ID NO: 13 cgtaaat trpE-ARO10-R GAATGTCAGCCATCAGAAAGTCTCCGTTTGTAG SEQ ID NO: 14 AAACGCAAAAAGGC 700trpE-D-L gcctttttgcgtttctacaaacGGAGACTTTCTG SEQ ID NO: 15 ATGGCTGACATTC 700trpE-D-R GGTAATAGATCTAAGCTTCTGCAGGTCGACGCT SEQ ID NO: 16 GAAAACAGCTGGTGGCT TTC 500trpE-U-L CCAGACCGTGGAAATTTCCACG SEQ ID NO: 17 500trpE-D-R GAGAATGGATTCCGGATGGAACTGG SEQ ID NO: 18 ΔtrpE-U-R GAATGTCAGCCATCAGAAAGTCTCCCGGGCTG SEQ ID NO: 19 GGTATCTGATTGCTT ΔtrpE-D-L AAGCAATCAGATACCCAGCCCGGGAGACTTTCT SEQ ID NO: 20 GATGGCTGACATTC sg-pabB GTCCTAGGTATAATACTAGTTAACCGGGGCTC SEQ ID NO: 21 CGAAAGTAGITTIAGAGCTAGAAATAGC sg-pabB-test TAACCGGGGCTCCGAAAGTA SEQ ID NO: 22 700pabB-U-L gagtcggtgctttttttgaattctctagaCCCTG SEQ ID NO: 23 GATTTCATTGGTGCC 700pabB-U-R ATTTACGACCTGCACAGCCATCAGTCCTGACTCT SEQ ID NO: 24 ACTGGCTATGTG pabB-ARO10-L CACATAGCCAGTAGAGTCAGGACTGatggctgt SEQ ID NO: 25 gcaggtcgtaaat pabB-ARO10-R AGGCTACGGTATTCCACGTCGTTTGTAGAAACG SEQ ID NO: 26 CAAAAAGGC 700pabB-D-L gcctttttgcgtttctacaaacGACGTGGAATACC SEQ ID NO: 27 GCTAGCT 700pabB-D-R GGTAATAGATCTAAGCTTCTGCAGGTCGACCAC SEQ ID NO: 28 GAATTATGCCTGCGGTC 500pabB-U-L GCCTGCTGTAATAGATAAAGCC SEQ ID NO: 29 500pabB-D-R GGCGACTGGC TTAACTATTCAC SEQ ID NO: 30 ΔpabB-U-R CAGGCTACGGTATTCCACGTCCAGTCCTGACTCT SEQ ID NO: 31 ACTGGCTATG ΔpabB-D-L CATAGCCAGTAGAGTCAGGACTGGACGTGGAA SEQ ID NO: 32 TACCGTAGCCTG sg-pabA GTCCTAGGTATAATACTAGTACGTTATTCGCCACT SEQ ID NO: 33 ATGCCGTTTTAGAGCTAGAAATAGC sg-pabA-test ACGTTATTCGCCACTATGCC SEQ ID NO: 34 700pabA-U-L gagtcggtgctttttttgaattctctagaGCCTTT SEQ ID NO: 35 AGTCACTCTTACTGCCGC 700pabA-U-R ATTTACGACCTGCACAGCCATGGCGGCTCCGGT SEQ ID NO: 36 ACAAAAGAAC pabA-ARO10-L GTTCTTTIGIAC SEQ ID NO: 37 CGGAGCCGCCATGGCTGTGCAGGTCGTAAAT pabA-ARO10-R GATCACCCTGTTACGCATAAACGTTTGTAGAAA SEQ ID NO: 38 CGCAAAAAGGC 700pabA-D-L gcctttttgcgtttctacaaacGTTTATGCGTAACAGGG SEQ ID NO: 39 TGATC 700pabA-D-R GGTAATAGATCTAAGCTTCTGCAGGTCGACTGG SEQ ID NO: 40 ATCGGCTCAACCACCA 500pabA-U-L GACCATTGAGCTTGGTCCGC SEQ ID NO: 41 500pabA-D-R CCACCCACCGAAACGGTAAAC SEQ ID NO: 42 ΔpabA-U-R GATCACCCTGTTACGCATAAACGGCGGCTCCGG SEQ ID NO: 43 TACAAAAGAAC ΔpabA-D-L GTTCTTTTGTACCGGAGCCGCCGTTTATGCGTA SEQ ID NO: 44 ACAGGGTGATC sg-pykF GTCCTAGGTATAATACTAGTATGGTTGCGGTAAC SEQ ID NO: 45 GTATGAGTTTTAGAGCTAGAAATAGC sg-pykF-test ATGGTTGCGGTAACGTATGA SEQ ID NO: 46 700pykF-U-L gagtcggtgctttttttgaattctctagaGGCT SEQ ID NO: 47 AATGCTGTACGTAATACGC 700pykF-U-R ATTTACGACC TGCACAGCCA TGTTGAGAAG SEQ ID NO: 48 GATGGGAGAAAC pykF-ARO10-L GTTTCTCCCATCCTTCTCAACATGGCTGTGCAGG SEQ ID NO: 49 TCGTAAAT pykF-ARO10-R CATCAGGGCGCTTCGATATACGTTTGTAGAAAC SEQ ID NO: 50 GCAAAAAGGC 700pykF-D-L gcctttttgcgtttctacaaacGTATA TCGAAGCGCC SEQ ID NO: 51 CTGATG 700pykF-D-R GGTAATAGATCTAAGCTTCTGCAGGTCGACCAG SEQ ID NO: 52 CAATGCGCCTTCAGTAG 500pykF-U-L CTGCACATTTCTCGGTACAGTTC SEQ ID NO: 53 500pykF-D-R CGCACAATGTGCGCCATTT SEQ ID NO: 54 ΔpykF-U-R GTTTCTCCCATCCTTCTCAACGTATATCGAAGCG SEQ ID NO: 55 CCCTGATG ΔpykF-D-L CATCAGGGCGCTTCGATATACGTTGAGAAGGAT SEQ ID NO: 56 GGGAGAAAC sg-yccx GTCCTAGGTATAATACTAGTGAAAGTCTGCATAA SEQ ID NO: 57 TTGCCTGTTTTAGAGCTAGAAATAGC sg-yccx-test GAAAGTCTGCATAATTGCCT SEQ ID NO: 58 700yccx-U-L gagtcggtgctttttttgaattctctagaGTGTCC SEQ ID NO: 59 GTGCTGAATATCCACC 700pykF-U-R ATTTACGACCTGCACAGCCA TTGCTGCTCT SEQ ID NO: 60 CCTTATCCTTAATGG yccx-ARO10-L ccattaaggataaggagagcagcaATGGCTGTGCAGG SEQ ID NO: 61 TCGTAAAT yccx-ARO10-R CCTGCCAAAACCGGTAAAATGTATGTTTGT SEQ ID NO: 62 AGAAACGCAAAAAGGC 700yccx-D-L gcctttttgcgtttctacaaacATACATTTTAC SEQ ID NO: 63 CGGTTTTGGCAGG 700yccx-D-R GGTAATAGATCTAAGCTTCTGCAGGTCGACCCA SEQ ID NO: 64 CCCGCAAAGATATGTCG 500yccx-U-L GATATTCTGC CCCAGCACTCAG SEQ ID NO: 65 500yccx-D-R GTGCCACGGT TAGCCTGTAT SEQ ID NO: 66

(14) III. Construction of a Strain YMGRA (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10*)

(15) A Red homologous recombination method is adopted, YMGR/pKD46 (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR/pKD46) is prepared into a competent cell, and the previously constructed lacI:ARO10* deletion expression cassette is transferred into the competent cell. A transformant is picked, colony PCR is carried out with primers YLACIL and YLACIR to verify the transformation situation, and the strain YMGR/pKD46 is used as a contrast. A plasmid pCP20 is transferred into the strain YMGR/pKD46 to eliminate kanamycin resistance. The high temperature of 42° C. is used for eliminating the plasmids pKD46 and pCP20. A strain YMGRA is obtained.

Example 2 Construction of a Strain YMGEA (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR ΔtrpE lacI:ARO10* trpE) and a Strain YMGR2A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10*)

(16) I. Construction of a trpE Deletion Cassette and a trpE::ARO10* Deletion Expression Cassette

(17) Primers 700trpE-U-L, ΔtrpE-U-R, ΔtrpE-D-L and 700trpE-D-R are designed according to the gene sequence of trpE, an E. coli MG1655 genome is used as a template, and fragments DtrpEUP and DtrpEDown are obtained through respective PCR amplification. 500trpE-U-L and 500trpE-D-R are used as primers, and a nested PCR method is adopted for amplification to obtain a gene trpE deletion cassette. Primers 700trpE-U-L, 700trpE-U-R, trpE-ARO10-L, trpE-ARO10-R, 700trpE-D-L and 700trpE-D-R are designed according to the gene sequence of trpE and a plasmid pKK223-ARO10*; the E. coli MG1655 genome and the plasmid pKK223-ARO10* are used as templates respectively for amplification to obtain fragments trpEUP, trpEDown, and ARO10. A plasmid pTarget is subjected to enzyme digestion with Xba I, and fragments are recovered. The four fragments are ligated by using a Vazyme one-step cloning kit to obtain a correct plasmid, and 500trpE-U-L and 500trpE-D-R are used as primers for PCR amplification to obtain a trpE::ARO10* deletion expression cassette.

(18) II. Construction of a Strain YMGEA (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR ΔtrpE lacI:ARO10* trpE) and a Strain YMGR2A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10*)

(19) The CRISPR-cas9 method is adopted for preparing a YMGRA/pCas (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10*/pCas) competent cell, and a sgRNA-containing plasmid sg-pTarget-trpE and the above trpE deletion cassette are transferred into the competent cell. A transformant is picked, colony PCR verification is carried out with primers 700trpE-U-L and 700trpE-D-R, and the strain YMGRA/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-trpE is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, and a strain YMGEA is obtained.

(20) The sgRNA-containing plasmid sg-pTarget-trpE and the trpE::ARO10* deletion cassette are transferred into the competent cell. A transformant is picked, colony PCR verification is carried out with primers 700trpE-U-L and 700trpE-D-R, and the strain YMGRA/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-trpE is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, and a strain YMGR2A is obtained.

Example 3 Construction of a Strain YMGB2A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR ΔpabB lacI:ARO10* trpE::ARO10*) and a Strain YMGR3A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10* pabB::ARO10*)

(21) A pabB deletion cassette and a pabB::ARO10* deletion expression cassette are constructed by using the strategy same as the construction of the deletion cassette and the trpE::ARO10* deletion expression cassette, YMGR2A/pCas is prepared into a competent cell by using the CRISPR-cas9 method, and a sgRNA-containing plasmid sg-pTarget-pabB and the constructed pabB deletion cassette are transferred into the competent cell for transformation. A transformant is picked, colony PCR verification is carried out with primers 700pabB-U-L and 700pabB-D-R, and the strain YMGR2A/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-pabB is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, the method is similar to that of Example 2, and a strain YMGB2A is obtained.

(22) YMGR2A/pCas is prepared into the competent cell by using the CRISPR-cas9 method, and the sgRNA-containing plasmid sg-pTarget-pabB and the constructed pabB::ARO10* deletion expression cassette are added into the competent cell for transformation. A transformant is picked, colony PCR verification is carried out with primers 700pabB-U-L and 700pabB-D-R, and the strain YMGR2A/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-pabB is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, the method is similar to that of Example 2, and a strain YMGR3A is obtained.

Example 4 Construction of a Strain YMGA3A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR ΔpabA lacI:ARO10* trpE::ARO10* pabB::ARO101 and a Strain YMGR4A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10* pabB::ARO10* pabA::ARO10*)

(23) A pabA deletion cassette and a pabA::ARO10* deletion expression cassette are constructed by using the strategy same as the construction of the trpE deletion cassette and the trpE::ARO10* deletion expression cassette, YMGR3A/pCas is prepared into an electrocompetent cell by using the CRISPR-cas9 method, and a sgRNA-containing plasmid sg-pTarget-pabA and the above pabA deletion cassette or the pabA::ARO10* deletion expression cassette are added into the competent cell for transformation. A transformant is picked, colony PCR verification is carried out with primers 700pabA-U-L and 700pabA-D-R, and the strain YMGR3A/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-pabA is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, and the method is similar to that of Example 2. Strains YMGA3A and YMGR4A are obtained.

Example 5 Construction of a Strain YMGF4A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR ΔpykF lacI:ARO10* trpE::ARO10* pabB::ARO10* pabA::ARO10*) and a Strain YMGR5A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10* pabB::ARO10* pabA::ARO10* pykF::ARO10*)

(24) A pykF deletion cassette and a pykF::ARO10* deletion expression cassette are constructed by using the strategy same as the construction of the trpE deletion cassette and the trpE::ARO10* deletion expression cassette, YMGR4A/pCas is prepared into a competent cell by using the CRISPR-cas9 method, and a sgRNA-containing plasmid sg-pTarget-pykF and the above pykF deletion cassette or the pykF::ARO10* deletion expression cassette are added into the competent cell for transformation. A transformant is picked, colony PCR verification is carried out with primers 700pykF-U-L and 700pykF-D-R, and the strain YMGR4A/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-pykF is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, and the method is similar to that of Example 2. Strains YMGF4A and YMGR5A are obtained.

Example 6 Shake Flask Fermentation of Microorganisms for Synthetizing Tyrosol

(25) Strains are subjected to streak culture on a non-resistant LB plate, a single colony is picked, 20 mL of a liquid LB culture medium is inoculated with the single colony, and a seed solution is cultured for 8-10 hours. 500 μL of the seed solution is taken, and 50 mL of a liquid LB culture medium is inoculated with the 500 μL of the seed solution for expanded culture, and then placed in a 200 r.Math.min.sup.−1 shaker for culturing at 37° C. for 10 hours. All cells are collected, a supernatant is removed after the cells are collected, and then the cells are cleaned once with normal saline. The cleaned cells are transferred into 50 mL of M9Y fermentation culture medium to make the cell density in the culture medium reach 6*10.sup.9 CFU/mL when the OD.sub.600 is about 5, and the cells are fermented in the 200 r.Math.min.sup.−1 shaker at 30° C. for 48 hours. Sampling is carried out every 12 hours. High performance liquid chromatography (HPLC) is used for detecting the yield of tyrosol. The yield result of tyrosol is shown as FIG. 1 and Table 2. The yield of tyrosol is gradually increased by knocking out relevant genes of competition pathways and appropriately increasing the copy number of the ARO10* gene. When the pykF gene is knocked out, the yield of tyrosol reaches 10.84. mM. When the pykF gene is knocked out and the ARO10* gene is integrated, the yield of tyrosol reaches 10.92 mM. It can be seen that continuous increase of the ARO10* gene has little effect on the yield of tyrosol.

(26) TABLE-US-00002 TABLE 2 The yield of tyrosol obtained by fermenting different strains Strains YMGRA YMGEA YMGR2A YMGB2A YMGR3A YMGA3A YMGR4A YMGF4A YMGR5A Yield of 3.11 3.29 6.64 7.97 8.5 9.42 9.94 10.84 10.92 tyrosol (mM)

Example 7 Culture of YMGR5A in a Fermenter to Produce Tyrosol

(27) YMGR5A is subjected to streak culture on an LB plate, a single colony is picked, 20 mL liquid LB culture medium is inoculated with the single colony, and a seed solution is cultured for 8-10 hours. The seed solution is taken, a 50 mL liquid LB culture medium is inoculated with the seed solution, the initial OD.sub.600 is controlled to be 0.05, and the liquid LB culture medium inoculated with the seed solution is placed in a 200 r.Math.min.sup.−1 shaker for expanded culture at 37° C. for 5 hours. When the OD.sub.600 reaches 0.25, a 5 L fermenter containing 2 L of an M9Y culture medium is inoculated with the seed solution, sampling is carried out every 4 hours, and appropriate amounts of glucose and yeast powder are added. High performance liquid chromatography (HPLC) is used for detecting the yield of tyrosol. The yield result of tyrosol is shown as FIG. 2. When fermentation is carried out for 48 hours, the yield of tyrosol in the fermenter reaches 27.96 mM.

Example 8 Construction of a Strain YMGR6A (E. coli MG1655 ΔfeaB ΔpheA ΔtyrB ΔtyrR lacI:ARO10* trpE::ARO10* pabB::ARO10* pabA::ARO10* pykF::ARO10* yccx::ARO10*)

(28) A yccx::ARO10* deletion expression cassette is constructed by using the expression strategy same as the construction of the trpE::ARO10* deletion expression cassette, YMGR5A/pCas is prepared into a competent cell by using the CRISPR-cas9 method, and a sgRNA-containing plasmid sg-pTarget-yccx and the yccx::ARO10* deletion expression cassette are added into the competent cell for transformation. A transformant is picked, colony PCR verification is carried out with primers 700yccx-U-L and 700yccx-D-R, and the strain YMGR5A/pCas is used as a contrast. IPTG is adopted for induction, the plasmid sg-pTarget-yccx is eliminated, the high temperature of 42° C. is used for eliminating the plasmid pCas, and the method is similar to that of Example 2. A strain YMGR6A is obtained, the yield of tyrosol obtained after shake flask fermentation reaches 11.74 mM, and the fermentation method is the same as that of Example 6.

(29) Culture in a fermenter to produce tyrosol: YMGR6A is subjected to streak culture on an LB plate, a single colony is picked, and 20 mL of a liquid LB culture medium is inoculated with the single colony, and a seed solution is cultured for 8-10 hours. The seed solution is taken, 50 mL of a liquid LB culture medium is inoculated with the seed solution, the initial OD.sub.600 is controlled to be 0.05, and the liquid LB culture medium inoculated with the seed solution is placed in a 200 r.Math.min.sup.−1 shaker for expanded culture at 37° C. for 5 hours. When the OD.sub.600 reaches 0.25, a 5 L fermenter containing 2 L of an M9Y culture medium is inoculated with the seed solution, sampling is carried out every 4 hours, and appropriate amounts of glucose and yeast powder are added. High performance liquid chromatography (HPLC) is used for detecting the yield of tyrosol. The yield result of tyrosol is shown as FIG. 3. When fermentation is carried out for 48 hours, the yield of tyrosol reaches 32.3 mM.

(30) Although the present disclosure has been disclosed as above as exemplary examples, it is not intended to limit the present disclosure. Any of those skilled in the art may make various alterations and modifications without departing from the spirit and scope of the present disclosure. Therefore, the protection scope of the present disclosure shall be as defined in the claims.