GB2107717A - Cloning vectors - Google Patents

Abstract

Selectable pairs of recombinant DNA cloning vectors for use in Streptomyces and related organism are described. A pair of recombinant DNA closing vectors comprises: a) plasmid pEL7, and b) a second plasmid that is functionally dependent upon plasmid pEL7, said second plasmid comprising a restriction fragment of plasmid pEL7 and one or more different DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell, said host cell being susceptible to transformation, cell division, and culture. p

Description

SPECIFICATION Cloning vectors The present invention relates to novel pairs of recombinant DNA cloning vectors, each pair comprising plasmid pEL7 and a second plasmid comprising a restriction fragment of plasmid pEL7 and one or more DNA segments that convey resistance to antibiotics. The invention further relates to transformants of the aforementioned pairs of vectors.

The present invention provides antibiotic resistance conferring cloning vectors for use in Streptomyces and related host cells. Heretofore, the development and exploitation of recombinant DNA technology in the above organisms has been retarded and made especially difficult because of the general lack of selectable genetic markers on cloning vectors. The vectors of the present invention are functional and selectable in both Streptomyces and other host strains and therefore represent a significant advance in the technical art.

The present vectors are particularly useful because they are versatile and can be transformed and selected in any Streptomyces cell that is sensitive to an antibiotic for which resistance is conveyed. Since a high proportion of the clinically important antibiotics are produced by Streptomyces strains, it is especially desirable to develop cloning systems and vectors that are applicable to that industrially important group.

The present invention provides such vectors and thus allows for the cloning of genes into Streptomyces for increasing the yields of known antibiotics as well as for the production of new antibiotics and antibiotic derivatives.

The present invention provides vehicles for cloning DNA into Streptomyces host cells and also allows for the convenient selection of transformants. Since transformation is a very low frequency event, such a functional test is a practical necessity for determining which cell(s), of among the millions of cells, has acquired the plasmid DNA. This is important because DNA sequences that are non-selectable can be inserted onto the vectors and, upon transformation, cells containing the vector and the particular DNA sequence of interest cari be isolated by appropriate antibiotic selection.

For purposes of the present invention as disclosed and claimed herein, the following terms are as defined below.

Recombinant DNA Cloning Vector - any autonomously replicating agent, including but not limited to plasmids, comprising a DNA molecule to which one or more additional DNA segments can or have been added.

Transformation -the introduction of DNA into a recipient host cell that changes the genotype and consequently results in a stable and heritable change in the recipient cell.

Transformant - a recipient host cell that has undergone transformation.

Sensitive Host Cell - a host cell that cannot grow in the presence of a given antibiotic without a DNA segment that confers resistance thereto.

Restriction Fragment - any linear portion or whole of a plasmid generated by the action of one or more restriction enzymes on the plasm id.

Functionally Dependent - the condition whereupon plasmid replication and expression of resistance to one or more antibiotics requires the presence of a separate and different plasmid.

Insertional Isomer - one of two or more possible recombinant DNA molecules formed when a DNA fragment is inserted at one of two or more compatible sites on the recipient DNA.

Plasmid pLR2 1 .sky BamHI Restriction Fragment - the same 1 .6kb BamHI thiostrepton resistance conferring fragment contained in plasmid plJ6.

Plasmid pLR1 or pLR4 3.4kb BamHI Restriction Fragment - the same 3.4 kb BamHI neomycin resistance conferring fragment contained in plasmid plJ2.

Plasmid pLR1 3.5kb Pstl Restriction Fragment - the same 3.5kb Pstl neomycin resistance conferring fragment contained in plasmid plJ2.

AmpR - the ampicillin resistant phenotype.

Tets - the tetracycline sensitive phenotype.

ThioR - the thiostrepton resistant phenotype.

NeoR - the neomycin resistant phenotype.

The present invention provides a process for isolating plasmid pEL7 which comprises cultivating Streptomyces ambofaciensipEL7 NRRL 12523 under submerged aerobic conditions in a nutrient medium containing assimilable sources of carbon, nitrogen and minerals at a pH in the range of 5 to 9 and at a temperature in the range of 15 to 45"C, harvesting the cells thus formed, lysing the harvested cells, solvent extracting the lysate supernatant, precipitate the plasmid DNA from the extract, and separating the plasmid pEL7 from the precipitate.

The invention further provides a process for preparing a plasm id that is functionally dependent upon plasmid pEL7 which comprises ligating one or more different DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell onto a restriction fragment of plasmid pEL7, and self ligating the resulting recombinant DNA to produce said functionally dependent plasmid.

The invention further comprises transformants of the aforementioned pairs of vectors.

Vectors of the present invention are constructed by ligating one or more antibiotic resistance conferring DNA segments onto a restriction fragment of plasmid pEL7. Plasmid pEL7, from which the restriction fragments are constructed, is approximately 10.9kb and contains several restriction sites which are particularly advantageous for molecular cloning. Since the resistance conferring vectors of the present invention are functionally dependent on plasmid pEL7, a variety of different pEL7 restriction fragments can be used for their construction without regard for independent functionality. Thus, plasmid pEL7, useful directly as a cloning vector, is essential for both the construction and functioning of the present invention. A detailed restriction site and functional map of plasmid pEL7 is presented in Figure 1 of the accompanying drawings.For purposes of the present application, Figure 1 and all subsequent Figures are not drawn to scale.

Plasmid pEL7 can be conventionally isolated from Streptomyces ambofacienslpE17, a constructed strain deposited and made part of the stock culture collection of the Northern Regional Research Laboratory, Peoria, Illinois. It is available to the public, as a source and stock reservoir of the plasmid under the accession number NRRL 12523.

Although many different restriction fragments of plasmid pEL7 can be constructed, those exemplified herein for illustrative purposes, include the 10.9kb BamHI and the 10.9kb Pstl restriction fragments. These fragments are ligated to one or more antibiotic resistance conferring DNA fragments, exemplified herein for illustrative purposes by the thiostrepton resistance conferring 1 .6kb BamHI restriction fragment of plasmid pLR2 and the neomycin resistance conferring 3.5kb Pstl restriction fragment of plasmid pLR1 , to form vectors illustrative of the present invention.

Plasmid pLR2, the source of the thiostrepton resistance conferring fragment, is approximately 18.7kb and is constructed by ligating Hindlll treated plasmid plJ6, disclosed in Thompson etal., 1980, Nature 286:525, to Hindlll treated plasmid pBR322. Plasmid pLR1,the source of the neomycin resistance conferring fragment, is approximately 14.8kb and is similarly constructed, except that plasmid plJ2, disclosed in Thompson etna, 1980, is used instead of plasmid plJ6. Both plasmids pLR2 and pLR1 are functional in E. coil and therefore can be amplified and isolated conveniently for subsequent manipulation. An analogous construction, resulting in plasmid pLR4, is made by ligating BamHI treated plasmid pBR322 to BamHI treated plasmid pLR1.A restriction site and functional map of each of plasmids pLR1, pLR2, and pLR4 is presented respectively in Figures 2-4 of the accompanying drawings.

For convenience and ease of construction, the thiostrepton resistance conferring 1 .6kb BamHI fragment and the neomycin resistance conferring 3.5kb Pstl fragment are inserted into plasmid pEL7 respectively at the adjacent BamHI and Pstl restriction sites. The resulting recombinant DNA is then self ligated to produce plasmids illustrative of the present invention. Recombinant plasmids of two orientations result depending upon the orientation of the inserted DNA fragment. Thus, the insertion of the 1 .6kb Bath1 fragment into plasmid pEL7 results in illustrative plasmids pEL7.1 and pEL7.2; insertion of the 3.5kb Pstl fragment results in illustrative plasmids pEL7.3 and pEL7.4; and insertion of both of the fragments results in illustrative plasmids pEL7.5, pEL7.6, pEL7.7, and pEL7.8.

Various plasmid pEL7 restriction sites can be used for the insertion of DNA segments. Therefore, a particular antibiotic resistance conferring DNA segment is not limited to a single position but can be inserted at varying sites provided that the resultant plasmid is functionally dependent on plasmid pEL7.

Although the thiostrepton and neomycin antibiotic resistance conferring DNA segments exemplified herein are respectively the 1 .sky BamHI and 3.5kb Pstl restriction fragments of plasmids pLR2 and pLR1, those skilled in the art can construct and use, either individually or in combination, additional DNA segments that also confer resistance to thiostrepton and neomcyin. Additional thiostrepton resistance conferring DNA segments of plasmid pLR2 include, for example, the 1 3kb Pstl restriction fragment and also the Bcll subfragment of the 1 .6kb BamHI restriction fragment. Additional neomycin resistance conferring DNA segments of plasmid pLR1 include, for example, the 3.4kb BamHI restriction fragment and also the larger of the Sacl-Kpnl subfragments of the 3.4kb BamHI restriction fragment.Still other DNA segments conferring resistance to the same or to different antibiotics such as, for example, chloramphenicol, hygromycin, viamycin, tylosin, erythromycin, and the like can also be constructed and used. In addition, various functional derivatives of the above described antibiotic resistance conferring DNA segments can be constructed by adding, eliminating, or substituting certain nucleotides. Ligation of these derivatives or other antibiotic resistance conferring DNA segments to plasmid pEL7, in place of the resistance conferring DNA segments exemplified herein, results in plasmids that are within the scope of the present invention.

Both the restriction fragments of plasmid pEL7 and the various antibiotic resistance conferring DNA segments can be modified to facilitate ligation. For example, molecular linkers can be provided to either or both of a particular plasmid pEL7 restriction fragment and to particular resistance conferring DNA segments.

Thus, specific sites for subsequent ligation can be constructed conveniently. In addition, plasmid pEL7 and the restriction fragments thereof can also be modified by adding, eliminating, or substituting certain nucleotides to alter characteristics and to provide a variety of restriction sites for ligation of DNA. Those skilled in the art understand nucleotide chemistry and the genetic code and thus which nucleotides are interchangeable and which DNA modifictions are desirable for a specific purpose.

The present vectors such as, for example, plasmid pEL7 and illustrative plasmids pEL7.1, pEL7.2, pEL7.3, pEL7.4, pEL7.5, pEL7.6, pEL7.7, and pEL7.8 can be ligated to a functional replicon containing and antibiotic resistance conferring restriction fragment of an E. coli plasmid such as, for example, plasmid pBR322, pBR324, pBR325, and the like, to produce bifunctional plasmids for use in E. coli and plasmid pEL7 containing Streptomyces cells. These constructions, exemplified herein by plasmids pLR5 and pLR6, are particularly advantageous because amplification and manipulation of plasmids can be done faster and more conveniently in E. coil than in Streptomyces.Thus, after desired recombinant DNA procedures are accomplished within the E. coli host system, the particular Streptomyces DNA can be removed, re-constructed to plasmid form, and then transformed into a suitable Streptomyces or related host cell.

The recombinant DNA cloning vectors of the present invention are not limited for use in a single species or strain of Streptomyces. To the contrary, the vectors are broadly applicable and can be transformed into host cells of many Streptomyces taxa, particularly restriction less strains of economically important taxa that produce antibiotics such as aminoglycoside, macrolide,3-lactam, polyether, and glycopeptide antibiotics.

Such restrictionless strains are readily selected and isolated from Streptomyces taxa by conventional procedures well known in the art (Lomovskaya et al., 1980, Microbiological Reviews 44:206). Host cells of restrictionless strains lack restriction enzymes and therefore do not cut or degrade plasmid DNA upon transformation. For purposes of the present application, host cells containing restriction enzymes that do not cut any of the restriction sites of the present vectors are also considered restrictionless.

Preferred host cells of restrictionless strains of Streptomyces taxa that produce aminoglycoside antibiotics and in which the present vectors are especially useful and can be transformed, include restriction less cells of, for example: S. kanarnyceticus (kanamycins), S. chrestomyceticus (aminosidine), S. griseoflavus (antibiotic MA 1267), S. microsporeus (antibiotic SF-767), S, ribosidificus (antibiotic SF733), S. flavopersicus (spectinomycin), S. spectabilis (actinospectacin), S. rimosus forma paromomycinus (paromomycins, catenulin), S. fradiae var. italicus (aminosidine), S. bluensis var. bluensis (bluensomycin), S. catenulae (catenulin), S. olivoreticullvar. cellulophilus (destomycin A), S. tenebrarius (tobramycin, apramycin), S.

Iavendulae (neomycin), S. alborgriseolus (neomycins), S. albus var. metamycinus (metamycin), S.

hygroscopicus var. sagamiensis (spectinomycin), S. bikiniensis (streptomycin), S. griseus (streptomycin), S.

erythrochromogenes var. narutoensis (streptomycin), S. poolensis (streptomycin), S. galbus (streptomycin), S. rameus (streptomcyin), S. olivaceus (streptomycin), S. mashuensis (streptomycin), S. hydrogroscopicus var. limoneus (validamycins), S. rimofaciens (destomycins), S. hygroscopicus forma glebosus (glebomycin), S. fradiae (hybrimycins neomycins), S. eurocidicus (antibioticA16316-C), S. aquacanus (n-methyl hygromycin B), S. crystallinus (hygromycin A), S. noboritoenis (hygromycin), S. hydroscopicus (hygromycins), S. atrofaciens (hygromycin), S. kasugaspinus (kasugamycins), S. kasugaensis (kasugamycins), S.

netropsis (antibiotic LL-AM31), S. lividus (lividomycins), S. hofuensis (seldomycin complex), and S. can us (ribosyl paromamine).

Preferred host cells of restrictionless strains of Streptomyces taxa that produce macrolide antibiotics and in which the present vectors are especially useful and can be transformed, include restrictionless cells of, for example: S. caelestis (antibiotic M188), S. platensis (platenomycin), S. rocheivar. volubi/is (antibiotic T2636), S. venezuelae (methymycins), S. griseofuscus (bundlin), S. narbonensis (josamycin, narbomycin), S.

fungicidicus (antibiotic NA-181), S. griseofaciens (antibiotic PA133A, B), S. roseocitreus (albocycline), S.

bruneogriseus (albocycline), S. roseochromogenes (albocycline), S. cinerochromogenes (cineromycin B), S.

albus (albomycetin), S. felleus (argomycin, picromycin), S. rochei(lankacidin, borrelidin), S. violaceoniger (lankacidin), S. griseus (borrelidin), S. maizeus (ingramycin), S. albus var. coilmyceticus (coleimycin), S, mycarofaciens (acetylleukomycin, espinomycin), S. hygroscopicus (turimycin, relomycin, maridomycin, tylosin, carbomycin), S. griseospiralis (relomycin), S. Iavendulae (aldgamycin), S. rimosus (neutramycin), S.

deltae (deltamycins), S. fungicidicus var. espinomyceticus (espinomycins), S. furdicidicus (mydecamycin), S.

ambofaciens (foromacidin D), S. eurocidicus (methymycin), S. griseolus (griseomycin), S. flavochromogenes (amaromycin, shincomycins), S. fimbriatus (amaromycin), S. fasciculus (amaromycin), S.

erythreus (erythromycins), S. antibioticus (oleandomycin), S. olivochromogenes (oleandomycin), S.

spinichromogenes var. surgaoenis (kujimycins), S. kitasatoensis (leucomycin), S. narbonensis var.

josamyceticus (leucomycin A3, josamycin), S. albogriseolus (mikonomyin), S. bikiniensis (chalcomycin), S.

cirratus (cirramycin), S. djakartensis (niddamcyin), S. eurythermus (angolamycin), S. fradiae (tylosin, lactenocin, macrocin), S. goshikiensis (bandamycin), S griseoflavus (acumycin), S. ha/stedii(carbomycin), S.

tendae (carbomcyin), S. macrosporeus (carbomycin), S. thermotolerans (carbomycin), and S. albireticuli carbomycin).

Preferred host cells of restriction less strains of Streptomyces taxa that produce ss-klactam antibiotics and in which the present vectors are especially useful and can be transformed, include restrictionless cells of, for example: S. lipmanii (A16884, MM4550, MM13902), S. clavuligerus (A16886B, calvulanic acid), S.

lactamdurans (cephamycin C), S. griseus (cephamycin A, B), S. hygroscopicus (deacetoxycephalosporin C), S. wadayamensis (WS-3442-D), S. chartreusis (SF 1623), S. heteromorphus and S. panayensis (C2081 X); S.

cinnamonensis, S. fimbriatus, S. halstedii, S. rocheiand S. viridochromogenes (cephamycins A, B); S.

cattleya (thienamycin); and S. olivaceus, S. flavovirens, S. flavus, S. fulvoviridis, S. argenteolus, and S.

sioyaenis (MM 4550 and MM 13902).

Preferred host cells of restrictionless strains of Streptomyces taxa that produce polyether antibiotics and in which the present vectors are especially useful and can be transformed, include restrictionless cells of, for example: S. albus (A204, A28695A and B, salinomycin), S. hygroscopicus (A218, emericid, DE3936), A120A, A28695A and B, etheromycin, dianemycin), S. griseus (grisorixin), S. conglobatus (ionomycin), S.

eurocidicus var. asterocidicus (laidlomycin), S. lasaliensis (lasalocid), S ribosidificus (lonomycin), S. cacaoi var. asoensis (lysocellin), S. cinnamonensis (monensin), S. aureofaciens (narasin), S. ga/linarius (RP 30504), S. Iongwoodensis (lysocellin), S. flaveolus (CP38936), S. mutabilis (S-11743a), and S. violaceoniger (nigericin).

Preferred host cells of restriction less strains of Streptomyces taxa that produce glycopeptide antibiotics and in which the present vectors are especially useful and can be transformed, include restriction less cells of, for example: S. orientalis and S. haranomachiensis (vancomycin); S. candidus (A-35512, avoparcin), and S. eburosporeus (LL-AM 374).

Preferred host cells of other Streptomyces restriction less strains in which the present vectors are especially useful and can be transformed include restriction less cells of, for example: S. coelicolor, S.

granuloruber, S. roseosporus, S. lividans, S. espinosus, and S. azureus.

In addition to the representative Streptomyces host cells described above, the present vectors are also useful and can be transformed into cells of restriction stains of other taxa such as, for example: Bacillus, Staphylococcus, and related Actinomycetes including Streptosporangium, Actinoplanes, Nocardia, and Micromonospora. Thus, the vectors of the present invention have wide application and are useful and can be transformed into host cells of a variety of organisms.

While all the embodiments of the present invention are useful, some of the present recombinant DNA cloning vectors and transformants are more preferred than others. Accordingly, preferred vectors are plasmids pEL7, pEL7.1, pEL7.3, pEL7.5, pLR1, and pLR2; preferred pairs of vectors are plasmids pEL7 and pEL7.1, pEL7 and pEL7.3, and pEL7 and pEL7.5; and preferred transformants are Streptomyces ambofaciensipEL7, S. ambofaciensipEL7, pEL7.1, S. ambofaciensipEL7, pEL7.3, S. ambofaciensipEL7, pEL7.5, E. coli K12 HB1 01/pLR1, and E. coli K12 HBl0l/pLR2. Moreover, of this preferred group, plasmid pEL7, plasmid pairs pEL7 and pEL7.1, and pEL7 and pEL7.5, and transformants S. ambofacienslpEL7, S.

ambofacienslpEL7, pEL7.1, and S. ambofaciensipEL7, pEL7.5 are most preferred.

The recombinant DNA cloning vectors and transformants ofthe present invention have broad utility and help fill the need for suitable cloning vehicles for use in Streptomyces and related organisms. Moreover, the ability of the present vectors to confer resistance to antibiotics that are toxic to non-transformed host cells, also provides a functional means for selecting transformants. This is important because of the practical necessity for determining and selecting the particular cells that have acquired vector DNA. Additional DNA segments, that lack functional tests for their presence, can also be inserted onto the present vectors and then transformants containing the non-selectable DNA can be isolated by appropriate antibiotic selection.Such non-selectable DNA segments include, but are not limited to, genes that specify antibiotic modification enzymes and regulatory genes of all types.

More particularly, a non-selectable DNA segment that comprises a gene is inserted on a plasmid such as for example, illustrative plasmid pEL7.5, at the Pvull restriction site of the 1 .6kb BamHI resistance conferring fragment. Such an insertion inactivates the thiostrepton resistance gene and thus allows for the easy identification of transformants containing the recombinant plasmid. This is done by first selecting for neomycin resistance and, secondarily, identifying those neomcyin resistant transformants that are not resistant to thiostrepton. In a similar manner, insertion of a DNA segment of interest at, for example, the Kpnl restriction site of the 3.5kb Pstl resistance conferring fragment inactivates the neomycin resistance gene.

Thus, transformants carrying this recombinant plasmid also are identified easily by first selecting for thiostrepton resistance and, secondarily, identifying those thiostrepton resistant transformants that are not resistant to neomycin. Therefore, the ability to select for antibiotic resistance in Streptomyces and related cells allows for the efficient isolation of the extremely rare cells that contain the particular non-selectable DNA of interest.

The functional test for antibiotic resistance, as described herein above, is also used to search vast quantities of D NA for those segments that can act as control elements and direct expression of an individual antibiotic resistance gene. Such segments, including but not limited to, promoters, attenuators, repressors, inducers, ribosomal binding sites, and the like, are used to control the expression of other genes in cells of Streptomyces and related organisms.

The thiostrepton and neomcyin resistance conferring vectors of the present invention are also useful for insuring that linked DNA segments are stably maintained in host cells over many generations. These genes or DNA fragments, covalently linked to the thiostrepton or neomcyin resistance conferring fragment and propagated either in Streptomyces or in the cells of related organisms, are maintained by exposing the transformants to levels of thiostrepton or neomycin that are toxic to non-transformed cells. Therefore, transformants that lose the vector, and consequently any covalently linked DNA, cannot grow and are eliminated from the culture. Thus, the vectors of the present invention can stabilize and maintain any DNA sequence of interest.

The cloning vectors and transformants of the present invention provide for the cloning of genes to improve yields of various products that are currently produced in Streptomyces and related cells. Examples of such products include, but are not limited to, Streptomycin, Tylosin, Cephalosporins, Actaplanin, Narasin, Monensin, Apramcyin, Tobramycin, Erythromycin, and the like. The present invention also provides selectable vectors that are useful for cloning, characterizing, and reconstructing DNA sequences that code for commercially important proteins such as, for example, human insulin, human proinsulin, glucagon, interferon, and the like; for enzymatic functions in metabolic pathways leading to commercially important processes and compounds; or for control elements that improve gene expression. These desired DNA sequences include, but are not limited to, DNA that codes for enzymes that catalyze synthesis of derivatized antibiotics such as, for example, Streptomycin, Cephalosporin, Tylosin, Actaplanin, Narasin, Monensin, Apramycin, and Erythromycin derivatives, or for enzymes that mediate and increase bioproduction of antibiotics or other products. The capability for inserting and stabilizing such DNA segments thus allows for increasing the yield and availability of antibiotics that are produced by Streptomyces and related organims.

Streptomyces ambofaciensipEL7, as a source of plasmid pEL7, can be cultured in a number of ways using any of several different media. Carbohydrate sources which are preferred in a culture medium include, for example, molasses, glucose, dextrin, and glycerol, and nitrogen sources include, for example, soy flour, amino acid mixtures, and peptones. Nutrient inorganic salts are also incorporated and include the customary salts capable of yielding sodium, potassium, ammonia, calcium, phosphate, chloride, sulfate, and like ions.

As is necessary for the growth and development of other microorganisms, essential trace elements are also added. Such trace elements are commonly supplied as impurities incidental to the addition of other constituents of the medium.

Streptomyces ambofaciensipEL7 is grown under aerobic culture conditions over a relatively wide pH range of about 5 to 9 at temperature ranging from about 15 to 40"C. For production of plasmid pEL7 at the highest copy number, however, it is desirable to start with a culture medium at a pH of about 6.5 and maintain a culture temperature of about 30"C. Culturing Streptomyces ambofacienslpEL7, under the aformentioned conditions, results in a reservoir of cells from which plasmid pEL7 is isolated conveniently.

The following examples further illustrate and detail the invention disclosed herein. Both an explanation of and the actual procedures for constructing the invention are described where appropriate.

EXAMPLE 1 Isolation of plasmid plasmid pEL7 A. Cu/ture of Streptomyces ambofaciensipEL7 A vegetative inoculum of Streptomyces ambofaciensipEL7 (NRRL 12523) was conveniently prepared by growing the strain under submerged aerobic conditions in 50 ml. of sterilized vegetative medium with the following preferred composition.

Ingredient Amount Glucose 20 g./l.

Nutrisoyflour* 15 g./l.

Corn steep liquor* 10 g./l.

CACAO3 2 g./l.

Water (tap) 1.11.

*Nutrisoyflour is obtained from Archer Daniels Midland Company, 4666 Faries Parkway, Decatur, Illinois 62526.

*Corn steep liquor is obtained from CPC International, Corn Products, P.O. Box 3000, Englewood, N.J.

07632.

The vegetative inoculum was incubated for 48 hours at a temperature of 30"C. and a pH of 6.5. After incubation, about 1.0 ml. of the inoculum was tranferred to 50 ml. of sterilized cell production medium with the following preferred composition.

Ingredient Amount Trypticase soy broth* 30 g./l.

Glucose 5 g./l.

Glycine 5 g./l.

Deionized water 1 g./l.

*Trypticase soy broth is obtained from Difco Laboratories, Detroit, Michigan.

The inoculated cell production medium was incubated for about 20 hours at 30"C. The pH was not adjusted. After incubation, the Streptomyces ambofaciensipEL7 cells were ready for harvest and subsequent isolation of plasmid DNA.

B. Plasmid isolation About 10 g. (wet wgt) of Streptomyces ambofaciensipEL7 cells were harvested by centrifugation (10 minutes, 5"C, 10,000 rpm). The cells were homogenized using a tissue grinder, washed in TES buffer (0.05M tris(hydroxymethyl)aminomethane [tris], 0.005M EDTA, and 0.05M NaCI, pH 8.0), and then suspended in TES buffer containing 25% sucrose. After the addition of about 120 mg. of lysozyme in 20 ml. of TES-25% sucrose buffer, the suspension was incubated at 35-37"C. for about 20 minutes and, upon addition of 40 ml. of 0.25M EDTA, pH 8.0, the suspension was again incubated at 35 C. for 10 minutes.Following this, about 40 ml. of 5% SDS (sodium dodecyl sulfate) in TE buffer (0.01 M tris, 0.001 M EDTA, pH 8.0) was added and then, after the resultant mixture was again incubated at 35-37 C. for 20 minutes, about 50 ml. of 5M NaCI in deionized water was added. The mixture was stirred, placed on an ice bath for about 4 hours, and then centrifuged (30 minutes, 4 C., 10,000 rpm). About 0.313 volumes of 42% polyethylene glycol in deionized water were added to the NaCI supernatant and the resulting mixture was cooled at 4 C. for about 18 hours. The DNA precipitate was collected by centrifugation (5 minutes, 40C., 3000 rpm) and was then dissolved in TES buffer at pH 8.0.

Centrifugation (40 hours, 15"C, 35,000 rpm) using cesium chloride and ethidium chloride gradients separated the DNA into two well defined bands with the lower band constituting the desired plasmid pEL7. Following conventional procedures, the plasmid band was removed, washed twice with isoamyl alcohol, dialyzed over TE buffer at pH 8.0, and precipitated with ethanol. The thus isolated plasmid pEL7 DNA was dissolved in 0.4 ml. of TE buffer at pH 8.0, and was then frozen at -20 C. for storage.

EXAMPLE 2 Construction of plasmid pLR2 A. Hindlll Digestion of plasmid pIJ6 About 20 . (20 Ft9.) of plasmid plJ6 DNA, disclosed in Thompson et al/., 1980, Nature 286:525,5 yl. BSA (Bovine serum albumin, 1 mg./ml.), 19 Fti. water, 1 stl. of Hindlll (containing 3 new England Bio Lab Units) restriction enzyme*, and 5 Ftl. reaction mix** were incubated at 370C. for 2 hours. The reaction was terminated by the addition of about 50 Coil. of 4M ammonium acetate and 200 yl, of 95% ethanol.The DNA precipitate was washed twice in 70% ethanol, dried in vacuo, suspended in 20 . of TE buffer, and frozen at -20 C. for storage.

*Restriction enzymes can be obtained from the folowing sources: New England Bio Labs., Inc.

32 Tozer Rd.

Beverley, Massachusetts 01915 Boehringer-Mannheim Biochemicals 7941 Castleway Dr.

Indianapolis, Indiana 46250 **Reaction mix for Hindl l l restriction enzyme was prepared with the following composition.

600 mM NaCI 100 mM Tris-HCI, pH 7.9 70 mM MgC12 10 mM Dithiothreitol B. Hindlil Digestion of plasmid pBR322 About 8 l. (4 g.) of plasmid pBR322 DNA, 5 l. reaction mix, 5 yl. BSA (1 mgdml.), 31 Fti. water, and 1 stl. of Hindlll restriction enzyme were incubated at 37"C. for 2 hours. After the reaction was terminated by incubating at 600C. for 10 minutes, about 50 l. of ammonium acetate and 200 Ftl. of 95% ethanol were added.

The resultant DNA precipitate was washed twice in 70% ethanol, dried in vacuo, and suspended in 45 ul. of water.

C. Ligation of Hindlil digested plasmids plJ6 and pBR322 About 20 . of Hind III treated plasmid plJ6 (from Example 2A), 20 RI. of HindIII treated plasmid pBR322 (from Example 2B), 5 RI. BSA (1 mg./ml.), 1 l. of T4 DNA ligase*, and 5 . ligation mix*** were incubated at 16 C. for 4 hours. The reaction was terminated by the addition of about 50 pl. 4M ammonium acetate and 200 l. of 95% ethanol. The resultant DNA precipitate was washed twice in 70% ethanol, dried in vacuo, and suspended in TE buffer. The suspended DNA constituted the desired plasmid pLR2.

*T4 DNA ligase can be obtained from the following source: New England Bio Labs., Inc.

32 Tozer Rd.

Beverley, Massachusetts, 01915 **Ligation mix was prepared with the following composition: 500 mM Tris - HCl, pH 7.8 200 mM Dithiothreitol 100 mM MgCl2 10 mM ATP EXAMPLE 3 Construction of E. coli K 12 HB 10 1/pLR2 About 10 ml. of frozen competent E. co/i K1 2 HB101 cells (Bolivar etal., 1977, Gene 2:75-93) were pelleted by centrifugation and then suspended in about 10 ml. of 0.01 M sodium chloride. Next, the cells were pelleted again, resuspended in about 10 ml. of 0.03M calcium chloride solution, incubated on ice for 20 minutes, pelleted a third time, and finally, resuspended in 1.25 ml. of 0.03M calcium chloride solution. The resultant cell suspension was competent for subsequent transformation.

Plasmid pLR2 in TE buffer (prepared in Example 2C) was ethanol precipitated, suspended in 150 FI. of 30mM calcium chloride solution, and gently mixed in a test tube with about 200 yl. of competent E. coli K12 HB101 cells. The resultant mixture was incubated on ice for about 45 minutes and then at 420C. for about 1 minutes. Next, about 3 ml. of L-broth (Bertani. 1951, J. Bacteriology 62:293) containing 50 Fg./ml. of ampicillin was added. The mixture was incubated with shaking at 37 C. for 1 hour and then plated on L-agar (Miller, 1972, Experiment in Molecular Genetics, Cold Spring Harbor Labs, Cold Spring Harbor, New York) containing ampicillin.Surviving colonies were selected and tested for the expected phenotype (ampR, Tets,) and constituted the desired E. coli K12 HBl0l/pLR2 transformants.

EXAMPLE 4 Construction of plasmid pLR1 Plasmid pLR1 was prepared in substantial accordance with the teaching of Example 2A-C except that plasmid plJ2, disclosed in Thompson eta/., 1980, Nature 286:525, was used in place of plasmid plJ6. The desired plasmid pLR1 was suspended in TE buffer.

EXAMPLE 5 Construction of E. coliK12 HB1011pLR1 The desired construction was carried out in substantial accordance with the teaching of Example 3 except that plasmid pLR1, rather than plasmid pLR2, was used for transformation. Surviving colonies were selected and tested for the expected phenotype (ampR, Tets,) and constituted the desired E. coli K12 HB1 01/pLR1 transformants.

EXAMPLE 6 Construction of plasmid pLR4 A. Partial Bam Hl digestion of plasmid pLR7 About 10 yl. (10 g.) of plasmid pLR1, 5 l. BSA (1 mg.lml.),291l1. of water, 1 IlI. of BamHI (diluted 1:4 with water) restriction enzyme, and 5 l. reaction mix* were incubated at 37 C. for 15 minutes. The reaction was terminated by the addition of about 50 ssI. of 4M ammonia acetate and 200 ill. of 95% ethanol. The resultant DNA precipitate was washed twice in 70% ethanol, dried in vacuo, and suspended in 20 ZI. of water.

*Reaction mix for BamHI restriction enzyme was prepared with the following composition.

1.5M NaCI 60mM Tris-HCI, pH 7.9 60mM MgC12 B. BamHI Digestion of plasmid pBR322 The desired digestion was carried out in substantial accordance with the teaching of Example 2B except that BamHI restriction enzyme was used in place of Hindlll restriction enzyme. The digested plasmid pBR322 was suspended in 29 FI. of water.

C. Ligation ofpartial BamHI digested plasmid pLR1 1 and BamHl digestedplasmidpBR322 The desired ligation was carried out in substantial accordance with the teaching of Example 2C. The resultant ligated DNA was suspended in TE buffer and constituted the desired plasmid pLR4.

EXAMPLE 7 Construction of E. coli K12 HB 1011pLR4 The desired construction was carried out in substantial accordance with the teaching of Example 3 except that plasmid pLR4, rather than plasm id pLR2, was used for transformation. Surviving colonies were selected and tested for the expected phenotype (AmpR, Tets,) and constituted the desired E. coli K12 HB1 011pLR4 transformants.

EXAMPLE 8 Construction ofplasmids pEL 7.1 andpEL 7.2 A. BamHI digestion of plasmid pLR2 and isolation of the 1,6kb thiostrepton resistance conferring fragment About 50 g. of plasmid pLR2 DNA, 20 1. reaction mix,10 l. 0.1M dithiothreitol, 20 I. BSA (1 mg./ml.),100 l. water, and 5 RI. (4 unitslyl.) of BamHI restriction enzyme were incubated at 37 C. for 2 hours. After adding an equal volume of 4M ammonium acetate and 2 volumes of 95% ethanol, the mixture was cooled at -20 C.

for about 18 hours to precipitate the DNA. The DNA precipitate was collected by centrifugation and then suspended in about 501l1. of TE buffer. The desired 1.6kb BamHI restriction fragment was isolated conventionally from the DNA suspension by gel electrophoresis. Following isolation, the fragment was resuspended in about 20 FI. of TE buffer for subsequent ligation.

B. BamHl digestion of plasmid pEL7 The desired digestion was carried out in substantial accordance with the teaching of Example 8A except that plasmid pEL7, rather than plasmid pLR2, was used. In addition, the DNA digest was notelectrophoresed but was suspended directly in 20 Coil. of TE buffer for subsequent ligation.

C. Ligation A mixture of about 20 yg. of BamHi restricted plasmid pEL7 DNA, 10 g. of the 1.6kb BamHI restriction fragment of plasmid pLR2, 5 . BSA (1 mg./ml.), 10 yl. ligation mix, 45 stl. water, and 3.5 yl. T4 DNA ligase were incubated at about 16 C. for about 18 hours. After adding 0.1 volume of 3M ammonium acetate and 2 volumes of cold ethanol, the mixture was cooled to -200C. for about 18 hours to precipitate the DNA.The DNA precipitate was collected by centrifugation, washed with 70% ethanol, collected again, and then suspended in 50 yl. of medium P (Hopwood and Wright, 1978, J. Molecular and General Genetics 162:307) for subsequent transformation.

Recombinant plasmids of two orientations result depending upon the orientation of the inserted 1.6kb BamHI thiostrepton resistance conferring fragment. In addition plasmid pEL7 is also restored by self ligation.

Plasmid pEL7.1 designates the resultant recombinant plasmid in which the Pvull restriction site of the resistance conferring fragment is inserted closest to the flanking Sphl site of plasmid pEL7. Plasmid pEL7.2 designates the recombinant plasmid with the reverse orientation. Thus, the final DNA suspension contains plasmids which include plasmids pEL7, pEL7.1, and pEL7.2. In addition, the insertional isomers of plasmids pEL7.1 and pEL7.2 are also produced since plasmid pEL7 has two BamHI restriction sites for the insertion of the thiostrepton resistance fragment. A restriction site and functional map of each of plasmids pEL7. 1 and pEL7.2 is respectively presented in Figures 5 and 6 of the accompanying drawings.

EXAMPLE 9 Construction of Streptomyces ambofaciens pEL 7, pEL 7.1 and Streptomyces ambofacienslpEL7, pEL 7.2 Using about 20 g. DNA from Example 8C and 1 x 108 protoplasts of Streptomyces ambofaciens, a strain deposited and made part of the stock culture collection of the Northern Regional Research Laboratory, Peoria, Illinois, from which it is available to the public under the accession number NRRL 2420, the desired constructions were carried out in substantial accordance with the teaching of Internationl Publication (of International Patent Application No. PCTIGB 79/00095) No. WO79/01169, Example 2. The desired transformants were selected for thiostrepton resistance by plating on Bennett's Modified Medium* containing about 50 ijgdml. of antibiotic thiostrepton.The resultant Streptomyces ambofaciensipEL7, pEL7.1 and S. ambofaciensi pEL7, pEL7.2 thiostrepton resistant colonies were isolated, cultured, and then conventionally identified by restriction enzyme and gel electrophoretic analysis ofthe constitutive plasmids.

*Bennett's medium (Agar), disclosed in Waksman, 1961, The Actinomycetes, Volume II, The Williams and Wilkins Company, Baltimore, Maryland, was modified by adding CoCI2-H20 (0.01 g./L.) and by replacing glucose with dextrin.

EXAMPLE 10 Construction ofplasmids pEL7.3 and pEL7.4 A. Pstl digestion of plasmid pLR 1 and isolation of the 3.5kb Neomycin resistance conferring fragment About 50 g. of plasmid pLR1 DNA, 20 l. reaction mix*, 10 ijI. 0.1 M dithiothreitol, 20 Fti. BSA (1 mg./ml.), 100 Fti. water, and 5 l. (4 units/tl.) of Pstl restriction enzyme* were incubated at 37"C. for 2 hours. After adding an equal volume of 4M ammonium acetate and 2 volumes of 95% ethanol, the mixture was cooled at -20 C. for about 18 hours to precipitate the DNA.The DNA precipitate was collected by centrifugation and then suspended in about 50 Ftl. of TE buffer. The desired 3.5kb Pstl restriction fragment was isolated conventionally from the DNA suspension by gel electrophoresis. Following isolation, the fragment was resuspended in about 20 Fti. of TE buffer for subsequent ligation.

*Reaction mix for Pstl restriction enzyme was prepared with the following composition.

50 mM NaCL 6 MM Tris-HCI, pH7.4 6 mM MgC12 6 mM 2-mercaptoethanol 100 ygJml. BSA **Restriction enzymes can be obtained from the sources listed in Example 2.

B. Pstl digestion of plasmid pEL7 The desired digestion was carried out in substantial accordance with the teaching of Example 1 OA except that plasmid pEL7, rather than plasmid pLR1,was used. In addition, the DNA digest was not electrophoresed but was suspended direction in 20 Ftl. of TE buffer for subsequent ligation.

C. Ligation The desired ligation is carried out by reacting about 20 g. of Pstl restricted plasmid pEL7 DNA and about 19 g. of the 3.5 kb Pstl restriction fragment of plasmid pLR1 in substantial accordance with the teaching of Example 8C.

Recombinant plasmids of two orientations result depending upon the orientation of the inserted 3.5kb Pstl neomycin resistance conferring fragment. In addition, plasmid pEL7 is also restored by self ligation. Plasmid pEL7.3 designates the recombinant plasmid in which the Sacl restriction site of the resistance conferring fragment is inserted closest to the flanking Kpnl site of plasmid pEL7. Plasmid pEL7.4 designates the recombinant plasmid with the reverse orientation. Thus, the final DNA suspension contains plasmids which include plasmids pEL7, pEL7.3, and pEL7.4. In addition, the insertional isomers of plasmids pEL7.3 and pEL7.4 are also produced since plasmid pEL7 has two Pstl restriction sites for the insertion of the neomycin resistance fragment.A restriction site and functional map of each of plasmids pEL7.3 and pEL7.4 is respectively presented in Figures 7 and 8 of the accompanying drawings.

EXAMPLE 11 Construction of Streptomyces ambofacienslpEL 7, pEL7.3 and Streptomyces ambofaciensipEL7, pEL7.4 Using about 20 yg. DNA from Example 10C and 1 x 108 protoplasts of Streptomyces ambofaciens, (NRRL No. 2420), the desired constructions are carried out in substantial accordance with the teaching of International Publication (of International Patent Application No. PCT/GB 79/00095) No. W079/01 169, Example 2. The desired transformants are selected for neomycin resistance by plating on Bennett's Modified Medium containing about 1 gdml. of antibiotic neomycin*.The resultant Streptomyces ambofaciensipEL7, pEL7.3 and S. ambofaciens pEL7, pEL7.4 neomycin resistant colonies are isolated, cultured, and then conveniently identified by restriction enzyme and gel electrophoretic analysis of the constitutive plasmids.

*Antibiotic neomycin can be obtained from Sigma, St. Louis, Missouri.

EXAMPLE 12 Construction ofplasmidspEL7.5andpEL7.6 A. Isolation ofplasmidspEL7andpEL7.1 The desired plasmids are isolated from Streptomyces ambofaciensipEL7, pEL7.1 (prepared in Example 9 and cultured according to the teaching of Example 1A) in substantial accordance with the isolation procedure of Example 1 B. The thus isolated plasmid pEL7 and pEL7.1 DNA is suspended in TE buffer at pH 8.0 for subsequent restriction enzyme digestion.

B. Pstldigestion ofplasmidspEL7andpEL7.1 The desired digestion is carried out in substantial accordance with the teaching of Example 1 OA, except that a mixture of plasmid pEL7 and pEL7.1 DNA is used instead of plasmid pLR1 DNA. The thus digested DNA is suspended in 20 Coil. of TE buffer for subsequent ligation with the 3.5kb Pstl restriction fragment of plasmid pLR1.

C. Ligation The desired ligation is carried out by reacting about 20 yg. of the Pstl restricted mixture of plasmid pEL7 and pEL7.1 DNA and about 10 Fg. of the 3.5kb Pstl restriction fragment (prepared in Example 10A) in substantial accordance with the teaching of Example 1 0C.

A mixture of recombinant plasmids is produced since the 3.5kb Pstl fragments are ligated with either or both of plasmids pEL7 and pEL7.1. The recombinant plasmids, as previously described, are also of two orientations depending upon the orientation of the 3.5kb Pstl neomycin resistance conferring fragment.

Thus, ligation with plasmid pEL7 results in plasmids pEL7.3 and pEL7.4 and ligation with plasmid pEL7.1 results in the desired plasmids pEL7.5 and pEL7.6. In addition, plasmids pEL7 and pEL7.1 are also restored by self ligation.

Plasmid pEL7.5 designates the recombinant plasmid in which the Sacl restriction sites of the 3.5kb Pstl neomycin resistance conferring fragment is inserted closest to the Pvull restriction site of the 1.6kb BamHI thiostrepton resistance conferring fragment. Plasmid pEL7.6 designates the recombinant plasmid in which the 3.5kb Pstl neomycin resistance conferring fragment has the reverse orientation. Thus, the final DNA suspension contains plasmids which include plasmids pEL7, pEL7.1, pEL7.3, pEL7.4, pEL7.5, pEL7.6, and, for the reasons described in Examples 8 and 10, the insertional isomers of plasmids pEL7.3, pEL7.4, pEL7.5, and pEL7.6. A restriction site and functional map of each of the desired plasmids pEL7.5 and pEL7.6 is respectively presented in Figures 9 and 10 of the accompanying drawings.

EXAMPLE 13 Construction of Streptomyces ambofaciensipEL7, pEL7,5and S. ambofaciensipEL7, pEL7.6 Using 20 yg. of DNA from examples 1 2C and 1 x 108 protoplasts of Streptomyces ambofaciens, (NRRL No.

2420), the desired constructions are carried out in substantial accordance with the teaching of International Publication (of International Patent Application No. PCT/GB 79/00095) No. WO79/01 169, Example 2. The desired transformants are selected for thiostrepton and neomycin resistance by plating on Bennett's Modified Medium containing about 50 Fg./ml. of antibiotic thiostrepton and 1 Fg./ml. of antibiotic neomcyin.

The resultant Streptomyces ambofaciensipEL7, pEL7.5 and S. ambofaciensi pEL7, pEL7.6 thiostrepton and neomycin resistant colonies are conventionally isolated, cultured, and then identified by restriction enzyme and gel electrophoretic analysis of the constitutive plasmids.

EXAMPLE 14 Construction ofplasmids pEL 7.4 andpEL 7.8 The desired plasmids are constructed in substantial accordance with the teaching of Example 12A-C, except that a mixture of plasmid pEL7 and pEL7.2 DNA (isolated from the Streptomyces ambofacienslpEL7.

pEL7.2 prepared in Example 9) is used instead of the mixture of plasmid pEL7 and pEL7.1 DNA.

A mixture of recombinant plasmids is produced since the 3.5kb Pstl fragments are ligated with either or both of plasmids pEL7 and pEL7.2. The recombinant plasmids, as previously described, are also of two orientations depending upon the orientation of the 3.5kb Pstl neomycin resistance conferring fragment.

Thus, ligation with plasmid pEL7 results in plasmids pEL7.3 and pEL7.4 and ligation with plasmid PEL7.2 results in the desired plasmids pEL7.7 and pEL7.8. In addition, plasmids pEL7 and pEL7.2 are also restored by self ligation.

Plasmid pEL7.7 designates the recombinant plasmid in which the Sall (flanking BamHI) restriction site of the 3.5kb Pstl neomycin resistance conferring fragment is inserted farthest from the Pvull restriction site of the 1 .6kb BamHI thiostrepton resistance conferring fragment. Plasmid pEL7.8 designates the recombinant plasmid in whch the 3.5kb Pstl neomycin resistance conferring fragment has the reverse orientation. Thus, the final DNA suspension contains plasmids which include plasmids pEL7, pEL7.2, pEL7.3, pEL7.4, pEL7.7, pEL7.8, and, for the reasons described in Examples 8 and 10, the insertional isomers of plasmids pEL7.3, pEL7.4, pEL7.7, and pEL7.8. A restriction site and functional map of each of the desired plasmids pEL7.7 and pEL7.8 is respectively presented in Figures 11 and 12 of the accompanying drawings.

EXAMPLE 15 Construction of Streptomyces ambofacienslpEL 7, pEL7. 7and S. ambofacienslpEL7, pEL7.8 Using DNA prepared in Example 14, the desired transformants are constructed in substantial accordance with the procedure of Example 13. The resultant Streptomyces ambofaciensipEL7, pEL7.7 and S.

ambofaciensipEL7, pEL7.8 thiostrepton and neomycin resistant colonies are conventionally isolated, cultured, and then identified by restriction enzyme and gel electrophoretic analysis of the constitutive plasmids.

EXAMPLE 16 Construction ofplasmidpLR5 and plasmid pLR6 Plasmids pLR5 and pLR6 are prepared in substantial accordance with the teaching of Example 6A-C except that plasmid pEL7 is used in place of plasmid pLR1. Recombinant plasmids of two orientations result depending upon the orientation of the inserted plasmid pEL7 DNA. In addition, for the reasons described in Example 8, insertional isomers of plasmids pLR5 and pLR6 are also produced. A restriction site and functional map of each of the plasmids pLR5 and pLR6 is presented in Figures 13 and 14 ofthe accompanying drawings.

EXAMPLE 17 Construction ofE. coli K12 HB 10 1/pLR5 and E. coli K12 HB1O 1/pLR6 The desired construction is carried out in substantial accordance with the teaching of Example 3 except that plasmids pLR5 and pLR6 (from example 16), rather than plasmid pLR2, are used for transformation.

Surviving colonies are selected and tested for the expected phenotype (AmpR, Tets) and constitute the desired E. coli K12 HB1 01/pLR5 and E. coli K12 HB1 01/pLR6 transformants. The resistant transformant colonies are isolated, cultured according to known procedures, and then conventionally identified by restriction enzyme and gel electrophoretic analysis of the constitutive plasmids.

EXAMPLE 18 Construction of Streptomyces ambofaciensipEL7, pLR5 Plasmid pLR5 is conventionally isolated from E. co/I K12 HB101/pLR5 (prepared in Example 17) and then transformed into Streptomyces ambofaciensipEL7 in substantial accordance with the teaching of Example 13. Colonies are selected and the desired Streptomyces ambofaciensipLR5 transformants identified by restriction enzyme and gel electrophoretic analysis of the constituent plasmids.

Representative plasmids that can be constructed according to the foregoing teaching include the following listed below.

Plasmid names designate and also encompass all the insertional and orientational isomers resulting from a particular construction.

Plasmid Name Construction pLR7 pBR322 and pEL7.1 pLR8 pBR322 and pEL7.2 pLR9 pBR322 and pEL7.3 pLR10 pBR322 and pEL7.4 pLR11 pBR322 and pEL7.5 pLR12 pBR322 and pEL7.6 pLR13 pBR322 and pEL7.7 pLR14 pBR322 and pEL7.8 Representative transformants of plasmids pLR7 through pLR1 4 include the following listed below, E. coliK12 HB101/pLR7 E. coliK12 HB101/pLR8 E. coliK12 HB101/pLR9 E. coli K12 HB101/pLR10 E. coliK12 HB101/pLR11 E. coliK12 HB101/pLR12 E. coliK12 HB101/pLR13 E. coliK12 HB101/pLR14 Streptomyces ambofacienslpEL7, pLR7 Streptomyces ambofacienslpEL7, pLR9 Streptomyces ambofaciensipEL7, pLR11

Claims (39)

1. A pair of recombinant DNA cloning vectors, said pair comprising: a) plasmid pEL7, and b) a second plasmid that is functionally dependent upon plasmid pEL7, said second plasmid comprising a restriction fragment of plasmid pEL7 and one or more different DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell, said host cell being susceptible to transformation, cell division, and culture.

2. The pair of claim 1 wherein the one or more DNA segments in the second plasmid are segments that convey resistance to either or both of antibiotics thiostrepton and neomycin.

3. The recombinant DNA cloning vector which is plasmid pEL7.

4. A recombinant DNA cloning vector which is a plasmid that is functionally dependent upon plasmid pEL7, said plasmid comprising a restriction fragment of plasmid pEL7 and one or more different DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell, said host cell being susceptible to transformation, cell division, and culture.

5. The vector of claim 4 which is plasmid pEL7.1, pEL7.2, pEL7.3, pEL7.4, pEL7.5, pEL7.6, pEL7.7, or pEL7.8.

6. A recombinant DNA cloning vector which is plasmid pLR1, pLR2, or pLR4.

7. A recombinant DNA cloning vector that is function is E. coliand is functionally dependent upon plasmid pEL7 when transformed into Streptomyces comprising: a) a functional E. coli replicon containing an antibiotic resistance conferring restriction fragment of an E.

coli plasmid, and b) a restriction fragment of a member of the pair of recombinant DNA cloning vectors recited in Claim 1.

8. The vector of claim 7 which is plasmid pLR5, pLR6, pLR7, pLR9 or pLR1 1.

9. A transformed restrictionless host cell comprising the vector of claim 3.

10. The cell of claim 9 which comprises a pair of recombinant DNA cloning vectors of claim 1 or 2.

11. The cell of claim 10 which comprises a vector of claim 4 or 5.

12. The cell of claim 9, 10 or 11 which is a restrictionless cell of Streptomyces, Streptosporangium, Actinoplanes, Nocardia, Micromonospora, Bacillus, or Staphylococcus.

13. A transformed restrictionless host cell comprising the recombinant DNA cloning vector of claim 7 or 8.

14. The cell of claim 13 which is E. coli.

15. The cell of claim 13 which is Streptomyces.

16. The cell of claim 12 or 15 which is Streptomyces of species fradiae, aureofaciens, coelicolor, or ambofaciens.

17. The cell of claim 16 which is Streptomyces ambofaciens.

18. A process for isolating plasmid pEL7 which comprises a cultivating Streptomyces ambofaciensipEL7 NRRL 12523 under submerged aerobic conditions in a nutrient medium containing assimilable sources of carbon, nitrogen and minerals at a pH in the range of 5 to 9, and at a temperature in the range of 15 to 45"C., harvesting the cells thus formed, lysing the harvested cells, solvent extracting the lysate supernatant, precipitating the plasmid DNA from the extract, and separating the plasmid pEL7 from the precipitate.

19. A process for preparing plasmid pLR1 which comprises ligating Hindlll treated plasmid plJ2 to Hindlll treated plasmid pBR322.

20. A process for preparing plasmid pLR2 which comprises ligating Hindlll treated plasmid plJ6 to Hindlll treated plasmid pBR322.

21. A process for preparing plasmid pLR4 which comprises ligating BamHI treated plasmid pLR2 to BamHI treated plasmid pBR322.

22. A process for preparing a plasmid that is functionally dependent upon plasmid pEL7 which comprises ligating one or more different DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell onto a restriction fragment of plasmid pEL7, and self ligating the resulting recombinant DNA to produce said functionally dependent plasmid.

23. The process of claim 22 wherein the DNA segment conveys resistance to antibiotic thiostrepton.

24. The process of claim 23 for preparing plasmids pEL7.1 and pEL7.2 which comprises ligating BamHI treated plasmid pLR2 to BamHI treated plasmid pEL7.

25. The process of claim 22 wherein the DNA segment conveys resistance to the antibiotic neomycin.

26. The process of claim 25 for preparing plasmids pEL7.3 and pEL7.4 which comprises ligating Pst1 treated plasmid pLR1 to Pst1 treated plasmid pEL7.

27. The process of claim 22 where the DNA segment conveys resistance to the antibiotics thiostrepton and neomycin.

28. The process of claim 27 for preparing plasmids pEL7.5 and pEL7.6 which comprises ligating a mixture of Pst1 treated plasmid pEL7, Pst1 treated plasmid pEL7.1, and Pst1 treated plasmid pLR1.

29. The process of claim 27 for preparing plasmids pEL7.7 and pEL7.8 which comprises ligating a mixture of Pst1 treated plasmid pEL7,Pst1 treated plasmid pEL7.2, and Pstl treated plasmid pLR1.

30. A process for preparing a plasmid that is functional in E. coliand is functionally dependent on plasmid pEL7 when transformed into Streptomyces which comprises ligating a) a functional E. coli replicon containing an antibiotic resistance conferring restriction fragment of an E.

coli plasmid, and b) a restriction fragment of a member of the pair of recombinant DNA cloning vectors recited in Claim 1.

31. The process of claim 30 for preparing plasmids pLR5 and pLR6 which comprises ligating BamHI treated plasmid pEL7 to BamHI treated plasmid pBR322.

32. A pair of recombinant cloning vectors substantially as hereinbefore described with particular reference to Examples 9,11,13, 15 and 18.

33. A recombinant DNA cloning vector which is a plasmid that is functionally dependent upon plasmid pEL7 substantially as hereinbefore described with particular reference to Examples 8,10,12 and 14.

34. A recombinant DNA cloning vector that is functional in E. coli and is functionally dependent on plasmid pEL7 when transformed into Streptomyces substantially as hereinbefore described with particular reference to Example 16.

35. A recombinant DNA cloning vector which is plasmid pLR1, pLR2, or pLR4 substantially as hereinbefore expressed with particular reference to Examples 2, 4, and 6.

36. A transformed restrictionless host cell substantially as hereinbefore described with particular reference to Examples 2, 5,7,9, 11, 13, 15, 17 and 18.

37. A process for isolating plasmid pEL7 substantially as herein before described with particular reference to Example 1.

38. A process for preparing a plasmid that is functionally dependent on plasmid pEL7 substantially as hereinbefore described with particular reference to Examples 8, 10, 12 and 14.

39. A process for preparing a plasmid that is functional in E. coli and is functionally dependent on plasmid pEL7 when transformed into Streptomyces substantially as herein before described with particular reference to Example 16.