JPH08131162A - Gene for coding phosphoenolpyruvic carboxylase - Google Patents

Abstract

PURPOSE: To obtain the subject new gene having a specific amino acid sequence, coding phosphoenolpyruvic carboxylase, useful as a reagent for measuring a carbon dioxide gas as an enzyme for clinical examination agent, capable of producing the enzyme having excellent stability. CONSTITUTION: This new gene has an amino acid sequence containing an amino acid sequence of the formula, codes phosphoenolpyruvic carboxylase, is useful as a reagent for measuring a carbon dioxide gas as an enzyme for clinical examination and is capable of producing the enzyme having excellent stability. The gene is obtained by separating chromosomal DNA from Acetobacter hansenii IFO14,820 by a conventional method, treating it with a restriction enzyme, bonding a formed fragment to a vector, transducing the vector to Escherichia coli, screening the prepared transformant with an antibody, selecting a clone containing phosphoenolpyruvic carboxylase gene, recovering the DNA and treating it with a restriction enzyme.

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to a gene encoding a novel phosphoenolpyruvate carboxylase, which is suitable for measuring the carbon dioxide concentration in a sample, and its use.

[0002]

BACKGROUND OF THE INVENTION Phosphoenolpyruvate carboxylase is an enzyme that acts on phosphoenolpyruvate and bicarbonate ions to catalyze the reaction that produces oxaloacetate and phosphate ions. In particular, it has been conventionally used as a reagent for measuring bicarbonate ion in serum and plasma. As a source of this phosphoenolpyruvate carboxylase, it has been reported that it is present in many plants, protozoa, and most bacteria ("Protein, nucleic acid, enzyme" Vol.22, No.14 (1977)). . However, most of these phosphoenolpyruvate carboxylases require expensive acetyl-coenzyme A, fructose-1,6-diphosphate and glucose-6-phosphate as activators for activity expression, and they are used as enzymes for clinical laboratory tests. Had a problem. Phosphoenolpyruvate carboxylase, which does not require an activator, has been found in some bacteria and C4 plants, but it has a problem in stability as an enzyme for clinical laboratory tests.

As a result of intensive studies to solve the above problems, it was found that a kind of acetic acid bacterium does not require an expensive activator and produces stable phosphoenolpyruvate carboxylase (special feature). 5-1132
No. 48).

[0004]

When phosphoenolpyruvate carboxylase is produced from the above-mentioned acetic acid bacterium,
Since the productivity is low and many purification steps are required, the manufacturing cost is high, which is a problem as a source of enzyme for clinical laboratory drugs. An object of the present invention is to provide a means capable of supplying a large amount of a novel phosphoenolpyruvate carboxylase in pure form by a genetic engineering method in order to solve the above problems.

[0005]

[Means for Solving the Problems] In order to achieve the above-mentioned object, the inventors of the present invention have identified acetobacter hansenii as a phosphoenolpyruvate carboxylase-producing bacterium.
acter hansenii) IFO14820 was selected, the phosphoenolpyruvate carboxylase gene was successfully isolated from the chromosomal DNA extracted from the cells, and the total structure of the DNA was determined. Furthermore, the phosphoenolpyruvate carboxylase was successfully produced in a transformant at a high level by a genetic engineering technique, and a large amount of highly pure phosphoenolpyruvate carboxylase could be supplied inexpensively.

That is, the present invention is a DNA fragment encoding phosphoenolpyruvate carboxylase, which comprises a DNA encoding the amino acid sequence set forth in SEQ ID NO: 1 of the Sequence Listing.

The present invention is also a recombinant vector containing the above DNA fragment.

Further, the present invention is a transformant transformed with the above recombinant vector.

The present invention comprises culturing the above transformant in a medium,
A method for producing phosphoenolpyruvate carboxylase, which comprises producing phosphoenolpyruvate carboxylase and collecting the phosphoenolpyruvate carboxylase.

The gene of the present invention originates from, for example, Acertobacter hansenii IFO 14820. As a medium for culturing this strain, a carbon source,
A medium containing a nitrogen source, inorganic ions, and optionally nitrates, phosphates, etc. is used. As the carbon source, sugars such as glucose and lactose or sugar alcohols such as glycerol and sorbitol can be used. As the nitrogen source, polypeptone, tryptone,
Meat extract, yeast extract, etc. can be used. In culturing the bacterium, an inducer or the like is not particularly necessary, and the phosphoenolpyruvate carboxylase production is maximized by culturing at a temperature and a pH at which the strain grows best under aerobic conditions. Incubate until time point.

The following method is used to purify phosphoenolpyruvate carboxylase from cultured cells. Collect the cells from the culture by centrifugation,
Then, the cells are crushed to extract phosphoenolpyruvate carboxylase. Examples of the method for disrupting the cells include treatment with a cell wall lysing enzyme such as lysozyme, and physical treatment such as ultrasonic disruption, glass bead disruption, French press disruption. The crude enzyme extract thus obtained is subjected to nucleic acid removal treatment by, for example, polyethyleneimine treatment, and then the phosphoenolpyruvate carboxylase fraction is recovered by ammonium sulfate precipitation. The phosphoenolpyruvate carboxylase fraction thus obtained is desalted by, for example, G-25 gel filtration, and then DEAE Sepharose CL-6B.
(Pharmacia LKB) → Hydroxyl apatite (Seikagaku Corporation) → Sephadex G-200 gel filtration (Pharmacia LKB) → MonoP HR5 / 5 chromatofocusing (Pharmacia LKB) etc.

The protein purified by the present inventors is SD
S-polyacrylamide gel showed electrophoretically uniform bands. The specific activity of phosphoenolpyruvate carboxylase at this time was 84 units (U) / mg protein. still,
Although the combination of column chromatography does not have to be limited to the above steps, several steps of column chromatography operation are required to obtain an electrophoretically uniform band.

The physicochemical properties of the above phosphoenolpyruvate carboxylase are as follows. (1) Action: It catalyzes the following reaction.

Phosphoenolpyruvate + HCO ₃
^- → Oxaloacetate + HPO ₄ ^2-

(2) Optimum action pH: 7.5-8.0 (3) pH stability: pH 5.0-8.0 (25 ° C, 24
Time treatment) pH 7.5 to 8.5 (25 ° C. for 24 hours in Tris buffer containing 10 mM MgSO ₄ ) (4) Optimum temperature: 60 ° C. (5) Thermal stability: 45 ° C. or less (pH 7. (6) Molecular weight: 390,000 ± 10,000 (gel filtration method) 100,000 ± 5,000 (SDS-PAGE) (7) Specific activity: 84 units / mg protein (8) Acetyl Not activated by CoA.

The gene encoding the novel phosphoenolpyruvate carboxylase of the present invention may be extracted from the bacterium of Acetobacter hansenii IFO 14820 or it may be chemically synthesized. As the gene sequence, for example, a DNA sequence encoding the amino acid sequence described in SEQ ID NO: 1 or a DNA having the base sequence described in SEQ ID NO: 2 or a sequence described in SEQ ID NO: 2 is mutated. DNAs that have been changed by

The gene of the present invention includes, for example, a product obtained by separating and purifying chromosomal DNA of Acetobacter hansenii IFO 14820, then sonicating, cleaving the DNA using a restriction enzyme, and a linear expression vector. The blunt end or sticky end of the DNA is ligated and closed with a DNA ligase to give a recombinant vector. The recombinant vector thus obtained is transferred to a replicable host microorganism and then screened using the marker of the vector and the expression of phosphoenolpyruvate carboxylase protein as an index to obtain a microorganism carrying the recombinant DNA vector. As a screening method for phosphoenolpyruvate carboxylase protein expression, a method by an antigen-antibody reaction using an antibody of the protein, a method of directly measuring the activity of the protein, and an auxotrophic complementation method using a deletion mutant of the protein Can be used. A microorganism expressing the protein may be cultured, the recombinant vector may be separated and purified from the cultured cells, and then the phosphoenolpyruvate carboxylase gene may be collected from the recombinant vector.

The DNA derived from the gene donor, Acetobacter hansenii IFO 14820, is specifically collected as follows. That is, for example, a culture obtained by stirring and culturing a donor microorganism in a liquid medium for about 1 to 3 days is collected by centrifugation, and then lysed to prepare a lysate containing a phosphoenolpyruvate carboxylase gene. You can do it. As a lysing method, for example, a treatment with a lysing enzyme such as lysozyme or β-glucanase is performed, and if necessary, a protease or other enzyme and a surfactant such as sodium lauryl sulfate (SDS) are used together, and further freeze-thawing It may be combined with a physical crushing method such as or French press treatment.

DNA from the lysate thus obtained
In order to separate and purify the product, a method such as deproteinization treatment with phenol treatment or protease treatment, ribonuclease treatment, alcohol precipitation treatment and the like can be appropriately combined according to a conventional method. The DNA separated and purified from the microorganism can be cleaved by, for example, sonication or restriction enzyme treatment, but a type II restriction enzyme acting on a specific nucleotide sequence is preferable.

Suitable vectors are those constructed for gene recombination from phages or plasmids capable of autonomous growth in host microorganisms. As the phage, for example, when Escherichia coli is used as a host microorganism, λgt · 10, λgt · 1
1 etc. can be used. As a plasmid, for example, when Escherichia coli is used as a host microorganism, pBR
322, pUC19, pBluescript, etc. can be used. Such a vector can be cleaved with the restriction enzyme used for cleaving the phosphoenolpyruvate carboxylase gene donor microbial DNA described above to obtain a vector fragment.
It is not necessary to use the same restriction enzyme as that used for the cleavage of The method for ligating the microbial DNA fragment and the vector DNA fragment may be a method using a known DNA ligase. For example, after annealing the cohesive ends of the microbial DNA fragment and the vector fragment, a suitable D
A recombinant vector of a microbial DNA fragment and a vector fragment is prepared by using NA ligase. If necessary, the recombinant vector can be prepared by using the in-vivo DNA ligase by transferring into a host microorganism after annealing.

[0021] As the host microorganism, it is sufficient that the recombinant vector is capable of stable and autonomous growth and capable of expressing a foreign gene. Generally, Escherichia coli W3110, Escherichia coli C600, Escherichia collie JM109, Escherichia collie H
B101 or the like can be used.

As a method for introducing the recombinant vector into the host microorganism, for example, when the host microorganism is a microorganism belonging to the genus Escherichia coli, the competent cell method by calcium treatment or the electroporation method can be used. . It was found that the thus obtained transformant microorganism can stably produce a large amount of phosphoenolpyruvate carboxylase by culturing in a nutrient medium. The selection as to whether or not the target recombinant vector is transferred into the host microorganism is carried out by selecting the drug resistance marker of the vector carrying the target DNA and acetyl CoA.
It is only necessary to search for a microorganism that simultaneously expresses a phosphoenolpyruvate carboxylase activity that does not require an activator such as phosphoenolpyruvine that grows in a selective medium based on a drug resistance marker and does not require an activator. A microorganism that produces acid carboxylase may be selected.

The nucleotide sequence of the phosphoenolpyruvate carboxylase gene obtained by the above method was deciphered by the dideoxy method described in Science, 214, 1205-1210 (1981). The amino acid sequence was deduced from the base sequence. The recombinant vector carrying the phosphoenolpyruvate carboxylase gene thus selected once can be easily taken out from the transformed microorganism and transferred to another microorganism. In addition, a DNA which is a phosphoenolpyruvate carboxylase gene is excised from a recombinant vector having a phosphoenolpyruvate carboxylase gene by a restriction enzyme and the like, and the fragment is ligated with a vector fragment obtained by cleaving the DNA by the same method to prepare a host. Transfer to microorganisms is also easy.

The culturing form of the host microorganism which is a transformant may be selected by considering the culturing conditions in consideration of the nutritional physiological properties of the host. Usually, in most cases liquid culture is carried out, but industrially aeration stirring It is advantageous to carry out culturing. As the carbon source of the medium, those usually used for culturing microorganisms can be widely used. It is sufficient that the host microorganism can assimilate, and for example, glucose, sucrose, lactose, maltose, fructose, molasses, pyruvic acid and the like can be used. The nitrogen source may be any nitrogen compound that can be utilized by the host microorganism, for example, organic nitrogen compounds such as peptone, meat extract, casein hydrolyzate and soybean meal alkali extract, and ammonium sulfate and ammonium salt. Inorganic nitrogen compounds can be used. In addition, salts such as phosphates, carbonates, sulfates, magnesium, calcium, potassium, iron, manganese and zinc, specific amino acids, specific vitamins and the like can be used as necessary.

The culturing temperature can be appropriately changed within the range where the host microorganism grows and produces phosphoenolpyruvate carboxylase, but in the case of Escherichia coli, it is preferably about 20 to 42 ° C. Although the culturing time varies somewhat depending on the culturing conditions, it may be completed at a suitable time in consideration of the time when the maximum yield of phosphoenolpyruvate carboxylase is reached, and it is usually about 20 to 48 hours. The pH of the medium can be appropriately changed within the range where the host microorganism grows and produces phosphoenolpyruvate carboxylase, but it is usually preferably about pH 6.0 to 9.0. The cells can be collected from the culture broth by a commonly used method, for example, centrifugation or filtration. When phosphoenolpyruvate carboxylase in the culture medium is secreted outside the cells, this cell separation solution may be used, and phosphoenolpyruvate carboxylase can be separated and purified according to the method after cell disruption below. . When phosphoenolpyruvate carboxylase is present in the cells, it can be crushed and extracted by the enzymatic or physical crushing method described above. The phosphoenolpyruvate carboxylase-containing solution thus obtained is treated with a hydrophilic polymer such as polyethyleneimine to remove nucleic acid, and then the phosphoenolpyruvate carboxylase fraction is recovered by ammonium sulfate precipitation. This crude enzyme solution is usually used, for example, dialysis using a semipermeable membrane or Sephadex G-25.
(Pharmacia LKB) Desalination can be performed by gel filtration or the like. After this operation, the enzyme solution is combined with various chromatographies, preferably DEAE Sepharose CL-6B (Pharmacia LKB), Butyl Toyopearl.
A purified enzyme preparation can be obtained by separation and purification by 650M (Toyo Soda) column chromatography. This purified enzyme preparation was purified to the extent that it showed almost a single band on SDS-PAGE electrophoresis.

The protein having phosphoenolpyruvate carboxylase activity of the present invention has the following properties. (1) Action: It catalyzes the following reaction.

Phosphoenolpyruvate + HCO ₃
^- → Oxaloacetate + HPO ₄ ^2-

(2) Optimum action pH: 7.5 to 8.0 (3) pH stability: pH 5.0 to 8.0 (25 ° C, 24
Time treatment) pH 7.5-8.5 (treatment in Tris buffer containing 10 mM MgSO4 at 25 ° C for 24 hours) (4) Optimum temperature: 60 ° C (5) Thermal stability: 45 ° C or less (pH 7.0) , Treatment for 15 minutes) (6) Molecular weight: 390,000 ± 10,000 (gel filtration method) 100,000 ± 5,000 (SDS-PAGE) (7) Specific activity: 110 units / mg protein (8) Acetyl CoA Not activated by.

The enzyme is Acetobacter hansenii IFO
Compared with the enzyme produced by 14820, it differs in stability and specific activity in the reagent for measuring carbon dioxide. That is,
The enzyme produced by Acetobacter hansenii IFO 14820 has a specific activity of 84 units / mg protein and a residual activity ratio of about 30% after storage in a reagent for measuring carbon dioxide at 25 ° C. for 7 days. The protein having a phosphoenolpyruvate carboxylase activity of 110 has a specific activity of 110 units / m 2.
The activity residual rate after storage for 7 days at 25 ° C. in a reagent for measuring g protein and carbon dioxide is about 95%.

[0030]

EXAMPLES The present invention will be specifically described below with reference to examples. In the examples, the phosphoenolpyruvate carboxylase activity was measured as follows. That is,
50 mM Tris-HCl (pH 8.0), 10 mM
Na ₂ CO ₃ , 3.2 mM phosphoenolpyruvate potassium salt, 10 mM MgSO ₄ , 0.14 mM N
2.9 ml of a reaction mixture containing ADH and 10 U / ml malate dehydrogenase is prepared in a cuvette (d = 1 cm), and preheated at 30 ° C. for about 5 minutes. Next, 0.1 ml of enzyme solution was added and mixed gently, and water was used as a control at 30 ° C.
Change the absorbance at 340 nm with a spectrophotometer controlled to 2
Record for ~ 3 minutes and determine the change in absorbance per minute from the initial linear portion (ΔODtest). In the blind test, instead of the enzyme solution, 50 mM potassium phosphate buffer, pH 7.0
Is added and the same operation is performed to determine the change in absorbance per minute (ΔODblank). Regarding the activity of phosphoenolpyruvate carboxylase, the amount of the enzyme that consumes 1 micromol NADH per minute under the above-mentioned conditions is 1 unit (U).

Reference Example 1 From Acetobacter hansenii IFO 14820 strain
Purification of phosphoenolpyruvate carboxylase Phosphoenolpyruvate carboxylase-producing bacterium Acetobacter hansenii IFO 14820 was cultured in a 10 L jar fermenter. Medium composition is polypeptone 0.5
%, Yeast extract 0.5%, glucose 0.5%, magnesium sulfate 0.5%, medium (pH 7.0) 100 m
1 to a 500 ml Sakaguchi flask, 121 ° C, 15
It was autoclaved for a minute. Acetobacter hansenii IFO 14820 was inoculated as an inoculum with 1 platinum loop, at 30 ℃,
It was cultured for 48 hours to obtain a seed culture solution. Next, add 6 L of medium to 10
The mixture was transferred to an L-volume jar fermenter and autoclaved at 121 ° C. for 15 minutes. After release, 100 ml of the seed culture solution was transferred and cultured at 300 rpm, aeration 2 L / min, and 30 ° C. for 48 hours. The phosphoenolpyruvate carboxylase activity in the culture medium at this time was 0.2 U / ml.

The culture broth was collected by centrifugation and suspended in 50 mM potassium phosphate buffer, pH 7.0. This solution was treated with a French press and centrifuged to obtain a crude enzyme fraction of phosphoenolpyruvate carboxylase. The crude enzyme fraction thus obtained was subjected to Sephadex G-25 after ammonium sulfate fractionation.
(Pharmacia LKB) After desalting by gel filtration, DEAE
Sepharose CL-6B (Pharmacia LKB), Hydroxyl apatite (Seikagaku Corporation), Sephadex G-200 gel filtration (Pharmacia LKB), MonoP HR5 / 5
Four types of chromatography, chromatofocusing (Pharmacia LKB), were performed. The phosphoenolpyruvate carboxylase preparation was purified until it showed a uniform band on SDS-PAGE. The specific activity of phosphoenolpyruvate carboxylase at this time is 84U.
/ Mg protein. Table 1 below shows a summary of the purification so far. Table 2 shows the physicochemical properties of phosphoenolpyruvate carboxylase obtained by the above method.

[0033]

[Table 1]

[0034]

[Table 2]

[0035] Chromosomal DNA isolation Acetobacter Hanzenii IFO fourteen thousand eight hundred twenty of Example 1 Chromosomal DNA
Were separated by the following method. The strain was cultured with shaking in 150 ml of a normal broth medium at pH 5.0 at 30 ° C. for 48 hours and then collected by centrifugation (8000 rpm, 10 minutes). 10% sucrose, 50 mM Tris-H
Solution 5 containing Cl, pH 8.0, 50 mM EDTA 5
1 ml lysozyme solution (10 mg / m
l) was added and incubated at 37 ° C for 15 minutes, then 10% S
The DS solution was added. To this solution, add an equal volume of chloroform / phenol (1: 1), stir and mix, and add 10,000
The aqueous layer and the solvent layer were separated by centrifugation at rpm for 3 minutes, and the aqueous layer was separated. The aqueous layer was gently overlaid with 2 volumes of ethanol, and the DNA was wound around the glass rod while gently stirring with a glass rod to separate the DNA. This is 1 mM EDTA
It was dissolved in 10 mM Tris-HCl, pH 8.0 (hereinafter abbreviated as TE) containing After treating this with an equal volume of chloroform / phenol solution, the aqueous layer was separated by centrifugation, twice the amount of ethanol was added, the DNA was separated again by the above method, and dissolved with 2 ml TE. Escherichia Collie JM109 competent cell is Hanahan
Was prepared by the method described above and used as a host for library preparation.

Phosphoenolpyruvate Carboxyler
Set having a DNA fragment containing a gene encoding ze
Preparation of recombinant vector 20 μg of the DNA obtained by the above method was added to the restriction enzyme Sau3AII.
After partial decomposition with I (manufactured by Toyobo Co., Ltd.), a 3-10 kbp fragment was separated and collected by a sucrose density gradient centrifugation method, concentrated by ethanol precipitation, and redissolved by TE to a concentration of 1 μg / μl. 1 μg of this DNA fragment was added to SalII
PUC190.5 μg cut with I (manufactured by Toyobo) and M.
Backfilling method of G. Loftus et al. (Biotechniques Vol. 12,
According to No. 2 (1992), T4 DNA ligase (Toyobo)
The DNA was ligated by reacting with 1 unit at 16 ° C. for 12 hours. The ligated DNA is Escherichia coli JM109.
Transformation was performed using the competent cells of. Used D
About 1 × 10 ⁵ transformant colonies were obtained per 1 μg of NA.

Phosphoenolpyruvate carboxylate
Transformant containing a DNA fragment encoding the ze gene
Screening of transformants containing a DNA fragment containing the phosphoenolpyruvate carboxylase gene from the transformants obtained by the method described above was carried out using an antibody specific to phosphoenolpyruvate carboxylase derived from Acetobacter hansenii IFO 14820. The enzyme immunoassay used was used. The preparation of the phosphoenolpyruvate carboxylase antibody derived from Acetobacter hansenii IFO 14820 and the enzyme label on the antibody was carried out in the following manner according to a conventional method. 10 ml of the serum of a rabbit immunized with phosphoenolpyruvate carboxylase derived from Acetobacter hansenii IFO 14820 was purified with protein A-Sepharose CL-6B (Pharmacia LKB) to collect an IgG fraction. Next, 8 mg of this IgG and 5 mg of peroxidase (manufactured by Toyobo) were used to prepare an IgG-peroxidase conjugate by the new Nakane method, and TSK G3000SW (Toyo Soda)
Purification was performed by gel filtration. The IgG-peroxidase conjugate obtained by the above method has a sensitivity capable of detecting 0.1 ng of phosphoenolpyruvate carboxylase protein and does not react with phosphoenolpyruvate carboxylase derived from Escherichia coli. It was The method for screening the phosphoenolpyruvate carboxylase gene using the phosphoenolpyruvate carboxylase antibody-peroxidase conjugate obtained by the above method was performed as follows.

The transformant colonies obtained by the above method are
After replicating on a vinyl sheet coated with phosphoenolpyruvate carboxylase antibody, it was cultured at 37 ° C. overnight to form colonies again, and then stored as a master plate. On the other hand, the bacterial cells on the replicated vinyl sheet were exposed to chloroform vapor for about 20 minutes to lyse them. After lysis procedure, 10 mM PBS containing 0.1% BSA
(2.3 mM KH ₂ PO ₄ , 7.7 mM Na ₂ HP
O ₄ .12H ₂ O, 150 mM NaCl, pH 7.
The cells were washed in 2) to remove the cell residue. This vinyl sheet was immersed in 10 mM PBS containing 0.1% phosphoenolpyruvate carboxylase antibody-peroxidase conjugate and 0.1% BSA at room temperature for 3 hours. Then 0.1% BSA and 0.05% Tween
It was washed with PBS containing 20 and further with distilled water, and then air-dried. The air-dried vinyl sheet was used as a gelatin plate (3 mg / ml 3,3'-5,5'-tetramethylbenzidine, containing a color-developing substrate for peroxidase,
10 mg / ml dioctyl sodium sulphate,
0.4 g / ml gelatin, 50% methanol, 50 mM
It was placed on a citrate buffer solution (pH 5.0), and a spot that developed a green color was detected. The colored spots were compared with the positions of the colonies on the master plate, and the matching colonies were selected as transformants containing the phosphoenolpyruvate carboxylase gene.

As a result of screening about 20,000 transformants by the above method, two antibody-positive strains were obtained. As a result of extracting a plasmid from these two strains and creating a restriction enzyme map, a common DNA fragment of about 2.7 kbp was confirmed.

Determination of nucleotide sequence Among the recombinant plasmids obtained by the above method, the inserted DNA
The plasmid having a small DNA size was designated as pEPC11, and the nucleotide sequence of the inserted DNA (about 4.2 kbp) was determined. Various subclones and deletion mutants were prepared according to the standard method using Nonradioactive Sequencing
t (manufactured by Toyobo). The determined nucleotide sequence and amino acid sequence are shown in Sequence Listing and SEQ ID NOs: 1 and 2.
The molecular weight of the protein determined from the amino acid sequence is about 10
3,000 and the Acetobacter Hansenii IFO 1
It was in good agreement with the molecular weight of phosphoenolpyruvate carboxylase of 4820 (about 100,000).

Preparation of Escherichia coli Transformant After transforming competent cells of Escherichia coli JM109 with pEPC11, transformant Escherichia coli.
Cory JM109 (pEPC11) was obtained.

Phosphoenolpyruvate carboxylate
Preparation of TB medium (1.2% bactotryptone, 2.4% bacto yeast extract, 0.4% glycerol, 17%
6 L of mM KH ₂ PO ₄ , 72 mM K ₂ HPO ₄ ) was dispensed into a 10 L-jar fermenter, and 121 ° C., 1
After autoclaving for 5 minutes and allowing to cool, 6 ml each of 50 mg / ml ampicillin (manufactured by Nacalai Tesque) and 100 mM isopropyl-1-thio-β-D-galactoside (IPTG, manufactured by NIPPON SEIKA CO., LTD.), Which were separately aseptically filtered, were added. LB medium (1% bactotryptone,
0.5% Bacto yeast extract, 1.0% Na
60 ml of a culture solution of Escherichia coli JM109 (pEPC11) which had been shake-cultured with Cl, pH 7.4) at 30 ° C. for 16 hours in advance was inoculated, and the mixture was aerated with stirring at 30 ° C. for 24 hours. The phosphoenolpyruvate carboxylase activity of the culture medium at the end of the culture was 5.4 U / ml. 6 L of the culture solution was collected by centrifugation, suspended in 3 L of 20 mM potassium phosphate buffer, pH 7.0, disrupted by a French press according to a conventional method, and then centrifuged at 8,000 rpm for 20 minutes, and phosphoenolpyruvate. A crude enzyme solution of carboxylase was obtained. The crude enzyme solution thus obtained was treated with polyethyleneimine to remove nucleic acid, and then the phosphoenolpyruvate carboxylase fraction was recovered by ammonium sulfate precipitation. Next, after desalting by Sephadex G-25 (Pharmacia LKB) gel filtration, DEAE Sepharose CL-6B (Pharmacia LKB) column chromatography and Butyl-Toyopearl 650M column chromatography were performed, and the product was concentrated and purified by ammonium sulfate precipitation. A phosphoenolpyruvate carboxylase preparation was obtained. This phosphoenolpyruvate carboxylase purified preparation is
SDS-PAGE electrophoresis showed a single band, and the activity recovery rate was 33.2%. Table 3 below shows a summary of the purification so far. Table 4 shows the physicochemical properties of the phosphoenolpyruvate carboxylase obtained by the above method.

[0043]

[Table 3]

[0044]

[Table 4]

Comparing Tables 1 and 3 above, the phosphoenolpyruvate carboxylase of the present invention shows that the phosphoenolpyruvate carboxylase of the present invention is produced in a high yield in a high yield by a simple method as compared with the method for producing the wild strain Acetobacter hansenii IFO 14820. Can be recovered. Table 2 above
Comparing Table 4 with Table 4, it can be seen that the phosphoenolpyruvate carboxylase of the present invention is of higher purity than the phosphoenolpyruvate carboxylase derived from the wild strain Acetobacter hansenii IFO 14820.

Reference Example 2 Phosphoenols derived from Escherichia coli JM109
Carbon dioxide measurement using a pyruvate carboxylase preparation Using the phosphoenolpyruvate carboxylase preparation derived from Escherichia coli JM109 purified in Example 1, the following reagent for measuring carbon dioxide was prepared. Tris-HCl, pH8.0 50 mM MgSO 4 10 mM phosphoenolpyruvate potassium salt 3.2 mM NADH 0.5 mM malate dehydrogenase 50 U / ml phosphoenolpyruvate carboxylase 3 U / ml the reagent 3ml and bicarbonate ions 0.05 ml of a sample containing 0 to 20 mM was added, and the mixture was reacted at 37 ° C. for 5 minutes.
The amount of decrease in absorbance at 0 nm for 5 minutes was measured (a bicarbonate ion concentration of 0 mM was subtracted as a blank). The relationship between the concentration of bicarbonate in the sample and the amount of decrease in absorbance during 5 minutes is shown in FIG. There was a linear relationship between bicarbonate concentration and absorbance change.

Reference Example 3 Phosphoenols derived from Escherichia coli JM109
Pyruvate carboxylase standard solution for carbon dioxide measurement
Stability in Acetobacter hansenii IFO 1 purified in Comparative Example 1
Phosphoenolpyruvate carboxylase preparation derived from 4820 and Escherichia coli JM1 purified in Example 1
The phosphoenolpyruvate carboxylase preparation derived from 09 was used to compare the stability in a test solution for measuring carbon dioxide at 25 ° C. The result is shown in FIG. As is clear from FIG. 2, the phosphoenolpyruvate carboxylase preparation of the present invention is a wild strain, Acetobacter hansenii I.
The storage stability at 25 ° C was significantly improved as compared to FO 14820-derived phosphoenolpyruvate carboxylase.

[0048]

INDUSTRIAL APPLICABILITY According to the present invention, the nucleotide sequence and amino acid sequence of the novel phosphoenolpyruvate carboxylase gene have been clarified, and it has become possible to industrially mass-produce it. Further, according to the production method of the present invention, compared to phosphoenolpyruvate carboxylase produced by a wild strain,
It has become possible to obtain high-purity phosphoenolpyruvate carboxylase with high yield. Furthermore, by using the phosphoenolpyruvate carboxylase obtained by the production method of the present invention, it became possible to prepare a reagent for measuring carbon dioxide having excellent stability.

[0049]

[Sequence list]

SEQ ID NO: 1 Sequence length: 933 Sequence type: Amino acid Topology: Linear Sequence type: Protein Origin organism name: Acetobacter hanzeni
nsenii) Strain name: IFO14820 Sequence Met Ser Gln Ala Ser Ala Pro His Ala Thr Asp Met Leu Gln Gln Gln 1 5 10 15 Ala Arg Glu Leu Val Ala Ile Pro Ala Leu Ser Asp Asn Pro Val Met 20 25 30 Thr Leu Ala Arg Ser Ile Gly Gln Gln Ile Asp Arg Gly Ser Leu Ser 35 40 45 Thr Asp Ala Leu Glu Ala Trp Val Arg Arg Leu Arg Asp Ala Ala Phe 50 55 60 Ala Arg Arg Ala Cys His Ile Ala Ala Tyr Val Gly Gly Val Asp Asp 65 70 75 80 Ala Val Ile Asp Gln Arg Met Arg Asp Val Ala Arg Arg Ile Met Gln 85 90 95 Pro Asp Pro Asn Asp Ser Pro Val Pro Ile Ala Arg Phe Arg Ala Ala 100 105 110 Thr Glu Arg Ser Arg Phe Ala Ala Val Phe Thr Ala His Pro Thr Phe 115 120 125 Ala Leu Ala Ser Pro Val Tyr Asp Cys Leu Ala Asp Met Ala Thr Gln 130 135 140 Asn Pro Gln Gln Pro Pro Thr Asp Val Pro Ala Phe Ile Thr His Arg 145 150 155 160 Arg Ala Ala Pro Pro Thr Leu Asp Glu Glu Phe Thr Leu Ala Thr Gln 165 170 175 Ala Ile Leu Arg Gly Arg Asn Ala Leu Asp Arg Leu Thr Arg Val Leu 180 185 190 Leu Thr Glu Ala Arg Ala His Trp Pro Gln Leu Trp Ala Thr Leu Ala 195 200 205 Pro Arg Pro Ile Ile Met Thr Ser Trp Val Gly Tyr Asp Thr Asp Gly 210 215 220 Arg Thr Asp Ile Gly Trp Trp Asp Thr Leu Arg Leu Arg Val Arg Met 225 230 235 240 Lys His Met Gln Leu Thr Arg Leu Asn Ala Gln Ile Gly Pro Val Ala 245 250 255 Ser Val Pro Asn Asp Leu His Glu Arg Val Asn Arg Ala Ile Gln Ala 260 265 270 Val Glu Ala Gln Ile Ala Ala Cys Pro Gly Ser Ala Asp Pro Gln Ala 275 280 285 Val Ala Asp Phe Ala Ala Val Leu Ile Gly Arg Arg Glu Glu Ala Met 290 295 300 Thr Ser Ser Asn Asp Leu Ala Pro Thr Phe Ala Glu Ala Ile Asp Ala 305 310 315 320 Ala Thr Leu Asp Asp Lys Met Thr Leu Ala Val Ala Arg Ala Gly Phe 325 330 335 Met Ala His Gly Leu Ser Ala Ala His Thr His Val Arg Leu Asn Ser 340 345 350 Thr Gln Leu His Asn Val Ala Arg Gln Arg Leu Gly Ile Thr Asp Asn 355 360 365 Pro Asp Ile His Ala Gln Arg Arg Ala Arg Ile Ala Arg Ile Asp Glu 370 375 380 Ala Leu Asp Thr Thr Gln Pro Ile Asp Ile Asp Phe Gly Ser Leu Leu 385 390 395 400 Val Glu Gln Ser Thr Ala Gly Arg Leu Met Met Thr Val Arg Gln Ile 405 410 415 Leu His His Ile Asp Arg Thr Thr Pro Ile Arg Phe Leu Ile Ala Glu 420 425 430 Thr Glu Thr Gly Tyr Thr Leu Leu Thr Ala Leu Trp Leu Ala Arg Leu 435 440 445 Leu Gly Val Glu Asp Met Ile Glu Ile Ser Pro Leu Phe Glu Thr Gln 450 455 460 Asp Ala Leu Glu Gln Gly Glu His Leu Ile Glu Glu Ala Leu His Ser 465 470 475 480 Pro His Trp Arg Ala Tyr Leu His Arg Thr Arg Lys Leu Ser Leu Gln 485 490 495 Phe Gly Phe Ser Asp Ser Gly Arg Tyr Val Gly Gln Leu Ala Ala Thr 500 505 510 Tyr Leu Ile Glu Arg Leu Arg Leu Lys Val Cys Asp Leu Leu Arg Gln 515 520 525 Trp Asp Leu Ala Phe Val Glu Val Ile Leu Phe Asp Thr His Gly Glu 530 535 540 Ser Ile Gly Arg Gly Ala His Pro Tyr Ser Leu Ala Glu Arg Phe Asp 545 550 555 560 Tyr Leu Ser Pro Pro His Ala Arg Met Arg Phe Leu Gln Ala Gly Ile 565 570 575 Arg Leu Arg Glu Glu Thr Ala Phe Gln Gly Gly Asp Gly Tyr Leu Leu 580 585 590 Phe Gly Thr Gln Pro Leu Ala Asp Ala Thr Val Ser Val Ile Ala Glu 595 600 605 His Ala Phe Ala Thr Thr Ser Ile Asp Glu Asp Pro Val Tyr Asp Glu 610 615 620 Pro Asp Phe Ser Ala Asp Phe Phe Ser Ala Ile Ala Arg Gly Met Thr 625 630 635 640 Gly Leu Val Glu Asp Pro Gly Tyr Ala Ala Leu Leu Gly Ala Phe Gly 645 650 655 Pro Ser Leu Ile Asp Lys Thr Gly Ser Arg Pro Ser Ala Arg Gln Ser 660 665 670 Asp Thr Ala Ala Ile Thr Thr Arg Ile Arg His Pro Ser Gln Leu Arg 675 680 685 Ala Ile Pro Asn Asn Ala Ile Leu Gln Gln Leu Gly Trp Cys Ala Asn 690 695 700 Thr Leu Gln Gly Leu Gly Thr Ala Ala Ala Arg His Pro Asp Thr Phe 705 710 715 720 720 Glu Arg Tyr Leu Asn Asp Ser Pro Arg Phe Arg Arg Ala Leu Asp Phe 725 730 735 Ala Ala His Gly Leu Ala His Ser Ser Asp Gly Val Leu Arg Gly Val 740 745 750 Ile Arg Leu Leu Asp Pro Asp Met Trp Leu Gln Arg Ala Thr Ala His 755 760 765 His Asp Pro Lys Arg Gln Asp Ala Cys Leu Thr Leu Met His Gly Leu 770 775 780 Glu Arg Leu Asp Phe Trp Ala Cys Thr Gln Ser Met Phe Arg Arg Leu 785 790 795 800 Gln Ser Asp His Leu Ala Leu Arg Asn Ala Trp Pro Ser Ala Pro Arg 805 810 815 Met Glu Ala Asp Glu Met Leu Leu His Ala Ile Arg Ile Ala Ile Ile 820 825 830 Glu Gln Ile Trp Met Leu Ser Thr Arg Ile Pro Tyr Phe Ala Pro Arg 835 840 845 Asn Ala Phe Thr Arg Asp Val Leu Thr Ala Lys Val Leu Cys Leu Glu 850 855 860 Ile Pro Asp Val Leu Lys Glu Leu Glu His Ile Phe Pro Tyr His Ala 865 870 875 880 Asp Arg Ser Phe Asp Leu Asp Phe His Glu Pro His Gly Pro Arg Asp 885 890 895 Glu Gly Thr Tyr Met Arg Glu Tyr Thr Glu Ile Phe Glu Pro Met Gln 900 905 910 Arg Leu Phe Thr Leu Val Arg Glu Ile Ser Thr Gly Val Met His His 915 920 925 Val Gly Ala Phe Gly 930 933

SEQ ID NO: 2 Sequence length: 2802 Sequence type: Nucleic acid (DNA) Number of strands: Double strand Topology: Linear Sequence type: GenomicDNA Origin Biological name: Acetobacter hazenii
nsenii) Strain name: IFO14820 Sequence ATG TCC CAG GCC TCT GCC CCT CAT GCA ACA GAC ATG CTG CAG CAG CAG 48 Met Ser Gln Ala Ser Ala Pro His Ala Thr Asp Met Leu Gln Gln Gln 1 5 10 15 GCC CGC GAA CTT GTG GCG ATC CCT GCC CTT TCC GAC AAC CCG GTC ATG 96 Ala Arg Glu Leu Val Ala Ile Pro Ala Leu Ser Asp Asn Pro Val Met 20 25 30 ACG CTG GCA CGC AGC ATC GGA CAG CAG ATC GAC CGG GGC AGC CTG TCG 144 Thr Leu Ala Arg Ser Ile Gly Gln Gln Ile Asp Arg Gly Ser Leu Ser 35 40 45 ACC GAC GCG CTG GAG GCC TGG GTC CGC CGC CTG CGC GAC GCC GCG TTC 192 Thr Asp Ala Leu Glu Ala Trp Val Arg Arg Leu Arg Asp Ala Ala Phe 50 55 60 GCC CGC CGC GCC TGC CAT ATC GCC GCG TAT GTC GGG GGG GTG GAT GAT 240 Ala Arg Arg Ala Cys His Ile Ala Ala Tyr Val Gly Gly Val Asp Asp 65 70 75 80 GCC GTC ATC GAC CAG CGC ATG CGT GAC GTG GCG CGC CGC ATC ATG CAG 288 Ala Val Ile Asp Gln Arg Met Arg Asp Val Ala Arg Arg Ile Met Gln 85 90 95 CCC GAC CCA AAT GAC AGC CCG GTG CCC ATC GCC CGG TTC CGC GCC GCG 336 Pro Asp Pro Asn Asp Ser Pro Val P ro Ile Ala Arg Phe Arg Ala Ala 100 105 110 ACC GAA CGC AGC CGC TTT GCC GCC GTG TTC ACC GCG CAT CCC ACG TTT 384 Thr Glu Arg Ser Arg Phe Ala Ala Val Phe Thr Ala His Pro Thr Phe 115 120 125 GCG CTG GCC AGC CCC GTC TAT GAC TGC CTT GCC GAC ATG GCG ACG CAA 432 Ala Leu Ala Ser Pro Val Tyr Asp Cys Leu Ala Asp Met Ala Thr Gln 130 135 140 AAC CCG CAG CAG CCC CCG ACC GAT GTC CCG GCA TTC ATA ACG CAT CGC 480 Asn Pro Gln Gln Pro Pro Thr Asp Val Pro Ala Phe Ile Thr His Arg 145 150 155 160 CGC GCC GCG CCG CCG ACG CTG GAT GAG GAA TTC ACG CTG GCG ACG CAG 528 Arg Ala Ala Pro Pro Thr Leu Asp Glu Glu Phe Thr Leu Ala Thr Gln 165 170 175 GCG ATC CTG CGC GGG CGC AAT GCA CTC GAT CGC CTG ACG CGG GTT CTC 576 Ala Ile Leu Arg Gly Arg Asn Ala Leu Asp Arg Leu Thr Arg Val Leu 180 185 190 CTG ACC GAG GCA CGG GCA CAC TGG CCG CAA CTG TGG GCC ACG CTG GCG 624 Leu Thr Glu Ala Arg Ala His Trp Pro Gln Leu Trp Ala Thr Leu Ala 195 200 205 CCG CGT CCC ATT ATC ATG ACA AGC TGG GTC GGA TAC GAC ACG GAC GGA 672 Pro Arg Pro Ile Ile M et Thr Ser Trp Val Gly Tyr Asp Thr Asp Gly 210 215 220 CGC ACC GAT ATC GGG TGG TGG GAC ACG CTG CGG CTG CGC GTG CGC ATG 720 Arg Thr Asp Ile Gly Trp Trp Asp Thr Leu Arg Leu Arg Val Arg Met 225 230 235 240 AAG CAC ATG CAG TTA ACC CGC CTG AAT GCA CAG ATT GGC CCC GTC GCC 768 Lys His Met Gln Leu Thr Arg Leu Asn Ala Gln Ile Gly Pro Val Ala 245 250 255 TCC GTC CCC AAT GAC CTG CAC GAA CGC GTC AAT CGC GCC ATA CAG GCG 816 Ser Val Pro Asn Asp Leu His Glu Arg Val Asn Arg Ala Ile Gln Ala 260 265 270 GTG GAG GCA CAG ATC GCC GCA TGC CCC GGC AGT GCC GAC CCG CAG GCG 864 Val Glu Ala Gln Ile Ala Ala Cys Pro Gly Ser Ala Asp Pro Gln Ala 275 280 285 GTG GCC GAT TTT GCC GCG GTC CTG ATC GGT CGC CGC GAA GAG GCC ATG 912 Val Ala Asp Phe Ala Ala Val Leu Ile Gly Arg Arg Glu Glu Ala Met 290 295 300 ACC AGC AGC AAC GAC CTC GCC CCC ACT TTT GCC GAA GCC ATT GAT GCC 960 Thr Ser Ser Asn Asp Leu Ala Pro Thr Phe Ala Glu Ala Ile Asp Ala 305 310 315 320 GCG ACG CTG GAC GAC AAG ATG ACG CTG GCG GTC GCA CGC GCG GGT TTC 1008 Ala Thr Leu Asp Asp Lys Met Thr Leu Ala Val Ala Arg Ala Gly Phe 325 330 335 ATG GCC CAT GGC CTG TCG GCG GCG CAT ACG CAT GTA CGC CTC AAT TCC 1056 Met Ala His Gly Leu Ser Ala Ala His Thr His Val Arg Leu Asn Ser 340 345 350 ACG CAA TTA CAC AAT GTC GCC CGC CAG CGC CTG GGC ATT ACC ACC GAC AAT 1104 Thr Gln Leu His Asn Val Ala Arg Gln Arg Leu Gly Ile Thr Asp Asn 355 360 365 CCC GAT ATC CAT GCC CAG CGT CGC GCC CGG ATC GCA CGC ATT GAC GAG 1152 Pro Asp Ile His Ala Gln Arg Arg Ala Arg Ile Ala Arg Ile Asp Glu 370 375 380 GCG CTG GAT ACA ACG CAG CCA ATC GAC ATT GAT TTC GGC TCC CTG CTG 1200 Ala Leu Asp Thr Thr Gln Pro Ile Asp Ile Asp Phe Gly Ser Leu Leu 385 390 395 400 GTG GAA CAG TCA ACG GCG GGG CGG CTG ATG ATG ACG GTG CGC CAG ATC 1248 Val Glu Gln Ser Thr Ala Gly Arg Leu Met Met Thr Val Arg Gln Ile 405 410 415 CTG CAC CAT ATC GAC CGC ACC ACG CCC ATC CGT TTC CTG ATC GCG GAA 1296 Leu His His Ile Asp Arg Thr Thr Pro Ile Arg Phe Leu Ile Ala Glu 420 425 430 ACG GAA ACC GGC TAT ACG CTG CTG ACG GCA CTG TGG CTT GC G CGC CTG 1344 Thr Glu Thr Gly Tyr Thr Leu Leu Thr Ala Leu Trp Leu Ala Arg Leu 435 440 445 CTG GGC GTG GAA GAC ATG ATC GAA ATC TCC CCC CTG TTT GAA ACG CAG 1392 Leu Gly Val Glu Asp Met Ile Glu Ile Ser Pro Leu Phe Glu Thr Gln 450 455 460 GAC GCG CTG GAA CAG GGG GAA CAC CTG ATC GAA GAA GCG CTG CAT TCA 1440 Asp Ala Leu Glu Gln Gly Glu His Leu Ile Glu Glu Ala Leu His Ser 465 470 475 480 CCG CAC TGG CGC GCC TAC CTG CAT CGT ACG CGC AAG CTG AGC CTG CAA 1488 Pro His Trp Arg Ala Tyr Leu His Arg Thr Arg Lys Leu Ser Leu Gln 485 490 495 TTC GGT TTT TCG GAT TCG GGA CGT TAT GTG GGA CAG CTT GCC GCG ACC 1536 Phe Gly Phe Ser Asp Ser Gly Arg Tyr Val Gly Gln Leu Ala Ala Thr 500 505 510 TAC CTG ATC GAA CGG CTG CGG CTG AAG GTC TGC GAC CTT CTG CGG CAA 1584 Tyr Leu Ile Glu Arg Leu Arg Leu Lys Val Cys Asp Leu Leu Arg Gln 515 520 525 TGG GAC CTC GCC TTC GTG GAA GTC ATC CTG TTC GAC ACC CAT GGG GAA 1632 Trp Asp Leu Ala Phe Val Glu Val Ile Leu Phe Asp Thr His Gly Glu 530 535 540 AGC ATC GGC CGC GGG GCA CAT CCC TAC AGC CTT GCC GAA CGT TTC GAC 1680 Ser Ile Gly Arg Gly Ala His Pro Tyr Ser Leu Ala Glu Arg Phe Asp 545 550 555 560 TAT CTC TCC CCC CCG CAT GCG CGC ATG CGT TTC CTG CAG GCA GGC ATT 1728 Tyr Leu Ser Pro Pro His Ala Arg Met Arg Phe Leu Gln Ala Gly Ile 565 570 575 CGC CTG CGC GAG GAA ACG GCC TTT CAG GGG GGG GAT GGC TAC CTC CTG 1776 Arg Leu Arg Glu Glu Thr Ala Phe Gln Gly Gly Asp Gly Tyr Leu Leu 580 585 TTC GGG ACG CAG CCC CTT GCG GAT GCA ACT GTC AGC GTG ATC GCG GAA 1824 Phe Gly Thr Gln Pro Leu Ala Asp Ala Thr Val Ser Val Ile Ala Glu 595 600 605 CAC GCC TTT GCC ACG ACC TCC ATC GAC GAA GAC CCG GTT TAC GAC GAA 1872 His Ala Phe Ala Thr Thr Ser Ile Asp Glu Asp Pro Val Tyr Asp Glu 610 615 620 CCC GAT TTC TCT GCC GAT TTC TTT TCC GCC ATC GCG CGC GGC ATG ACA 1920 Pro Asp Phe Ser Ala Asp Phe Phe Ser Ala Ile Ala Arg Gly Met Thr 625 630 635 640 GGA CTG GTG GAG GAT CCA GGC TAT GCC GCG CTG CTG GGT GCG TTC GGG 1968 Gly Leu Val Glu Asp Pro Gly Tyr Ala Ala Leu Leu Gly Ala Phe Gly 645 650 655 CCG TCA CTA ATC GAC AAG ACG GGT TCA CGC CCC TCC GCC CGG CAG AGC 2016 Pro Ser Leu Ile Asp Lys Thr Gly Ser Arg Pro Ser Ala Arg Gln Ser 660 665 670 GAT ACG GCC GCC ATC ACC ACG CGC ATC CGC CAT CCC AGC CAG TTG CGC 2064 Asp Thr Ala Ala Ile Thr Thr Arg Ile Arg His Pro Ser Gln Leu Arg 675 680 685 GCC ATC CCC AAC AAC GCC ATC CTC CAG CAG CTT GGC TGG TGC GCC AAT 2112 Ala Ile Pro Asn Asn Ala Ile Leu Gln Gln Leu Gly Trp Cys Ala Asn 690 695 700 ACG TTG CAG GGG CTG GGC ACG GCG GCC GCG CGT CAT CCC GAT ACG TTC 2160 Thr Leu Gln Gly Leu Gly Thr Ala Ala Ala Arg His Pro Asp Thr Phe 705 710 715 720 Glu Arg Tyr Leu Asn Asp Ser Pro Arg Phe Arg Arg Ala Leu Asp Phe 725 730 735 GCC GCC CAT GGC CTG GCC CAT TCC AGC GAC GGC GTC CTG CGT GGT GTG 2256 Ala Ala His Gly Leu Ala His Ser Ser Asp Gly Val Leu Arg Gly Val 740 745 750 ATC CGG CTG CTG GAC CCG GAC ATG TGG TTG CAA CGC GCA ACG GCG CAT 2304 Ile Arg Leu Leu Asp Pro Asp Met Trp Leu Gln Arg Ala Thr Ala His 755 760 765 CAC GAC CCG AAA CGG CAG GAT GCG TGC CTG ACG CTG ATG CAC GGG CT G 2352 His Asp Pro Lys Arg Gln Asp Ala Cys Leu Thr Leu Met His Gly Leu 770 775 780 GAA CGG CTG GAT TTC TGG GCC TGT ACG CAA TCC ATG TTC CGC CGC CTG 2400 Glu Arg Leu Asp Phe Trp Ala Cys Thr Gln Ser Met Phe Arg Arg Leu 785 790 795 800 CAA TCG GAC CAT CTG GCG TTA CGC AAC GCA TGG CCC AGC GCA CCA CGG 2448 Gln Ser Asp His Leu Ala Leu Arg Asn Ala Trp Pro Ser Ala Pro Arg 805 810 815 ATG GAG GCG GAT GAA ATG CTG CTG CAT GCC ATC CGC ATC GCC ATC ATT 2496 Met Glu Ala Asp Glu Met Leu Leu His Ala Ile Arg Ile Ala Ile Ile 820 825 830 GAA CAG ATA TGG ATG CTG TCC ACC CGG ATC CCG TAT TTT GCG CCG CGC 2544 Glu Gln Glu Trp Met Leu Ser Thr Arg Ile Pro Tyr Phe Ala Pro Arg 835 840 845 AAT GCG TTC ACC CGC GAC GTG CTG ACG GCG AAG GTC CTG TGC CTG GAA 2592 Asn Ala Phe Thr Arg Asp Val Leu Thr Ala Lys Val Leu Cys Leu Glu 850 855 860 ATC CCC GAT GTG CTG AAG GAG CTG GAG CAT ATC TTC CCC TAT CAC GCG 2640 Ile Pro Asp Val Leu Lys Glu Leu Glu His Ile Phe Pro Tyr His Ala 865 870 875 880 GAC CGC AGC TTC GAC CTG GAT TTC CAT GAA CCG CAC GGG CCC CGC GAT 2688 Asp Arg Ser Phe Asp Leu Asp Phe His Glu Pro His Gly Pro Arg Asp 885 890 895 GAA GGG ACG TAT ATG CGC GAA TAC ACG GAA ATT TTC GAA CCG ATG CAA 2736 Glu Gly Thr Tyr Met Arg Glu Tyr Thr Glu Ile Phe Glu Pro Met Gln 900 905 910 CGG CTG TTC ACA CTG GTG CGC GAA ATC AGC ACC GGC GTG ATG CAC CAT 2784 Arg Leu Phe Thr Leu Val Arg Glu Ile Ser Thr Gly Val Met His His 915 920 925 GTC GGG GCC TTT GGC TGA 2802 Val Gly Ala Phe Gly *** 930 933

[Brief description of drawings]

FIG. 1 shows the relationship between bicarbonate ion concentration and absorbance change.

FIG. 2 shows the stability in a test solution for measuring carbon dioxide.

─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. ⁶ Identification code Internal reference number FI technical display location // (C12N 9/00 C12R 1:19) (C12N 1/21 C12R 1:19) (72) Inventor Kazumi Yamamoto 10-24 Toyo-cho, Tsuruga-shi, Fukui Prefecture Toyobo Co., Ltd. in the Tsuruga Bio Research Laboratory (72) Inventor Yoshihisa Kawamura 10-24 Toyo-cho, Tsuruga-city, Fukui Toyobo Co., Ltd.

Claims (6)

[Claims] 1. A DNA fragment encoding phosphoenolpyruvate carboxylase, which comprises a DNA encoding the amino acid sequence set forth in SEQ ID NO: 1 of the Sequence Listing. 2. A DNA encoding phosphoenolpyruvate carboxylase according to claim 1, which contains the nucleotide sequence shown in Sequence Listing / SEQ ID NO: 2.
fragment. 3. A DNA encoding phosphoenolpyruvate carboxylase, characterized in that it encodes a polypeptide having phosphoenolpyruvate carboxylase activity which has been altered by mutation to the DNA sequence according to claim 2. fragment. 4. A recombinant vector containing the DNA fragment according to claim 2 or 3. 5. A transformant transformed with the recombinant vector according to claim 4. 6. A phosphoenolpyruvate carboxylase, which comprises culturing the transformant according to claim 5 in a medium to produce phosphoenolpyruvate carboxylase and collecting the phosphoenolpyruvate carboxylase. Manufacturing method.