CN1079002A

CN1079002A - Chicken growth hormone gene and the expression in intestinal bacteria thereof

Info

Publication number: CN1079002A
Application number: CN 93102099
Authority: CN
Inventors: 曹重明; 朴荣烈; 林宽烈; 诸勋成; 李弘均; 崔形培
Original assignee: Lucky Ltd
Current assignee: LG Corp
Priority date: 1992-05-09
Filing date: 1993-03-05
Publication date: 1993-12-01
Anticipated expiration: 2013-03-05
Also published as: KR100229420B1; TW367364B; CN1072720C; KR930023463A

Abstract

The present invention relates to the purifying of the chicken growth hormone of chicken growth hormone gene and its expression method and expression, the CGH gene that has particularly related to energy scale operation hormone in intestinal bacteria, with the colibacillary method of described expression vector conversion, and the method for producing the method for chicken production hormone and the chicken production hormone that the purifying Bacillus coli cells is produced with the intestinal bacteria transformant.

Description

Chicken growth hormone gene and the expression in intestinal bacteria thereof

The present invention relates to the purifying of the chicken growth hormone of a chicken growth hormone gene and its expression and expression.Be meant that more specifically the present invention relates to one is used in the chicken growth hormone gene that carries out the mass production chicken growth hormone in the intestinal bacteria, with this gene constructed expression vector, the Bacillus coli cells that transforms with this expression vector, and produce the method for chicken growth hormone and purifying is produced chicken production hormone by intestinal bacteria method with this intestinal bacteria transformant.

Up to the present, in cattle breeding, improved efficiency of feed utilization greatly and made the domestic animal weight increase by in conventional feed, sneaking into high protein material or steroid hormone, yet, the source of high protein material is limited, use steroid hormone because it is residual over a long time in animal body, may produce certain side effect to human body, thereby controlled by strictness.

By contrast, the animal growth hormone that has been developed in the recent period is but in animal body not residual, and has specificity, and it is harmless therefore being considered to the mankind.In view of the above, animal growth hormone is considered to promoting that aspect the fast growth of animal be a kind of desirable material.

Animal growth hormone is a kind of sub-thread chain sphaeroprotein, approximately form (referring to Barrinton etc. by 190 to 200 amino acid, Academic Press, N.Y., 2(1979)), thus it is participate in to regulate lipid and carbohydrate and protein metabolism to promote one of some protein hormone of animal tissues's growth.

At the tethelin that the animal brain prepituitary gland produces is ripe and get from the tethelin precursor that contains segment signal order at aminoterminal.The tethelin precursor just becomes sophisticated functional growing hormone (Davies etc., Nature 283,433-438(1980)) through cutting a segment signal sequence when by endoplasmic reticulum.

Tethelin stimulates translating of mRNA simultaneously by promoting that amino acid enters the balanced growth of accelerating animal in the cell, impels the division growth of cell, and this is an important factors for growth.Thereby the animal of injection tethelin is not increasing forage volume when improving the means of tissue protein, and it is fast that body weight is still carried nice and high.

The complete sequence amino-acid sequence of present most of animal growth hormones determined, some animal growth hormone genes clone and expressing in intestinal bacteria is also arranged, for example people, ox, pig and rat (Miller etc., JBC 255,7521-7524; Martial etc., Science 205,602-607(1979); Seeburg etc., Nature 270,486-494(1977)).Method that up to the present still can not using gene engineering is produced chicken growth hormone on a large scale in intestinal bacteria.

The chicken growth hormone of producing in the intestinal bacteria transformant usually forms an inclusion body, thereby its solubilization of inclusion bodies could should be isolated chicken growth hormone from the intestinal bacteria transformant.Yet known have several dissolving methods, for example, use urea, guanidinesalt or sodium lauryl sulphate (Sodium dodecylsulfate) etc., but they all have some defective relevant with following factor, and as purifying expense height, purge process is too complicated and yield poorly etc.

In addition, also have some purification process, for example, the monoclonal antibody affinity chromatography method (B.Houston etc., J.Endocr.125,207-215(1990)) and the combined utilization (L.M.Souza etc. of negatively charged ion, cation-exchange chromatography, J.Exp.Zoology, 232,465-474(1984))., the monoclonal antibody affinity chromatography method is not suitable for large scale purification because of manufacture order clonal antibody cost is very high.The method high complexity of Souza, the problem that will remove the heat source substance of Escherichia coli source in addition.

The purpose of this invention is to provide one and be designed to effective expression and the chicken growth hormone gene that can be used for scale operation chicken growth hormone (CGH) in intestinal bacteria.

Another object of the present invention provides a kind of Bacillus coli cells that contains said CGH expression carrier and transform with this carrier.

Further purpose of the present invention provides a kind of method of producing CGH with the intestinal bacteria transformant.

Another object of the present invention provides the method for the CGH that a kind of effective separation and purifying produce on the intestinal bacteria transformant, mainly adopted in the method with alkali reagent and be dissolved in the CGH inclusion body that produces in the Bacillus coli cells.

Correspondingly, with one aspect of the present invention be the nucleotide sequence that shows the CGH gene at Fig. 1, this sequence is designed in intestinal bacteria to produce ripe CGH.

Another aspect of the present invention provides a Bacillus coli cells that contains described CGH expression carrier and transform with this carrier.

A further aspect of the invention provides a method of producing CGH on the intestinal bacteria transformant, and this mainly is to cultivate the intestinal bacteria transformant under the culture condition of CGH gene and obtain CGH being fit to express.

For another aspect of the present invention provides the method for a kind of purifying CGH, it comprises: separatin non-soluble inclusion body from the intestinal bacteria transformant of producing chicken growth hormone; Wash insoluble inclusion body with the solution that contains tensio-active agent and ethylenediamine tetraacetic acid (EDTA) (EDTA), then, further with damping fluid that contains NaCl or distillation washing; The inclusion body that suspension had been washed in a kind of basic solution is collected at dissolving forgives intravital CGH; Centrifugal this suspension is collected supernatant liquor, carries out ultrafiltration, promptly contains dissolved CGH in the filtrate; Analyse post by a cation exchange resin layer again.

CGH gene of the present invention is to be that basic design is come out with (J.of Exp.Zoology 232,465-473(1984)) described aminoacid sequences such as L.M.Souza, and is specific as follows:

(ⅰ) before the-terminal amino acid Threonine password of ripe CGH, put into the initiation codon of a methionine(Met).

(ⅱ) behind the password of the C-of ripe CGH end amino acid Isoleucine, put into two termination codon TAG and TAA so that stop at the Isoleucine place when translating.

(ⅲ) recognition site of several restriction enzymes is introduced into this gene so that make this gene of modification convenient, and these sites are: SacI(5 '-GAGCTC-3 ', contain the arginic password of the 17th amino acids), EcoRI(5 '-GAATTC-3 '; The password that contains the 31st amino acids L-glutamic acid), the Bal II (5 '-GAGTCT-3 '; The password that contains the 115th amino acids aspartic acid) and the Hind III (5 '-AAGCTT-3 '; The password that contains the 121st amino acids glutamine); And,

(ⅳ) can form the nucleotide sequence of secondary structure or subsequence and be modified, being expressed in of CGH transcribed and the level of translating reaches optimum regime by substituting some Nucleotide.

The complete nucleotide sequence of CGH gene can as with dna synthesizer or polymerase chain reaction (PCR), be synthesized into by known ordinary method.

The present invention is used for can adapting to colibacillary various expression system by use in the described CGH expression carrier of escherichia coli expression and prepares.

For example, can use the ptrp322H-HGH carrier to prepare, this carrier has description (the host cell intestinal bacteria W3110 that contains described ptrp322H-HGH carrier has been preserved in Korea S microbial strains preservation center, and code name is KFCC-10667) in Korea S publication publication No.91-457.Be exactly specifically this preparing carriers be to be used in the CGH gene shown in Fig. 1 to replace human growth hormone gene in ptrp322H-HGH, this will be described in the embodiment of back.

The CGH expression carrier that contains of Huo Deing is named as ptrp-CST like this.The intestinal bacteria W3110(ATCC 27325 of Zhuan Huaing thus) is deposited in Korea S microbial strains preservation center for the patented procedure purpose on June 26th, 1991 by international microbial preservation budapest treaty, is numbered KCCM-10005.

Cultivate under the condition that can make CGH genetic expression with the Bacillus coli cells that contains the conversion of CGH expression carrier, further determine by the feature of carrier and intestinal bacteria recipient cell.

For example, in containing the M9 substratum of penbritin, cultivate,, add indole acrylic acid and continue to cultivate when optical density value (OD) under 650nm when reaching 0.5 with the intestinal bacteria W3110 cell that the ptrp-CST expression vector transforms.

The CGH that produces in the intestinal bacteria transformant can separate and purifying by series of steps, and these steps comprise cell rupture, centrifugal, dissolving, transfer pH to alkalescence, filter and chromatography.

Specifically be exactly to carry out ultrasonic again with smudge cells by in cultured cell, adding N,O-Diacetylmuramidase.Broken cell centrifugation precipitation is collected the throw out that contains the CGH inclusion body.

This throw out is washed once with containing with tensio-active agent (as: 0.1%-1% Triton (Triton) X-100) and the damping fluid of EDTA, then, uses another damping fluid again instead and (as: contains 100-500mM NaCl or NH ₄The pH7.2 solution of Cl) or distillation washing to remove cytolemma and other foreign protein.The CGH inclusion body of Huo Deing is suspended in the distilled water again like this, slowly adds alkaline solution (NaOH or KOH solution) then, the limit edged stirs, and pH is adjusted between 11.5 to 13.0, is preferably 11.8 to 12.3.This suspension is further centrifugal to remove insoluble impurities.The supernatant suspension obtains to contain the solution of solubility CGH with ultra-filtration filters, transfers between the filtrate pH to 8.5 and 10.5, is preferably 9.0 to 9.5.Joining the anion-exchange chromatography post through adjusted filtrate, be preferably the DEAE(diethylaminoethylcellulose) to carry out chromatography be high-purity CGH 95% or more and the intracellular toxin that is lower than 10 units/milligram concentration to obtain purity to post.

The present invention has overcome the deficiency of CGH production method in the prior art, has obtained a kind of chicken growth hormone of high purity low endotoxin content.

The following examples will specify content of the present invention in being not limited to scope of the present invention.The test method of Shi Yonging should be undertaken by the content that reference example is given if not otherwise specified in an embodiment.

Brief Description Of Drawings is as follows:

Fig. 1 shows CGH gene nucleotide series of the present invention and the aminoacid sequence of deriving thus;

Fig. 2 has described the scheme that obtains CGH gene shown in Figure 1.

Fig. 3 has shown to make up to contain and has been useful on the expression carrier at expression in escherichia coli CGH.

Fig. 4 is presented at the intestinal bacteria transformant SDS-PAGE(sodium dodecyl sulfate-polyacrylamide gel electrophoresis of cultivating under the condition that is fit to CGH genetic expression) the result.

Fig. 5 provides in the intestinal bacteria of cultivating the SDS-PAGE result of CGH behind the purifying under being fit to CGH genetic expression condition.

Fig. 6 has disclosed the HPLC(of purifying CGH from effect liquid phase chromatogram) the result.

Unless the solid composition in the solid mixture of mentioning especially otherwise occurring in following, liquid composition in the solution and the solid composition in the liquid are respectively with w/w (wt/wt), and volume/volume (vol/vol) and weight/volume (wt/vol) are the basis.

Reference example 1: restriction endonuclease dna digestion

Restriction endonuclease used herein and reaction buffer be all available from NEB(New England Biolabs, Jolla, and MA, U.S.A.).

This reaction is carried out in the Eppendorf of sterilization pipe usually, reaction volume is at 50 μ l-100 μ l, 37 ℃ of reactions 1-24 hour, afterwards, this reaction mixture carries out thermal treatment in 15 minutes (or with phenol extracting, ethanol sedimentation to prevent the effect of heat resistance restriction endonuclease) at 65 ℃ and is used for the deactivation restriction endonuclease.

The 10X reaction buffer that is used for the restriction endonuclease reaction is made up of following:

10X NEB reaction buffer 1:100mM double Tris pronane hydrochloric acid (bis Tris propane-HCl), 100mM magnesium chloride (MgCl ₂), the 10mM dithiothreitol (DTT) (dithiothreitol, DTT), pH7.0;

10X NEB reaction buffer 2:100mM Tris-HCl, 100mM MgCl ₂, 500mM NaCl, 10mM DTT, pH7.0;

10X NEB reaction buffer 3:100mM Tris-HCl, 100mM MgCl ₂, 1000mM NaCl, 10mM DTT, pH7.0;

10X NEB reaction buffer 4:200mM Tris-acetate, 100mM magnesium acetate, 500mM potassium acetate, 10mM DTT, pH7.0.

Reference example 2: phenol extracting and ethanol sedimentation

After finishing enzyme reaction, reaction mixture phenol extracting its objective is the effect of wanting the deactivation restriction endonuclease and obtains DNA in the reaction mixture.Here it is to be noted that the phenol that uses needs in advance with containing 10mM Tris-HCl(pH8.0) and 10mM EDTA(ethylenediamine tetraacetic acid (EDTA)) the damping fluid balance.The phenol extractive process is pressed the step and is carried out: mix isopyknic phenol solution and sample liquid, concuss; With 15000rpm centrifugal mixture 5 minutes; Again water is changed in the new pipe, repeat said process 2-3 time.

Then, with equal-volume chloroformic solution (chloroform: extracting water isopropylcarbinol=24: 1), isolate water again, the 3M sodium acetate solution and 2.5 volume of ethanol that inwardly add 0.1 volume, put-70 ℃ of stops 30 minutes or stopped 12 hours so that nucleic acid is separated out at-20 ℃, afterwards, at 4 ℃, with 15000 rpm centrifugal mixtures 20 minutes, collecting precipitation.

Reference example 3: ligation

The DNA ligation is the T that uses available from NEB ₄(pH 7.8,0.5M Tris-HCl, 0.1M MgCl for ligase enzyme and 10X ligase enzyme damping fluid ₂, 0.2M DTT, 10mM ATP, 0.5mg/ml bovine serum albumin (BSA)) carry out.Reaction volume is generally 20 μ l, the T of 10 units ₄Ligase enzyme is used to connect the sticky end of DNA, and 100 units are used to connect the DNA of blunt end.

Being reflected at 16 ℃ carries out carrying out more than 14 hours in 5 hours or 4 ℃.After reaction finished, this reaction mixture heated 15 minutes with deactivation T at 65 ℃ ₄Dna ligase.

Reference example 4: colibacillary conversion

The coli strain that uses among the following embodiment comprises intestinal bacteria HB101(ATCC 33694): intestinal bacteria W 3110(ATCC 27325) and intestinal bacteria JM105(ATCC 47016).A kind of method well known in the art has been used in colibacillary conversion, promptly at Maniatis etc., Molecular Cloning:A Laboratory Manual, Cold Spring Harbor Press, N.Y.(1982) or Cohen, Proc.Natl.Acad.Sci.U.S.A., 69, the method for the transformed into escherichia coli of being introduced on 2110(1972).

Reference example 5: oligonucleotide fragment synthetic

The synthetic of oligonucleotide fragment is with an automatic solid phase phosphamidon chemical method (automatic solid phase phosphoamidite chemistry) dna synthesizer (Applied Biosystems Inc., 3808, U.S.A.) finish.

Synthetic oligonucleotide denaturing polyacrylamide gel (2M urea, 12% acrylamide and two fork acrylamide (29: 1), 50mM Tris, 50mM boric acid, 1mM EDTA) electrophoresis and SEP-PAK(Waters Inc., U.S.A.) column chromatography carries out purifying, determines its content by measure optical density(OD) (O.D.) value at the 260nm place.

Reference example 6: polymerase chain reaction (PCR)

Give and add following material: 10 μ l 10X Taq polymeric enzyme reaction damping fluid (10mM Tris-HCl, 500mM KCl, 15mM MgCl in the template DNA mixture of 10-100ng ₂0.1%(w/v) gelatin, pH8.3), 10 μ l dNTP ' s mixtures (at each 1.25mM of dGTP, dATP, dTTP and dCTP), 2 each primer of μ g are (usually, 2 kinds of primers are used in reaction, in case use 4 kinds of primers, being positioned at intermediary primer usage quantity is 0.02 μ g) and 0.5 μ l Ampli Taq archaeal dna polymerase (Perkin Elmer Cetus, U.S.A.), transferring to cumulative volume with distilled water is 100 μ l, adds 50 μ l mineral oil again to prevent the hybrid reaction evaporation.

PCR is that (Perkin Elmer Cetus carries out in U.S.A), suitably repeats repeatedly by the thermal cycling program, and circular order is: ℃ 30 second → 72,95 ℃ of 30 second → 55 ℃ 1 minute at a thermal cycler; Last circulation time is reflected at 72 ℃ and carried out 10 minutes.

After reaction is finished, mixture phenol extracting, the PCR product goes out with ethanol sedimentation, this throw out is dissolved in the 20 μ l TE damping fluids (10mM Tris-HCl, 1mM EDTA pH7.5) again.

Embodiment 1: the preparation of chicken growth hormone gene

(1-A): the design of the oligonucleotide of structure CGH gene and synthetic

For prepare to be contained in 5 '-recognition site of the restricted property restriction endonuclease Nde I recognition site of end and 2 termination codons and restriction enzyme Sal I, describe with reference example 5

Oligonucleotide CGH1 5 '-end contains the recognition site of a restriction enzyme Nde I: 5 '-CATATG-3 ' and 3 '-end has 5 of 20 nucleotide residues and CGH2 '-end complementation.

5 of CGH3 '-end has 20 nucleotide residues and CGH4 3 '-end complementation, 5 of CGH5 '-end has 3 of 20 nucleotide residues and CGH6 '-end complementary, 5 of CGH7 '-end has 3 of 20 nucleotide residues and CGH8 '-end complementary, and 5 of CGH9 '-end has 3 of 20 nucleotide residues and CGH10 '-end complementary.

(1-B): the preparation of full CGH gene

＜the first step 〉

Carry out the following PCR reaction first time by reference example 6: give to add 2 μ g CGH1,0.02 μ g CGH2,0.02 μ g CGH3 and 2 μ g CGH4 among the reaction tubes A; Give and add 2 μ g CGH5,0.02 μ g CGH6,0.02 μ g CGH7 and 2 μ g CGH8 among the reaction tubes B; Give and add 2 μ g CGH9 and 2 μ g CGH10 among the reaction tubes C.Give again respectively and add 10 μ l 10X Taq polymerase buffer (100mM Tris-HCl, pH8.3,500mM KCl, 15mM MgCl in above-mentioned 3 pipes ₂, 0.1%(w/v) gelatin), 10 μ l dNTP ' s mixtures (dGTP, dATP, dTTP, each 1.25mM of dCTP), 0.5 μ l(5 unit/μ l) Ampli Taq archaeal dna polymerase and 67 μ l distilled water.Thermal cycling is in proper order: ℃ 30 second → 72,95 ℃ of 30 second → 55 ℃ 1 minute, repeat this order 4 times after, should be further after this carry out in 10 minutes at 72 ℃.Last reaction mixture application of sample carries out electrophoretic separation in polyacrylamide gel and goes out PCR product for the first time.This product is further used Elutip-D(Schleicher ﹠amp; Schuell, U.S.A.) purifying is dissolved in the 20 μ l TE damping fluids (10mM Tris-HCl, pH7.5,1mM EDTA).

＜the 2 step 〉

With the 1st PCR product by following the 2nd polymerase chain reaction (PCR) process of carrying out.

About 100ng PCR product in reaction tubes A is blended among the reaction tubes D with the about 100ng PCR product in reaction tubes B, add 2 μ gCGH1 again, 2 μ g CGH8,10 μ l 10X Taq polymerase buffers, 10 μ l dNTP ' s mixtures, 0.5 μ l(5 unit/μ l) Ampli Taq archaeal dna polymerase and 67 μ l distilled water.This mixture carries out 20 PCR circulations.The PCR product of Huo Deing is by＜the 1 step like this〉identical method processing, at last product is dissolved among the 20 μ l TE damping fluids.

＜the 3 step 〉

Press with the 2nd PCR product and to give an account of the program that continues and carry out the 3rd PCR reaction.

Each reactant below in reaction tubes E, adding: the PCR product among the product of the PCR among about 100ng reaction tubes D, the about 100ng reaction tubes C, 2 μ g CGH1,2 μ gCGH10,10 μ l 10X Taq polymerase buffers, 10 μ l dNTP ' s mixtures, 0.5 μ l(5 unit/μ l) Ampli Taq archaeal dna polymerase and 67 μ l distilled water.This mixture carries out 20 PCR circulations.The 3rd the PCR product of Huo Deing is by＜the 1 step like this〉identical method processing, obtain a fragment (being called the CGH fragment here) at last and contain complete CGH gene or total length CGH gene, be dissolved in too in the 20 μ l TE damping fluids.The segmental all processes of preparation CGH illustrates in Fig. 2.

Embodiment 2: preparation of expression vectors

(2-A): the segmental preparation of CGH-N/L, PL and PN

The CGH fragment that about 2 μ g obtain in embodiment 1 uses restriction endonuclease Nde I (10 unit) in 37 ℃ of digestion in 50 μ l 10X NEB reaction buffers 4, carries out phenol extracting and ethanol sedimentation afterwards.The throw out that contains nucleic acid is dissolved in further uses restriction enzyme Sal I (10 unit) to handle 2 hours at 37 ℃ in the 5 μ l 10X NEB reaction buffers 3.

On the other hand, 2 μ g are with intestinal bacteria W3110(KFCC-10667) isolated plasmid ptrp322H-HGH mode same as described above restriction endonuclease Pst I and the digestion of Sal I, other 2 μ g plasmid ptrp322H-HGH digest with restriction endonuclease Pst I and Nde I.Postdigestive plasmid all on 0.7% sepharose electrophoresis isolate 0.6Kb, 1.5Kb and 0.8Kb fragment, respectively called after CGH-N/L fragment, PL fragment and PN fragment.

(2-B): CGH-N/L, PL is connected with PN is segmental

Give about 100ng CGH-N/L fragment, approximately add the T of 2 μ l 10X ligase enzyme damping fluids and 10 units in 100ng PL fragment and the about segmental mixed solution of 100ng PN ₄Dna ligase; Then, it is 20 μ l that adding distil water is adjusted to cumulative volume, and this mixture solution was reacted 12 hours at 16 ℃.After finishing this reaction, with reaction mixture transformed into escherichia coli HB 101(ATCC 33694); Filter out the intestinal bacteria bacterium colony that transforms with the ptrp-CST that contains the CGH gene fragment.From transform thalline, isolate plasmid ptrp-CST, use primer 2 090(5 '-CATCACCGAAACGCGCGAG-3 ' again) and primer ptrpl(5 '-GACAATTAATCATCGAACTA-3 ') ptrp-CST is carried out dideoxy dna sequential analysis (Sanger, F.et al, P.N.A.S.74,5463(1977)) to determine the nucleotide sequence of total length CGH gene.

Embodiment 3: with expression vector transformed into escherichia coli and expression CGH gene

The ptrp-CST plasmid transformation escherichia coli W3110(ATCC 27325 that obtains in embodiment 2), the method for use is identical with the method for reference example 4; Transformed bacteria 37 ℃ of concussions in the LB substratum that contains 50 μ g/ml penbritins (every liter contains 10g Bacto-Tryptones (Bacto-triptone), 15g yeast extract, 5g sodium-chlor) were cultivated 12 hours.Getting the 5ml nutrient solution is transferred to 11 capacity and is 5 liters and contains 1L40 μ g/ml penbritin M ₉Substratum (40mM K ₂HPO ₄), 22mM KH ₂PO ₄, 8.5mM NaCl, 18.7mM NH ₄Cl, 1% glucose, 0.1mM MgSO ₄, 0.1mM CaCl ₂, 0.4% casamino acids, 10 μ g/ml vitamins Bs ₁) under 37 ℃, swing in the culturing bottle and cultivated 3-4 hour.When the optical density value (O.D.) of culture reaches 0.5 at 650nm place in each is cultivated, add with the indole acrylic acid (IAA) of various concentration and to make CGH genetic expression (IAA makes IAA concentration in the nutrient solution from 0mM to 1.0mM with the concentration of each 0.1mM of raising).After adding IAA5 hour (do not add IAA, can increase incubation time), with whizzer (Beckman J to 12-24 hour ₆-B, rotary head JS 4.2) the centrifugal culture of 3000rpm is 25 minutes, obtains the Bacillus coli cells throw out.The cell precipitation thing is suspended in the sample buffer, presses Laemmli method (Laemmli, Nature 227,680(1970)) and carry out electrophoresis to determine this expression of gene on 12% polyacrylamide gel, the result is referring to Fig. 4.

The the 1st and the 4th capable having shown do not contain CGH gene Bacillus coli cells sample protein matter gel pattern among Fig. 4; The 2nd and 3 behaviors contain CGH gene intestinal bacteria and cultivate cell sample protein gel collection of illustrative plates after 12-24 hour when not adding IAA, and the 5th line display is cultivated when adding IAA concentration reaches 0.1mM and contained CGH gene intestinal bacteria 5 hour cell sample protein matter gel patterns.

As seen in fig. 4, can find that CGH albumen band spectrum clearly can occur on the 2nd, 3 and 5 row 22Kd positions, expression amount accounts for 30% of whole coli somatic protein content at least.

Embodiment 4: the CGH purifying that intestinal bacteria are produced

(4-A): separation of C GH inclusion body from culture of Escherichia coli

(50mM Tris, 50mM EDTA pH7.4), use Polytron agitator (Lightnin, Model TS 1515) to stir 3 minutes then to give 4 liters of damping fluids of adding in 1 kilogram of culture of Escherichia coli.This liquid was handled 3 minutes with ultrasonic generator (Cole-Pamer, Model 4720), added 0.4g N,O-Diacetylmuramidase (these product are from the egg white part) again and make that concentration reaches 0.1g/L in solution, 37 ℃ of stirrings are 30 minutes then.

Add 200ml 20% triton x-100 in this solution, about 5 minutes of vigorous stirring is used centrifugal 30 minutes of whizzer (Beckman JM-21), supernatant discarded, collecting precipitation.(100mM NaCl, 10mM Tris pH7.2) wash throw out, and centrifugation goes out the CGH inclusion body again with 2 liters of damping fluids.

(4-B): the dissolving of CGH inclusion body

The CGH inclusion body that obtains in above-mentioned (4-A) is suspended in 8 liters of distilled water; In it, add 1N NaOH solution then in batches and make pH reach about 12.3, further stirred 3 hours, the last centrifugal insoluble impurities of removing.

(4-C): ultrafiltration and anion-exchange chromatography

Obtaining 8 in above-mentioned (4-B), to go up clear liquid be 3 * 10 with the molecular cut-off size ⁵Filter membrane carry out ultrafiltration, be concentrated into 1 liter of residual solution.It is 3 * 10 to obtain about 40 liters of molecular weight that this process repeats 4-5 time ⁵Or be lower than 3 * 10 ⁵Filtrate, this filtrate is 1 * 10 with molecular weight current-carrying size again ⁴Filter membrane be concentrated into below 20 liters or 20 liters, transfer pH to 9.0 with 1N HCl solution.The concentrated solution that contains CGH is splined on the DEAE-Sepharose chromatography column.This post uses 10mM glycine buffer (pH 9.0) balance to wash post in advance, about 10 liters/hour of elution flow rate, wash 5 column volume 10mM glycine buffers after, use the glycine buffer wash-out that contains 90mM NaCl again instead.The elutriant of Huo Deing (pH 9.0) is 1 * 10 with molecular weight current-carrying size like this ⁴Or be lower than 1 * 10 ⁴The filter membrane ultrafiltration and concentration be 99.7% to obtain about 3.6g 93% pure monomer CGH(purity), endotoxin content is 10 unit/milligrams or is lower than this value.

Fig. 5 shows the SDS-PAGE result who expresses CGH intestinal bacteria transformant cell extract and purifying CGH.

In Fig. 5, A behavioral standard molecular weight of albumen marker protein; CGH intestinal bacteria transformant whole-cell protein is not expressed in the B behavior; CGH intestinal bacteria transformant whole-cell protein is expressed in the C behavior; D behavior purifying CGH shows as one and is about the 23.5Kd band clearly.

Purifying CGH further uses efficient liquid phase chromatographic analysis, and the result shows that purity reaches 99.7%, and the result of HPLC is in Fig. 6 and table 1.

Table 1

Peak number order 123 amounts to

Retention time 4.656 9.278 11.284

The component ripple

Concentration (ng/ml) 0.0000 0.0000 0.0000 0.0000

Complanation concentration 0.0000 0.0000 0.0000 0.0000

Peak area 0.05533 124.30640 0.32342 124.68514

Peak height 0.00038 0.18592 0.00157 0.18787

Matrix sign indicating number BCB BCB BCB

Reply coefficient 0.0000 0.0000 0.0000 0.0000

Relative retention time 0.0000 0.0000 0.0000 0.0000

Peak area percentage value 0.044 99.697 0.259 100.000

Peak height percentage value 0.205 98.959 0.836 100.000

Though the present invention has obtained describing by above-mentioned specific embodiment, also should be realized that the person skilled in the art also can do various obviously relevant with the present invention operational technology and change and variation simultaneously.These changes and change and also to belong to category of the present invention, will be in the claims in addition clear and definite.

Claims

1, the chicken growth hormone gene that has following nucleotide sequences:

2, the expression vector that contains chicken growth hormone gene in the claim 1, wherein chicken growth hormone gene is placed on the position that can express on Bacillus coli cells.

3, as the expression vector in the claim 2, it is ptrp-CST.

4, the Bacillus coli cells that transforms with the expression vector described in the claim 2.

5, as the Bacillus coli cells in the claim 4, it is to use ptrp-CST(KCCM-10005) the intestinal bacteria W3110 that transforms.

6, a kind of method of producing chicken growth hormone comprises and cultivating as the intestinal bacteria in claim 4 or 5.

7, a kind of method of purifying chicken growth hormone comprises:

The separatin non-soluble CGH inclusion body of under the condition that is fit to CGH genetic expression, cultivating the intestinal bacteria transformant described in claim 4;

Wash inclusion body with the solution that contains tensio-active agent and ethylenediamine tetraacetic acid (EDTA), then, again with containing NaCl or NH ₄The damping fluid of Cl or distilled water clean;

In pH value scope is that the suspend inclusion body washed of 11.5 to 13.0 basic solution is collected at dissolving and forgives intravital CGH;

Centrifugal this suspension is to obtain supernatant liquor;

Supernatant liquor is carried out uf processing to obtain to contain the filtrate of dissolved chicken growth hormone;

With this filtrate by anion exchange resin layer being analysed post to obtain the chicken growth hormone of purifying.

8, method as claimed in claim 7, wherein said tensio-active agent are 0.1 to 1% triton x-100 (Triton X-100) for the final concentration scope.

9, method as claimed in claim 7, wherein said ultrafiltration are meant with a kind of ultra-filtration membrane carries out, this film only allow molecular weight be 3 * 105 or the material that is lower than this value pass through.

10, method as claimed in claim 7, wherein said anionite-exchange resin are the DEAE(diethylaminoethyl-) resin.

11, method as claimed in claim 7, wherein said anion-exchange chromatography have used 70-150mM NaCl solution as elutriant.