前苏联专利SU1523055A3 Method of producing strains of bacteria esherichia coli and pseudomonas putida as producers of cleat

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专利摘要:
Ein neuer Mikroorganismus der Gattung E. coli oder Pseudomonas putida bildet konstitutiv Creatinamidinohydrolase. Bevorzugte können enthalten: das Plasmid pBT 2a-1, DSM 3148P oder das Plasmid pBT 306.16, DSM 3149P.
公开号:SU1523055A3
申请号:SU864002500
申请日:1986-01-03
公开日:1989-11-15
发明作者:Шумахер Гюнтер；Букель Петер；Бокамп Клаус
申请人:Берингер Маннхайм Гмбх (Фирма)；
IPC主号:

专利说明:

This invention relates to genetic engineering and relates to the production of creatine dihydrolases in the strains of the bacteria Escherichia coli and Pseudomonas putida.
The purpose of the invention is to obtain strains that constitutively produce creatine dihydrolase.
DNA was isolated from Pseudomonas putida, digested with an EcoRI endonuclease to isolate a 5.8 kV fragment, treated with endonuclease EcoRI and PvuII, and a 2.2 kV fragment was obtained, which was cloned into a digested vector, transformed into the corresponding E. coli and R. putida.
Example. The chromosomal DNA of Pseudomonas putida DSM 2106 was isolated after
cell destruction, DNA winding on a glass rod after two treatments with phenol and precipitation with ethanol, dissolve it at a concentration of 600 / U / ml.
10 Cg of chromosomal DNA is treated with 5 units of EcoRI and the degree of digestion in an agarose gel is analyzed,
E. coli ED DSM 2102 bacteria were incubated in the presence of 5-10 D phages of Sharon 10 for 20 minutes at 37 ° C and then allowed to grow until the bacteria began to lyse in 500 ml of complete medium, followed by isolation of phage,
10 gig Sharon 10 DNA completely digested with 1 mg of EcoRI endonuclease, cut the Pseudocide chromosomal DNA.

O4
The tnonas putida is incubated with 3 g of the phage Sharon 10 DNA cleaved by the EcoRI endonuclease with 40 units of T4 DNA ligase enzyme. The packaging of the bound DNA fragments of the phage head and tail proteins / is carried out in a test tube. About 0.5 Cg of bound and Pseudomonas DNA are incubated with the original mixture, 0.5 ml of SM buffer solution, 1/200 volume (2.5 (ql) of the original mixture in packaging incubated with an overnight strain of E. coli (in lO molar magnesium sulphate) aged overnight for 10 minutes at 37 ° C, the suspension of bacteria is then mixed with 3 ml of LB-agarose: (0j8%) and added to the plate. About 15 phage holes (platelets) are obtained per 1 Hz g of the introduced DNA,
An immunoassay with an enzyme is used to identify phages that contain a creatinase-encoding gene. The indicator system consists of 6 mg / ml tetramethylbenzidine, 20 mg / ml dioctyl sodium sulfosuccinate and 0.01% in gelatin. For 1000 platelets, two positive signals are established.
Of the five positive in the immunoassay, a platelet enzyme test, the phage preparation DNA – DNA was obtained. The cleavage of five different DNAs by EcoRI made it possible to detect the DNA band in all five 5.8 kV phages of DNA.
Approximately 5 ill g of this EcoRI fragment was cleaved using PvuII endonuclease and 2.2 kV fragment was made. The generated DNA fragments were separated in a low melting agarose gel by their size and the EcoRI fragment was extracted from PvuIIa fusible agarose gels are made by cutting the appropriate lanes, transferring to a test tube (Eppendorf tube) and mixing with approximately two times the volume of water, then incubated at until 5 to 10 minutes until the agarose has melted, shake the sample From time to time and then vigorously shaken with half the volume of phenol (neutralized with 10 mmol TPA-HC1 with pH 7.5 and 1 mm EDTA. TE), Separate the phases by centrifugation for 10 minutes at 15000 g and extract the upper aqueous phase again.
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khivanii with phenol. After centrifuging for 10 minutes at 15,000 g, the upper phase is extracted twice by shaking with ether (1 ml each), the ether is evaporated at 65 ° C. and the precipitate is precipitated with 1/10 volume of 3 M sodium acetate pH 7.2 and 2.5 times the volume of ethanol at 20 ° C. The DNA is precipitated by centrifugation for 10 minutes at 15,000 g, dried under vacuum, and introduced into 10 ~ (TE), All further described fragments are produced in the same way.
About 4 C | g pBR 322 DNA was digested with EcoRI and PvuII and a 2.3 kV fragment was isolated. A 0.2 / ug of this pBR 322 fragment is incubated overnight in the presence of five units of T4 DNA ligase and a 0.5 | Ur EcoRI - PvuII fragment of 2.2 kV from the described-L phages. The resulting plasma MIDU is called rVT-3-2, it encodes in E, coli biologically active creatinease.
Example 2. A DNA fragment encoding creatinease from plasmid pBT-3-2 was treated with nitrosoguanidine. Plasmid DNA was isolated after cell lysing using the CSCI ethyl bromide method. Cells of strain E, coli ED 8654 are transformed with plasmid DNA and placed on complete medium plates (LB) containing 20 Y4H / ml ampicillin. After incubation overnight, nitrocerol filter paper is placed on a BB plate. After incubation for 37 hours at 37 ° C, the nitrocellulose filter with the colonies is removed and transferred to a glass Petri dish (W 20 cm), into which 1 ml of a mixture of chloroform and toluene (1: 1) was added, Incubation wire t for 20 min at 37 ° С. Then the nitrocellulose filter is placed on the indicator agarose plate so that direct contact between the cells and the indicator plate occurs.
Color reaction occurs depending on the time and amount of creatine in individual clones of creatine clones. From the filtering system described, the clone ED was selected with the pVT plasmid, DSM 3143 "This plasmid encodes creatinease, which is about 50% of the dissolved protein of the cells.
As an alternative to the described direct YC mutagenesis, an increase in the level
51523
Creatinase expressiveness can be achieved with lac-npoMOTopa (the latter can be made from commercially available plasmids, for example, pUC-plasmids). For this, plasmid rWT-3-2 is treated with EcoRI-endonuclease, lease, treated with the Bal 31 endonuclease in such a way that it removes about 10-100 times. each side. Then, the 1ac promoter is injected using the T4 ligase enzyme, which binds the ends, to the truncated plasmid WT 3-2. This DNA is mutagenized with nitrosoguanidine, is then used to transform an ED strain, and the clones are tested for high expression of the gene.
Mentioned indicator agarose plate is a test system for screening activity, the principle of which is that creatine is cleaved by the enzymes creatine dinogydrolase and Sarcinozinoxylase to form H, 0 through peroxidase at 1/2 0 and performs the reaction of oxygen with. system color indicator, for example, from 4-aminoantipirin (4AAN) and N-ethyl-N- (sulfoethyl) -3-methylaniline ,. salt est. A bluish-violet staining is formed, which, with an excess of sarcasinoxylase and peroxidase enzymes, represents the degree of synthesis. bath in colonies of creatinine hydrolase.
Test prints:
creatinidine
Creatine + sarcosine hydrolase + urea
Registry - CD,
Sarkozin + 0 (2 + HgO glycine + formaldehyde +
Pod
4-AAP + EST
35
The composition of the filtering activity of creatinine hydrolase is shown in Table 1.30.
The reagents mentioned in paragraphs 1.-7 are dissolved and mixed with the same volume of low-melting agarose (2%), 6 ml is poured into a Petri dish, the plates can be stored for about 2 weeks at dark.
Example 3 For cloning and providing expressiveness of cloned creatine dihydrolase in dO
Pseudomonas putida used the plasmid RSF 1010. RSF 1010 was linearized by Pstll and from the plasmid raCUS 177 after HAE11 cleavage
1.4 kV fragment, 0.2 | Cyg RSF 1010 DNA dd bind to 1 / and g Nae 11-fragment using T4 ligase, I get
Plasmid plasmid is a pBT 306.1 RSF 1010 and derivatives of this plasmid have a wide range of host and are suitable, for example, for Pseudomonaden and E. coli, pBT 2a-1 plasmid is cleaved by Pvul and
PvuII, a 2.8 kV fragment. - pBT 306.1 the plasmid was digested with Pvul and Smal and a 10 kV fragment was isolated. 0.5 (U g vector Dac is bound to 0.5 (C g Pvu I-Pv, uII fragment. A. E. coli ED is transformed
dye + 2H20
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ABOUT
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and identify creatine encoding clones by selecting activity on the plates. Plasmid DNA is obtained from one of the positive clones by the method of C8C1-etsh1-bromide. The plasmid is called rBT 306.16, DSM 3149 R.
Transform plasmid DNA into Pseudomonas putida 2440,
By filtering with a selection of activity on the plates, positive clones are identified. This is possible in Pseudomonas putida 2440, although this strain contains chromosomal-encoded creatine dynohydrolase, since the expressiveness of the encoded plasmid creatine dinohydrolase is structurally manifest. This distinguishing feature allows a distinction to be made between the encoded chromosome and the encoded plasmid creatinine hydramine.
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Example 4. The determination of the activity of creatinine hydrolase is carried out by detecting ammonium ions formed as a result of reactions with urease with a urea test combination.
Wild type Pseudomonas putida 2440 to determine the activity of creatinamine hydrolase is incubated overnight in B-medium (5 ml), which contains 1% creatine.
Cells are harvested by centrifugation and washed once in 50 mM phosphate buffer solution pH 7.5. The cells in the initial volume were introduced into a phosphate buffer solution (50 mM with a pH of 7.5) and dissolved by sonication (4) SDR s).
Cultivation and dissolution of cells that contain a plasmid encoding creatine dihydrolase is carried out in an optimal manner, with the exception that the medium does not contain creatine for induction and that is taken with the addition of ampicillin (20 jUr / ml for plasmid pBT) or streptomycin (20 mg / ml for plasmid pBT 306.16). Crop growth occurs for Pseudomonas putida at 30 ° C5 for Ebdol.i - at 37 C.
The data show that as a result. The cloning of creatinine hydrolase in E. coli bacteria acquires a new property to synthesize creatinine hydrolase, and this expressiveness, in contrast to the original Pseudomonas putida strain, is manifested structurally for both E. coli and Pseudomonas putida. Due to the mutagenesis of DNA coding for creatinine hydrolase, particularly high expressivity can be achieved.
. In E coli U / pBT 2A-1 DSM 3143, the activity is 500 units / g of biomass (wet) 5. specific activity is 4.5 units, / mg protein As the specific activity of highly purified protein is 9 units / mg, this means that creatinamide hydrolase in E.coli is 50% soluble protein. Analysis of the crude extract indicates that creatine disodium hydrolysis is the major band of the soluble protein fraction.
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Example 5. Dd cultivation. “Three different Eecoli host systems are used in the fermenter, namely E. coli W 3350, E. coli AU 8654 and E.ccli CHI Ppaemidu rVT is transformed into the appropriate competent cells. Separately, the culture colonies are grown in DYT medium, which contains 20 jyr / i-in ampicillin, overnight at. The fermentation medium (DYT) is inoculated with a preliminary culture (1% inoculum) and left without selection for the content of plasmid for 1 h at 37 ° C for - growth. Creatinamide hydrolase activity after 25 hours of incubation
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Lakes about 600 units / g wet weight or 4.5 units / mg protein.
Plasmid pBT 306.16 transform into cells of Pseudomonas putida strain 2440, and get P. putida DSM N3147.

权利要求:
Claims (1)
[1]
After purification of individual colonies, the culture is incubated in DYT medium, which contains 200 Kg / ml of strepto mycin at 30 ° C overnight. The fermentation medium (FLS) is seeded (1% inoculum) and the culture is left to grow for 30-30 hours at 30 ° C. Activity after 25 hours is about 220 units / g fresh weight, activity 1.8 units / mg Protein Formula of the invention
The method of obtaining bacteria of Escherichia coli and Pseudomonas putida - creatine creatinine hydrolase producers, consisting in that chromosomal DNA from Pseudomonas putida DSM 2106 and DIC of phage Sharon 10 is treated with Eco endonuclease. RI, ligate the obtained fragments, pack hybrid DNAs in the presence of phage shell proteins, transform the obtained hybrid phages into E. coli DSM 2102 cells, which are pretreated overnight 0, with maltose solution and dissolved in 0.1 M / L MgSO4 , further, phages are identified by expressing creatine dihydrolase with an indicator system containing 6 mg / ml of tetramethylbenzidine, 20 mg / ml of dioctyl sodium succinate and 0.01%, in 6% gelatin, phages that give a positive reaction are isolated, DNA these phage ob- (work endonuk Eco.RI lease followed by isolation of a 5.8 kV fragment that is treated with the PvuII endonuclease, Eco.RI PvuII is a 2.2 kV fragment that is ligated with the digested EcORI and PvuII vector pBR 322, and the resulting recombinant DNA is transformed into cells E. coli DSM 2102 bacteria, select cells that constitutively produce creatine, cells are treated with 25 mg / ml nitroseguanidine, plasmid DNA is isolated ,. which translates into E. coli DSM 2102 cells, selects bacteria containing the plasmid pBT 2a-1, and the plasmid DNA obtained is transformed into E. coli DSM 2102 and processed
endonucleases Pvul and PvuII, a fragment of 2.8 kV is inserted, which is ligated with a Pvul - Smal fragment of 10 kV of the pVT 306.1 vector, obtained by processing plasmid pSE 1010 and ligating with
Table
Creatinome hydrolase in Pseudomonas putida and E.Coli
05510
The 1.4 kV Haell fragment of the plasmid pACC177 obtained by recombinant DNA transforms P.putida DSM 2440 cells and isolated clones that constitutively produce creatine-dine-hydrolase.
T b .a ..

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引用文献:

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US4039384A|1975-04-05|1977-08-02|Noda Institute For Scientific Research|Creatinine amidohydrolase and creatine amidinohydrolase and process for producing them|

JPS528395B2|1975-04-05|1977-03-09|

DE3500184A1|1985-01-04|1986-08-14|Boehringer Mannheim Gmbh, 6800 Mannheim|MICROORGANISM AND PLASMID FOR CONSTITUTIVE CREATINAMIDINOHYDROLASE FORMATION AND METHOD FOR PRODUCING THE SAME|DE3500184A1|1985-01-04|1986-08-14|Boehringer Mannheim Gmbh, 6800 Mannheim|MICROORGANISM AND PLASMID FOR CONSTITUTIVE CREATINAMIDINOHYDROLASE FORMATION AND METHOD FOR PRODUCING THE SAME|

DE3803175A1|1987-05-12|1988-11-24|Boehringer Mannheim Gmbh|STABLE CREATINAMIDINOHYDROLASE MUTANTS|

JP2527035B2|1989-06-16|1996-08-21|東洋紡績株式会社|A DNA fragment containing a gene encoding creatinine amide hydrolase, a recombinant vector having the DNA fragment, a transformant having the recombinant vector, and a method for producing creatinine amide hydrolase|

法律状态:

优先权:

申请号 | 申请日 | 专利标题

DE19853500184|DE3500184A1|1985-01-04|1985-01-04|MICROORGANISM AND PLASMID FOR CONSTITUTIVE CREATINAMIDINOHYDROLASE FORMATION AND METHOD FOR PRODUCING THE SAME|LV930466A| LV5533A3|1985-01-04|1993-06-02|Panemiens for the production of escherichia coli and pseudomonas putida strains - creatine amidinhydrolase producers|

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