Patent Grant
11773383
This application claims the benefit of priority to Chinese patent application No. 2020112083956, filed Nov. 3, 2020, the content of which is hereby incorporated by reference in its entirety.
The invention belongs to the field of genetic engineering, enzyme engineering and microbial engineering. It particularly relates to methods for promoting extracellular expression of proteins in Bacillus subtilis (B. subtilis) using a cutinase.
Extracellular expression of exogenous proteins can simplify the downstream purification process, save production costs, and has great advantages in large-scale industrial production. An intracellularly localized protein is expressed inside cells, and the cells need to be disrupted by physical or chemical methods to obtain the target protein. The subsequent extraction process is cumbersome and costly, so it has become the goal of researchers to find an effective way to simplify the downstream extraction steps and reduce the purification cost of products.
It was found that cutinase can promote extracellular secretion of proteins in an Escherichia coli system without signal peptide mediation. Although the “secretion” mechanism has not been fully understood, it is speculated that this phenomenon is related to the enhanced membrane permeability caused by the limited phospholipid hydrolysis activity of the cutinase. It is also found that, when the cutinase is co-expressed with intracellular proteins in E. coli, it can also trigger extracellular release of proteins that are normally localized inside cells. No obvious cell lysis phenomenon is found in this process, and no obvious adverse effect will be generated on the downstream separation and extraction process. When the cutinase and natural intracellularly localized protein are co-expressed in E. coli, cutinase can hydrolyze the phospholipid component of the cell membrane to a certain extent and increase the permeability of the cell membrane. In this way, the natural intracellularly localized protein is secreted outside the cell without compromise of cell membrane integrity, which provides a new method for extracellular expression of recombinant intracellularly localized enzyme. However, E. coli is not considered a food safety grade strain, so its application in food industry is limited.
B. subtilis is a gram-positive bacterium, has the advantages of non-pathogenicity, good environmental compatibility, and does not develop drug resistance easily. B. subtilis also has a good fermentation foundation, and its cultivation is simple and fast. B. subtilis has been recognized as a food safety grade strain GRAS (Generally recognized as safe) by the U.S. Food and Drug Administration and relevant Chinese authorities. B. subtilis is widely used in the production of various industrial enzymes.
When the inventor tried to using the same strategy of co-expressing a cutinase and an intracellular target protein in a B. subtilis expression system, the effect of extracellular secretion of the target protein is not good. This is due to the difference in the composition of the cell membrane of E. coli and that of B. subtilis. Therefore, there is an urgent need to develop a safe and efficient method for extracellular secretion of natural intracellularly localized protein in a B. subtilis expression system.
In view of the aforementioned problems in the use of E. coli expression systems to obtain extracellular expression of intracellular proteins, the disclosure aims to provide a safe and efficient method for extracellular secretion of natural intracellularly localized proteins. Firstly, a cutinase mutant is provided, which is obtained by mutating one or more sites at the amino acid residue positions 175, 177, 178, 207, 209, 213 and 214 of a cutinase having the amino acid sequence of SEQ ID NO: 1.
In one embodiment of the invention, the cutinase is derived from Thermobifida fusca.
The nucleotide sequence of the cutinase is set forth in SEQ ID NO: 2.
In one embodiment of the invention, the cutinase mutant is a single amino acid mutation obtained by mutating the amino acid at the positions 175, 177, 178, 207, 209, 213 or 214 of the cutinase having the amino acid sequence of SEQ ID NO: 1 to alanine, and is named as: L175A, T177A, I178A, T207A, F209A, I213A and P214A, respectively.
In one embodiment of the invention, the cutinase mutation is a double amino acid mutation L175A/T177A obtained by mutating the leucine (Leu) at position 175 to alanine (Ala) and the threonine (Thr) at position 177 to Ala.
In one embodiment of the invention, the cutinase mutation is a double amino acid mutation T207A/F209A obtained by mutating the Thr at position 207 to Ala and the phenylalanine (Phe) at position 209 to Ala.
In one embodiment of the invention, the cutinase mutation is a double amino acid mutation I213A/P214A obtained by mutating the isoleucine (Ile) at position 213 to Ala and the phenylalanine (Phe) at position 214 to Ala.
In one embodiment of the invention, it provides a gene for encoding a mutant cutinase.
In one embodiment of the invention, it provides a vector carrying the gene encoding the mutant cutinase.
In one embodiment of the invention, it provides a recombinant cell carrying the cutinase mutant gene or the vector containing the cutinase mutant gene.
In one embodiment of the invention, the recombinant cell takes B. subtilis as an expression host.
In one embodiment of the invention, it provides a recombinant B. subtilis that co-expresses the cutinase mutant and an intracellular protein.
The intracellular protein is an exogenous protein that is synthesized in ribosome and is localized in the cytoplasm with the help of chaperone proteins under the natural condition.
In one embodiment of the invention, the intracellular protein includes but not limited to xylose isomerase, 4,6-α-glucosyltransferase, 4-α-glucosyltransferase, trehalose synthase and branching enzyme.
In one embodiment of the invention, the amino acid sequence of the xylose isomerase is set forth in SEQ ID NO: 3.
In one embodiment of the invention, the nucleotide sequence of the xylose isomerase is set forth in SEQ ID NO: 4.
In one embodiment of the invention, the amino acid sequence of the 4,6-α-glucosyltransferase is set forth in SEQ ID NO: 5.
In one embodiment of the invention, the nucleotide sequence of the 4,6-α-glucosyltransferase is as shown in SEQ ID NO: 6.
In one embodiment of the invention, the amino acid sequence of the 4-α-glucosyltransferase is as shown in SEQ ID NO: 7.
In one embodiment of the invention, the nucleotide sequence of the 4-α-glucosyltransferase is as shown in SEQ ID NO: 8.
In one embodiment of the invention, the amino acid sequence of the trehalose synthase is SEQ ID NO: 9.
In one embodiment of the invention, the amino acid sequence of the branching enzyme is SEQ ID NO: 10.
In one embodiment of the invention, any one of B. subtilis WS5, B. subtilis 168, B. subtilis W600, B. subtilis W800 and B. subtilis RIK1285 is taken as the expression host.
In one embodiment of the invention, any one of pHY300PLK, PUB110, pBE-S and pWB980 is taken as an expression vector.
In one embodiment of the invention, it provides a method for constructing the recombinant B. subtilis, including: linking the gene encoding the cutinase mutant and the gene encoding the intracellular protein to an expression vector to obtain a recombinant expression vector, and then transforming the recombinant expression vector into an expression host.
In one embodiment of the invention, the method includes the following steps:
(1) Linking the genes encoding the cutinase and the intracellular protein with the plasmid pHY300PLK to obtain a recombinant plasmid; using the recombinant plasmid as a template for site-directed mutation, and designing a mutation primer for performing the site-directed mutation; and constructing a recombinant mutant plasmid containing the gene encoding the cutinase mutant;
(2) Transforming the recombinant mutant plasmid obtained in step (1) into B. subtilis WS5; and
(3) Selecting positive clones in step (2) for performing fermentation culture, centrifugating the fermentation broth and collecting the fermentation supernatant, wherein the fermentation supernatant is the crude solution containing the intracellular protein.
The B. subtilis WS5 has been preserved in the China Center for Type Culture Collection on Sep. 29, 2016 with a preservation number of CCTCC NO: M 2016536; and the preservation address is Wuhan University, Wuhan, China.
The B. subtilis WS5 is described in the patent application with the publication number of CN106754466A and the application number of 201611025858.9.
In one embodiment of the invention, it provides methods of using the cutinase mutant, the gene there of, or the vector thereof in promoting extracellular expression of the natural intracellularly localized target protein in B. subtilis. The method comprises co-expressing genes of the cutinase mutant and the intracellular target protein in different vectors, or linking the cutinase gene and the intracellular target protein gene in the same vector and transfer the vector into a B. subtilis to obtain a recombinant B. subtilis.
In one embodiment of the invention, the method further comprises performing fermentation of the recombinant B. subtilis with the cutinase mutant and the intracellular target protein and obtaining the target protein in the fermentation broth outside B. subtilis cells.
In one embodiment of the invention, it provides a method for producing extracellular protein, comprising: inoculating the recombinant B. subtilis into a seed medium to obtain a seed liquid; inoculating the seed liquid into a fermentation medium for performing fermentation; and performing centrifugation and collecting the fermentation supernatant containing the target protein.
In one embodiment of the invention, it provides a method for producing extracellular proteins, comprising the following steps: the recombinant B. subtilis cells are inoculated into a seed medium and cultured at 35-38° C. and 180-220 rpm for 8-10 hours to obtain a seed liquid, and the seed liquid is then inoculated into a fermentation medium and cultured at 30-37° C. and 180-220 rpm for 20-26 hours.
In one embodiment of the invention, the components of the seed medium include 8-12 g/L peptone, 4-6 g/L yeast powder and 8-12 g/L sodium chloride.
In one embodiment of the invention, the components of the fermentation medium include 20-25 g/L yeast extract, 5-10 g/L soy peptone and 4-6 g/L glycerol; and the initial pH of the fermentation medium is 6-7.
In one embodiment of the invention, it provides methods of using the cutinase mutant, the gene, the vector, the recombinant cells, or the recombinant B. subtilis in enzyme production or enzymatic catalytic reaction.
(1) The invention provides a method for promoting extracellular secretion of recombinant intracellular enzymes by co-expressing a cutinase mutant in a B. subtilis system. Taking xylose isomerase, 4,6-α-glucosyltransferase, 4-α-glucosyltransferase, trehalose synthase and branching enzyme as examples, the method successfully achieves extracellular expression of the xylose isomerase, 4,6-α-glucosyltransferase, 4-α-glucosyltransferase, trehalose synthase and branching enzyme. The invented method can simplify the downstream purification process, save costs and have great advantages in large-scale production of industrial proteins.
(2) When xylose isomerase is expressed alone, the extracellular enzyme activity of the xylose isomerase is not detected. With the technical solution provided by the invention, the maximum extracellular enzyme activity of the xylose isomerase can reach 5.6 U/mL.
(3) When 4,6-α-glucosyltransferase is expressed alone, the extracellular enzyme activity of the 4,6-α-glucosyltransferase is not detected. With the technical solution provided by the invention, the maximum extracellular enzyme activity of the 4,6-α-glucosyltransferase can reach 745.2 U/mL, achieving efficient extracellular secretion of the recombinant intracellular enzyme.
(4) When 4-α-glucosyltransferase is expressed alone, the extracellular enzyme activity of the 4-α-glucosyltransferase is not detected. With the technical solution provided by the invention, the maximum extracellular enzyme activity of the 4-α-glucosyltransferase can reach 11.4 U/mL.
The media involved in the following examples are as follows:
LB solid medium: 10 g/L peptone, 5 g/L yeast extract, 10 g/L NaCl and 0.2 g/L agar powder.
LB liquid medium: 10 g/L peptone, 5 g/L yeast extract and 10 g/L NaCl.
Seed medium: 10 g/L peptone, 5 g/L yeast extract and 10 g/L sodium chloride.
Fermentation medium: 24 g/L yeast extract, 12 g/L soy peptone, 5 g/L glycerol, 12.54 g/L K2HPO4 and 2.31 g/L KH2PO4; and the initial pH is 6-7.
The detection methods involved in the following examples are as follows:
Detection Method of Enzyme Activity of Xylose Isomerase
100 μL of a solution to be tested was added to a reaction system (containing a 3 mol·L−1 substrate, 100 μL of a glucose solution, 100 μL of a 50 mmol·L−1 MgSO4 solution, 100 μL of a 0.3 mol·L−1 Na2HPO4—KH2PO4 buffer with pH 7.5, and 600 μL of H2O). After reacting at 70° C. for 10 min, 1 mL of 0.5 mol·L−1 HClO4 was added to stop the reaction. 500 μL of the reaction solution was taken, and 100 μL of a cysteine hydrochloride solution (15 g·L−1), 3 mL of 75% concentrated H2SO4 and 100 μL of a carbazole-alcohol solution were added, and the mixed solution was shaken and mixed well. Color was developed at 60° C. for 10 min. Cooling was performed in an ice bath, and the absorbance was determined at a wavelength of 560 nm (using the inactivated enzyme solution subjected to the same operations as a blank control).
The enzyme activity is defined as the amount of enzyme required to produce 1 μmol of fructose per minute under the above reaction conditions.
(1) Preparation of substrate: 2 mL of distilled water was added to 40 mg of amylose to fully moisten the amylose, and then 2 mL of a 2 M NaOH solution was added. Vortex shaking was performed to fully dissolve the enzyme to prepare an amylose mother liquor. 500 μL of the amylose mother liquor was added with 250 μL of a 2 M HCl solution, and then 3250 μL of a phosphoric acid-citric acid buffer (pH 7.0) was added to prepare a 0.125% substrate.
(2) Preparation of iodine color solution: 0.26 g of iodine and 2.60 g of potassium iodide were put in a 10 mL volumetric flask, add water to the volumetric flask to the mark (prepared 3 days in advance to ensure that the iodine was completely dissolved) to obtain Lugol's iodine solution. When it is time to perform the assay, 100 μL of the Lugol's iodine solution was added to 50 μL of a 2 M HCl solution, and then water was added to 26 mL to prepare the iodine color solution.
(3) 200 μL of the substrate prepared in step (1) was taken in a 1.5 mL centrifuge tube and placed in a warm bath at 35° C. for 10 min. 200 μL of an enzyme solution to be tested was added and reacted at 35° C. for 10 min. After the reaction, 200 μL of the reaction solution was added to 3800 μL of the iodine color solution for color development for 5 min, and the absorbance at 660 nm was determined by a spectrophotometer.
As a control, 200 μl buffer, instead of the enzyme solution, was added to 3800 μL of the iodine color solution for color development.
The unit of enzyme activity is defined as: the absorbance value decreased by one percent per unit time is a unit of enzyme activity.
Detection Method of Enzyme Activity of Trehalose Synthase:
400 μL of an enzyme solution diluted to a suitable multiple was taken and 400 μL of a 5% (w/v) maltose solution prepared with a phosphate buffer (20 mmol/L, pH7.0) was added to obtain a mixed solution. The mixed solution was reacted at 30° C. for 30 min, then the enzyme reaction was terminated in a boiling water bath for 10 min, and the content of trehalose produced was determined by HPLC.
The HPLC detection conditions were: a mobile phase contained acetonitrile and water in a ratio of 80:20, the flow rate was 0.8 mL/min, the column temperature was 40° C., and a NH2 column and a differential detector were used.
Definition of enzyme activity: Under the above reaction conditions, the amount of enzyme required to form 1 μmol of trehalose per minute is defined as 1 unit of enzyme activity.
Detection Method of Enzyme Activity of Branching Enzyme:
(1) Preparation of substrate: 0.01 g of amylose (0.1 g of amylopectin) and 0.2 mL of 96% ethanol were taken, 0.5 mL of a 2 mol·L−1 NaOH solution was added after 3-4 min, 10 mL of water was added, the mixed solution was stirred for 10 min to dissolve the starch, then 0.5 mL of a 2 mol·L−1 HCL solution was added, and a phosphate buffer (50 mmol·L−1, pH 6.5) was added to volume to 10 mL to adjust the pH (prepared when used).
(2) Preparation of termination reaction solution: Lugol's iodine solution (mother liquor): 0.26 g of iodine and 2.60 g of potassium iodide were dissolved in a 10 mL volumetric flask, and stored at room temperature and protected from light. 0.1 mL of the Lugol's iodine solution was added, and 50 μL of a 2 mol·L−1 hydrochloric acid solution was added, and water was added to volume to 26 mL (prepared when used).
(3) 50 μL of a crude enzyme solution was taken and 50 μL of a substrate was added, and the mixed solution was placed in a water bath at 60° C. for 30 min. After adding 2 mL of the termination reaction solution, the absorbance at 660 nm was determined after being placed at room temperature for 20 min.
Definition of enzyme activity: At room temperature, the absorbance value at 660 nm decreased by 1% per minute is as a unit of enzyme activity.
25 μL of a 0.02% (w·v−1) potato amylose solution (dissolved in 90% dimethyl sulfoxide) was taken in a test tube, and preheated in a water bath at 70° C. for 10 min. 25 μL of a diluted enzyme solution (dissolved in a 50 mmol·L−1 Na2HPO4-citrate buffer with pH 5.5) was added, and the mixed solution was shaken and mixed well. After reacting at 70° C. for 30 min, 1 mL of an iodine solution (0.1 mL of original iodine solution+0.1 mL of 1 N HCl, diluted to 26 mL) was added to terminate the reaction. The original iodine solution was 26% KI+2.6% I2.
Definition of unit of enzyme activity: Under the enzyme activity measurement system, the amount of enzyme required to decrease the absorbance value A660 by 0.1 per minute.
(1) Plasmid pHYPMLd4P (the plasmid contains pullulanase pμL and chaperone protein prsA genes, and the construction method is recorded in the doctoral dissertation “Modification of Bacillus subtilis Strain, Promoter Optimization and High-Level Expression of Pullulanase”, of Zhang Kang, Jiangnan University, 2018) stored in the laboratory was used as a template to design forward and reverse primers, respectively:
An expression vector pHY300PLK-prsA fragment was amplified.
(2) Plasmid xylA/pET24a (+) (the construction method of the plasmid is recorded in Chinese Patent ZL201210581801.2) stored in the laboratory was used as a template to design forward and reverse primers, respectively:
A xylose isomerase gene fragment was amplified.
(3) The expression vector pHY300PLK-prsA fragment obtained in step (1) and the xylose isomerase gene fragment obtained in step (2) were linked by Infusion. The linked product was transformed into an E. coli JM109 competent cell to obtain a transformed product. The plasmid in the transformed product was extracted and verified by Hind III restriction enzyme digestion and sequenced to obtain the recombinant plasmid pHY300PLK-xylA-prsA.
The recombinant plasmid pHY300PLK-xylA-prsA was used as a template to design forward and reverse primers, respectively:
An expression vector pHY300PLK-xylA fragment was amplified.
(4) Plasmid pET20b-Tfu_0883 (the construction method of the plasmid is recorded in Chen S, Tong X, Woodard R W, Du G C, Wu J, Chen J, Identification and Characterization of Bacterial Cutinase, Journal of Biological Chemistry, 2008, 283(28):25854-25862) stored in the laboratory was used as a template to design forward and reverse primers, respectively:
A cutinase gene cut was amplified.
The expression vector pHY300PLK-xylA fragment obtained in step (3) and the cutinase gene fragment were linked by Infusion. The linked product was transformed into an E. coli JM109 competent cell to obtain a transformed product. The plasmid in the transformed product was extracted and verified by Hind III restriction enzyme digestion and sequenced to obtain the recombinant plasmid pHY300PLK-xylA-cut.
(5) The recombinant plasmid pHYPMLd4 (the plasmid contains pullulanase pul gene, and the construction method is recorded in the doctoral dissertation “Modification of Bacillus subtilis Strain, Promoter Optimization and High-Level Expression of Pullulanase”, of Zhang Kang, Jiangnan University, 2018) was used as a template, and an expression vector pHY300PLK fragment was amplified using the forward and reverse primers (pHY300PLK-F1 and pHY300PLK-R1). Plasmid xylA/pET24a (+) (disclosed in a patent with the patent number of ZL201210581801.2) stored in the laboratory was used as a template, and a xylose isomerase gene fragment was amplified using the forward and reverse primers (xylA-F and xylA-R). The expression vector pHY300PLK fragment and the xylose isomerase gene fragment were linked by Infusion. The linked product was transformed into an E. coli JM109 competent cell to obtain a transformed product. The plasmid in the transformed product was extracted and verified by Hind III restriction enzyme digestion and sequenced to obtain the recombinant plasmid pHY300PLK-xylA.
The recombinant plasmid pHY300PLK-xylA-cut obtained in step (4) of Example 1 was used as a template, and according to the gene sequences of cutinase, primers introducing mutations of L175A/T177A, T207A/F209A, I213A/P214A, I178A, L175A, T177A, T207A, F209A, I213A and P214A were designed and synthesized. The cutinase genes were subjected to site-directed mutation and verified by sequencing to obtain recombinant expression vectors containing the cutinase mutant genes: pHY300PLK-xylA-L175A/T177A, pHY300PLK-xylA-T207A/F209A, pHY300PLK-xylA-I213A/P214A, pHY300PLK-xylA-I178A, pHY300PLK-xylA-L175A, pHY300PLK-xylA-T177A, pHY300PLK-xylA-T207A, pHY300PLK-xylA-F209A, pHY300PLK-xylA-I213A, pHY300PLK-xylA-P214A.
The site-directed mutation primer introducing the L175A/T177A mutation was:
The site-directed mutation primer introducing the T207A/F209A mutation was:
The site-directed mutation primer introducing the I213A/P214A mutation was:
The site-directed mutation primer introducing the I178A mutation was:
The site-directed mutation primer introducing the L175A mutation was:
The site-directed mutation primer introducing the T177A mutation was:
The site-directed mutation primer introducing the T207A mutation was:
The site-directed mutation primer introducing the F209A mutation was:
The site-directed mutation primer introducing the I213A mutation was:
The site-directed mutation primer introducing the P214A mutation was:
(1) Preparation of Competent Cells
Cryopreserved B. subtilis WS5 was taken by dipping with an inoculating loop, then streaked on an LB solid medium, and cultured overnight at 37° C. for activation. A single colony was picked, inoculated in 10 mL of LB liquid medium, and cultured overnight at 37° C. and 200 rpm for 8 h to obtain a culture solution. 2.5 mL of the culture solution was transferred to 40 mL of LB liquid medium containing 0.5 M sorbitol, and cultured at 37° C. and 200 rpm for 4-5 h to obtain a bacterial solution. The obtained bacterial solution was placed in an ice-water bath for 10 min, and then centrifuged at 4° C. and 5000 rpm for 5 min, and bacterial cells were collected. The bacterial cells were resuspended in 50 mL of a pre-cooled electroporation transformation buffer, and centrifuged at 4° C. and 5000 rpm for 5 min. The supernatant was removed, and the bacterial cells were rinsed 4 times according to the above steps. The washed bacterial cells were resuspended in 1 mL of the electroporation transformation medium and dispensed into 1.5 mL EP tubes with 200 μL per tube to obtain the competent cells.
(2) Transformation of Competent Cells
The recombinant plasmids obtained in Examples 1 and 2 were added to the competent cells obtained in step (1). After being placed in an ice bath for 18 min, the competent cells and the recombinant plasmids were added to a pre-cooled electroporation cuvette (2 mm) and shocked (at 2.4 kv, 25 μF, 200Ω) once. After the electric shock is completed, 1 mL of a pre-cooled RM medium (RM medium components: peptone 10 g/L, yeast powder 5 g/L, NaCl 10 g/L, sorbitol 91 g/L and mannitol 69 g/L) was added immediately. After resuscitating at 37° C. and 200 rpm for 3 h, the competent cells were applied to a plate containing tetracycline resistance (50 μg/mL) to obtain recombinant bacteria:
Bacillus subtilis WS5/pHY300PLK-xylA, Bacillus subtilis WS5/pHY300PLK-xylA-cut, Bacillus subtilis WS5/pHY300PLK-xylA-L175A/T177A, Bacillus subtilis WS5/pHY300PLK-xylA-T207A/F209A, Bacillus subtilis WS5/pHY300PLK-xylA-I213A/P214A, Bacillus subtilis WS5/pHY300PLK-xylA 4178A, Bacillus subtilis WS5/pHY300PLK-xylA-L175A, Bacillus subtilis WS5/pHY300PLK-xylA-T177A, Bacillus subtilis WS5/pHY300PLK-xylA-T207A, Bacillus subtilis WS5/pHY300PLK-xylA-F209A, Bacillus subtilis WS5/pHY300PLK-xylA4213A, Bacillus subtilis WS5/pHY300PLK-xylA-P214A.
(1) The recombinant B. subtilis strains obtained in Example 3 were inoculated into the seed culture media, and cultured at 35-38° C. and 180-220 rpm for 8-10 h to obtain the seed liquids.
(2) The seed liquids obtained in step (1) were transferred to the fermentation media at an inoculum concentration of 5% (v/v), and cultured at 33° C. and 200 rpm for 24 h. Then the culture solutions were centrifuged at 12000 r·min−1 for 10 min to obtain fermentation supernatant. The fermentation supernatant was tested for the enzyme activity of xylose isomerase. The test results are shown in Table 1:
Bacillus subtilis WS5/pHY300PLK-xylA
Bacillus subtilis WS5/pHY300PLK-xylA-cut
Bacillus subtilis WS5/pHY300PLK-xylA-L175A/
Bacillus subtilis WS5/pHY300PLK-xylA-T207A/
Bacillus subtilis WS5/pHY300PLK-xylA-I213A/
Bacillus subtilis WS5/pHY300PLK-xylA-I178A
Bacillus subtilis WS5/pHY300PLK-xylA-L175A
Bacillus subtilis WS5/pHY300PLK-xylA-T177A
Bacillus subtilis WS5/pHY300PLK-xylA-T207A
Bacillus subtilis WS5/pHY300PLK-xylA-F209A
Bacillus subtilis WS5/pHY300PLK-xylA-I213A
Bacillus subtilis WS5/pHY300PLK-xylA-P214A
It can be seen from the test results that when the xylose isomerase was expressed alone, the extracellular enzyme activity of the xylose isomerase was not detected. When co-expressed with the cutinase or mutants thereof, the extracellular enzyme activity was detected, proving that the technical solution of the disclosure realizes the extracellular secretion of the xylose isomerase in B. subtilis. At the same time, the enzyme activity when the xylose isomerase and cutinase mutant I213A/P214A were co-expressed is 7 times the enzyme activity when the xylose isomerase and wild-type cutinase were co-expressed.
(1) Recombinant plasmids pHY300PLK-gtfB, pHY300PLK-gtfB-cut, pHY300PLK-gtfB-L175A/T177A, pHY300PLK-gtfB-T207A/F209A, pHY300PLK-gtfB-I213A/P214A, pHY300PLK-gtfB-I178A, pHY300PLK-gtfB-L175A, pHY300PLK-gtfB-T177A, pHY300PLK-gtfB-T207A, pHY300PLK-gtfB-F209A, pHY300PLK-gtfB-I213A and pHY300PLK-gtfB-P214A were constructed by the methods of Examples 1-3 and transformed into B. subtilis WS5 to obtain recombinant bacteria:
Bacillus subtilis WS5/pHY300PLK-gtfB, Bacillus subtilis WS5/pHY300PLK-gtfB-cut, Bacillus subtilis WS5/pHY300PLK-gtfB-L175A/T177A, Bacillus subtilis WS5/pHY300PLK-gtfB-T207A/F209A, Bacillus subtilis WS5/pHY300PLK-gtfB-I213A/P214A, Bacillus subtilis WS5/pHY300PLK-gtfB-I178A, Bacillus subtilis WS5/pHY300PLK-gtfB-L175A, Bacillus subtilis WS5/pHY300PLK-gtfB-T177A, Bacillus subtilis WS5/pHY300PLK-gtfB-T207A, Bacillus subtilis WS5/pHY300PLK-gtfB-F209A, Bacillus subtilis WS5/pHY300PLK-gtfB-I213A, Bacillus subtilis WS5/pHY300PLK-gtfB-P214A.
(2) The recombinant B. subtilis strains were inoculated into the seed culture media, and cultured at 35-38° C. and 180-220 rpm for 8-10 h to obtain the seed liquids.
(3) The seed liquids obtained in step (2) were transferred to the fermentation media at an inoculum concentration of 5% (v/v), and cultured at 33° C. and 200 rpm for 24 h. Then the culture solutions were centrifuged at 12000 r·min−1 for 10 min to obtain fermentation supernatant. The fermentation supernatant was tested for the enzyme activity of 4,6-α-glucosyltransferase. The test results are shown in Table 2:
Bacillus subtilis WS5/pHY300PLK-gtfB
Bacillus subtilis WS5/pHY300PLK-gtfB-cut
Bacillus subtilis WS5/pHY300PLK-gtfB-L175A/
Bacillus subtilis WS5/pHY300PLK-gtfB-T207A/
Bacillus subtilis WS5/pHY300PLK-gtfB-I213A/
Bacillus subtilis WS5/pHY300PLK-gtfB-I178A
Bacillus subtilis WS5/pHY300PLK-gtfB-L175A
Bacillus subtilis WS5/pHY300PLK-gtfB-T177A
Bacillus subtilis WS5/pHY300PLK-gtfB-T207A
Bacillus subtilis WS5/pHY300PLK-gtfB-F209A
Bacillus subtilis WS5/pHY300PLK-gtfB-I213A
Bacillus subtilis WS5/pHY300PLK-gtfB-P214A
It can be seen from the test results that when the 4,6-α-glucosyltransferase was expressed alone (Bacillus subtilis WS5/pHY300PLK-gtfB), the extracellular enzyme activity of the 4,6-α-glucosyltransferase was not detected.
The enzyme activity when the 4,6-α-glucosyltransferase and cutinase mutant I213A/P214A were co-expressed (Bacillus subtilis WS5/pHY300PLK-gtfB-I213A/P214A) is 6 times the enzyme activity when the 4,6-α-glucosyltransferase and wild-type cutinase were co-expressed (Bacillus subtilis WS5/pHY300PLK-gtfB-cut).
(1) Recombinant plasmids pHY300PLK-4GT, pHY300PLK-4GT-cut, pHY300PLK-4GT-L175A/T177A, pHY300PLK-4GT-T207A/F209A, pHY300PLK-4GT-I213A/P214A, pHY300PLK-4GT-I178A, pHY300PLK-4GT-L175A, pHY300PLK-4GT-T177A, pHY300PLK-4GT-T207A, pHY300PLK-4GT-F209A, pHY300PLK-4GT 4213A and pHY300PLK-4GT-P214A were constructed by the methods of Examples 1-3 and transformed into B. subtilis WS5 to obtain recombinant bacteria:
Bacillus subtilis WS5/pHY300PLK-4GT, Bacillus subtilis WS5/pHY300PLK-4GT-cut, Bacillus subtilis WS5/pHY300PLK-4GT-L175A/T177A, Bacillus subtilis WS5/pHY300PLK-4GT-T207A/F209A, Bacillus subtilis WS5/pHY300PLK-4GT I213A/P214A, Bacillus subtilis WS5/pHY300PLK-4GT-I178A, Bacillus subtilis WS5/pHY300PLK-4GT-L175A, Bacillus subtilis WS5/pHY300PLK-4GT-T177A, Bacillus subtilis WS5/pHY300PLK-4GT-T207A, Bacillus subtilis WS5/pHY300PLK-4GT-F209A, Bacillus subtilis WS5/pHY300PLK-4GT 4213A, Bacillus subtilis WS5/pHY300PLK-4GT-P214A.
(2) The recombinant B. subtilis strains were inoculated into the seed culture media, and cultured at 35-38° C. and 180-220 rpm for 8-10 h to obtain the seed liquids.
(3) The seed liquids obtained in step (2) were transferred to the fermentation media at an inoculum concentration of 5% (v/v), and cultured at 33° C. and 200 rpm for 24 h. Then the culture solutions were centrifuged at 12000 r·min−1 for 10 min to obtain fermentation supernatant. The fermentation supernatant was tested for the enzyme activity of 4-α-glucosyltransferase. The test results are shown in Table 3:
Bacillus subtilis WS5/pHY300PLK-4GT
Bacillus subtilis WS5/pHY300PLK-4GT-cut
Bacillus subtilis WS5/pHY300PLK-4GT-L175A/
Bacillus subtilis WS5/pHY300PLK-4GT-T207A/
Bacillus subtilis WS5/pHY300PLK-4GT-I213A/
Bacillus subtilis WS5/pHY300PLK-4GT-I178A
Bacillus subtilis WS5/pHY300PLK-4GT-L175A
Bacillus subtilis WS5/pHY300PLK-4GT-T177A
Bacillus subtilis WS5/pHY300PLK-4GT-T207A
Bacillus subtilis WS5/pHY300PLK-4GT-F209A
Bacillus subtilis WS5/pHY300PLK-4GT-I213A
Bacillus subtilis WS5/pHY300PLK-4GT-P214A
It can be seen from the test results that when the 4-α-glucosyltransferase was expressed alone (Bacillus subtilis WS5/pHY300PLK-4GT), the extracellular enzyme activity of the 4-α-glucosyltransferase was not detected.
The enzyme activity when the 4-α-glucosyltransferase and cutinase mutant T207A/F209A were co-expressed (Bacillus subtilis WS5/pHY300PLK-4GT-T207A/F209A) is 4.6 times the enzyme activity when the 4-α-glucosyltransferase and wild-type cutinase were co-expressed (Bacillus subtilis WS5/pHY300PLK-4GT-cut).
(1) Recombinant plasmids were constructed by the methods of Examples 1-3 and transformed into B. subtilis WS5 to obtain recombinant bacteria:
Bacillus subtilis WS5/pHY300PLK-treS, Bacillus subtilis WS5/pHY300PLK-treS-cut, Bacillus subtilis WS5/pHY300PLK-treS-L175A/T177A, Bacillus subtilis WS5/pHY300PLK-treS-T207A/F209A, Bacillus subtilis WS5/pHY300PLK-treS-I213A/P214A, Bacillus subtilis WS5/pHY300PLK-treS-I178A, Bacillus subtilis WS5/pHY300PLK-treS-L175A, Bacillus subtilis WS5/pHY300PLK-treS-T177A, Bacillus subtilis WS5/pHY300PLK-treS-T207A, Bacillus subtilis WS5/pHY300PLK-treS-F209A, Bacillus subtilis WS5/pHY300PLK-treS-I213A, Bacillus subtilis WS5/pHY300PLK-treS-P214A (wherein the literature involved in plasmid construction is: doctoral dissertation “Study on B. subtilis Strain Modification, Promoter Optimization and Efficient Preparation of Pullulanase” of Zhang Kang, Jiangnan University, 2018; Luo Feng, Duan Xuguo, Su Lingqia, Wu Jing, Cloning Expression and Fermentation Optimization of Thermobifida fusca Trehalose Synthase Gene, Journal of Chinese Biotechnology, 2013, 33 (8): 98-104).
(2) The recombinant B. subtilis strains were inoculated into the seed culture media, and cultured at 35-38° C. and 180-220 rpm for 8-10 h to obtain the seed liquids.
(3) The seed liquids obtained in step (2) were transferred to the fermentation media at an inoculum concentration of 5% (v/v), and cultured at 33° C. and 200 rpm for 24 h. Then the culture solutions were centrifuged at 12000 r·min−1 for 10 min to obtain fermentation supernatant. The fermentation supernatant was tested for the enzyme activity of trehalose synthase. When the trehalose synthase was expressed alone, the extracellular enzyme activity of the trehalose synthase was not detected. When co-expressed with the cutinase or mutants thereof, the extracellular enzyme activity was detected.
(1) Recombinant plasmids were constructed by the methods of Examples 1-3 and transformed into B. subtilis WS5 to obtain recombinant bacteria:
Bacillus subtilis WS5/pHY300PLK-TtSBE, Bacillus subtilis WS5/pHY300PLK-TtSBE-cut, Bacillus subtilis WS5/pHY300PLK-TtSBE-L175A/T177A, Bacillus subtilis WS5/pHY300PLK-TtSBE-T207A/F209A, Bacillus subtilis WS5/pHY300PLK-TtSBE-I213A/P214A, Bacillus subtilis WS5/pHY300PLK-TtSBE-1178A, Bacillus subtilis WS5/pHY300PLK-TtSBE-L175A, Bacillus subtilis WS5/pHY300PLK-TtSBE-T177A, Bacillus subtilis WS5/pHY300PLK-TtSBE-T207A, Bacillus subtilis WS5/pHY300PLK-TtSBE-F209A, Bacillus subtilis WS5/pHY300PLK-TtSBE-1213A, Bacillus subtilis WS5/pHY300PLK-TtSBE-P214A (wherein the literature involved in plasmid construction is: Master's thesis of Liu Jun, Jiangnan University, 2017).
(2) The recombinant B. subtilis strains were inoculated into the seed culture media, and cultured at 35-38° C. and 180-220 rpm for 8-10 h to obtain the seed liquids.
(3) The seed liquids obtained in step (2) were transferred to the fermentation media at an inoculum concentration of 5% (v/v), and cultured at 33° C. and 200 rpm for 24 h. Then the culture solutions were centrifuged at 12000 r·min−1 for 10 min to obtain fermentation supernatant. The fermentation supernatant was tested for the enzyme activity of branching enzyme. When the branching enzyme was expressed alone, the extracellular enzyme activity of the branching enzyme was not detected. When co-expressed with the cutinase or mutants thereof, the extracellular enzyme activity was detected.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202011208395.6 | Nov 2020 | CN | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20140187468 | Estell | Jul 2014 | A1 |
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| Studer. Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes. Biochem. J. (2013) 449, 581-594. |
| H6WX58_9ACTN. UnitProtKB Database. Oct. 10, 2018. |
| A0A2TOT7X1_9PSEU. UnitProtKB Database. Oct. 10, 2018. |
| Number | Date | Country | |
|---|---|---|---|
| 20220135957 A1 | May 2022 | US |
