PREPARATION METHOD OF HIGH-STABILITY SUPEROXIDE DISMUTASE WITH TRANSMEMBRANE CAPABILITY

Abstract

The present disclosure belongs to the technical field of genetic modification of an enzyme preparation and particularly relates to a preparation method of a high-stability superoxide dismutase with a transmembrane capability. The method includes the following steps: extracting mRNA from Geobacillus stearothermophilus, synthesizing cDNA by a reverse transcription method, amplifying a large number of coding regions of the cDNA by designing a specific primer, ligating the coding regions to an E. coli expression vector, and transforming the coding regions into engineering bacteria BL21 (DE3). A point mutation technology is used to enhance stability of the superoxide dismutase and a flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11) is designed, such that a soluble fusion expression of a transmembrane peptide YGRKKRRQRRR (SEQ ID NO: 10) and the superoxide dismutase is successfully realized.

Claims

1. A preparation method of a high-stability superoxide dismutase with a transmembrane capability, comprising the following steps: extracting mRNA from Geobacillus stearothermophilus, synthesizing cDNA by a reverse transcription method, amplifying a large number of coding regions of the cDNA by designing a specific primer, ligating the coding regions to an E. coli expression vector, and transforming the coding regions into engineering bacteria BL21 (DE3).

2. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, comprising the following steps: (1) designing a specific primer sequence extracting a sequence encoding the superoxide dismutase from natural Geobacillus stearothermophilus; (2) successfully ligating the sequence of the superoxide dismutase cloned in (1) to a prokaryotic expression vector and designing a primer for identifying a positive clone; (3) obtaining an expression strain, wherein the superoxide dismutase cloned from the Geobacillus stearothermophilus has an amino acid sequence as follows (SEQ ID NO: 1): TABLE-US-00010 MPFELPALPYPYDALEPHIDKETMNIHHTKHHNTYVTNLNAALEGHPDL QNKSLEELLSNLEALPESIRTAVRNNGGGHANHSLFWTILSPNGGGEPT GELADAINKKFGSFTAFKDEFSKAAAGRFGSGWAWLVVNNGELEITSTP NQDSPIMEGKTPILGLDVWEHAYYLKYQNRRPEYIAAFWNVVNWDEVAK RYSEAKAK; (4) mutating aspartic acid at position 20 to glycine and mutating leucine at position 141 to asparagine; and (5) coupling a cell penetrating peptide (CPP) sequence YGRKKRRQRRR (SEQ ID NO: 10) with a transmembrane capability on an HIV-1 peptide segment with the superoxide dismutase for expression to enable the superoxide dismutase to have the transmembrane capability, wherein the CPP sequence is a trans-activating transcriptional activator sequence.

3. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein in step (1) of designing the specific primer sequence, an RNA extraction kit is used to extract the mRNA from the Geobacillus stearothermophilus, a reverse transcription kit is used to synthesize the cDNA of the microorganism, a specific primer is optimized according to restriction endonuclease sites, and the sequence encoding the superoxide dismutase is captured and the optimized specific primer has sequences as follows: a captured upstream primer sequence for the superoxide dismutase: TABLE-US-00011 (SEQ ID NO: 2) 5′-CATATGCCCTTTGAACTACCAGCAT-3′, and a captured downstream primer sequence for the superoxide dismutase: TABLE-US-00012 (SEQ ID NO: 3) 5′-AAGCTTCTTCGCTTTCGCCTCGCTG-3′.

4. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein in (1), the captured sequence, that is, the coding sequence of the superoxide dismutase to be expressed in the next step is as follows (SEQ ID NO: 4): TABLE-US-00013 ATGCCCTTTGAACTACCAGCATTACCCTATCCCTATGATGCTCTAGAAC CGCACATTGACAAGGAGACCATGAACATCCACCACACCAAGCACCACAA CACCTACGTGACCAACCTGAACGCGGCGCTGGAGGGTCACCCGGACCTG CAGAACAAAAGCCTGGAGGAACTGCTGAGCAACCTGGAGGCGCTGCCGG AAAGCATCCGTACCGCGGTTCGTAACAACGGTGGCGGTCACGCGAACCA CAGCCTGTTTTGGACCATCCTGAGCCCGAACGGCGGTGGCGAGCCGACC GGTGAACTGGCGGACGCGATTAACAAGAAATTCGGCAGCTTTACCGCGT TCAAGGATGAGTTTAGCAAAGCGGCGGCGGGTCGTTTCGGTAGCGGTTG GGCGTGGCTGGTTGTGAACAACGGCGAGCTGGAAATCACCAGCACCCCG AACCAGGACAGCCCGATCATGGAGGGCAAGACCCCGATTCTGGGCCTGG ATGTGTGGGAACACGCGTACTATCTGAAATACCAAAACCGTCGTCCGGA ATATATTGCGGCGTTCTGGAATGTGGTGAACTGGGACGAGGTGGCGAAG CGTTACAGCGAGGCGAAAGCGAAGTGAAAGCTT.

5. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein in step (2), a pET30a vector is selected as the expression vector, an amplified sequence and the vector are digested with HindIII and NdeI, an obtained digested product is recovered with a DNA gel recovery kit, the recovered digested product is ligated with a DNA ligase at 16° C. for 12 h at a ratio of a DNA fragment and a plasmid of 2:1, a ligated linker is transformed into the competent E. coli engineering bacteria BL21 (DE3) by heat shock at 42° C., the transformed engineering bacteria are spread on an LB-resistant plate containing 50 μg/mL of kanamycin and incubated at 37° C. for 18-26 h to form a single clone and the clone is verified; and a primer for colony PCR has sequences as follows: an upstream primer sequence for colony PCR: 5′-TTACCCTATCCCTATGATGCTC-3′ (SEQ ID NO: 5), and a downstream primer sequence for colony PCR: 5′-CCCAACCGCTACCGAAAC-3′ (SEQ ID NO: 6).

6. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein in step (3) of obtaining the expression strain, a correctly verified single clone is selected for an expression verification and specifically an expression condition is as follows: 5 mL of a LB liquid medium is inoculated with a monoclonal colony, the medium contains 50 μg/mL of kanamycin, when an OD600 value reaches 0.7, IPTG is added to a final concentration of 0.5 mM, induction is conducted at different temperatures, bacterial cells are collected after the induction, an ultrasonic lysis is conducted and each component is detected by an electrophoresis by a sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) method.

7. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 5, an ultrasonic lysis is conducted at an ultrasonic volume of 1 mL and specifically, is conducted for 2 sec and stopped for 3 sec with a total ultrasonic time of 10 min.

8. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein in step (5), a flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11), GGGGS (SEQ ID NO: 12), GGSGGS (SEQ ID NO: 13) or GGGGG (SEQ ID NO: 14) is used for an coupling expression of the superoxide dismutase; and after D20G and L141N are subjected to point mutations and the flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11) is used for a fusion expression of a YGRKKRRQRRR (SEQ ID NO: 10) sequence and the superoxide dismutase, the superoxide dismutase has an amino acid sequence as follows (SEQ ID NO: 7): TABLE-US-00014 MPFELPALPYPYDALEPHIGKETMNIHHTKHHNTYVTNLNAALEGHPDL QNKSLEELLSNLEALPESIRTAVRNNGGGHANHSLFWTILSPNGGGEPT GELADAINKKFGSFTAFKDEFSKAAAGRFGSGWAWLVVNNGENEITSTP NQDSPIMEGKTPILGLDVWEHAYYLKYQNRRPEYIAAFWNVVNWDEVAK RYSEAKAKGGGSGGGSYGRKKRRQRRR.

9. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, in step (3), an activity of the superoxide dismutase in a lysed supernatant is determined in the following steps: determining the activity by a WST-8 method, then purifying by a glycerin-assisted heating method, a salting-out method, an organic solvent precipitation method and a dialysis method, concentrating and then detecting the activity by a WST-8 kit method; and in a thermal stability test, placing the purified superoxide dismutase in a water bath at 4° C., 75° C., 80° C., 85° C., 90° C. and 95° C. for 3 h respectively and detecting the enzyme activity.

10. The preparation method of a high-stability superoxide dismutase with a transmembrane capability according to claim 1, wherein a glycerin-assisted heating method comprises the following steps: heating to 75° C. in 15% glycerol to inactivate impure proteins.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0048] FIG. 1 is a photo of a monoclonal colony;

[0049] FIG. 2 shows identification of positive clones by colony PCR;

[0050] FIG. 3 shows an expression of a target protein in a designed system by the present disclosure identified by using an SDS-PAGE method;

[0051] FIG. 4 shows determination of an activity of a superoxide dismutase by using a WST-8 method;

[0052] FIG. 5 shows the activity the superoxide dismutase measured after the superoxide dismutase obtained in the present disclosure is incubated at different temperatures;

[0053] FIG. 6 shows the activity the superoxide dismutase measured after the superoxide dismutase obtained by using a point mutation modification is incubated at different temperatures;

[0054] FIG. 7 shows comparison of thermal stability before and after mutation of D20G&L141N;

[0055] FIG. 8 shows a soluble expression and a transmembrane secretion expression of the coupled superoxide dismutase after introducing “a transmembrane peptide and a flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11)”;

[0056] FIG. 9 shows a verification of a thermal stability effect after introducing “a transmembrane peptide and the flexible polypeptide-GGGSGGGS (SEQ ID NO: 11)”;

[0057] FIG. 10 shows the tolerance of the superoxide dismutase of the present disclosure to different pH environments;

[0058] FIG. 11 shows the tolerance of the superoxide dismutase of the present disclosure to a denaturant SDS;

[0059] FIG. 12 shows the tolerance of the superoxide dismutase of the present disclosure to a digestive enzyme;

[0060] FIG. 13 shows the tolerance of the superoxide dismutase of the present disclosure to a preservative potassium sorbate;

[0061] FIG. 14 shows the verification of the function of the superoxide dismutase of the present disclosure on skin repair after sun exposure;

[0062] FIG. 15 shows the verification of the effect of the superoxide dismutase of the present disclosure on repairing and preventing solar dermatitis;

[0063] FIG. 16 shows the superoxide dismutase of the present disclosure having the enzyme activity of 50,000 U/mL or more; and

[0064] FIG. 17 shows half-life test results at room temperature and 50° C.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0065] To energy enable those skilled in the art to better understand the present disclosure, the present disclosure further stated in conjunction with specific embodiment.

[0066] The kits or raw materials used in the present disclosure have the following manufacturers or purchasing channels:

[0067] 1. an RNA extraction kit, a reverse transcription kit and a DNA gel recovery kit: Tiangen Biotech;

[0068] 2. a pET30a vector: Youbio;

[0069] 3. a kit for determining activity by a WST-8 method: purchased from Beyotime;

[0070] 4. HindIII and NdeI: purchased from Abclonal; and

[0071] 5. a point mutation Q5 site-directed mutagenesis kit: purchased from NEB (New England BioLabs) company.

Example 1

[0072] A preparation method of a high-stability superoxide dismutase with a transmembrane capability included the following steps.

[0073] (1) an RNA extraction kit (purchased from Tiangen Biotech) was used to extract mRNA from Geobacillus stearothermophilus, a reverse transcription kit (purchased from Tiangen Biotech) was used to synthesize the cDNA of the microorganism, a specific primer (the primer sequence was as follows) was optimized according to restriction endonuclease sites, and the sequence encoding the superoxide dismutase was captured.

[0074] A captured upstream primer sequence for the superoxide dismutase was:

TABLE-US-00006 (SEQ ID NO: 2) 5′-CATATGCCCTTTGAACTACCAGCAT-3′, and

[0075] a captured downstream primer sequence for the superoxide dismutase was:

TABLE-US-00007 (SEQ ID NO: 3) 5′-AAGCTTCTTCGCTTTCGCCTCGCTG-3′.

[0076] (2) A pET30a vector (purchased from Youbio) was selected as the expression vector, an amplified sequence and the vector were digested with HindIII and NdeI (purchased from Abclonal), an obtained digested product was recovered with a DNA gel recovery kit (purchased from Tiangen Biotech), the recovered digested product was ligated with a DNA ligase at 16° C. for 12 h at a molar ratio of a DNA fragment and a plasmid of 2:1, a ligated linker was transformed into the competent E. coli engineering bacteria BL21 (DE3) by heat shock at 42° C., and the transformed engineering bacteria were spread on an LB-resistant plate containing 50 μg/mL of kanamycin and incubated at 37° C. for 18-26 h to form a single clone; after the single clone was formed (FIG. 1), a colony PCR method was used (sequences of colony PCR primers as follows) to verify the clone (FIG. 2).

[0077] FIG. 1 is a diagram of ligation of an amplified superoxide dismutase fragment and the expression vector. A ligated linker was transformed into competent E. coli engineering bacteria BL21 (ED3), and the transformed engineering strain was spread on an LB-resistant plate containing 50 μg/mL of kanamycin and incubated at 37° C. for 24 h to form a single-clone colony;

[0078] FIG. 2 shows identification of positive clones by a colony PCR method, where 1, 2, 3, 4, 5, 6, 9 and 10 are positive clones.

[0079] An upstream primer sequence for colony PCR was: 5′-TTACCCTATCCCTATGATGCTC-3′ (SEQ ID NO: 5); and

[0080] a downstream primer sequence for colony PCR was: 5′-CCCAACCGCTACCGAAAC-3′ (SEQ ID NO: 6).

[0081] (3) A correctly verified single clone was selected for an expression verification and specifically an expression condition was as follows: 5 mL of a LB liquid medium (the medium contains 50 μg/mL of kanamycin) was inoculated with a monoclonal colony, when an OD600 value reached 0.7, IPTG was added to a final concentration of 0.5 mM (a preferred concentration), and induction was conducted at different temperatures (preferably, 16° C. and 37° C.); bacterial cells were collected after the induction and an ultrasonic lysis was conducted at an ultrasonic volume of 1 mL and specifically, was conducted for 2 s and stopped for 3 s with a total ultrasonic time of 10 min.

[0082] After the experiment, each component was detected by an electrophoresis by using an SDS-PAGE method (FIG. 3).

[0083] FIG. 3 shows an expression of a target protein in a designed system by the present disclosure identified by using the SDS-PAGE method; Lane 1 and Lane 2 in FIG. 3 were the 5th component (BSA-V) spotted with different amounts of bovine serum albumin (BSA) and technical internal references, indicating that the SDS-PAGE was in good working; from Lane 3 to Lane 5 in the figure, the system expressed the target protein well; from Lane 6 to Lane 8 in the figure, the target protein expressed by the system had fair solubility; from Lane 9 to Lane 11 in the figure, the target protein expressed by the system had certain inclusion bodies; comparing Lane 8 and Lane 11, the protein expressed by the system was soluble proteins, which enabled the protein to have an anti-oxidation ability;

[0084] FIG. 3 proves that the protein obtained by the present disclosure is solublely expressed, which is a key step for the success of the present disclosure; if the solublely expressed protein cannot be obtained or the obtained protein was insoluble, it proves that the method has no practical use significance.

[0085] An activity of the superoxide dismutase in an obtained lysate supernatant was determined by using a WST-8 method (a kit was purchased from Beyotime). After the activity was determined, a purification method was explored. A glycerin-assisted heating method (heating to 75° C. in 15% glycerol to inactivate impure proteins), a salting-out method, an organic solvent precipitation method and a dialysis method were used for purification, and a WST-8 kit method was used to detect the activity and the activity was 24,747 U/mL (See FIG. 4).

[0086] FIG. 4 uses the WST-8 method to determine the activity of the superoxide dismutase. According to the kit instructions, when an absorbance value of a sample tube to be tested reaches ½ of a positive oxidation tube, the measured data is the most accurate. As shown in the figure, a first hole represents a “negative oxidation tube control” not containing an oxidation starter; a second hole represents the positive oxidation tube (oxygen free radicals could catalyze a substrate to produce yellow products and darker yellow color meant more severe oxidation); third to sixth holes almost has no color, indicating that the enzyme activity is too high to be accurately estimated; in a seventh hole and an eighth hole, the measured value is close to ½ of the positive oxidation tube; and after calculation, the activity is 24,747-28,055 U/mL.

[0087] In a thermal stability test, the purified superoxide dismutase was placed in a water bath 4° C., 75° C., 80° C., 85° C., 90° C. and 95° C. for 3 h respectively and the enzyme activity was detected (See FIG. 5). FIG. 5 shows the superoxide dismutase obtained in the present disclosure, and the activity of the superoxide dismutase was measured by using the WST-8 method after the superoxide dismutase was incubated in water bath at different temperatures for 3 h respectively. It was concluded from FIG. 5 that the enzyme obtained by the present disclosure had relatively good thermal stability but lost the activity significantly when the temperature exceeded 80° C.;

[0088] (4) Stability of the superoxide dismutase is improved.

[0089] In order to improve the thermal stability of the superoxide dismutase, characteristics of an amino acid sequence were analyzed, key amino acid sites having an impact on the thermal stability were screened out, and the superoxide dismutase was mutated to improve the thermal stability; after a pre-test experiment and study, it was finally found that after aspartic acid at position 20 was mutated to glycine and leucine at position 141 was mutated to asparagine, the thermal stability of the enzyme could be maximized (FIG. 6 and FIG. 7).

[0090] FIG. 6 shows the superoxide dismutase obtained after the modification by the point mutation, and the activity of the superoxide dismutase was measured by using the WST-8 method after the superoxide dismutase was incubated in water bath at different temperatures for 3 h respectively. It could be seen from the result histogram that the enzyme of the present disclosure had an excellent thermal stability and had the activity not decreased by more than 20% even if heated in an environment of 90° C. for 3 h; and

[0091] FIG. 7 compares the thermal stability before and after the mutation of D20G&L141N. From the result histogram, it could be seen that after the sequence was mutated the thermal stability was greatly enhanced.

[0092] (5) The transmembrane capability of the superoxide dismutase is improved.

[0093] The cell membrane has a natural barrier function, and specifically can maintain a relatively stable intracellular environment and regulate and select substances entering and leaving the cell. The cell membrane is composed of a bilayer of phospholipids, such that non-fat-soluble substances, polypeptides and protein biological macromolecules cannot enter the cell freely. Due to the barrier function of the cell membrane, many medicinal biologically active macromolecules in vitro cannot enter the cell. It was analyzed that the superoxide dismutase did not have a transmembrane signal region and thus had extremely low transmembrane capability; the present disclosure needed to develop a superoxide dismutase with a transmembrane capability.

[0094] Recently, it is found that a class of short peptides, namely CPPs, are capable of spontaneously crossing the cell membranes and carrying biological macromolecules into cells, and have a relatively strong transmembrane capability; the CPPs are a class of short peptides composed of tens of amino acids, can deliver biologically active substances into cells to exert biological activity and produce therapeutic effects, do not cause permanent damage to cell membranes, and are non-irritating, such that the CPPs are used as a highly favored new drug delivery vehicle. A CPP sequence YGRKKRRQRRR (SEQ ID NO: 10), that was a trans-activating transcriptional activator, with a transmembrane capability on an HIV-1 peptide segment was coupled with the superoxide dismutase for expression to enable the superoxide dismutase to have the transmembrane capability. However, a problem of protein expression spatial conformation should be considered when a coupling expression was conducted. In order to prevent the CPP sequence from affecting the correct spatial conformation of the superoxide dismutase, a flexible polypeptide linker-GGGSGGGS (SEQ ID NO: 11) (other optional flexible polypeptide linkers GGGGS (SEQ ID NO: 12), GGSGGS (SEQ ID NO: 13) and GGGGG (SEQ ID NO: 14)) was introduced in the present disclosure to maximize a soluble expression and a transmembrane secretion expression of the coupled superoxide dismutase (FIG. 8).

[0095] FIG. 8 shows the maximized soluble expression and the transmembrane secretion expression of the coupled superoxide dismutase after introducing “a transmembrane peptide and a flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11)”.

[0096] It could be seen from FIG. 8 that the left picture shows that the transmembrane peptide and flexible polypeptide linker GGGSGGGS (SEQ ID NO: 11) was added, and a target protein was concentrated in the culture medium instead of mainly in the bacteria. As a control, the transmembrane peptide and an AAASAAAS (SEQ ID NO: 15) sequence were added in the right picture, however a desired effect cannot be achieved. A red arrow marked location of the target protein.

[0097] A method for introducing the flexible peptide linker and the CPP sequence was as follows: the Q5 Site-directed mutagenesis kit was purchased from the NEB company, primers were designed as follows, the ability of a high-fidelity ultra-length DNA polymerase Q5 was used to amplify a plasmid in a reverse manner, and KLD brought by the kit connected the newly amplified plasmid into a circle.

[0098] Primer 1 was as follows:

TABLE-US-00008 (SEQ ID NO: 8) 5′-CCATAACTTCCTCCTCCACTTCCTCCTCCAAGCTTTCACTTCGCTT TCG-3′;

[0099] Primer 2 was as follows:

TABLE-US-00009 (SEQ ID NO: 9) 5′-TCGTAAGAAGCGCCGTCAACGTCGCCGTATTCGCCGGCCTGAGCT C-3′.

[0100] The flexible peptide linker and the CPP sequence were used for the coupled expression with the superoxide dismutase to achieve the soluble expression and the transmembrane secretion expression, and then the thermal stability (FIG. 9), the pH stability (FIG. 10), the denaturant tolerance (FIG. 11), the resistance to enzymatic hydrolysis (FIG. 12) and the compatibility with potassium sorbate (FIG. 13) of the obtained product was continuously verified. The results showed that the superoxide dismutase had good thermal stability and could maintain more than 80% of the activity even if heated at a high temperature of 90° C. for 3 h.

[0101] FIG. 9 shows the verification of the thermal stability after introducing “the transmembrane peptide and the flexible polypeptide GGGSGGGS”. As shown in the figure, the superoxide dismutase had excellent thermal stability.

[0102] FIG. 10 shows the tolerance of the superoxide dismutase of the present disclosure to different pH environments. It could be seen from the result histogram that the superoxide dismutase could tolerate a wide range of pH, especially had strong tolerance to alkaline environments, was relatively weak tolerance to acidic environments, and could maintain vitality only in weakly acidic environments.

[0103] FIG. 11 shows the tolerance of the superoxide dismutase of the present disclosure to a denaturant SDS. It could be seen from the result histogram that the superoxide dismutase had very strong tolerance to the ionic surfactant SDS and could be applied in products such as daily chemical products.

[0104] FIG. 12 shows the tolerance of the superoxide dismutase of the present disclosure to a digestive enzyme. 2 h and 5 h respectively represented digestion by a trypsin (purchased from Gibco) for 2 h and for 5 h. It could be seen from the result histogram that the superoxide dismutase had strong tolerance to the trypsin and the vitality of the superoxide dismutase was not weakened even in a high concentration of the trypsin for digestion for 5 h (left picture). The molecular weight of the superoxide dismutase would decrease slightly with the extension of trypsin digestion time, but the vitality remained unchanged, which indicated that the trypsin could only degrade a part of side chains of the superoxide dismutase, but did not affect an active center.

[0105] FIG. 13 shows the tolerance of the superoxide dismutase of the present disclosure to a preservative potassium sorbate. The potassium sorbate was a commonly used preservative in food and cosmetics, and had a common final use concentration of 0.05%-0.2%. After the superoxide dismutase was incubated with different concentrations of the potassium sorbate for 24 h, the enzyme activity was detected. It could be seen from the result histogram that the superoxide dismutase had a good compatibility with the potassium sorbate and the activity of the superoxide dismutase was not weakened even incubated in a high concentration of the potassium sorbate for 24 h, which indicated that in the terminal product containing the superoxide dismutase, the potassium sorbate could be used as a preservative.

[0106] After an excellent enzymatic performance of the superoxide dismutase was verified, in a mouse sunburn repair model, the repair effect of the superoxide dismutase after sun exposure was verified (FIG. 14 and FIG. 15). The superoxide dismutase could scavenge oxygen free radicals. Since ultraviolet radiation would enable the skin to produce a large number of free radicals, after nude mice were subjected to ultraviolet radiation, a repair experiment was used to verify after transdermal absorption and antioxidant properties of the superoxide dismutase;

[0107] FIG. 14 shows the verification of the function of the superoxide dismutase of the present disclosure on skin repair after sun exposure. Two groups of the nude mice (BalB/C nude) were irradiated with ultraviolet rays for 45 min, respectively. After the sun exposure, the mice in a repair group were quickly applied with 200 μl of the superoxide dismutase with the activity of 300 U/mL, while the mice in a control group were not applied with the product. After 4 days, there were obvious differences in the skin of the nude mice: the skin of the nude mice in the control group had obvious browning, wrinkling, hardening, etc., while the skin of the nude mice in the repair group remained healthy. It could be seen that the product could effectively repair skin problems caused by the ultraviolet radiation.

[0108] FIG. 15 shows the functions of the superoxide dismutase of the present disclosure on repairing and preventing solar dermatitis. Two groups of the nude mice were irradiated with ultraviolet rays for 40 min each day. After the sun exposure, the mice in the repair group were quickly applied with 200 μl of the superoxide dismutase with the activity of 300 U/mL, while the mice in the control group were not applied with the product. After the operation was repeated for 3 days, the solar dermatitis occurred in the control group, while the skin of the mice in the repair group had no abnormalities. It could be seen that the product could effectively repair the solar dermatitis caused by the ultraviolet radiation.