Expression control sequences

Abstract

Expression control sequences are provided for the expression of proteins from a gene of interest. The gene may express viral, prokaryotic, or eukaryotic proteins. These control sequences are produced by combining phage promoter and operator/repressor systems. Expression vectors containing such expression control sequences, microorganisms transformed with such expression vectors and methods for producing viral, prokaryotic, and eukaryotic proteins using the expression control sequences, expression vectors and transformed microorganisms are also provided.

Description

[0001] This is a continuation in part of U.S. application Ser. No. 08/941,020 filed Sep. 30, 1997.

FIELD OF THE INVENTION

[0002] The present invention relates to highly efficient and highly repressible expression control sequences, expression vectors which contain these expression control sequences, microorganisms transformed with these expression vectors, and methods for their production by means of recombinant DNA technology. The present invention also relates to methods for the production of viral, prokaryotic, and eukaryotic proteins and fragements thereof using these highly repressible expression control sequences, expression vectors and transformed microorganisms.

BACKGROUND OF THE INVENTION

[0003] The level of production of a protein in a host cell is determined by three major factors: the number of copies of its structural gene within the cell, the efficiency with which the structural gene copies are transcribed and the efficiency with which the resulting messenger RNA (“mRNA”) is translated. The transcription and translation efficiencies are, in turn, dependent on nucleotide sequences which are normally situated ahead of the desired structural genes or the translated sequence. These nucleotide sequences (expression control sequences) define, inter alia, the location at which the RNA polymerase binds (the promoter sequence to initiate transcription; see also EMBO J. 5:2995-3000 (1986)) and at which the ribosomes bind and interact with the mRNA (the product of transcription) to initiate translation.

[0004] Not all expression control sequences have the same efficiency. It is therefore often advantageous to separate the specific coding sequence for a desired protein from its adjacent nucleotide sequences and to link it with other expression control sequences to achieve a higher expression rate. After this linkage has been accomplished, the newly combined DNA fragment can be inserted into a plasmid capable of achieving a high copy number or a derivative of a bacteriophage to increase the structural gene copies within the cell, thereby improving the yield of the desired protein.

[0005] The constitutive expression of overproduction of both toxic and normally nontoxic gene products is often harmful to the host cells, thereby, lowering the stability of a specific host cell-vector system. Therefore, an expression control sequence should, in addition to improving the transcription and translation efficiency of a cloned gene, be regulatable to permit the regulation of the expression during the growth of the microorganisms. Some regulatable expression control sequences can be switched off during the growth of the host cells and then can be switched on again at a desired point in time, to favor the expression of large amounts of the desired protein.

[0006] Various expression control sequences have been used to regulate the expression of DNA sequences and genes which code for desired proteins. See, e.g., Itakura et al.(1977) Science 198:1056-1063; Goeddel et al. (1979) Proc. Natl. Acad. Sci. U.S.A. 76:106-110; Emtage et al. (1980) Nature 283:171-174; Bernard et al. (1979) Sciences 205:602-607; Ammann et al. (1983) Gene 25:167-178; de Boer et al. (1983) Proc. Natl. Acad. Sci. U.S.A. 80:21-25; European Patent Application Publication Nos. 41767 and 186069.

SUMMARY OF THE INVENTION

[0007] In accordance with the invention, highly efficient and highly repressible expression control sequences can be produced by combining promoter sequences with operator/repressor sequences. The present invention provides for expression control sequences for the expression of polypeptides from a gene or polynucleotide of interest. The gene or polynucleotide may express a viral, prokaryotic, or eukaryotic polypeptide. These control sequences are produced by combining bacterial or phage promoter and operator/repressor systems.

[0008] More particuarly, the present invention provides for DNA expression control sequences comprising at least a portion of one or more lac operator sequences and a phage promoter comprising a −30 region, having a sequence represented by the sequence 5′ TTGMYW 3′ (where M=A or C and Y=C or T and W=A or T), and a −12 region, having a sequence represented by the sequence 5′ TAWRMT (where R=A or G).

[0009] The present invention further provides for DNA expression control sequences comprising at least a portion of one or more lac operator sequences and a phage promoter comprising a −30 region, having a sequence represented by the sequence 5′ TTGAYA 3′ (where Y=C or T), and a −12 region, having a sequence represented by a sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′ (where W=A or T and M=A or C), and 5′ TAARMT 3′.

[0010] The present invention further provides for DNA expression control sequences comprising at least a portion of one or more lac operator sequences and a phage promoter comprising a −30 region, having a sequence represented by the sequence 5′ TTGMTW 3′ (where M=A or C and W=A or T), and a −12 region, having a sequence represented by a sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′, and 5′ TAARMT 3′.

[0011] The present invention further provides for DNA expression control sequences comprising at least a portion of one or more lac operator sequences and a phage promoter comprising a −30 region, having a sequence represented by the sequence 5′ TTGCTW 3′ (where Y=C or T and W=A or T), and a −12 region, having a sequence represented by a consensus sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′ (where M=A or C), and 5′TAARMT 3′.

[0012] The present invention further provides for DNA expression control sequences comprising at least a portion of one or more lac operator sequences and a phage promoter comprising a −30 region, having the sequence 5′ TTGACT 3′, and a −12 region, having the sequence 5′ TAAGAT 3′.

[0013] The present invention further provides for expression vectors comprising the above expression control sequences, host cells transformed with such expression vectors, and methods for producing viral, prokaryotic, and eukaryotic polypeptides using the disclosed expression control sequences.

BRIEF DESCRIPTION OF THE FIGURES

[0014] FIG. 1 shows the nucleotide sequence of expression control sequences of the present invention designated: M, M+D, U+D, M+D1, and M+D2. The start of transcription is represented by the bolded letter A labelled with an arrow and is designated as +1. The promoter regions −35 to −30 and −12 to −7 are bolded. Operator sequences are underlined. Underlined bases of the promoter regions share the same sequence as the operator and are, therefore, designated as both operator and promoter sequences.

[0015] FIG. 2 shows the nucleotide sequence of an expression vector comprising expression control sequence M+D1 and the MPIF-1&Dgr;23 gene and illustrates relevant features of the expression vector.

DETAILED DESCRIPTION OF THE INVENTION

[0016] Promoter sequences which can be used in this invention include natural promoter sequences and functional variants, which have been specifically altered by mutation or synthesis, and combinations of these promoter sequences. The promoter sequences can routiney be obtained from: gram-negative organisms, including but not limited to, gram negative bacteria, such as E coli; from gram-positive organisms, such as B. subtilis and B. stearothermophilis; and from the corresponding phages that infect these organisms. Preferred promoter sequences are those from T-coliphages. Espeically preferred, are T5 phage promoter sequences.

[0017] Operator/repressor systems that can be used according to the present invention include all systems that are directly inducible by chemical inducers which produce, in the natural state or after corresponding variations (e.g., by mutation), repression factors. In preferred embodiments, the directly inducible systems of the present invention are not inducible by SOS function (lexA/recA system) or by temperature, such as the PL operator/repressor system.

[0018] Examples of systems which are directly regulatable by chemical induction include, but are not limited to, the regulation units of the lactose, galactose, tryptophan and tetracycline operons, and other negatively controllable operons (i.e., operons which are regulatable by an operator/repressor action. See, e.g., Miller et al., The operon (Cold Spring Harbor Laboratory 1980); Hillen et al., (1984) J. Mol. Biol. 172:185-201. Especially preferred operator/repressor systems are the natural lac-operator/repressor system, see, e.g., Miller et al., The operon (Cold Spring Harbor Laboratory 1980), and variants of the above-named operator/-repressor systems, which are specifically modified by mutation.

[0019] LacIq is an allele of the lacI gene which confers tight regulation of the lac operator. See E. Amann et al., (1988) Gene 69:301-305; M. Stark Gene (1987) 51:255-267. The lacIq gene encodes a repressor protein which binds to lac operator sequences and blocks transcription of down-stream (i.e., 3′) sequences. However, the lacIq gene product dissociates from the lac operator in the presence of either lactose or certain lactose analogs, e.g., isopropyl B-D-thiogalactopyranoside (IPTG). An expression vector comprising a gene of interest under the control of the expression control sequences which comprise the lac operator will not produce appreciable quantities of protein in uninduced host cells. Induction of host cells by the addition of an agent such as IPTG, however, results in the expression of the protein encoded by the gene of interest.

[0020] The phage promoter sequences can be used with one or more operator/repressor system(s) to produce the desired expression control sequences. When a single operator/repressor system is used, a full or partial operator sequence can be located either within or outside the promoter sequence, can partially replace the promoter, or can be located before or after the promoter sequence. In preferred emobodiments, a full or partial operator/repressor system is integrated into the promoter sequence. In an especially preferred emobodiment, the integration position of the operator sequence is the spacer region between position −12 and −30 (nomenclature as in FIG. 1), wherein +1 is designated as the start of transcription and −1 is designated as the adjacent base 5′ to the start of transcription.

[0021] When two or more operator/repressor systems are used, both operators can be located within or outside the promoter sequence, or alternatively one operator can be situated within and another outside the promoter sequence. The operator sequence located outside the promoter spacer may be either 5′ or 3′ of the promoter region. That is, the operator may be either upstream of the −30 promoter region or downstream of the −12 promoter region. Preferably, one operator/repressor is integrated into the spacer region (between the −12 and −30 promoter regions) and a second operator/repressor is integrated either upstream or downstream (5′ or 3′) of the promoter regions (−30 and −12). More preferably, one operator/repressor is integrated into the spacer region and the other is integrated downstream (3′) of the −12 promoter region, so that repressor binding will create maximal cooperatively between the two operator sequences of the operator/repressor systems.

[0022] The invention further provides for a ribosome binding site (Shine-Dalgarno (S/D) sequence) downstream of the start of transcription and upstream from the start of translation, (usually about 10 nucleotide bases). Preferred ribosome binding site sequences comprise the sequence 5′-GAGGAC-3′. A more preferred ribosome binding site sequence comprises the sequence 5′-ATTAAAGAGGAGAAATTA-3′ (SEQ ID NO: 1).

[0023] The invention additionally provides for one or more restriction enzyme sites downstream of the ribosome binding site sequence for cloning and expressing a gene or polynucleotide of interest. A preferred restriction enzyme site is NdeI which recognizes and cleaves the sequence 5′-CATATG-3′. A preferred location for the NdeI site is at the 5′-ATG-3′ initiation codon downstream of the ribosome binding site sequence which will permit proper positioning of the gene of interest for translation at the correct codon and in the correct frame.

[0024] As discussed above, the T5 promoter sequences of the present invention comprise two critical elements located between positions −30 to −35, called the −30 region, and −7 to −12, called the −12 region. In a preferred enbodiment the −30 region comprises any sequence represented by the sequence 5′TTGMYW 3′ (where M=A or C, Y=C or T, and W=A or T). More preferred are any −30 sequences represented by sequences 5′ TTGATA 3′, 5′ TTGMTW 3′, or 5′ TTGCTW 3′. Even more preferrably the −30 region comprises the sequence 5′ TTGACA 3′

[0025] In a preferred enbodiment the −12 region comprises any sequence represented by the sequence 5′TAWRMT 3′ (where R=A or G). In a more preferred embodiment, the −12 region promoter is represented by the sequences, 5′ TATAMT 3′, 5′ TAWAMT 3′, 5′ TAARAT 3′, or 5′ TAWAMT 3′. In a most preferred embodiment, the −12 region promoter comprises the sequence 5′ TAAGAT 3′ and the −35 region comprises the sequence 5′ TTGACT 3′. The invention also provides for the exclusion of any −30 promoter region represented by the sequence 5′ TTGMYW 3′ and any −12 promoter region represented by the sequence 5′TAWRMT 3′.

[0026] The lac operator sequences of the present invention comprises the entire lac operator sequence represented by the sequence 5′ AATTGTGAGCGGATAACAATTTCACACA 3′ (SEQ ID. NO:2) or a portion thereof that retains at least partial activity. Activity is routinely determined using techniques well known in the art to measure the relative repressability of a promoter sequence in the absence of an inducer such as IPTG. This is done by comparing the relative amounts of protein expressed from expression control sequences comprising portions of the lac operator sequence and full length lac operator sequence. The partial operator sequence is measured relative to the full length lac operator sequence (SEQ ID NO:2). In one embodiment, partial activity for the purposes of the present invention means activity not less then 100 fold reduced relative to the full length sequence. In alternative embodiments, partial activity for the purpose of the present invention means activity not less than 75, 50, 25, 20, 15, and 10 fold reduced relative to the full length lac operator sequence. In a preferred embodiment, the ability of a partial sequence to repress is not less than 10 fold reduced relative to the fall length sequence.

[0027] In a preferred enbodiment the expression control sequences comprise a T5 phage promoter sequence and two lac operator sequences wherein at least a portion of the full length lac operator sequence (SEQ ID NO:2) is located within the spacer region between −12 and −30 of the expression control sequences. A preferred portion of an operator sequence comprises at least the sequence 5′-GTGAGCGGATAACAAT-3′ (SEQ ID NO:3). The precise location of operator sequences are designated using the nomenclature as in FIG. 1, wherein the 5′ base position of the sequence 5′-GTGAGCGGATAACAAT-3′ is described. In another preferred embodiment, the operator sequences comprise the sequence 5′-GTGAGCGGATAACAAT-3′, wherein the 5′ G occupies any base position between −75 and +50. An example of this preferred embodiment is the expression control sequence M+D1 wherein the operator sequences comprise the sequence 5′-GTGAGCGGATAACAAT-3′ and are located at positions −28 and +5.

[0028] The expression control sequences of the present invention can be produced by recombinant DNA techniques, or alternatively, can be synthesized in whole or in part, using chemical methods known in the art. See, e.g., Caruthers et al. (1980) Nuc. Acids. Res. 7:215-233; Crea and Hom, (1980) Nuc. Acids. Res. 9(10):2331; Matteucci and Caruthers, (1980) Tetrahedron Letters 21:719. Expression control sequences of the present invention have been obtained by chemical DNA synthesis, whereby functional parts of the lac-operator sequence have been combined with functional parts of a T5 promoter sequence. Preferred are expression control sequences, M (SEQ ID NO:4), M+D (SEQ ID NO:5), U+D (SEQ ID NO:6), M+D1 (SEQ ID NO:7), and M+D2 (SEQ ID NO:8), (See FIG. 1.)

[0029] The previously mentioned lac-operator sequences are negatively regulated by the lac-repressor. The corresponding repressor gene can be introduced into the host cell in a vector or through integration into the chromosome of a bacterium by known methods, such as by integration of the laciq gene. See, e.g.,Miller et al, supra; Calos, (1978) Nature 274:762-765. The vector encoding the repressor molecule may be the same vector that contains the expression control sequences and a gene or polynucleotide of interest or may be a separate and distinct vector. Preferably, the repressor gene is encoded on the vector containing the expression control sequences and a gene or polynucleotide of interest. An advantage of having the repressor gene encoded on same vector that contains the expression control sequences and gene of interest is that the ratio of repressor protein to plasmid copy number may be more consistent than the other alternatives above. This may allow better regulation of repression and also provide for greater predictability of the extent of repression. Another advantage is that it is not necessary to maintain multiple vectors in a single host cell or to integrate the repressor gene into the bacterial chromosome.

[0030] The expression control sequences of the invention can routinely be inserted using procedures known in the art into any suitable expression vector which can replicate in gram-negative and/or gram-positive bacteria. See, e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual (Cold Spring Harbor, N.Y. 2nd ed. 1989); Ausubel et al., Current Protocals in Molecular Biology (Green Pub. Assoc. and Wiley Intersciences, N.Y.). Suitable vectors can be constructed from segments-of chromosomal, nonchromosomal and synthetic DNA sequences, such as various known plasmid and phage DNA's. See, e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual (Cold Spring Harbor, N.Y. 2nd ed. 1989). Especially suitable vectors are plasmids of the pDS family. See Bujard et al, (1987) Methods in Enzymology, 155:416-4333. Examples of preferred suitable plasmids are pBR322 and pBluescript (Stratagene, La Jolla, Calif.) based plamids. More preferred examples of suitable plasmids are pUC based vectors including pUC18 and pUC 19 (New England Biolabs, Beverly, Mass.) and pREP4 (Qiagen Inc., Chatsworth, Calif.). Portions of vectors encoding desired functions may also be combined to form new vectors with desired characteristics. For lexample, the origin of replication of pUC19 may be recombined with the kanamycin resistance gene of pREP4 to create a new vector with both desired characteristics.

[0031] Preferably, vectors comprising the expression control sequences also contain sequences that allow replication of the plasmid to high copy number in the host bacteria of choice. Additionally, vectors comprising the expression control sequences may further comprise a multiple cloning site immediately downstream of the expression control sequences and ribosomal binding site.

[0032] Vectors comprising the expression control sequences may further comprise genes conferring antibodic resistance. Preferred genes are those conferring resistance to ampicillian, chloramphenicol, and tetracyclin. Espeically preferred genes are those conferring resistance to kanamycin.

[0033] The expression control sequences of the invention can also be inserted into the chromosome of gram-negative and gram-positive bacterial cells using techniques known in the art. In this case, selection agents such as antibiotics, which are generally required when working with vectors, can be dispensed with.

[0034] In another embodiment, vectors containing the expression control sequences of the invention aditionaily contain polynucleotide sequences expressed under the control of the expression control sequences. In a spceific embodiment, host cells are transformed with vectors containing the expression control sequences of the invention and multiple copies of the vectors are harvested from the transformants.

[0035] Polynucleotide sequences which can be expressed using the expression control sequences of the invention include those which code in vivo or in vitro for viral, prokaryotic, or eukaryotic proteins. For example, such DNA sequences can code for: enzymes; hormones; proteins having immunoregulatory, antiviral or antitumor activity; antibodies and fragments thereof (e.g., Fab, F(ab), F(ab)2, single-chain Fv, disulfide-linked Fv); antigens; and other useful viral, prokaryotic, or eukaryotic proteins.

[0036] In one embodiment of the invention, a desired protein is produced by a method comprising:

[0037] (a) transforming a bacterium such as E. coli, S. typhimurium or B. subtilis, with an expression vector in which DNA which codes for a desired viral, prokaryotic, or eukaryotic protein is operably linked to an aforementioned expression control sequence;

[0038] (b) culturing the transformed bacterium under suitable growth conditions; and

[0039] (c) isolating the desired protein from the culture.

[0040] In another embodiment of the invention, a desired protein is produced by a method comprising:

[0041] (a) inserting an aforementioned expression control sequence, which is operably linked to the coding sequence of a desired viral, prokaryotic, or eukaryotic protein, into the chromosome of a suitable bacterium;

[0042] (b) cultivating of the thus-obtained bacterium under suitable growth conditions; and

[0043] (c) isolating the desired protein from the culture.

[0044] The selection of a suitable host organism is determined by various factors which are well known in the art. Factors to be considered include, for example, compatibility with the selected vector, toxicity of the expression product, expression characteristics, necessary biological safety precautions and costs.

[0045] Suitable host organisms include, but are not limited to, gram-negative and gram-positive bacteria, such as E. coli, S. typhimurium, and B. subtilis strains. Preferred E. coli strains include DH5&agr; (Gibco-BRL, Gaithersberg, Md.), XL-1 Blue (Stratagene), and W3110 (ATCC No. 27325). Other E. coli strains that can be used according to the present invention include other generally available strains such as E. coli 294 (ATCC No. 31446), E. coli RR1 (ATCC No. 31343) and M15.

EXAMPLES

[0046] The examples which follow are set forth to aid in understanding the invention but are not intended to, and should not be construed to, limit its scope in any way. The examples do not include detailed descriptions for conventional methods employed in the construction of vectors, the insertion of genes encoding polypeptides of interest into such vectors or the introduction of the resulting plasmids into bacterial hosts. Such methods are described in numerous publications and can be carried out using recombinant DNA technology methods which are well known in the art See, e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual (Cold Spring Harbor, N.Y. 2nd ed. 1989); Ausubel et al., Current Protocals in Molecular Biology (Green Pub. Assoc. and Wiley Intersciences, N.Y.).

[0047] Expression control sequences M (SEQ ID NO:4), M+D (SEQ ID NO:5), U+D (SEQ ID NO:6), M+D1 (SEQ ID NO:7), and M+D2 (SEQ ID NO:8), represented in FIG. 1, comprising a T5 and lac operator sequences were designed de novo and then chemically synthesized. Restricion enzyme sites (e.g. HindIII and NdeI) were designed at the 5′ and 3′ ends of the oligonucleotides to facilitate cloning. The sequences were synthesized as single stranded fragments and hybridized as complementary fragments to produce overlapping double stranded fragements. The overlapping fragments were then extended using DNA polymerase, cleaved with restriction enzymes, and cloned into a plasmid vector. The plasmid vector was constructed by ligating a 2.7 Kb HindIII to SalI fragment comprising the kanamycin resistance gene and the lac repressor from pREP4 (Qiagen Inc., Chatsworth, Calf.) with the origin of replication from the pUC19 vector (LTI, Gaithersburg, Md.). Expression vectors were assembled by individually ligating the chemically synthesized expression control sequences with the vector comprising the kanamycin resistance gene, lac repressor, and pUC19 origin of replication.

[0048] To determine the relative promoter strengths and level of repressibility between the expression control sequences, a gene was ligated in an NdeI site approximately 10 bases 3′ of the ribosome binding site. The gene used was the MPIF-1&Dgr;23 gene which codes for a novel human &bgr;-chemokine. The mature form of MPIF-1&Dgr;23 is a 76 amino acid peptide. The expression vector pHE4-5 comprising the expression control sequence M+D1 and the MPIF-1&Dgr;23 gene is represented in FIG. 2 (SEQ ID NO:9).

[0049] To express protein from the expression vectors E. coli cells were transformed with the expression vectors and grown in overnight (O/N) cultures supplemented with kanamycin (25 ug/ml) to an opitical density 600 &lgr;(O.D. 600) of between 0.4 and 0.6. IPTG was then added to a final concentration of 1 mM. IPTG induced cultures were grown for an additional 3-4 hours. Cells were then harvested using methods known in the art and the level of protein was detected using Western blot analysis. The results varied with the expression control sequence M+D 1 demonstrating unexpectedly high levels of repression, in the absence of IPTG, and high levels of induced expression in the presence of IPTG.

[0050] Two other plasmids, pHE4-0 (SEQ ID NO: 10) and pHE4a (SEQ ID NO: 11) were constructed to facilitate cloning of other genes or polynucleotides of interest. pHE4-0 was constructed using an expression vector comprising the expression control sequence M+D 1 and the MPIF-1&Dgr;23 gene. pHE4-0 was constructed by removing the sequence between the NdeI and Asp718 sites, comprising the MPIF-1&Dgr;23 gene, and replacing it with a polylinker comprising a Bam-HI site. pHE4a was constructed in a similar manner, but the sequence between the NdeI and Asp718 sites, comprising the MPIF-1&Dgr;23 gene, was replaced by a polylinker comprising XbaI, BamHI, and XhoI restriction sites and an additional “stuffer”fragment of approxmately 300 bp in length. The stuffer fragment is used to indictate whether the polylinker (multiple cloning site) has been efficiently digested when two restriction enzymes are used in cloning a gene or polynucleotide of interest. For example, after digesting the DNA with the appropriate restriction enzymes, e.g. NdeI and Asp718, a portion of the digested vector is assayed by agarose gel electrophoresis. The presence of an approxamelty 300 bp fragment indicates the vector was properly cleaved with both enzymes.

Deposit of Microorganisms

[0051] Plasmid pHBE4a has been deposited with the American Tissue Type Culture Collection, 12301 Parklawn Drive, Rockville, Md., 20852 on Feb. 25, 1998 under accession number 209645. These cultures have been accepted for deposit under the provisions the Budapest Treaty on the International Recognition of Microorganisms for the Purposes of Patent Proceedings. Applicants have directed that the plasmids be made available without restriction to the general public upon the issuance of a United States patent.

[0052] The disclosure of all publications (including patents, patent applications, journal articles, laboratory manuals, books, or other documents) cited herein are hereby incorporated by reference in their entireties.

[0053] The present invention is not to be limited in scope by the specific embodiments described herein, which are intended as single illustrations of individual aspects of the invention. Functionally equivalent methods and components are within the scope of the invention, in addition to those shown and described herein and will become apparant to those skilled in the art from the foregoing description and accompanying drawings. Such modifications are intended to fall within the scope of the appended claims.

Claims

1. A DNA expression control sequence comprising: at least one lac operator sequence comprising the sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3); a −30 region having a sequence represented by the sequence 5′ TTGMYW 3′ (where M=A or C and Y=C or T and W=A or T); and a −12 region having a sequence represented by the sequence 5′ TAWRMT (where R=A or G); with the proviso that if the −30 region sequence is 5′ TTGACW 3′ then the −12 region is not 5′ KATAMT 3′ (where K=G or T); and further with the proviso that if the −30 region sequence is 5′ TTGCCT 3′ then the −12 region is not 5′ TTGCTT 3′.

2. A DNA expression control sequence comprising: at least one lac operator sequence comprising the sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3); a −30 region having a sequence represented by the sequence 5′ TTGAYA 3′ (where Y=C or T); and a −12 region having a sequence represented by a sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′ (where W=A or T and M=A or C), and 5′ TAARMT3′.

3. A DNA expression control sequence comprising: at least one lac operator sequence comprising the sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3); a −30 region having a sequence represented by the sequence 5′ TTGMTW 3′ (where M=A or C and W=A or T); and a −12 region having a sequence represented by a sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′, and 5′ TAARMT 3′.

4. A DNA expression control sequence comprising: at least one lac operator sequence comprising the sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3); a −30 region having a sequence represented by the sequence 5′ TTGCTW 3′ (where Y=C or T and W=A or T); and a −12 region having a sequence represented by a consensus sequence selected from the group consisting of: 5′ TAWRTT 3′ (where R=A or G), 5′ TAWGMT 3′ (where M=A or C), and 5′TAARMT 3′.

5. A DNA expression control sequence comprising: at least one lac operator sequence comprising the sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3); a −30 region having the sequence 5′ TTGACT 3′; and a −12 region having. the sequence 5′ TAAGAT 3′.

6. A DNA expression control sequence of claim 1 wherein said lac operator sequence begins at position −28.

7. A DNA expression control sequence of claim 1 wherein said lac operator sequence begins between nucleotide positions +1 and +6.

8. A DNA expression control sequence of claim 1 wherein the expression control sequence comprises two said lac operator sequences.

9. A DNA expression control sequence of claim 8 wherein a first lac operator sequence 5′ GTGAGCGGATAACAAT 3′ is located at nucleotide position −28 and a second lac operator sequence 5′ GTGAGCGGATAACAAT 3′ (SEQ ID NO:3) is located downstream of the start of transcription.

10. A DNA expression control sequence of claim 8 wherein said second lac operator sequence begins between nucleotide position +1 and +6.

11. A DNA expression control sequence selected from the group consisting of: expression control sequence M (SEQ ID NO:4); expression control sequence M+D (SEQ ID NO:5); expression control sequence U+D (SEQ ID NO:6); expression control sequence M+D 1 (SEQ ID NO:7); and expression control sequence M+D2 (SEQ ID NO:8).

12. An expression vector comprising a DNA expression control sequence of claim 1.

13. The expression vector pHE4-0 (SEQ ID NO: 10).

14. The expression vector pHE4a (SEQ ID NO: 11).

15. A host cell comprising an expression vector of any one of claim 12.

16. A method of using an expression vector of claim 12 comprising:

(a) transforming a bacterium with an expression vector of claim 12, wherein the expression control sequences are operably linked to the coding sequence of a viral, prokaryotic, or eukaryotic polypeptide to form a recombinant cell;

(b) growing the cell such that the protein is expressed by the cell; and

(c) recovering the expressed protein.

17. The method of claim 16 wherein the bacterium is selected from the group consisting of: E. coli, S. typhimurium, and B. subtilis.

18. A method of producing a protein comprising:

(a) inserting the expression vector of any one of claims 12, wherein the expression control sequences of the vector are operably linked to the coding sequence of a desired viral, prokaryotic, or eukaryotic protein, into the chromosome of a bacterium to form a recombinant cell;

(b) growing the recombinant cell such that the protein is expressed by the cell; and

(c) recovering the expressed protein.

19. The method of claim 14 wherein the bacterium is selected from the group consisting of: E. coli, S. typhimurium, and B. subtilis.