US 4,824,786 AGrant
Methylotroph Cloning Vehicle
Issue Date:1989-04-25
•3 Claims
•3 Drawing Sheets
Abstract
A cloning vehicle comprising: a replication determinant effective for replicating the vehicle in a non-C.sub.1 -utilizing host and in a C.sub.1 -utilizing host; DNA effective to allow the vehicle to be mobilized from the non-C.sub.1 -utilizing host to the C.sub.1 -utilizing host; DNA providing resistance to two antibiotics to which the wild-type C.sub.1 -utilizing host is susceptible, each of the antibiotic resistance markers having a recognition site for a restriction endonuclease; a cos site; and a means for preventing replication in the C.sub.1 -utilizing host. The vehicle is used for complementation mapping as follows. DNA comprising a gene from the C.sub.1 -utilizing organism is inserted at the restriction nuclease recognition site, inactivating the antibiotic resistance marker at that site. The vehicle can then be used to form a cosmid structure to infect the non-C.sub.1 -utilizing (e.g., E. coli) host, and then conjugated with a selected C.sub.1 -utilizing mutant. Resistance to the other antibiotic by the mutant is a marker of the conjugation. Other phenotypical changes in the mutant, e.g., loss of an auxotrophic trait, is attributed to the C.sub.1 gene. The vector is also used to inactivate genes whose protein products catalyze side reactions that divert compounds from a biosynthetic pathway to a desired product, thereby producing an organism that makes the desired product in higher yields.
Metadata
Assignee
- The Regents of the University of Minnesota
Inventors
- Richard S. Hanson
- Larry N. Allen
Application Information
Application Number:US 1072447
Filing Date:1987-11-13
Priority Date:1984-09-14
Art Unit:185
Classifications
IPC:
C12N 120C12N 1500
Field of Search:
435935172.3;253;32026;29;72
Patent Drawings (3 sheets)
Description
DESCRIPTION OF THE PREFERRED EMBODIMENT
We turn now to a description of the preferred embodiment of the invention, first briefly describing the drawings.
FIG. 1 is a flow diagram of a process for producing the cloning vector pLA2901.
FIG. 2 is a flow diagram of a process for producing the cloning vectors pLA2905, pLA2910, and pLA2917.
FIG. 3 is a flow diagram of a process for producing the cloning vector pLA2920.
The preferred cloning vehicles are illustrated by the following descriptions of specific vehicles denoted pLA2920, pLA2905, pLA2910, and pLA2917; the two most preferred vehicles are pLA2917 and pLA2920. The latter two vehicles have been deposited with the American Type Culture Collection and given accession nos. 39840 and 39841, respectively. Applicants recognize their obligation to notify the ATCC of the issuance of a patent on this application, to make the above deposits publicly available thereafter, and to replace the deposit should it die during the effectiveness of any patent issuing on this application.
We will describe first the construction of pLA2917 and the derivation of pLA2920 from it, thereby providing a detailed description of the elements of thos plasmids.
We will then describe complementation analysis using those plasmids to characterize the genome of a C.sub.1 -utilizing microorganism, exemplified by a strain of Methylobacterium organophilum; we then will describe engineering selected genes of the C.sub.1 -utilizing microorganism and integration of those genes in the chromosome of that or another C.sub.1 -utilizing microorganism.
Finally, we will describe production of a desired product, exemplified by production of L-phenylalanine, by culturing the engineered C.sub.1 -utilizing microorganism on a C.sub.1 carbon source.
GENERAL TECHNIQUES
Except as noted below or as noted elsewhere in this application, the experimental techniques that can be used to accomplish the engineering described in this application are described in Maniatis Molecular Cloning, Cold Spring Harbor Laboratory, 1983.
Escherichia coli is routinely cultured on LB medium as described in Miller (1972) Experiments in Molecular Genetics, P. 433 (Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.). Unless otherwise specified, M. organophilum ATCC 27886, M. organophilum DSM 760, and Ps. AM 1 strains are grown on MacLennan salts (see Maclennan et al. (1971) J. Gen. Microbiol. 69:395-404) supplemented with sodium succinate (0.1% weight/vol.) or methanol (0.5% vol/vol).
Antibiotics, when added, are used at final concentrations of 25 .mu.g/ml (kanamycin) and 20 .mu.g/ml (tetracycline) for E. coli and 10 .mu.g/ml each for methylotrophs.
Preparative amounts of plasmid DNA are isolated from E. coli HB101 essentially by the method of Birnboim (1983) Methods Enzymol. 100:243-255. Cells are lysed in alkaline SDS followed by high salt precipitation. This material is centrifuged (8,000 rpm, 30 minutes) and the plasmid DNA is precipitated by the addition of 0.55 vol of col isopropanol. Plasmid DNA is then further purified by banding twice in ethidium bromide/CsCl dye bouyant density gradients.
Plasmid DNA from recombinant clones is screened by the miniprep procedure of Crosa et. al. ["Plasmids" (pp. 266-282) Manual Of Methods for General Biochemistry, Gerhardt e., Am. Soc. Microbiol. Wash, D.C., 1981] except that following isopropanol precipitation, restrictable plasmid preps are obtained by two successive precipitations with ethanol. Chromosomal DNA from wild-type strain xx is purified from cells lysed in the following manner. A late log phase culture of M. organophilum grown on Penassay broth is harvested by centrifugation (8,000 rpm, 10 minutes) and washed once by centrifugation with 1 M NaCl. The pellet is resuspended in 1 M NaCl (20 ml/gm wet weight) and incubated at 55.degree. C. for 30 minutes. EDTA (ethylenediaminetetraacetate) is added to 0.1 M and the incubation at 55.degree. C. is continued for 15 minutes. Cells are collected by centrifugation (8,000 rpm, 10 minutes) and resuspended in TES (10 nM TRIS(hydroxymethyl-amino methane)-HCl pH 8.0, 1 mM EDTA, 0.15 M NaCl) plus 10 mg/ml lysozyme. The cell suspensions are incubated at 37.degree. C. for 45 minutes followed by the addition of sodium dodecyl sulfate (SDS) to 1% (wt/vol). After addition of SDS, the cells are incubated for 45 minutes at 65.degree. C. Chromosomal DNA from cells lysed in the manner described above is purified by the method of Marmur (1961) J. Mol. Biol. 3:208-218.
Where indicated, DNA is purified from agarose gels by electroelution onto dialysis membranes according to the method of Yang et al (1979) Methods Enzymol. 68:176-182.
Restriction endonucleases are used according to manufacturers' recommedations (Bethesda Research Laboratories (BRL), Rockvill, MD and Promega Biotech Inc., Madison, Wisc.).
Nuclease Ba131 (BRL) is incubated with DNA at 0.09 units/.mu.g DNA (500 .mu.l) at 32.degree. C. in 20 mM TRIS-HCl pH 8.0, 12 mM CaCl.sub.2, 12 mM MgCl.sub.2, 1 mM EDTA, 200 mM NaCl and 250 .mu.g/ml BSA. Samples (22.mu.l) are taken at regular intervals and the reaction stopped by the addition of 2 .mu.l of 200 mM ethylene glycol-bis(B-amino ethyl ether)-N,N'-tetracetate(EGTA).
T.sub.4 DNA polymerase (BRL) and deoxynucleotide triphosphates are used to generate blunt ends in Ba131 treated molecules. T.sub.4 DNA ligase (Promega Biotech, Inc.) and Bacterial Alkaline Phosphatase (BRL) are used according to manufacturers' recommendations.
Bateriophage lamgda packaging extracts and in vitro packaging is performed by the method of Hohns (1979) Methods Enzymol. 68:299-309 as modified by Ostrow et al. (1983) J. of Invest. Dermatol. 80:436-440.
THE VEHICLES
FIG. 1 outlines the steps in the construction of pLA2901 from pRK290, which is then modified as shown in FIG. 2 to yield pLA2905, pLA2910, and pLA2917.
FIG. 3 outlines the steps in forming pLA2920 from pLA2917.
Plasmid pLA2917 is based on the broad host range mobile cloning vector pRK290 reported by Ditta et al. PNAS USA 77:7347-7351. pRK290 is a 20 kbp plasmid that can be mobilized from E. coli to several gram negative bacteria by RK2-derived plasmid pRK2013. Specifically, pLA2917 and pLA2920 include the kanamycin resistance gene of the Tn5 transposon, described below.
In order to incorporate the kanamycin resistance element of Tn5 into pRK290, pBR322 is digested with HindIII, and the HindIII fragment of transposon Tn5 is cloned into pBR322.
Next the kanamycin resistance element is excised from the resulting plasmid with BamHl. This element is inserted into pRK290 [Ditta et al. (1980) PNAS USA 77:7347-7351] by a BamHl/BglII fusion to yield a 22.4 kbp plasmid, pLA2901.
Plasmid pLA2901 harbors genes coding for resistance to kanamycin and tetracycline. It contains 5 unique restriction sites: the EcoRl site of pRK290, the HindIII site of pBR322, and the BglII, BstEII, and XhoI sites of Tn5. DNA insertions at the unique BglII site can be detected by inactivation of Km resistance.
More versatile cosmid vectors, pLA2910 and pLA2917, are then constructed from pLA2901 in the following manner. In order to generate unique restriction sites for PstI and SalI, pLA2901 is linearized with XhoI and treated with Ba131 Nuclease. The extent of Ba131 digestion is followed by subcutting samples at 2 minute intervals with PvuII and monitoring the PvuII fragment (originally 730 bp) of Tn5 on 4% polyacrylamide gels according to the method of Rothstein et al. (1980) Cell 19:795-805. An increase in the mobility (decrease in size) of this fragment indicates that Ba131 activity has proceeded past the SalI and adjacent PstI sites and into the region of the PvuII fragment.
The cohesive ends (cos site) of bacteriophage lambda are then introduced in order to generate a vector with increased DNA insert capacity. The origin of the lambda cos site in pLA2910 and pLA2917 is pMF517 disclosed by Feiss et al. (1972) Gene 17:123-130. This plasmid is linearized with HindIII, treated with Nuclease Ba131 to reduce the size of the resulting cos fragment by approximately 800 bp, and blunt ends are generated with T4 DNA polymerase plus dNTP's. The resulting DNA is subcut with PvuII, separated on a 0.7% agarose gel and the gel-purified cos fragment is ligated to pLA2901 which is treated as described above.
Cosmid pLa2917 is shown in FIG. 2; cosmid pLA2910 is the same as pLA2917, except that the lambda cos fragment is in the opposite orientation. The cos site allows in vitro packaging into bacteriophage lambda of inserts up to 30 kbp in length. Cosmid pLA2917 (21 kbp) contains 6 unique restriction enzyme cleavage sites: BglII, (Km), BstEII, HindIII, HpaI, Pstl, (Km), and SalI (Tc). Several possible cassettes exist for the Km resistance gene. For example, a PhaI, EcoRV fragment of 1.4 kbp contains unique restriction sites for BglII, HindIII and Pstl.
Plasmid pLA2920 is created from pLA2917 by deleting the kanamycin resistance segment to avoid internal rearrangement when the transposon segment moves and to permit selection of conjugants that have a Tn5 insertion. To construction pLA2920 from pLA2917, the latter was treated with HindIII and HpaI, and then with phage T4 DNA polymerase and the resulting strand was ligated as shown in FIG. 3.
The above-described vectors carry resistance determinants for kanamycin and/or tetracycline and have multiple unique restriction endonuclease cleavage sites. Insertional inactivation of kanamycin (BglII and Pstl) and tetracycline (SalI) can be used to detect inserts. These vectors can transfer efficiently to a broad host range including E. coli HB101, M. organophilum strain xx, M. organophilum DSM 761. Pseudomonas AM 1, Pseudomonas putida and Pseudomonas aeruginosa. The previously described pVK100 series cosmids also have multiple drug resistance markers; however, the cosmids described here have the additional advantage of utilizing Sau3A generated partials of insert DNA to clone into the BglII site. The tetranucleotide recognition sequence of Sau3A allows the cloning of a more complete random set of partial digestion products than does a restriction endonuclease with a hexanucleotide recognition sequence. Indeed, examples of BglII or Sau3A inserts greater than 26 kbps with no internal sites for BglII and/or HindIII have been found in this laboratory. These libraries would not contain the entire genome.
CHARACTERIZATION OF THE C.sub.1 UTILIZER'S GENOME
A C.sub.1 -utilizing organism is selected to be transformed to the ultimate fermentation host. For example, a strain of Methylobacterium organophilum (ATCC 27886), a facultative methlylotroph that prefers methanol as a carbon and energy source, is a suitable starting strain. Other suitable organisms include Methylophilus methylotrophus, Pseudomonas aeruginosa mutants, Pseudomonas AM 1, Methylobacterium organophilum DSM761, and Pseudomonas putida.
Once the ultimate fermentation host has been selected, its genome can be mapped and characterized to enable engineering that will enhance further the yield of the desired compound. Such complementation mapping is illustrated by the following description of mapping M. organophilum.
M. organophilum is naturally resistant to trimethoprin (100 .mu.g/ml), mutates spontaneously at high frequency to streptomycin resistance, and due to the extended period necessary to select transconjugants (10-12 days), ampicillin is not sufficiently stable to allow selection of resistant colonies. As a result, these three antibiotics, frequently used for selection in genetic studies of other gram negative bacteria, cannot be used with this organism. M. organophilum strain xx is very sensitive (<10 .mu.g/ml) to kanamycin and a convenient source of this antibiotic resistance determinant is the neomycin phosphotransferase gene of Tn5 as described by Beck et al. (1982) Gene 19:326-336. These factors, in addition to convenient restriction enzyme cleavage sites available for the isolation of this gene, are desirable factors.
A genomic library of M. organophioum strain xx DNA is constructed in the BglII site of pLA2917. A Sau3A partial digest of strain xx chromosomal DNA is size fractionated on a 0.5% agarose gel (500 ml) and partial digestion products ranging from 22 to 30 kbp are isolated. pLA2917 is linearized with BglII, treated with bacterial alkaline phosphatase, mixed with the M. organophilum strain xx DNA fragments, and the DNA mixture is treated with DNA ligase. Vector and chromosomal DNA are ligated at a vector-to-insert ratio of 2:1 and a total DNA concentration of 300 .mu.g/ml. The ligation mixture is packaged into bacteriophage lambda and the resulting phage particles are used to infect E. coli HB101 (ATCC No. 33694). Several thousand transfectants can be obtained, and 2,000 are picked for further study. Tc.sup.R clones contain insert DNA with an average size of 28 kbp.
Complementation assays can be performed by patch plate matings. Fifty recombinant E. coli HB101 donors containing pLA2917 with inserts, arranged in a grid pattern on a master plate, can be replica plated onto a lawn of E. coli HB101 (pRK2013) and a Ps. aeruginosa auxotroph. Matings are incubated at 37.degree. C. for nin hours and then replica plated onto selective media. In this way, mutant clones exhibiting a particular phenotypical trait (such as auxotraphes for some, but not all, aromatic amino acids) are complemented by specific clones containing specific recombinant plasmids, thus enabling identifications and mapping of the gene responsible for that trait.
Thus, the ability of recombinant molecules to complement mutants unable to grow without an amino acid is determined by patch plate matings. Plates are examined and donors are scored for the ability to complement markers in the recipients i.e., to restore ability to grow without the amino acid.
DNA from complementing clones is subcloned into pLA2920 and mutagenized in vivo with Tn5 in E. coli HB101 as described below. Since Tn5 does not appear to transpose in M. organophilum, these can be mobilized into strain xx wild type to create mutants by marker exchange. This establishes which functions are coded for by each cloned fragment and enables determination of linkages between other C-1 markers in M. organophilum strain xx.
ENGINEERING THE C.sub.1 -UTILIZING HOST
Where production of a specific compound is desired, mutants of the organism that are resistant to analogs of the product can be selected. For example, where phenylalanine production is sought, the original Methylotrophs are mutated chemically (for example, with N-nitrosoguanidine) and the mutants are exposed to 5-fluorophenylalanine. Resistant mutants such as ATCC No. 39866 are selected.
Having identified and cloned a gene for a side reaction which lessens product yield as described above, that gene can be rendered inactive as follows.
A plasmid such as pLA2920 containing the gene of interest is inserted into E. coli and is mutagenized by transposition of Tn5, a discrete 5.7 kilobase segment of bacterial DNA which can insert at high frequency into numerous sites in gram negative bacteria. It encodes resistance to kanamycin and neomycin in bacteria. Tn5 is disclosed in Berg et al. Bio/Technology July, 1983, pp. 417-435. A suitable source of Tn5 is plasmid pJBJI reported by Beringer et al. (1978) Nature 276:633-634. The transposon can move to new locations in DNA molecules without relying on extensive DNA sequence homology between the inserted element and the insertion site, and without relying on rec genes needed for classical homologous crossing over. That transposition is marked by an antibiotic resistance marker on Tn5 transposon plasmid. By restriction mapping techniques, it is possible to select events in which the transposon has inserted into the gene of interest.
The selected E. coli organisms are then conjugated with the ultimate C.sub.1 -utilizing host, and the gene of interest containing the inactivating insert integrates into the chromosome to replace the wild-type active gene.
In this way, genes whose protein products catalyze undesired side reactions are inactivated. The resulting C.sub.1 -utilizing organism provides enhanced yields of desired compounds.
FERMENTATION
The engineered C.sub.1 -utilizing microorganism may be cultured according to known techniques using a C.sub.1 compound, preferably methanol as the primary source of carbon and energy. The desired compound is harvested according to known techniques. For example, the fermentation conditions described at p. 1089 in Demain at al. (1981) Appl. and Env. Microbiol 41:1088-1096 may be used, and the product recovery technique described at p. 777 in Yamada et al. (1981) Appl. and Env. Microbiol 42:773-778 may be used.
OTHER EMBODIMENTS
Other embodiments are within the following claims. For example, other transposons, other antibiotic resistance traits, and other replicons may be used. Similarly, other C.sub.1 -utilizing organisms may be used, and other desired compounds may be produced.
Claims
What is claimed is:
1. A cloning vehicle selected from the group consisting of the following plasmids: pLA 2917 as deposited in E. coli strain HB101 as ATCC 39840; pLA 2920 as deposited in E. coli strain HB101 as ATCC 39841; pLA 2901; pLA 2905; pLA 2910; and derivatives engineered therefrom.
2. A C.sub.1 -utilizing microorganism of the species Methylobacterium organophilium, the species Pseudomonas aeruginosa, or the strain Pseudomonas AM 1, and wherein said microorganism comprising a cloning vehicle selected from the group consisting of the following plasmids; pLA 2917 as deposited in E. coli strain HB101 as ATCC 39840; pLA 2920 as (deposited in E. coli strain HB101 as ATCC 39841; pLA 2901; pLA 2905; pLA 2910; and derivatives engineered therefrom.
3. The microorganism of claim 2 wherein said microorganism is Methylobacterium organophilum deposited as ATCC 39866 or a derivative thereof.
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| US3907637 | 1975-09-01 | Nakayama | |
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| JPX29791/75 | 1980-11-01 |
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