• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    An improved process for producing a thermostable alpha-amylase enzyme is described. The gene coding for the alpha-amylase is incorporated into a chimeric plasmid which is produced in multiple copies by a host microorganism.
    公开号:SU1200853A3
    申请号:SU823383349
    申请日:1982-01-14
    公开日:1985-12-23
    发明作者:Р.Миленз Джонатан；Миккел Сьюзен
    申请人:Спс Интернэшнл Инк (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to genetic engineering, namely, to the production of r-microorganisms containing the genetic code of the enzyme heat-resistant al fah amylase. Example 1. Obtaining plasmid containing the genes of alpha-amylase resistant to the antibiotic. All DNA containing alpha-amylase genes is isolated from the plexus of Bacillus stearotherraophilus ATCC No. 31783 using the well-known method of Burns and Thomas. In accordance with the proposed method, cells i-yi: no; M, inivioi (: H in a mixture of 50 mM tr .. hydrochloride with (oxime1) aminomethane (tris-HC1 ;, 0.6 mM ethylenediaminetetraacetic acid (EDTA) and 25% pacib.jpa of sucrose of standard salt citrate at pH 8 , 0. In addition, cells are treated with lysozyme (2 mg / ml) for 1 hour at 0 ° C before lysis. Plasmid pBR 322 DNA, restriction enzyme Hind III and DNA of phage T4 ligase were obtained from laboratories at the Beta Food Research Center, Maryland A mixture of 7.5 / and g from the entire DNA of the strain of Bac. Stcajothermophilus restriction enzyme Hind III and 10 / U g of albumen per serum in 100 ju l of solution that contains 50 m NaCl, 6 mM at pH 7.5 and 6 mM MgQ, incubated at 37 ° C for 30 NIN. 2.2 cc. DNA plasmid pBR 322 and 7 units (E) of Hind III are digested in 20 ml of the same solution for 1 hour at 37 ° C, DNA analysis on agar gel shows that the process of your-1 was completed. Then 6.75 / IG of the treated DNA of You stearothermophilus and I. The DNA of the treated pBR 322 are mixed with 0.3 ml of a solution containing 6, 6 Trio-HC1 (pH 7.6), 6.6 mM Mga2, 10 mM dithiothreitol and 0.067 mM Trifafata adenosine (ATP), and combined using 0.28 units of phage T. DNA ligase. Analysis on agar gels DNA after ligation indicates that ligation Completed and the remaining linear DNA molecules pB 322 were not detected. Example 2. Transformation of plasmids containing alpha-amylase genes and a marker resistant to antibiotic effects in K, Coli. 53 Culture E. co 1 i RH. , obtained as PRC 399 strain from the Plasmid Species Center. The University Medical Center in Stanform, California, is grown in an environment containing g / l ;; trypton 10.0; Yeast Extract 5.0 Sodium Chloride 5, Oglukoza, 0. The culture is grown in vitro overnight at. It is then diluted with 9 parts of the same medium and incubated at 37 ° C for an additional 135 minutes with vigorous stirring. The cells are collected by centrifuging by 1-1 and washed with a 0.1 M cold solution of NaCl. Collected E. coli cells are processed before transformation in accordance with the known procedure proposed by Kozny and others. Half of the DNA that is ligated (obtained in Example 1) is transferred into E. cells with 1i RRI. Cells are cultured on plates containing the same medium E. coli cells were grown on, except that the medium contains ampicillin with a concentration of 50 L (g / ml. As a result, only E. coli cells containing the plasmid pBR 322 (with genes responsible for ampicillin resistance) are obtained As a means to determine the numbers of cells containing their recombined DNA cells ampicillin-resistant are analyzed for tetracycline resistance. Since the introduction of the DNA fragment into the dissecting section of the Hind III enzyme pBR 322 strain generally deactivates the plasmid gene responsible for resistance to tetracycline, the amount of sensitivity to tetracycline gives the number of cells containing recombinant purulent DNA present in the cell population; Transformation yields 3.6 x 10 ampicillin-resistant cells per millimeter and 3.0 X 10 1 tetracycline-resistant cells per millimeter. Consequently, approximately 16% of the cells are sensitive to tetracycline, which indicates that they contain a plasd with recombinant DNA. Example 3. Isolation of E. coli colonies synthesizing alpha-amylase. . A medium of the same composition as that used for the cultivation of E. coli is prepared, except for adding 15 g / l of agar plus ampicillin (g / ml). This c; food is placed on 130 Petri plates and the diluted transformed culture of E. co 1i is grafted onto it, obtained in Example 2. These plates give an average of 113 colonies per plate. Colonies are grown until they reach a diameter of about 1-2 mm, and then are copied on plates with a starch medium of the following composition, g / l: 6; KH2PO 3, NaCl 0.5; one; yeast extract 1, peptone 10; agar 15; Lintner starch 10. After being grown for 3 hours. bacteriophage T, ATCC No. 11303-B4, is added to plates coated with starch-containing medium. Approximately 1x is used to release all intracellular enzymes. x10 T for each plate. After growing overnight and lysing, 2.5% iodine Lugol iodine solution is applied to the plates in order to detect all transparent zones formed under the action of amylase activity. Of the approximately 15,000 colonies present, 18 colonies form transparent zones, indicating the presence of amylase. The colonies exhibiting amylase activity are replicated on the plates, - and at the same time the activity of amylase reappears, however, only after the addition of the bacteriophage T4 to the lysed cells. This fact indicates that amyl for is obtained inside the cells. Subsequent experiments showed that D-cyclo-losser is effective for producing lysed cells if this preparation is added to a medium with a concentration of 600 g / ml. The E. coli strain RRI containing the plasmid pBR 322 vector with the amylase gene is known as ATCC No. 31789. Example 4. Transformation of plasmids containing alpha-amylase genes and an antibiotic-resistant marker in E. coli strain C600, ATCC No. 23724. E. coli C600 ATSS culture No. 23724 is grown, cells are harvested and prepared for transformation according to Example 2. Five different amylase clones are grown as described in Example 3, and recombinant plasmids are released: using the same procedure to clarify the lysate Clevell and Helinski. Partially purified plasmid ZNAs are suspended in a mixture of 10 mM HNS-HC1 and 1.0 mM ELTC with pH 7.5 immediately before being transferred into E. coli cells treated with CaC. This DNA is analyzed to determine that it is sterile. Thus, no amylase synthesizing colonies can appear due to copying of cells introduced with DNA. Transformed cells are grown on a medium containing ampicillin so that only cells containing plasmids continue to grow. When testing colonies for amylase activity, a 100% correlation is established between the presence of plasmids and amylase activity. This indicates that plasmid DNA transforms both strains of E. coli and transforms them into amylase producers. Thus, it does not depend on the strain, but requires a recombinant plasmid for its implementation. The strain E. coli C600, containing the vector of the plasmid pBR 322 with the amylase gene, is known as ATCC No. 31,788. Example 5. Heat resistance of alpha-amhase. Four amylase clones, prepared as described in Example 3, and one E. coli RRI control culture are grown in 15 ml of the medium described in Example 2. The cells are dissolved by adding D-cycloserine, and then the remaining cells are removed by centrifugation. Sodium acetate and calcium chloride are added to a liquid located on the surface in order to obtain a concentration of 50 mM and 2.5 mM, respectively, the pH is adjusted to 6.0. Enzyme solutions are placed in tubes with screw caps connected to a Teflon tape. The solutions are analyzed for the activity of alacid, and then kept at 90 ° C for 45 minutes. The amylase activity is determined by the rate of starch hydrolysis, which is manifested in a rate of decrease in the ability to dye iodine, measured spectrophotometrically according to a well-known procedure B.U. Smith and JG Row. The control strain E. coli does not possess amylase activity. In order to obtain standards, heat
    K0 (,: - il-: Н КС) НТрОЛ1 PYY LIZLT E. CO 1 1
    to do kpch; purified amylase from 5ac;; -. ATSS No. 31783 ,, v-MVii, P i g, obtained from r} Sigma Kemkelkel Co., St. Louis, Missouri, under the name Sigma A6380 and Termyl methylstone alpha amnlachu, obtained from Novo Laboratories, Wilton, Conn,
    The results of the tests are given in i4i6js,.
    Amylase, synthesized by clones, is just as heat resistant as the enzyme synthesized by donor B. ste-V 1G1 G:;} 1kP-1z, It is comparable in hectare) (t: available by Mi.iuj.U-HHOc; Ifj -c black-resistant alpha-amy. casoG) tetramyl and superior in germ / resistance to al) β-amylase, which (on an industrial scale, is cultured by B. subtilis,
    The hydrolysates obtained from the starch treatment of each amylase are analyzed by thin layer chromatography in order to determine the amount of sugars with a low molecular weight. The relative amount of HHSKHN sugars with a molecular weight produced by the action of amylases synthesized by E. cli clones is similar to the amounts of sugars obtained by exposure to known alpha-amylases used as controllers.
    The results show that the heat-resistant enzyme gene, obtained from extremely thermophilic organisms, is well copied in a mesophilic bacterial host and gives a heat-resistant enzyme product. Thus, it was found that the gene from extremely hermophilic bacteria can be copied to mesophilic bacteria with using recombinant DIC methods. In addition, the synthesis of a heat-resistant active enzyme is carried out with normal mesophilic tagged patterns (approximately 20-40 C1
    Example 6: Isolation of naturally occurring plasmids containing alpha-amylase genes.
    All DNA is released from you cells. stearothermohilus ATCC No. 31783, as described in Example 1, plasmid DNA is separated from all DNA using ultracentrifugation using cesium chloride, ethidium chloride and
    known procedure; 1, uzzy, P 1 d11zhripoy R. Redlos1kh} 1st, U. Bau rum and Lk. R / and hail.
    The fact that ilHlv rvruii gpasmid contains Go.n alpha-amylase is established as follows: the LI of the glt-plasmid is dissected using the restriction enzyme i-.itid as in Pe 1. Thiyuns are obtained by, removing this DNA in E, col: agially with Examples 1-3. Ap.chiz fepot1-P1a CTOIIKOSTy to chetratsik.gppgu pshsazal that 3.3% of the cells of the cell are tetracycline and, therefore, contain cloned DNA. After the cells were isolated from the actuality of alphamylase, it showed that 0.42% or approximately one of the ka}: {D15Gx cells and cells that contain clonronophageal LNK have an amylase gene. Plasmold dissection) B. Bleago1: G1H; O:) 1 Bottom with Kind ITT gives) i.e. fragments of DICs that are separated by n; .i eight easily detected; kvaye1-nd regiments: by electrophoresis pa agarops; gel. The frequency of cloning a; a - ilase (I / B) is equal to approx. Plc) available, if one of the eight predominant bands contains hep amplases. The analysis of such plasmid bands shows that o and dpa from the bands are approximately 3.6 md, i.e. this is a TITT of the same size as the klongrovapnye pieces of DNA, which are obtained when aparalyzing the plasmid of example 1
    This experiment shows that at least one hepatitis 1 amylase is located on a naturally occurring plasmid in the B. stea-rotTiermcTihilns strain used,
    Example 7. The preparation and isolation of strains E, 1 i, s: objadi, various hybrid plasmids.
    A, A culture of amylase-producing E. coli, isolated as described in Example 3, ATCC No. 31,789, grown overnight in the medium used in Example 2, plasmidgl DNA is amplified by noMOiiiii of the known procedure Clevell D. using chloro-amphenicol per milli esr. The following medium is used for amplification, g / lt. Ha iiJ-Q ,, 6,0; 3.0 NaCl 0.5; . 1, 0, casein amino acids slots 5.0, glucose 2.0 and CaClj 2 0.015, - / P 0.246, vitamin B, 0.001.
    DN (plasmids are then isolated using the standard clearing method for Clevell and Helinski lysates. Isolated plasmids are purified using ethidium bromo MIDA, CsCl as described in Example 6, and then using isopropanol and deep dialysis in 10 mM tris-HC1 plus 1 mM EDTA with a pH of 7.5.
    A culture of E. coli RRT, PRC 399 containing 3.9 Md, plasmid pVP 325 is grown, and the plasmid DNA is amplified, distributed and purified by the indicated method.
    The DNA of the two obtained plasmids are cut with the Hind III restriction enzyme. Solutions of dissected plasmids are mixed and ligated at 0 ° C for 18 hours using the general procedure of Example 1,
    The DNA after ligation is transferred to E. coli RRI using the method described in Example 2. The cells are diluted and applied onto agar plates containing 20pg / ml of chloramphenicol. As a result of this procedure, E. coli cells containing only the pBH plasmid are obtained 325 (with genes responsible for chloramphenicol resistance). The colo-dai cells that are prepared are screened for amylase activity using the method described in example 3dl cell dissolution using 1) -cycloserine.
    The recombinant DNA plasmids from three colonies that have amylase activity and show resistance to chloramphenicol 5 are extracted by clarifying the cellate described in Example 4. The isolation of recombinant plasmids on agar gels showed that they have the expected size for a pV 325 plus 3 plasmid combination , 6 MD fragment containing the amylase gene. The impact on the plasmid with the Hind TIT enzyme gives a 3.6 Md fragment and the linear form of the plasmid pBR 325. This suggests that the amylase gene can replicate on various vectors, pBH 325, without losing its activity on amylase synthesis. The resulting E. coli strain is known as ATCC No. 31,792,
    B. A hybrid plasmid, chloramphenicol and ampicillin resistant, obtained in Part A, is used as a donor of a DNA fragment that contains the alpha-amylase gene. This fragment is connected to the 10 Md plasmid of the BpWL 625 vector indicated in Part A me / o. Plasmid pV / L 625 is described by W. Goebel and others. It can be isolated from the culture of E. coli strain ATCC No. 31787 using the plasmid isolation procedure used in Part A. This vector is made resistant to antibiotics, ampicillin and kanamycin. Injecting DNA in pWL 625 into the Hind ITT area destroys kanamycin resistance.
    E. coli RRI cells, which are transformed by the introduction of recombinant DNA, are grown on agar plates containing ampicillin. Those colonies that are resistant to ampicillin, but are not resistant to chloramphenicol due to the presence of pBR 325, and show amylase activity are selected for analysis. Plasmid DNAs are isolated from colonies. An analysis on agar gels before and after exposure to the Hind TIT enzyme showed that the DNA fragment containing the amylase gene is copied onto the plasmid pWL 625 and gives a new plasmid. E. coli strain containing such a hybrid
    The plasmid is known as ATCC No. 31791.
    %
    Example 8. Transformation of two different hybrid plasmids in the same E. coli strain.
    E. coli papamm is synthesized, which synthesizes amylase obtained in Example 7B; it is then prepared for transformation using the procedure of Example 2. The purified plasmid obtained in Example 7A is transformed into these cells. When growing chloramphenicol containing agar plates, all colonies showed amylase activity. Plasmid DNA was selected from one of the colonies and analyzed on agar gels. It is established that both Hybrid plasmids are described as described in Example 7A and 7B. This experiment shows that the E.coli culture can continue to grow and simultaneously contain two different hybrid plasmids containing alpha-amylase genes. Stability for the duration of this combination has not been determined. The E. coli strain containing these two hybrid plasmids is known as ATCC No. 31790 I p and m ep 9. Graigformpi r Jia4Nni; i containing an antibiotic in pggammo II; G., 11Pt .. L. Obtaining a DNA donor, Hybrid nllsmide, obtained in Example 7K, is used as a donor of a DNA fragment that contains the gene, F-A, and Pylla. It is extracted using the procedure ocBej.-ie, neither Kleve lysate. And Helinski, the DNA of this plasmid is dissected with the restriction enzyme Kind TIT. The lilucleus product is mixed with a small amount of ethyl bromide and is isolated using the well-known method of sucrose gradient, presumed El-Gyuli and Helly}, 3.6 Md fragment containing the alpha-amide gene ;.y., extracted twice butyl alcohol, is precipitated with an equal volume of isodroic alcohol and is suspended in cm si 10 mM rice plus 1 mM EDTA with a pH of about 7.8, kept at -20 ° C before use. B, Vector Preparation (nepeHOC4HK Strain p., Subtil.is, obtained from the Genetic Center for Bacillus Storage, Faculty of Microbiology, Oraiio State University, strain No. 1E17, containing 2.0 Md of plasmid pC 9A, which contains a gene that is resistant and chloramphenicol is applied strips on a plate containing Difco Tryptic Soybean agar, obtained from Difco, Detroit, Michiten and 50 pg / ml laborative laboratories.Further, cells are grafted on 150 ml of Penasse broth (Difco) in a 1-liter flask and grown overnight at 37 ° C shaking The cells are granulated and resuspended in 10 ml of 25% sucrose protoplast buffer, 0.1 M Nad — 0.05 M trisNA at pH 7.5 and 0.05 M EDTA at pH 8.3), 5 mg of white lysozyme montej (Sigm Chemical Company) is added for 30 minutes at 37 ° C, then 13 ml of 2% sodium dodecyl sulfate solution in 0.7 M NaCl are vigorously stirred, and then 2.5 ml of 5 M NaCl solution. The mixture is cooled in ice water and centrifuged with; acceleration 12 1000 X g for 20 min. DNA is precipitated with an equal volume of isopropyl alcohol. The solid residue is held in ice-cold water for 60 hours. It is surrounded by zeolite (1) by a bath and suspended at another. into a solution containing 0.01 M tone of hydrochloride and 0.001 M EDTA at RP 7.5, the plasmid DNA is isolated using ul1-centrifugation, using et-iodi bromide, CsCl using the Rdloff method and others, 2 Md of the plasmid is processed by extraction from - tropyl alcohol and deep dialysis in 10 mM Tris plus 1 mM EDTA at pH 7.5, C. Preparation of the hybrid plasmid, 2 MD-vector of Part B is dissected using Hind 11 restriction enzyme-1 and mixed with 3.6 MD-DNA fragment parts A, Concentration of the vector and donor DNA 5 and 17.01 g / ml respectively, and in Example 1, The absence of any linear 3.6 Md fragment after lngatsii (this fact ustanav :: ivaets by electrophoresis on agarose gel) indicates that ligadi completed. G, Transformation of a hybrid plasmid into B, subtilis. Culture B, subtilis, ATCC No. 31735, which does not contain the amylase gene, is grown overnight on a plate containing agar based on blood tryptosis (Difco and 1% solution of soluble starch. Add 2 ml of growth medium to the plate ,%: CNH 0.2V K2HP04 1.4; 0.6; sodium citrate 2 ° O 0.1; M) 1-. 0.12; glucose 0,5; casein acids (Difco 0.02 G, -tryptophan 0.005, Approximately 0.1 ml of cell suspension, thus obtained, is added to 10 ml of the same medium: in a 250 ppm flask and incubated at 37 ° C for vigorous stirring for A h Then, 1 ml of the culture is added to 9 ml of pre-heated dd transformation medium at 37 ° C and the incubation with shaking is continued for 90 m. The transformation medium is the same as the growth medium, with the exception that contains a 0.01% solution of casein amino acids and a 0.0005% solution of L-tritstophan, 0.25 mp of cell culture with a density of approximately 1x10 cells current / ml of added elc 5 / q of the hybrid plasmid solution of part B containing plasmid. The mixture is vigorously shaken at 37 ° C for 30 minutes, diluted with an equal volume of broth Penasse (Difco) and shaken for an additional 90 min. A portion of cells in 0.1 ml is applied onto plates containing blood-based tryptone agar (Difco, soluble starch and chloramphenyl solution,%). As control samples of cell B. -subtilis without plasmid and B. subtilis cells with plasmid vector pC194 are applied to the same Wednesday No colonies were noted on the plates, where the cells did not contain the added plasmids. Three colonies were marked on plates where the cells contained plasmid rs194, but none of the colonies showed amylase activity. One of the colonies was marked on plates that bear cells containing the hybrid plasmid DNA part B. It gave a transparent zone when exposed to iodine vapor, This indicates that cells synthesize an extracellular amylase fragment. The cells appeared to require the presence of fenicol chlorine for stability. This culture is known as ATSS No. 31786. A sample of DP1K amylase-containing colonies was obtained using an electro-agar gel electrophoresis. A plasmid band of about 5.6 Md is noted. This corresponds to the size of the hybrid plasmid from part B. t The purified hybrid plasmid is cut with the Hind III restriction enzyme and subjected to agar gel electrophoresis. The result is two fragments of approximately 2.0 and 3.6 Md. They correspond to the size of the donor DNA of part A and the DNA of part B. B. Transformation of the hybrid plasma in the second strain of B. subtilis. The hydride plasmid containing the amylase gene is isolated from the amylase-synthesizing colony cells from part B using the procedure used to isolate the plasmir pC194 in part B, the isolated hybrid plasmid is transformed in another amylase-resistant i strain B. subtilis ( strain No. 1A289), obtained from the Genetic Center for Storage of Bacilli, Department of Microbiology, Ohio State University, Transformer 12 3 maci is carried out using the well-known method of photoplast fusion proposed by S. Chang and S.N. Koznom. As a result, and cells chasplastinkah method described in ti T, recorded approximately x10 kblony / ml on plates containing no chloramphenicol. Approximately -1x10 colonies / ml were also recorded on the plates containing chloramphenicol. Using starch-iodine testing, it was found that all these colonies contain amylase. Such amylase-containing B. subtilis is known under the name of ATCC No. 31784. Example 10 Thermal stability of alpha-amylase synthesized by B. subtilis strain containing the hybrid plasmid. Cells B, subtilis, containing the hybrid plasmid, from example 9D, ATCC No. 31784, are grown in 1 l of medium in a 2.8 l Fernbach flask using medium of the following composition,%: corn starch 9.0, maize liqueur 6, OJ yeast autosilate (Primex-154, obtained from the laboratories of Amber Juneau Wisconsin) O, 35; (1.0; 0.1; 0.06; MPS, - 4F20 0.05; corn oil, 1.0; termamyl, O., 05 U / mp. The medium is kept in an autoclave for 30 minutes at a temperature that destroys thermamyl activity, and then cooled to room temperature. Next, 0.01 mg of chloramphenicol per milliliter is added to the cell medium before grafting. The broth is centrifuged and the heat resistance is tested using a diluted sample of the upper liquid layer and the general procedure of Example 5, For comparison, measure also the heat resistance of amylase cultures of B. stearothermophilus, B, subtilis, as well as of known termamyl amylase in incubation medium containing 50 mM sodium acetate and 2.5 mM CaCJ2 (3TO amylases used for comparison in example 5, the test results are shown in Table 2. In this test amylase synthesized by B. subtilis clone ATCC No. 31 784, possesses no less heat resistance than the enzyme synthesized
    1312008531
    bath culture donor B. stearo. alpha-amylase, termamyl and transmothermophilus. It is comparable in thermo-heat resistance of alpha-amine resistance with the known heat-resistant
    Zu in. subtilis.
    Table
    E.coli (control)
    Control + oi-amylase
    V. stearothermophilus
    Table
    权利要求:
    Claims (1)
    [1]
    METHOD FOR CONSTRUCTING A HYBRID PLASMID, CONTAINING THE HEAT-RESISTANT 'ALPHA-AMILASE GENETIC CODE, · Including hydrolysis of donor DNA by endonuclease to obtain a linear one. DNA sequences with an alpha-amylase-encoding gene, recipient hydrolysis with an endonuclease, vector to obtain a second linear DNA sequence, joining linear DNA sequences using DNA ligase, and natural or hybrid plasmids from Bacillus stearothermohilus strains are used as donor DNA. ATCC No. 31195 , 31196, 31197, 31198, 31199, 31783, and as a recipient vector, a plasmid selected from the group of plasmids including rVP 322, pBR 325, pWL · 625, and pC 194 is used; endonuclease Hind III is used, and from DNA ligaz - D K-T 4 ligase ._>
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US22528781A| true| 1981-01-15|1981-01-15|
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