Patent Application
20160319248
The present invention relates to the field of in vitro diagnostics, in particular, a fructose lysine oxidase mutant with a high thermostability, a method for determining levels of glycated albumin, and a test kit for determining the glycated albumin levels. The present invention can be used in clinical testing, and can accurately determine glycated albumin levels.
Diabetes is a metabolic disease occurring in people with high blood sugar, and can lead to serious damage to many systems of the body, especially the nerves and blood vessels. According to the expectation of the World Health Organization, the number of people with diabetes in China has been ranked first in the world. Diabetes will be the most serious public health problem in China in the next 50 years.
Glycated albumin (GA) is the product formed by a non-enzymatic reaction occurring between glucose and glycated N-terminus albumin in human serum. 90% of them reacts with albumin within the chain of lysine ε-NH2 residue. The reaction principle lies in, at first both of them form an unstable Glycosylamine or Schiff Base. Then, through irreversible Amadori rearrangement, the latter forms a stable amino ketone (ketone amine). Since the half-life of albumin is about 20 days, detection of glycated albumin can be used to detect the average level of blood sugar over the past 2-3 weeks. Currently, glycated albumin testing has become an essential test for diabetics. Compared with glycated hemoglobin, it is more suitable as an index for assessing the risk of hospitalization and death of diabetic patients who have had dialysis.
Therefore, how to accurately determine the amount of glycated albumin in human's serum has become the key of clinical detection of glycated albumin. Currently, the market mainly uses enzymatic method to detect glycated albumin in human's serum. The reaction principle lies in, using protease at first, glycated albumin is digested into glycated polypeptides with a low molecular weight. Then, using fructosyl amino acid oxidase to catalyze glycated polypeptides to perform the oxidation reaction to generate polypeptides (or amino acids), Arabino hexose and H2O2. Release of H2O2 is detected by an endpoint reaction colorimetric method. Absorbance at 600 nm is proportional to the concentration of glycated albumin. Specific reaction process is as follows:
As is known form the above reaction mechanism and reaction steps, fructosyl amino acid oxidase is the key enzyme of detecting glycated albumin, and fructosyl amino acid oxidase has become the key for whether glycated albumin in human's serum can be accurately detected.
Fructosyl amino acid oxidase can also be referred as Fructosyl amino acid enzyme. Amadoriase, ketone oxidase, and etc. Such fructosyl amino acid oxidase has already been found in many bacteria, yeasts, and fungi, for example, from Aspergillus, Penicillium, Fusarium, Pichia, Coniochaeta, Eupencillum, Corynebacterium, and etc. (non-patent document 1, Lin, Z. and J. Zheng (2010) “Occurrence, characteristics, and applications of fructosyl amine oxidases (amadoriases).” Appl Microbiol Biotechnol 86. (6): 1613-1619). The above fructosyl amino acid oxidases are all possible to be applied in the glycated albumin test kit. However, at the same time, since in practice the diagnostic test kit need to be stored for a certain period of time, the requirements for stability are relatively high. Thus, the raw material-enzymes used also need to be stable. However, the thermostability of the enzymes shown in the above public materials are not ideal. After a heating treatment at 45° C. for 10 minutes, fructosyl amino acid oxidase from Aspergillus terreus GP1 shows a residual enzyme activity of about 40% (Non-Patent Document 2: Yoshida, N., Y. Sakai, et al (1996) “. Primary structures of fungal fructosyl amino acid oxidases and their application to the measurement of glycated proteins” European Journal of Biochemistry 242 (3): 499-505). After a heating treatment at 45° C. for 5 minutes, fructosyl amino acid oxidase from Fusarium oxysporum S-1F4 shows a residual enzyme activity of about 10% (Non-Patent Document 3: Sakai, Y., N. Yoshida, et al (1995). “Purification and properties of fructosyl lysine oxidase from Fusarium oxysporum S-1F4” Bioscience, biotechnology, and biochemistry 59 (3): 487). After a heating treatment at 37° C. for 30 minutes, fructosyl amino acid oxidase from the Coniochaetidium savoryi ATCC36547 shows a residual enzyme activity of 80% (Japanese Patent Application Publication No. 2004-275013;). Because of the poor thermostabilities of existing fructosyl amino acid oxidases, the stability of glycated albumin test kits on the market nowadays cannot meet the requirements. In many cases, a large amount of stabilizer is added in the test kit, so as to increase the stability of the test kit (International Patent Application Publication No. WO02002061119A1). This leads to a higher viscosity of the reagent, as well as a series of other issues. It is not conducive to be applied in a biochemical analyzer.
Therefore, there is an urgent need to develop a fructosyl amino acid oxidase with high thermostability. Also, this fructosyl amino acid oxidase is used to develop a glycated albumin test kit having both high sensitivity and long-term stability.
For the above-mentioned deficiencies of the prior art, the present invention provides a fructosyl amino acid oxidase having a high thermostability.
Amadoriase I (its amino acid sequence is the sequence shown in sequence 1, i.e., SEQID. No. 1: its nucleotide sequence is sequence 2, i.e., the sequence shown in SEQID. No. 2) from Aspergillus fumigatus has the characteristic that the activity for a substrate fructose lysine is far greater than that of fructosyl valine (non-patent document 4: Mennella, C., R C Borrelli, et al (2005) “Substrate specificity of Amadoriase I from Aspergillus fumigatus.” Ann NYA cad Sci 1043: 837-844.). Such a characteristic makes it particularly suitable for the glycated albumin test kit. The glycosylation site of glycated albumin is a lysine residue, which is different from a valine residue of glycated hemoglobin. This helps to reduce interference in other factors in the test. Therefore, from this point, the enzyme is modified to improve its thermostability. The sequence of Amadorise I has a very low homology with sequences of FAOX-TE and FPOX-CE as previously reported (Non-Patent Document 5: Sakaue, R. and N. Kajiyama (2003) “Thermo stabilization of bacterial fructosyl-amino acid oxidase by directed evolution “Applied and environmental microbiology 69 (1): 139-145 Non-Patent document 6: Hirokawa, K., A. Ichiyanagi, et al (2008)”. Enhancement of thermos stability of fungalde glycating enzymes by directed evolution “Appl Microbiol Biotechnol 78 (5): 775-781). Therefore, it is impossible to obtain relevant information simply by the sequence comparison. However, information about the transformation of the enzyme must be obtained through a lot of creative research.
Specifically, the random mutating method is utilized, to increase the thermostability of Amadorise I. The method is as follows:
In the present invention, using the nucleotide sequence 2 as a template, designing primer sequence 3 (5′-atggcgccttcaattttgagcactg-3′) and primer sequence 4 (5′-ttacggacctctgctctctccaatc-3′), error-prone PCR is conducted. By reasonably controlling the concentration of manganese ions in a PCR reaction system, the mutagenesis frequency is controlled to 1 to 2 nucleotide mutageneses/1 Kb nucleotides. After the obtained fragment containing the mutant nucleotide is purified, using pET-22b plasmid containing the nucleotide sequence 2 as a template, the whole plasmid PCR (WHOP-PCR) is conducted (non-Patent Document 7: Miyazaki, K. (2003) Creating random mutagenesis libraries by mega primer PCR of whole plasmid (MEGAWHOP) Directed Evolution Library Creation, Springer: 23-28). The obtained product is enzyme digested using the restriction enzyme DpnI, so as to remove the template plasmid. Thereafter, TOP10 competent cells were transformed, and are applied to LB agar plate containing antibiotic ampicillin. The obtained clones are approximately 10,000. Therefore, the library capacity of the random mutagenesis is about 10,000.
After the obtained clones are mixed well with a coating bar, they are collected in the centrifuge tube. The plasmid is extracted. The obtained plasmid is transformed into BL21 (ED3), so as to be ready for use in the next step of screening Subsequently, the transformant is inoculated in a 96-well plate. The cultivation medium is 150 ul LB/per well, containing the antibiotic ampicillin. This plate is used as a retention plate. The next day, in the same order, it is transferred to another 96-well plate. The cultivation medium is 150 ul LB/per well. Meanwhile, the antibiotics ampicillin and IPTG are added for induction. It is cultivated for 6 hours at 37° C. Bacteria are harvested by a centrifugation of 3800 rpm. The medium is removed. The plate is used as the assay plate.
150 ul of lysis solution (100 mM Tris, pH 8.0; 0.4 mg/ml sodium deoxycholate; 0.8 mg/ml CTAB; 20 mM KCl; 80 mM MgSO4) is added into the assay plate. After being cleaved after for half an hour at room temperature, it is centrifugated at 3800 rpm for 15 minutes. 50 ul of lysate is taken into a new 96-well plate. Another 50 ul lysate is taken into 96-well PCR plates, and is put into a 96-well PCR instrument. It subjects to a heating treatment for 15 minutes at 50° C. It is transferred to another piece of 96-well plate. In the above-mentioned two plates, 100 ul of chromogenic solution (Tris, 100 mM, pH 8.0; TOOS solution, 15 mM; 4-APP, 0.5 mM; POD, 40 U/ml; fructose lysine, 15 mM) is added respectively. By the chromogenic treatment for 30 minutes, the absorbance value is recorded using a microplate reader. By calculating a ratio of both absorbances, the activity proportion of residual enzyme of crude enzyme solution after the heat treatment is determined. For mutant strains having improved thermostability, their theoretical activity residual rate will be higher than that of the wild type.
In the present invention, by screening more than 10000 mutant strains, six mutant strains with enhanced thermostability are obtained in total by screening. After the sequencing analysis, it is found that these six mutant strains are all single-base mutagenesis. Their nucleotide sequence mutageneses are 177G→T, 293A→C, 764G→C, 830A→C, 853G→C, 1063G→C, respectively. Corresponding amino acid sequence mutagenises are 59E→N, 98E→A, 225G→A, 277K→S, 285E→Q, and 355D→H, respectively.
Since mutagenesis of the above six sites have enhanced thermostability, if the above sites are mutated to other amino acids, the likelihood that the thermostability is higher than that of the wild type is also very high. Thus, the present invention tried numerous other mutagenesis of the above sites. At the same time, considering that if single site-directed mutageneses are superimposed, the thermostability may be further improved, a variety of combinations of different mutagenesis sites also have been tried.
For 59-site Glu, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that the thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, L, I, V, F, M, W, T, C, N, Y, D, and H.
For 98-site Glu, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that the thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, A, L 1, V, P, F, S, T, C, N, Y, D, and H.
For the 225-site Gly, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, A, L, F, M, W, S. N, and D.
For the 277-site Lys, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely. A, L, I, F, S, T, N, Y, R, and H.
For 277-site Lys, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that the thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, A, L, I, F, S, T, N, Y, R, and H.
For 285-site Glu, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that the thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, A, L, I, F, M, W, Q, and N.
For the 355-site Asp, by the site-directed mutagenesis method, it is substituted with other 19 kinds of amino acids respectively, so as to construct 19 kinds of mutant plasmids. These 19 kinds of mutant plasmids are transformed and expressed as strain BL21 (DE3) respectively. Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that the thermostability of a vast majority of mutants has been improved, wherein improvements of thermostabilities of following mutants are significant, namely, L, I, V, F, M, W, T, C, Y, R, and H.
By specific analysis for the above sites, it is found that these sites indeed have a greater contribution to the thermostability of these enzymes. For this reason, it is considered that if different mutagenesis sites are combined, it is very likely that the thermostability of enzymes can be further improve. Thus, combinations of different mutagenesis sites are further conducted, such as a combination of 2 sites, a combination of 3 sites, a combination of 4 sites, a combination of 5 sites, a combination of 6 sites. However, since each site has ten or even more amino acid mutageneses that can be selected, combinations of different sites will be an astronomical figure. It is impossible to carry out research on each one. Therefore, merely mutagenesis combinations that are relatively representative can be selected, so as to illustrate that the combination of the above sites are effective.
For the combination of 2 mutagenesis sites, by the site-directed mutagenesis method, it is mutated into the following mutants: 59E→F, 98E→C; 59E→F, 225G→D; 59E→F, 277K→N; 59E→F, 285E→F; 98E→P, 225G→N; 98E→P, 277K→S; 225G→L, 277K→A; 225G→L, 285E→I; 277K→Y, 355D→T; 285E→I, 355D→W. The constructed mutant strains are transformed to BL2 (DE3). Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostabilities of these mutant strains have been further improved.
For the combination of 3 mutagenesis sites, by the site-directed mutagenesis method, it is mutated into the following mutants: 59E→F, 98E→C, 225G→F; 59E→F, 225G→D, 277K→N; 59E→F, 277K→N, 285E→I; 98E→P, 225G→N, 285E→Q; 225G→L, 285E→I, 355D→T. The constructed mutant strains are transformed to BL21 (DE3). Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostabilities of these mutant strains have been further improved.
For the combination of 4 mutagenesis sites, by the site-directed mutagenesis method, it is mutated into following mutants: 59E→F, 98E→C, 225G→F, 277K→N; 59E→F, 225G→D, 277K→N, 285E→F. The constructed mutant strains are transformed to BL21 (DE3). Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostabilities of these mutant strains have been further improved.
For the combination of 5 mutagenesis sites, by the site-directed mutagenesis method, it is mutated into following mutants: 59E→F, 98E→C, 225G→F, 277K→N, 285E→F. The constructed mutant strains are transformed to BL21 (DE3). Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostabilities of these mutant strains have been further improved.
For the combination of 6 mutagenesis sites, by the site-directed mutagenesis method, it is mutated into following mutants: 59E→F, 98E→C, 225G→F, 277K→N, 285E→F, 355D→L. The constructed mutant strains are transformed to BL21 (DE3). Cultivating, inducing, expressing, purifying, and enzymatic characteristic analysis are conducted. As a result, it is found that thermostabilities of these mutant strains have been further improved.
Meanwhile, as a common measure, between two sequences with a high homology, their structures and functions are usually similar. Beneficial effects obtained by mutating one of the sequences, the same mutagenesis conducted on the other sequence with a high homology usually can achieve similar beneficial effects. Generally speaking, the homology is more than 80%, preferably, more than 90%, more preferably, more than 96%, most preferably, more than 99%. Therefore, in the present invention, on the above basis, with respect to sequences that have a homology of equal or more than 80% with the amino acid sequence of Sequence 2, a great amount of researches on mutageneses and combinations thereof have been conducted.
Fructosyl amino acid oxidase from following several strains are selected as experimental subjects, so as to illustrate that enzymes homologies of more than 80% with Sequence 1, mutageneses on corresponding sites also lead to thermostabilities of these enzymes increased. These strains are: Aspergillus niger CBS513.88, Aspergillus clavatus NRRL1, Neosartorya fischeri NRRL181, and Aspergillus fumigatus Af293, respectively. Correspondingly, homologies with Sequence 1 are 80%, 83%, 96%, and 99%, respectively.
Aspergillus clavatus NRRL1 has a homology of 83% with Sequence 1, and its corresponding mutagenesis sites are 59E, 98E, 225G, 277N, 285E, and 355D. By selectively choosing several kinds of single amino acid mutagenesis, and several kinds of combinations of different sites mutageneses, it is found that thermostabilities of these enzymes do have different degrees of increase. For example, improvements of thermostabilities of following mutant strains are particularly evident: 59E→F, 98E→C, 225G→F, 285E→F, and 355D→L.
Neosartorya fischeri NRRL181 has a homology of 96% with Sequence 1, and its corresponding mutagenesis sites are 59E, 98E, 225G, 277K, 285E, and 355D. By selectively choosing several kinds of single amino acid mutagenesis, and several kinds of combinations of different sites mutageneses, it is found that thermostabilities of these enzymes do have different degrees of increase. For example, improvements of thermostabilities of following mutant strains are particularly evident: 59E→F, 98E→C, 225G→F, 277K→N, 285E→F, and 355D→L.
Aspergillus fumigatus Af293 has a homology of 999% with Sequence 1, and its corresponding mutagenesis sites are 59E, 98E, 225G, 277K, 285E, and 355D. By selectively choosing several kinds of single amino acid mutagenesis, and several kinds of combinations of different sites mutageneses, it is found that thermostabilities of these enzymes do have different degrees of increase. For example, improvements of thermostabilities of following mutant strains are particularly evident: 59E→F, 98E→C, 225G→F, 277K→N, 285E→F, and 355D→L.
In the present invention, mutageneses of amino acids are all substituted with Acronym character, which is common knowledge. Specific meanings are as follows: glycine G, alanine A, leucine L, isoleucine I, valine V, proline P, phenylalanine F, methionine M, tryptophan W, serine S, glutamine Q, threonine T, cysteine C, asparagine N, tyrosine Y, aspartic acid D, glutamic acid E, lysine K, arginine R, and histidine H. In the present invention, 285E→F, represents that 285-site glutamic acid is mutated into phenylalanine, and the rest are also similar.
Hereinafter, it should be noted that, the vector used by the present research is pET-22b, and the host bacteria (host cells) are BL21 (DE3). According to common sense, any simple alternations of vector, for example, pET-20b, pET-28b, pET-32a, pQE30, pTrc99a, and etc., or alternations of host bacteria, for example, Rosetta, Origami, M15, and etc., should be all construed as having the same technical effects, and should be all construed as falling into the scope of claims. Behaviors of adding purified tags or signal peptides on N or C-terminus of any mutant enzymes, should be also construed as falling into the scope of claims.
Generally, the well-known enzyme expression purification technology can be used for preparing fructosyl amino acid oxidases. For example, corresponding mutant strains are inoculated. After OD600 grows to 0.5˜1, isopropyl thiogalactoside (IPTG) induction is performed. In this case, in order to facilitate the expression, the low-temperature induction can be selected, such as 25° C., 20° C., 16° C., and etc. According to the induction temperature and the expression situation, an optimal induction time is determined, so as to obtain the optimal expression amount. After the expression, conventional methods can be used for centrifugation, sonic disruption, SDS-PAGE detection of the expression amount, and etc. As for purification, the tag carried by the recombinase can be used to select the appropriate method. For example, if a recombinant plasmid contains a His-tag, the nickel column can be used to for affinity purification.
The above fructosyl amino acid oxidases having good thermostabilities can be used to develop a detection method of glycated albumin, and to further develop glycated albumin test kit.
The main principle lies in that, an appropriate buffer being selected, under the action of a protease, the glycated albumin is degraded to fructosyl amino acids or fructosyl polypeptides. At this time, under the action of the fructosyl amino acid oxidases, fructosyl amino acids or fructosyl polypeptides are oxidized into fructose, glucose, or they are oxidized into peptides, hydrogen peroxide. A certain amount of oxygen is consumed at the same time. Then, by determining the generation of the product or the consumption amount of the substrate, the content of glycated albumin in the sample is calculated.
Sample requirements: in theory, as long as samples contain glycated albumin, glycated peptides, or glycated amino acids, they can be used as samples for testing. Since this method is mainly used in clinical tests, the common sample is the serum. Theoretically, hemolysis should be avoided. After samples are collected, they should be stored at 2˜8° C. and promptly tested.
Buffer: buffers of any suitable concentration and pH can be used here, as long as they have no inhibition effect on the activity of the reaction during the test, and do not interfere with the test process. Typical buffers are: Tris hydrochloride buffer solution, acetic acid-sodium acetate buffer, phthalic acid-hydrochloric acid buffer, or glycine-hydrochloric acid buffer solution, and etc. The concentration of the buffer can be determined depending on circumstances, preferably, 20˜200 mmol/L, more preferably, 50˜100 mmol/L.
Protease: any protease capable of degrading glycated albumin can be used here, preferably trypsin, basophils, protease A, proteinase K, etc. The added protease should facilitate full degradation of glycated albumin. According to different sources, corresponding concentration should be 10˜00 KU/L, preferably 40 KU/L.
Generation of product: there are three types of products generated: glucose, amino acids, and hydrogen peroxide. By determining the levels of any one of these three types of products, the content of glycated albumin can be calculated.
The determination of glucose can be performed by the hexokinase method. The principle is, under the effect of catalytic hexokinase, phosphorylation reaction occurs between glucose and ATP, producing glucose-6-phosphate (G-6-P) and ADP. Under the catalytic effect of Glucose-6-phosphate dehydrogenase (G6PD), the former is dehydrogenized, producing 6-phosphogluconate (6-GP). Meanwhile, NADP is reduced into NADPH. The rate of formation of NADPH is proportional to the concentration of glucose. The absorbance increase rate is monitored at a wavelength of 340 nm, so as to calculate the concentration of glucose.
By the reaction with fluorescamine, the fluorescence is eventually determined, so as to determine the amount of the amino acid.
The hydrogen peroxide can be detected by generating H2O2 through a coupling peroxidase, then generating the color through Trinder reaction. Here chromogen may be N, N-di(4-sulfobutyl)-3-methylaniline disodium salt (TODB), N-ethyl-N-(3-sulfopropyl)-3-methylaniline sodium salt (TOPS), and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt (TOOS).
The consumption of substrate, the substrate mainly refers to O2. The consumption of O2 can be detected by the oxygen electrode.
With the above method, a corresponding glycated albumin test kit can be developed. The main principle lies in that, an appropriate buffer being selected, under the action of a protease, the glycated albumin is degraded to fructosyl amino acids or fructosyl polypeptides. At this time, under the action of the fructosyl amino acid oxidases, fructosyl amino acids or fructosyl polypeptides are oxidized into fructose, glucose, or they are oxidized into peptides or hydrogen peroxide. A Certain amount of oxygen is consumed at the same time. Then, by determining the generation of the product or the consumption of the substrate, the content of glycated albumin in the sample is calculated. In practice, the most common method is detecting the hydrogen peroxide in the product, that is, detecting through Trinder reaction. This is the coupling manner currently used in the vast majority of test kits. Embodiments in the present specification focus on using this method to perform the experiment, so as to illustrate. However, detecting other substances to achieve the detection of glycated albumin in the test kit is not excluded.
This glycated albumin test kit includes reagent 1 and reagent 2. Reagent 1 contains a buffer, protease, peroxidase, 4-amino antipyrine, and preservatives. Reagent 2 contains a buffer, fructosyl amino acid oxidases mutant strains, the chromogen, preservatives.
Buffer: buffers of any suitable concentration and pH can be used here, as long as they have no inhibition effect on the activity of the reaction during the test, and do not interfere with the test process. Typical buffers are: Tris hydrochloride buffer solution, acetic acid-sodium acetate buffer, phthalic acid-hydrochloric acid buffer, or glycine-hydrochloric acid buffer solution, and etc. The concentration of the buffer can be determined depending on circumstances, preferably, 20˜200 mmol/L, more preferably, 50˜100 mmol/L.
Protease: any protease capable of degrading glycated albumin can be used here, preferably, trypsin, basophils, protease A, proteinase K, and etc. The added protease should facilitate full degradation of glycated albumin. According to different sources, corresponding concentration should be 10˜100 KU/L, preferably 40 KU/L.
Peroxidase: this enzyme functions as coupling. The concentration of 10˜100 KU/L can be added according to requirements, preferably, 30 KU/L.
The purpose of preservatives is to avoid the breeding of bacteria in the test kit, so as to ensure that the sensitivity and etc. of the test kit will not be affected for long-term preservation. Preservatives include 2-methyl-4-isothiazolin-3-one, proclin 300, and etc. To effectively achieve this object, the adding amount of preservatives should be 0.01˜0.05%, preferably 0.02%.
Said fructosyl amino acid oxidases refer to fructosyl amino acid oxidases with high thermostabilities of the present invention. The adding amount of these enzymes should be able to make the substrate fructosyl amino acids or fructosyl polypeptides sufficiently react. The adding amount should be 10˜100 KU/L, preferably, 20˜50 KU/L, most preferably, 28 KU/L.
The chromogen of the present invention may be N, N-di(4-sulfobutyl)-3-methylaniline disodium salt (TODB), N-ethyl-N-(3-sulfopropyl) sodium 3-methylaniline (TOPS), and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt (TOOS,). The concentration of the chromogen in the test kit may be 1˜10 mmol/L, preferably 2 mmol/L.
The above test kit for determining glycated albumin of the present invention, the test kit includes reagent 1 and reagent 2, wherein concentrations of components of the reagents are:
reagent 1:
buffer 20˜200 mmol/L,
protease 10˜100 KU/L,
peroxidase 10˜100 KU/L,
4-amino-antipyrine 5˜50 mM/L, and
preservative 0.01 to 0.05%;
reagent 2:
buffer 20˜200 mmol/L,
fructosyl amino acid oxidases obtained after amino acid of one or more of the above six sites is substituted 10˜100 KU/L
chromogen 1˜10 mmol/L, and
preservative 0.01 to 0.05%.
If the detection of glycated albumin of the present invention and the detection of albumin are combined, a percentage value of the glycated albumin can be obtained through calculating the glycated albumin concentration divided by the albumin concentration.
Since its performance is better than prior fructosyl amino acid oxidases, not only that the test kit meets the requirement in terms of sensitivity, interference, and etc., but also that all aspects of performance do not significantly decrease after long-term preservation.
The present invention provides a stable, simple, fast, sensitive and accurate quantitative detection reagents, whose detection has good dilution linearity, accuracy, precision, and has a good consistency with HPLC test. Compared with the prior art, in the glycated albumin test kit using the present invention, glycated albumin is determined by the enzyme method. It can completely replace the HPLC, to be applied to clinical laboratories, to perform tremendous sample testing. Its operation is simple, with a wide linear range, low cost. It is very valuable in practice.
The present invention is further illustrated below with reference to Embodiments. However, the present invention is not limited to the following Embodiments.
1. For the sequence shown in Sequence 2, using whole gene synthesis method to perform the synthesis, and it is cloned into pET-22b vector. Restriction sites NdeI and XhoI are used. Thereby obtained plasmid pET-Ama is the following error-prone PCR and WHOP-PCR template.
2. Error-Prone PCR Reaction System and Conditions
Reaction conditions are:
95° C. 5 min; 94° C. 30 sec; 55° C. 30 sec; 72° C. 2 min; 30 cycles; 72° C. 10 min; 4° C. preservation.
The amount of the above MnCl2 can be adjusted as appropriate, in order to obtain a suitable mutagenesis frequency, i.e., 1 to 2 nucleotide mutageneses/1 Kb nucleotides.
3. WHOP-PCR Reaction System and Conditions
The error-prone PCR fragment with the size of about 1.4 Kb is recycled using gel, and is used as primers in the next round WHOP-PCR.
WHOP-PCR reaction conditions:
98° C. 30 sec; 98° C. 10 sec; 60° C. 10 sec; 72° C. 2.5 min; 24 cycles; 72° C. 5 min; 4° C. preservation.
4. Digestion and Transformation
1 ul of DpnI is added into 50 ul of WHOP-PCR product, to perform the enzyme digestion. At 37° C., the reaction lasts for 2 hours to completely remove the template DNA.
The digested product described above is divided into five tubes and transformed into TOP10 competent cells. The next day, a total library capacity of more than 10000 monoclone is obtained.
1. Cultivating, Inducing, and Expressing
The obtained clones, after mixing by a coating stick, are collected in a centrifuge tube. Plasmids are extracted. The obtained plasmids are transformed into BL21 (ED3), to be ready for the next screening use. Next, the transformants are inoculated in a 96-well plate, wherein the last well is inoculated with a wild-type strain as a control. The cultivation medium is 150 ul LB/per well, containing the antibiotic ampicillin. This well plate is used as a retention plate. The next day, in the same order, it is transferred to another 96-well plate. The cultivation medium is 150 ul LB/per well. Meanwhile, the antibiotic ampicillin and IPTG are added for induction. It is cultivated at 37 (C for 6 hours. Bacteria is harvested by a centrifugation of 3800 rpm. The medium is removed. This plate is used as an assay plate.
2. Screening
150 ul lysis solution (100 mM Tris, pH 8.0; 0.4 mg/ml sodium deoxycholate; 0.8 mg/ml CTAB; 20 m MKCl; 80 mM MgSO4) is added to the assay plate. After lysis at room temperature for half an hour, it is centrifuged at 3800 rpm for 15 minutes. Another 50 ul lysate is added to a new 96-well plate. Another 50 ul of lysis solution is taken in a 96-well PCR plate, which is placed in a 96-well PCR instrument. It is heat-treated at 50° C. for 15 minutes. It is transferred to another 96-well plate. In the above-mentioned two plates, 100 ul of chromogenic solution (Tris, 100 mM, pH8.0; TOOS solution, 15 mM; 4-APP, 0.5 mM; POD, 40 U/ml; fructose lysine, 15 mM) is added respectively. By the chromogenic treatment for 30 minutes, the absorbance value is recorded using a microplate reader. By calculating a ratio of both absorbance, the activity proportion of residual enzyme of crude enzyme solution after the heat treatment is determined. For mutant strains having improved thermostability, their theoretical activity residual rate will be higher than that of the wild type.
In the present invention, by screening more than 10000 mutant strains, six mutant strains with enhanced thermostability are obtained in total by screening. After the sequencing analysis, it is found that these six mutant strains are all single-base mutagenesis. Their nucleotide sequence mutageneses are 177G→T, 293A→C, 764G→C, 830A→C, 853G→C, 1063G→C, respectively. Corresponding amino acid sequence mutagenises are 59E→N, 98E→A, 225G→A, 277K→S, 285E→Q, and 355D→H, respectively.
In a buffer of 100 mM Tris, pH 8.0, purified fructosyl amino acid oxidase is diluted to approximately 10 ug/ml.
50 ul of fructosyl amino acid oxidase is taken into a 96-well PCR. It is heat-treated at 50° C. for 15 min. It is stored under 4° C.
50 ul of heat-treated fructosyl amino acid oxidase is transferred to a 96-well plate. Meanwhile, unheated 50 ul fructosyl amino acid oxidase is taken to a 96-well plate. It is incubated at 37° C. for 10 min.
Color developing solution which has previously been incubated to 37° C. (Tris, 100 mM, pH 8.0; TOOS solution, 15 mM; 4-APP, 0.5 mM; POD, 40 U/ml; fructose lysine, 15 mM) is added. The reaction is conducted at 37° C. for 30 min.
The absorbance at 555 nm is recorded using a microplate reader.
The absorbance value of heat-treated fructosyl amino acid oxidase is divided by the absorbance value of non-heat-treated fructosyl amino acid oxidase. The resulting value is the ratio of residual activity at this temperature.
Thermostability analysis is performed on these six mutant strains obtained from random mutageneses and wild-type fructosyl amino acid oxidases. The results are shown in Table 3.
1. Introducing 59-Site Amino Acid Site-Directed Mutagenesis
In the first round of the PCR, pET-Ama is used as a template, primer sequence 5 (5′-tgctagttattgctcagcgg-3′), Sequence 6 (5′-acaagattatgttacacagcgagctg-3′) containing the site-directed mutagenesis are used as upstream primers respectively. Fragment containing site-directed mutagenesis is obtained. PCR system is 50 ul:
PCR reaction conditions are:
98° C. 30 sec; 98° C. 10 sec; 60° C. 10 sec; 72° C. 30 sec; 30 cycles; 72° C. 5 min; 4° C. preservation.
After the obtained target fragment is purified, it is used as a primer in the next round WHOP-PCR. Specific reaction system is shown in Table 5
PCR reaction conditions are:
98° C. 30 sec; 98° C. 10 sec; 60° C. 10 sec; 72° C. 2.5 min; 24 cycles; 72° C. 5 min; 4° C. preservation.
1 ul of DpnI is added into 50 ul of WHOP-PCR product to perform enzyme digestion. The reaction last for 2 hours under 37° C., so that the template DNA is removed completely. Then, BL21 (DE3) is transformed. After sequencing correctly, it is used for thermostability analysis.
Thermostability after 2.59-Site Amino Acid Substitution
The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to a fresh LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG with a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced in the 98-site amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to a fresh LB medium containing ampicillin. After OD600 grown to about 0.8, IPTG with a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced in 225-site amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to a fresh LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG with a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced in 277-site amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced in 285-site amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced in the 355-site amino acids. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced on two different sites of the amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced on three different sites of the amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced on four different sites of the amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced on five different sites of amino acids. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
According to the above method, different site-directed mutageneses are introduced on six different sites of amino acid. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
As is known from Blast, the amino acid sequence of fructosyl amino acid oxidases from Aspergillus niger CBS513.88 and the amino acid sequence of fructosyl amino acid oxidases from Aspergillus fumigatus have a homology of 80%. Its amino acid sequence is shown a sequence 68. The nucleotide sequence of the sequence 69 is shown. Use whole gene synthesis method, sequences 69 are synthesized, and cloned into the NdeI and XhoI restriction sites of pET-22b vector.
After the sequence analysis, it is found that, corresponding to amino acids of sites 59, 98, 225, 277, 285, and 355 of Amadoriase I, corresponding sites on fructosyl amino acid oxidases of Aspergillus niger CBS513.88 are 59E, 98E, 225G, 277K, 285E, and 355D.
According to the above method of site-directed mutagenesis, these sites of fructosyl amino acid oxidases of Aspergillus niger CBS513.88 is single-base mutated or mutated on a combination of different sites. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
Thermostability analysis of mutageneses of fructosyl amino acid oxidases from Aspergillus clavatus NRRL1 and the combination thereof
As is known from Blast, the amino acid sequence of fructosyl amino acid oxidases from Aspergillus clavatus NRRL1 and the amino acid sequence of fructosyl amino acid oxidases from Aspergillus fumigatus have a homology of 83%. Its amino acid sequence is shown in sequence 70. The nucleotide sequence is shown in sequence 71. Using whole gene synthesis method, sequences 71 is synthesized and cloned into the NdeI and XhoI restriction sites of pET-22b vector.
After the sequence analysis, it is found that, corresponding to amino acids of sites 59, 98, 225, 277, 285, and 355 of Amadoriase I, corresponding sites on fructosyl amino acid oxidases of Aspergillus clavatus NRRL1 are 59E, 98E, 225G, 277N, 285E, and 355D.
According to the above method of site-directed mutagenesis, these sites of fructosyl amino acid oxidases of Aspergillus clavatus NRRL1 are single-base mutagenesis or mutated on a combination of different sites. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
As is known from Blast, the amino acid sequence of fructosyl amino acid oxidases derived from Neosartorya fischeri NRRL181 and the amino acid sequence of fructosyl amino acid oxidases from Aspergillus fumigatus have a homology of 96%. Its amino acid sequence is shown in sequence 72. The nucleotide sequence is shown in sequence 73. Using whole gene synthesis method, sequences 73 is synthesized and cloned into the NdeI and XhoI restriction sites of vector pET-22b.
After the sequence analysis, it is found that, corresponding to amino acids of sites 59, 98, 225, 277, 285, and 355 of Amadoriase I, corresponding sites on fructosyl amino acid oxidases of Neosartorya fischeri NRRL181 are 59E, 98E, 225G, 277K, 285E, and 355D.
According to the above method of site-directed mutagenesis, these sites of fructosyl amino acid oxidases of Neosartorya fischeri NRRL181 are single-base mutated or mutated on a combination of different sites. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8, IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
As is known from Blast, the amino acid sequence of fructosyl amino acid oxidases from the amino acid sequence of Aspergillus fumigatus A1293 and fructosyl amino acid oxidases from Aspergillus fumigatus have a homology of 99%. Its amino acid sequence is shown in sequence 74. The nucleotide sequence is shown in sequence 75. Using whole gene synthesis method, sequences 75 is synthesized, and is cloned into the NdeI and XhoI restriction sites of pET-22b vector.
After the sequence analysis, it is found that, corresponding to amino acids of sites 59, 98, 225, 277, 285, and 355 of Amadoriase I, corresponding sites on fructosyl amino acid oxidases of the Aspergillus fumigatus CBS513.88 are 59E, 98E 225G, 277K, 285E, and 355D.
According to the above method of site-directed mutagenesis, these sites of fructosyl amino acid oxidases of Aspergillus fumigatus Af293 are single-base mutated or mutated on a combination of different sites. The obtained mutant is inoculated overnight. The next day, in a proportion of 1%, it is transferred to LB medium containing ampicillin. After OD600 grows to about 0.8. IPTG having a final concentration of 0.4 mM is added. It is induced for about five hours. Bacteria are harvested by centrifugation, broken, and purified. Thermostability analysis as described above is performed on purified fructosyl amino acid oxidases. Detailed results are shown in the table below.
1. Obtaining the strain: when the strain containing different mutated genes has been cultivated to OD600 of about 0.8, IPTG is added. It is induced for 5 hours. The strain is harvested by centrifugation. The collected strain is re-suspended with the buffer, and is ultrasonically disrupted. The supernatant is collected by centrifugation.
2. Ammonium sulfate precipitation: using an ammonium sulfate solution, the supernatant obtained in step (1) is subjected to fractional precipitation. The final collected and obtained precipitate is dissolved in buffer A, so as to obtain a crude extracted solution.
Affinity chromatography: using buffer A balanced nickel column, the crude extract solution obtained in step (2) is adsorbed on a nickel column. After the absorption finishes, gradient elution is performed with an imidazole solution. The eluent is collected.
4. Dialysis: the eluate in step (3) is put into a dialysis bag. It is put in a dialysate at 4° C., and is dialyzed overnight with magnetic stirring.
Buffer A in step (2) is: 50 mM potassium phosphate buffer, pH 8.0, 500 mM NaCl.
Imidazole solution in step (3) is: 50 mM potassium phosphate buffer, pH 8.0, 500 mM NaCl, 20 mM˜1000 mM imidazole.
Dialyzate in step (4) is: 50 mM potassium phosphate buffer, pH 8.0, 500 mM NaCl.
Including reagent 1 and reagent 2, wherein:
Reagent 1:
Tris hydrochloride buffer 50 mmol/L
Protease K40 KU/L
Peroxidase 30 KU/L
4-amino-antipyrine 10 mmol/L
Methyl-4-isothiazolin-3-one 0.02%
Reagent 2:
Tris hydrochloride buffer 50 mmol/L
Mutants of fructosyl amino acid oxidases 28 KU/L
N. N-bis(4-sulfobutyl)-3-methylaniline (TODB) 2 mmol/L
Methyl-4-isothiazolin-3-one 0.02%
The mutant of fructosyl amino acid oxidase used in the present embodiment particularly is No. M76 mutant. In fact, other mutants also can be used.
Fresh serum samples should be used for the test. The hemolysis should be avoided. After the serum is collected, if not promptly tested, it should be stored at 4 CC. Theoretically, it should not be stored for more than two weeks.
Detection conditions: Main wavelength of 600 nm, sub-wavelength of 700 nm.
Detection steps: shown in Table 21
The linear range, shown in
The serum having high GA value is taken, and is diluted into different gradients using normal saline, and will be measured respectively.
The linear range of glycated albumin detected by this method is 21.0˜1200 umol/L, r2>0.990.
A high and low quality control and two serum samples are tested 20 times respectively. Mean values are 204 umol/L, 751 umol/L, 251 umol/L, 373 umol/L respectively. CVs are 1.1%, 0.7%, 0.8%, 0.6% respectively.
A high and low value quality control and two serum samples are continuously measured for 10 days respectively. Mean values are 204 umol/L, 751 umol/L, 251 umol/L, 373 umol/L, respectively. CVs are 1.2%, 0.7%, 1.3%, 1.0%, respectively.
On Hitachi biochemical analyzer, the open-bottle stability of the reagent can sustain for at least 4 weeks.
The glycated albumin detection test kit of the present invention and classical HPLC detection methods are used in the determination of the same sample, after comparison, it is found that the correlation is good, R2>0.995.
It is found that, when the concentration of vitamin C is less than 0.2 mmol/L, hemoglobin less than 1.6 g/L, bilirubin less than 0.32 mmol/L, uncoupling bilirubin less than 0.32 mmol/L, triglyceride less than 20 mmol/L, blood glucose less than 20 g/L, uric acid less than 36 g/L, their interference of the measured value of glycated albumin is less than 10%.
The detection of glycated albumin and the detection of albumin are combined, so as to obtain a percentage value of the glycated albumin through calculating the glycated albumin concentration divided by the albumin concentration.
The Albumin detection reagent is as follows
Reagent 3:
Succinate buffer 0.05 mol/L
Polyoxyethytene (23) lauryl ether 2.4 g/L
Bromocresol green 1.8×10−4 mol/L
Test conditions: main wavelength of 600 nm, sub-wavelength of 700 nm.
Reaction method: end-point method.
Detection steps: shown in Table 26
Using the above method, 20 samples of serum are detected. The percentage of glycated albumin is calculated, as shown in Table 27.
Typically, the reference value of glycated albumin is from 11% to 16%. An increased glycated albumin value is common in diabetes. The index can be used as a reference indicator of medium-term glucose control of diabetic patients.
Since mutants of fructosyl amino acid oxidases involved in the present invention are so many, it is impossible to verify them in the glycated albumin test kit one by one. Therefore, only a few of the most typical mutants of fructosyl amino acid oxidases are selected for the glycated albumin detection test kit. Their performances are evaluated. Mutants of fructosyl amino acid oxidases involved in the present invention that are suitable for the glycated albumin test kits are used to illustrate the present invention, and cannot limit the present invention. The detection method of the involved test kit, verification methods of linear range, the intra-batch precision, the precision inter-batch, the open-bottle stability, the correlation with HPLC, the anti-interference, and etc. are the same as those of Embodiments twenty to twenty-five.
Glycated albumin test kit includes reagent 1 and reagent 2, wherein:
Reagent 1:
Tris hydrochloride buffer 50 mmol/L
Protease K 40 KU/L
Peroxidase 30 KU/L
4-amino-antipyrine 10 mmol/L
Methyl-4-isothiazolin-3-one 0.02%
Reagent 2:
Tris hydrochloride buffer 50 mmol/L
Fructosyl amino acid oxidase mutant 28 KU/L
N, N-bis(4-sulfobutyl)-3-methylaniline (TODB) 2 mmol/L
Methyl-4-isothiazolin-3-one 0.02%
In this embodiment, the following representatives are selected from mutant strains of fructosyl amino acid oxidases to be tested: i.e., those prepared in the above embodiments, M1, M13, M28, M35, M50, M56, M64, M73, M79, M80, M81, M90, M100, M109, and M120.
Performances of the above mutants of fructosyl amino acid oxidases and their corresponding glycated albumin test kit are shown in the table below in details.
The above embodiments of the present invention are descriptions of the present invention, but not for limiting the present invention. Any change equivalent to the concept and scope of claims of the present invention should all be construed as falling within the scope of the claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201310744635.8 | Dec 2013 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2014/093580 | 12/11/2014 | WO | 00 |
