Immunogens comprising the non-lytic membrane spanning domain of bacteriophages MS2 or PhiX174

Abstract

The invention concerns a carrier-bound recombinant protein obtainable by expression of a fusion protein gene in gram-negative bacteria which codes for at least one hydrophobic non-lytically active protein domain capable of membrane integration as well as the recombinant protein and of a gene which codes for a lytically active membrane protein from bacteriophages or a lytically active toxin release gene or lytically active partial sequences thereof and isolation of the carrier-bound recombinant protein from the culture broth. The recombinant protein is thereby firmly incorporated into the cell wall complex of gram-negative bacteria via a target sequence. Furthermore the invention concerns a recombinant DNA for the production of the protein, the production process as well as the use of carrier-bound recombinant proteins according to the present invention for immunization and as vaccines.

Description

The invention concerns carrier-bound recombinant proteins, a process for their production and their use, in particular as immunogens and vaccines.

The main purpose of the immunological system in humans and animals is to resist and avoid pathological damages which arise as a result of degenerate cells of infectious viruses, bacteria, fungi or protozoa. A special characteristic of the immunological system is that an increasingly stronger resistance occurs after repeated infections with pathogens. The aim of immunization is to build up the power of the immunological system against particular pathogens without causing corresponding diseases.

Antibodies and cellular T and B lymphocytes are responsible for the specific resistance to pathogens. An essential prerequisite for this is the recognition of foreign structures such as e.g. those which occur on a bacterial cell. Depending on the stimulation of the immunological system a temporary or a lifelong immunity to pathogens can be built up in this process after immunization.

It is important for the quality of monoclonal and polyclonal antibodies as well as for the effectiveness of vaccines that the immunological response to the antigen occurs to a sufficient extent. However, viral antigens or recombinant human proteins often show a poor immunological response or none at all if they are used without further modification. For this reason these antigens are often linked to carriers (preferably to proteins) in order to amplify the immunological response. However, the antigens can be changed at or near the antigenic determinants by the binding of the antigens to the carrier. As a result the immunological response can be substantially weakened.

In order to improve the immunological response it is advantageous to incorporate such antigens into the outer membrane of bacteria and to use these complexes as immunogens (J. Immunol. 139 (1987) 1658-1664, Bacterial Vaccines and Local Immunity--Ann. Sclavor 1986, n. 1-2, pp. 19-22, Proceedings of Sclavo International Conference, Siena, Italy, 17-19 November 1986). Attenuated or dead pathogens (bacteria or viruses), treated partial components of pathogens (membrane proteins of bacteria, structural proteins of viruses) or recombinant live vaccines (viruses or bacteria) are also used.

A disadvantage of using live bacteria or viruses as immunogens for the immunization is that an undesired pathogenic spread of the germs cannot be excluded.

However, the antigenic determinant can be altered by killing or fragmenting the bacteria and viruses before their use as an immunogen or vaccine which can substantially reduce the immunological response.

The object of the present invention is therefore to provide immunogens and vaccines which do not have these disadvantages.

This object is achieved via a carrier bound, recombinant protein. This carrier bound, recombinant protein is obtained by expressing a first gene coding for a fusion protein and a second gene, hereinafter referred to as "lysis gene", which codes for one of: (a) a lytically-active, bacteriophage membrane protein, (b) a lytically-active, toxin release gene, or (c) a lytically active, partial sequence of one of these. The fusion protein comprises at least one hydrophobic, non-lytically active protein domain capable of membrane integration and a recombinant protein carrier bound, recombinant protein is then isolated from the culture broth.

The expression of the fusion protein gene and the lysis gene is preferably controlled by two different promoters (FIG. 1). The expression of the lysis gene is preferably delayed with respect to the expression of the fusion protein.

With this type of expression of fusion protein gene and lysis gene one obtains at first the integration of a multitude of fusion proteins into the membrane of the gram-negative bacteria used as the host organism and subsequently lysis of these bacteria takes place. The usually impermeable cell wall complex of the bacteria is made so permeable by this that the cytoplasmic components of the bacteria are released (Eur. J. Biochem. 180 (1989), 393-398). The morphology of the cells, for example the rod-form of E. coli cells, is preserved. A tunnel structure is merely formed in a localized area of the membrane. The tunnel formation is accompanied by a fusion of the inner and outer membrane at the edge of the tunnel. The bacterial coats formed in this way represent the carriers for the recombinant protein and are hereinafter denoted bacterial ghosts (FIG. 2 ).

The bacterial ghosts consist of a cytoplasmic (inner) membrane, periplasmic space and outer membrane whereby the integrity of the cell wall complex is preserved to a large extent. In the case of bacterial strains which have an additional S-layer coat (paracrystalline protein layer outside the outer membrane) this protein layer is also a component of the bacterial ghosts (Ann. Rev. Microbiol. 37 (1983), 311-339). The bacterial ghosts are therefore carriers of the recombinant proteins (immunogens) and, as a result of their composition (peptidoglycan, lipopolysaccharide), they at the same time constitute the adjuvant for amplifying the immunological response.

All gram-negative bacteria, preferably gram-negative pathogens such as e.g. Escherichia coli, Bordetella pertussis, Campylobacter jejuni, Corynebacterium diphteriae, Legionella pneumophilia, Listeria monocytogenes, Pseudomonas aeruginosa, Shigella dysenteriae, Vibrio cholerae, Yersinia enterolitica are suitable as host organisms (Schaechter, M., H. Medoff, D. Schlesinger, Mechanisms of Microbial Disease. Williams and Wilkins, Baltimore (1989)).

The carrier-bound recombinant proteins according to the present invention are surprisingly well suited as immunogens which results in pronounced immunological responses and very high antibody titres.

A particular advantage results from the fact that the recombinant protein is integrated into the membrane of the bacteria directly after the expression and thus the carrier binding is formed. As a consequence it is unnecessary to isolate the recombinant protein as such before production of the immunogen. Moreover, since it is sufficient for the production of bacterial ghosts containing immunogens when from several hundred up to the maximum possible number (ca. 50000) of recombinant antigens are integrated into the membrane of the bacterial ghosts, an over-expression of the recombinant protein is not necessary.

A further advantage of the process according to the present invention is that very many antigenic epitopes are presented in the cell wall complex of the bacterial ghosts. It has turned out that the target sequences for the recombinant proteins prefer certain regions within the bacterial cell wall complex for integration. These regions mainly constitute adhesion sites of the inner and outer membrane and are associated with the cell division of the bacteria. As a result the recombinant protein is not distributed uniformly but rather islet-type accumulations occur within the cell wall complex (cf. FIG. 2d). The clustered arrangement of the recombinant proteins within a relatively small region (cluster) has the advantage that the proliferation of B cells carrying immunoglobulin is stimulated. On the other hand the lipopolysaccharide present in the bacterial ghosts acts as a mitogen and also triggers a signal for the cell division. As a result one achieves an effective stimulation of the B-cell specific production of immunoglobulins.

In addition it has also turned out that the carrier-bound recombinant proteins according to the present invention are integrated into the bacterial membrane in their natural protein structures and thus in an active form.

This is particularly surprising since recombinant proteins are usually obtained in an inactive form as inclusion bodies (cf. EP-A- 0219 874, WO 89/03711) after expression in prokaryotes and can only subsequently be converted into the active form by denaturation and renaturation.

All proteins familiar to one skilled in the art are suitable as recombinant proteins. Human proteins and antigens, in particular viral antigens, are particularly preferably used. Their size is not limited. The molecular weight of the antigens is, however, preferably 2000 to 200000 Daltons.

The recombinant antigen has particularly preferably antigenic structures of human viruses and retroviruses such as e.g. of HIV (human immunodeficiency virus), HBV (hepatitis B virus), and EBV (Epstein Barr Virus)

The hydrophobic non-lytically active protein domains capable of membrane integration are hereinafter denoted target sequences. Complete sequences or partial sequences of membrane proteins which can, however, also be modified by amino acid substitutions are preferred as target sequences. Such a substitution should not, however, alter the structure of the corresponding protein.

Target sequences which are preferably used are those which--in contrast to the signal sequences of other membrane proteins--are not cleaved by proteases which are present in the membrane (e.g. signal peptidase and proteases of the periplasmic space). Target sequences can for example be derived from naturally occurring sequences of the lysis gene of the PhiXl74 phage group (for N-terminal targeting) as well as from the naturally occurring sequences of the lysis gene of the MS2 phage group (for C-terminal targeting) by protein engineering.

A hydrophobic alpha-helical protein domain consisting of 14 to 20 amino acids, which can be flanked N- and C-terminally by 2 to 30 arbitrary amino acids each, is preferred as the target sequence. At least one further protein domain can preferably be bound to this protein domain. The binding preferably takes place via flexible linker sequences. Flexible linker sequences are understood as hydrophilic amino acid sequences with 2 to 100 amino acids, preferably with 2 to 30 amino acids and with a disordered secondary structure (turn and random coil sequences).

The additional protein domains which are coupled to the first protein domain can be structured in an analogous manner to the first protein domain. It is, however, preferable that at least one of the additional domains posesses a .beta.-pleated sheet structure and is composed of 10 to 16 amino acids, preferably 11 to 13 amino acids. The construction and secondary structure of such .beta.-pleated sheet structures is preferably similar to amphipathic protein sequences which occur in porins of the outer membranes. For a N-terminal targeting it is preferable to use those target sequences which contain the amino acids 1 to 54 of protein E from the phage PhiXl74 (hereinafter denoted E' sequence) and which do not act lytically. For a C-terminal targeting it is preferable to use target sequences which contain the amino acids 21 to 75 of protein L from the phage MS2 (hereinafter denoted L' sequence) and which do not act lytically (for sequences compare EP-A 0 291 021). Sequences which are derived from the above-mentioned sequences of the E and L target sequences by a homologous amino acid substitution which does not cause an alteration in the secondary structure of the protein are also suitable.

Membrane proteins of bacteriophages are preferably understood as membrane proteins from bacteriophages of the Microviridae class, preferably from icosahedral phages, lytic phages and phages containing ssDNA, which can infect Enterobacteriacae. Examples of these are the phages PhiXl74, S13, G4, G6, G14, PhiA, PhiB, PhiC, PhiR which can infect E. coli C strains. Alpha 3 which can infect E. coli C and E. coli B strains is also suitable. The phages K9, St-1, PhiK, PhiXtB and U3 which can infect E. coli K12 strains are also suitable (Sinsheimer R. L. (1968) in: Prog. Nucl. Acid Res. Mol. Biol. (Davidson J. N. & Cohn W. W., eds) Vol.8, Academic Press, New York & London, pp. 115-169; Tessman E. S. & Tessmann I. (1978) in: The single-stranded DNA Phages (Denhardt D. T., Dressler D. & Ray D. S., eds.) Cold Spring Harbor Press, Cold Spring Harbor, pp. 9-29; Hayashi M., Aoyama A., Richardson D. L. & Hayashi M. N. (1987) in: The Bacteriophages, pp. 1-71).

Lysis proteins from the mentioned bacteriophages as well as other toxin release genes such as the colicin lysis gene (Microbiol. Sciences 1 (1984) 168-175 and 203-205) are preferably suitable as lytically active membrane proteins.

In a further, preferred embodiment, a binding partner for the recombinant protein is bound to it. This binding partner binds non-covalently. Examples of recombinant protein/binding partner pairs include, e.g., biotin and (strept)avidin, hapten and antibody, antigen and antibody, concanavalin and antibody, sugar and lectin, hapten and binding protein (e.g., thyroxin binding globulin and thyroxin), and oligopeptide and antibody. Additional substances may, in turn, be bound to the binding partner, either covalently or non-covalently.

Streptavidin, or avidin, and biotin are preferably used as the binding pair. Streptavidin or avidin is especially preferably used as the immobilized recombinant protein and biotinylated antigen is bound to it.

Furthermore, it is preferred that a protein be used as the recombinant protein which recognizes a chemical ligand. Examples for this are .beta.-galactosidase/p-aminophenyl-.beta.-D-thiogalactoside (a structural analogue of lactose), Gene 29 (1984) 27-31. Such substituted products are bound to the bacterial ghosts by the recognition of the active centre of the .beta.-galactosidase without cleavage of the substrate.

The invention also concerns a recombinant DNA which contains a first DNA sequence (DNA target sequence), which codes for at least one hydrophobic non-lytically active protein domain capable of membrane integration, a second DNA sequence (DNA protein sequence) which codes for a recombinant protein, as well as a DNA sequence (DNA lysis gene) which is under separate control from this which codes for a lytically active membrane protein from bacteriophages or a lytically active toxin release gene or for their lytically active parts.

DNA sequences are preferred as DNA target sequences which code for the L' protein or the E' protein. DNA sequences are also suitable which code for amino acid sequences which are derived from these proteins having the same secondary structure. These sequences are preferably connected by DNA sequences which code for hydrophilic protein domains having 2 to 30 amino acids and a disordered secondary structure.

In a preferred embodiment the DNA lysis sequence contains the DNA sequence of the E protein, the DNA sequence of the L protein or the DNA sequence of the EL hybrid protein (for sequences cf. EP-A 0 291 021). Partial sequences thereof which act lytically are also suitable.

The DNA protein sequence is preferably the DNA sequence of a viral antigen (e.g. HIV, HBV, EBV) or of a recombinant human protein.

The invention also concerns a process for the production of a carrier-bound, recombinant protein which is characterized in that a fusion protein which contains at least one hydrophobic non-lytically active protein domain capable of membrane integration as well as a recombinant protein, and a lytically active membrane protein from bacteriophages or a lytically active toxin release gene or lytically active partial sequences thereof are expressed in gram-negative bacteria and the carrier-bound, recombinant protein is isolated from the culture broth. The transformation and expression can be carried out according to processes familiar to one skilled in the art. The transformation is preferably carried out by electroporation or conjugation.

During the fermentation the activity of the lytic protein is preferably at first inhibited or the expression of the lysis gene is repressed and the inhibition or repression is only abolished at a desired time, preferably in the late logarithmic phase.

In a further preferred embodiment the carrier-bound recombinant protein obtained in this way is incubated with a binding partner for the protein which is derivatised, if desired, and the conjugate which is formed is isolated. The above-mentioned partners of the binding pairs are suitable as the binding partner.

In a further preferred embodiment the genes of at least two different recombinant proteins are expressed according to the present invention. In this way immunogens or vaccines can be obtained which have several antigenic structures. In this connection it is particularly preferred to use the antigenic determinants of different viruses or retroviruses (e.g. HIV1, HIV2, HBV and EBV) as the recombinant proteins. For the expression these genes can be arranged in an expression vector either as an open reading frame in the 3' direction after the gene for the target sequence or a special vector can be used for each of the recombinant proteins to be expressed. In this case it is, however, necessary that the vectors are each provided with separate origins of replication and separate resistance genes.

The invention also concerns a process for the production of antibodies which is characterized in that a mammal is immunized with a carrier-bound recombinant protein which is obtainable by expression of a fusion protein in gram-negative bacteria and which contains at least one hydrophobic non-lytically active protein domain capable of membrane integration as well as the recombinant protein, if desired, with a delayed expression of a lytically active membrane protein from bacteriophages or of a lytically active toxin release gene or lytically active partial sequences thereof and the antibodies are obtained from the serum or the spleen according to well-known methods.

In a preferred embodiment B lymphocytes of the immunized animals are fused with a suitable cell line in the presence of transforming agents, the cell line which produces the desired antibodies is cloned and cultured and the monoclonal antibodies are isolated from the cells or the culture supernatant.

It has turned out that the process according to the present invention is particularly suitable for the production of viral immunogens such as e.g. HIV immunogens, HBV immunogens.

In addition, it has surprisingly turned out that the activity and thus the antigenic structures of recombinant antigens, which are usually obtained in an inactive form as refractile bodies (e.g. human proteins such as TPA or G-CSF) when expressed in prokaryotes, are preserved when expressed according to the process according to the present invention. The process according to the present invention therefore proves to be particularly advantageous for the production of immunogenic recombinant human proteins.

The present invention also concerns the use of the carrier-bound recombinant proteins according to the present invention as vaccines and for the stimulation of T lymphocytes.

The vaccines according to the present invention can be produced and used in the usual manner.

The present invention also concerns a process for the production of vaccines using the carrier-bound recombinant proteins according to the present invention. The production of these vaccines can be carried out according to the well-known methods. However, the carrier-bound recombinant protein is preferably first lyophilised and subsequently suspended, if desired, with addition of auxiliary substances.

Furthermore, it is preferred to formulate the vaccine as a multivalent vaccine. For this the carrier-bound recombinant protein according to the present invention can contain several recombinant antigens immobilized on the membrane of the bacterial ghost.

The vaccination with the vaccine according to the present invention can be carried out according to methods which are familiar to those skilled in the art, for example intradermally, intramuscularly, intraperitoneally, intravenously, subcutaneously, orally and intranasally.

For the intramuscular or subcutaneous administration, the vaccine can for example be suspended in physiological saline. For the intranasal or intra-ocular application the vaccine can for example be applied in the form of a spray or an aqueous solution. For local, for example oral, administration it is often necessary to protect the immunogens temporarily against inactivation, for example against saccharolytic enzymes in the cavity of the mouth or against proteolytic enzymes in the stomach. Such a temporary protection can for example be effected by encapsulation of the immunogens. This encapsulation can for example be effected by coating with a protective agent (microencapsulation) or by embedding a multitude of immunogens according to the present invention in a protective carrier (macroencapsulation).

The encapsulation material can be semi-permeable or can become semi-permeable when introduced into the human or animal body. A biologically degradable substance is usually used as the carrier for the encapsulation.

The following examples figures and sequence protocols elucidate the invention further.

FIG. 1 shows diagrams of the plasmids pkSELS, pMLl and pMTVl

FIG. 2a-2d Diagram of a bacterial ghost as a carrier for recombinant proteins

a) longitudinal section through a gram-negative bacterium (om: outer membrane; pp: periplasmic space; im: inner (cytoplasmic) membrane, cp: cytoplasm). b) Formation of a transmembrane lysis tunnel. c) Cytoplasm flowing out through the lysis tunnel. d) Bacterial ghost with fusion proteins which are anchored in the cell wall complex via target sequences.

EXAMPLE 1

N-terminal membrane targeting for HIV 1 gp41.

A HIV 1 specific DNA fragment is isolated from plasmid pHF14 as a 1445 bp DNA fragment by partial digestion with HincII/PvuII. The fragment contains the complete sequence of gp41, (345 codons of gp41) linker sequences, the last 45 codons of gp120. It corresponds to the nucleotides 4 to 1448 from SEQ ID NO: 1.

After linearizing plasmid pKSEL5 (SEQ ID NO:6) with AccI and filling up the protruding DNA ends with Klenow polymerase the HIV1 specific DNA fragment is ligated with this linearized plasmid. The plasmid which formed is denoted pHIE1 and contains in frame a fusion of a partial sequence of the E gene (E' target sequence) of PhiX174 with the above-mentioned HIV1 fragment, in which the natural stop codon of the HIV1 env-gene is preserved.

EXAMPLE 2

N- as well as C-terminal membrane targeting of HIV1 gp41.

A 1059 bp HIV1 specific DNA fragment is isolated from the plasmid pHFl4 by digestion with HincII. This fragment contains linker sequences at the 5' side followed by 45 codons from gp120 as well as 301 codons from gp41. It corresponds to the nucleotides 4 to 1062 from SEQ ID NO:1. After linearizing plasmid pKSEL5 with AccI and filling up the protruding DNA ends with Klenow polymerase the HIV1 specific DNA fragment is ligated with this vector. The plasmid pHIE3 which formed contains an in frame fusion of a partial sequence of the E gene (E' target sequence) with a partial sequence of HIV and a partial sequence of the L gene (L' target sequence ).

EXAMPLE 3

C-terminal membrane targeting of HIV1 gp41.

A 1061 bp DNA fragment is isolated from plasmid pHF14 with SalI and HincII. This fragment contains linker sequences on the 5' side followed by 45 codons of gp120 as well as 301 codons of gp41. It corresponds to the nucleotides 2 to 1062 from SEQ ID NO: 1. After removing the E' sequence from the plasmid pKSEL5 by digestion with XhoI/AccI the protruding DNA ends of the vector and of the isolated HIV1 fragment are filled up with the aid of Klenow polymerase and, ligated. The plasmid pHIE5 which formed contains an in frame fusion of the first 5 codons of the lacZ gene, polylinker codons, gp120/gp41 codons and polylinker codons followed by the L' target sequence.

EXAMPLE 4

C-terminal membrane targeting of streptavidin.

The 498 bp XbaI fragment (FXaStrpA, nucleotide 2 to 499 of SEQ ID NO:2) from pFN6 filled up with Klenow polymerase is ligated into the filled up cleavage sites of the plasmid pKSEL5 from which the E' gene fragment was deleted by cleavage with HincII/XhoI. The plasmid obtained is denoted pAV5. This gives rise in the plasmid pAV5 to an in frame fusion of the first5 codons of the LacZ gene, 26 amino acid codons from the remaining polylinker sequence as well as of the amino acid sequences of the FXaStrpA part followed by the L' target sequence.

EXAMPLE 5

N-terminal membrane targeting of streptavidin.

The streptavidin gene extended on the 5' side by a factor Xa protease cleavage site is isolated as a 511 bp fragment from plasmid pFN6 after digestion with BamHI. It contains nucleotides 14 to 524 from SEQ ID NO:2. After filling up the ends with Klenow polymerase this DNA fragment is integrated into the filled up XbaI cleavage site of vector pKSEL5 between the E' and L' target sequences. An in frame gene fusion thereby results in plasmid pAV1 consisting of the E' target sequence and the FXaStrpA sequence. The stop codons occurring on the 3' side of streptavidin remain intact by the cloning which was carried out.

EXAMPLE 6

N- and C-terminal membrane targeting of streptavidin.

The stop codons 5'-TAATAA-3' which are located behind the streptavidin gene in plasmid pAV1 are removed by deletion of a 33 bp long DNA fragment which is produced by partial digestion with HincII and subsequent digestion with XbaI. The streptavidin-specific DNA sequence contains nucleotides 14 to 499 from SEQ ID NO:2. After filling up the plasmid ends with Klenow polymerase and religating, the L' target sequence included on the vector is fused in frame to the E' target sequence and the FXaStrpA sequence (plasmid pAV3). The corresponding gene product is thus provided with an N- as well as a C-terminal target sequence.

EXAMPLE 7

N-terminal membrane targeting of .beta.-galactosidase.

A 3124 bp DNA fragment (SEQ ID NO:3) is isolated from the plasmid pMC1403 (J. Bacteriol. 143 (1980) 971-980) with the aid of PstI and DraI and ligated in the correct orientation into the PstI and NruI restriction sites of the plasmid pKSEL5. The plasmid pLZl which formed contains the first 54 codons of the E' target sequence, 13 linker codons and 1015 codons of the LacZ gene. The PstI/DraI fragment used for plasmid pLZ1 extends in the sequence protocol SEQ ID NO:3 from nucleotide 26 to 3149 inclusive and comprises 3124 bp.

EXAMPLE 8

N- and C-terminal membrane targeting of .beta.-galactosidase.

The 3010 bp LacZ DNA fragment (PstI-EcoRI, nucleotides 26 to 3035 from SEQ ID NO: 3) is isolated from plasmid pMC1403 and is integrated in the correct orientation into the PstI/HindIII restriction site of pKSEL5 after filling up the EcoRI and HindIII ends. In the plasmid pLZ3 thus obtained this results in an in frame fusion of the E' target sequence with the LacZ gene and the L' target sequence.

EXAMPLE 9

C-terminal membrane targeting of .beta.-galactosidase.

Plasmid pLZ3 is digested with EcoRI and partially digested with AccI. The E' target sequence is thereby removed. The fragment contains the nucleotides 29-3035 from SEQ ID NO:3 and is 3007 bp long (after filling up the EcoRI cleavage site). After filling up the protruding DNA ends of the vector and religating, the vector pLZ5 results in which a lacZ-L' fusion gene is present and the gene product of which has a C-terminal membrane target sequence.

EXAMPLE 10

Production of the carrier-bound recombinant proteins via the plasmids pMTVl (SEQ ID NO:4), pkSEL and pMLl (SEQ ID NO:5).

A lysis cassette is present on the plasmids pMTVl and pMLl consisting of the lambda cI857 repressor gene, the lambda promotor/operator system pR on the right side as well as the PhiXl74 lysis gene E. The integration of the foreign gene can be carried out in the multiple cloning site mcs 2 for pMTVl or pkSEL5 (FIG. 1). This is carried out in an analogous manner to that described in Examples 1-9.

EXAMPLE 11

Fermentation and lysis

The plasmid is integrated into E. coli K12 (DSM 2093) and the culture is grown in a shaking flask up to OD 0.8-1.2 at 600 nm whereby the expression of the lysis gene E is repressed by cI857 repressor molecules (Eur. J. Biochem. 180 (1989) 393 to 398). The expression of gene E by thermal inactivation of cI857 repressor molecules is carried out by increasing the temperature to 42.degree. C. during the exponential growth phase of the bacteria. The lysis of E. coli caused by protein E starts between 10 and 30 min after increasing the temperature depending on the culture medium of the bacteria (total medium or minimum medium, under aeration in a shaking water bath). After a further 10 to 30 min the lysis is completed.

EXAMPLE 12

Modified protein E-lysis

The culture is as in Example 11 in which, however, the culture medium is made up to 0.2 mol/1 magnesium sulphate by adding magnesium sulphate solution 30 min prior to increasing the temperature from 28.degree. C. to 42.degree. C. This prevents the lysis of the bacteria despite the expression of gene E.

The cells are harvested by centrifugation 30 min after increasing the temperature. An instantaneous lysis of the cells is effected by resuspension of the cell pellet in low molar buffer (PBS, 1 mmol/1 phosphate buffer, 1 to 10 mmol/1 Tris-HCl pH 6-8) or water. The cell coats which are obtained in this process are denoted bacterial ghosts. Under these conditions, which correspond to a combination of protein E lysis and osmotic shock, a larger lysis structure is obtained in the bacteria. The morphology of the bacterial ghosts is also preserved to a large degree under these conditions.

The bacterial ghosts are washed 2.times. with PBS or 0.9% NaCl for purification (resuspending and centrifuging) and lyophilized.

EXAMPLE 13

Immunization

For the immunization, 10.sup.9 germs (corresponding to 1 mg dry weight of bacterial ghosts) per mouse are administered 4.times. intraperitoneally in 0.9% NaCl at monthly intervals. 8 days after the last immunization serum is obtained and the antibodies are isolated.

EXAMPLE 14

Binding of biotinylated HBc antigen

Bacterial ghosts produced according to example 4, into which streptavidin is integrated via target sequences, are lyophilized. 10 ml of a solution of 20 Ig/ml of a conjugate of hepatitis B core antigen and biotin (produced by reaction of HBcAg with N-hydroxysuccinimide-activated biotin) in 40 mmol/1 phosphate buffer, pH 7.4 is added to 1 mg of this lyophilisate, incubated for 30 min and subsequently washed several times with 40 mmol/1 phosphate buffer, pH 7.4. In this way a carrier-bound HBcAg immunogen is obtained which can be used for immunization and isolation of antibodies.

__________________________________________________________________________SEQUENCE LISTING(1) GENERAL INFORMATION:(iii) NUMBER OF SEQUENCES: 6(2) INFORMATION FOR SEQ ID NO: 1:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 1451 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1:GTCGACCTGC AGGCATGCAAGCTGATCTTCAGACCTGGAGGAGGAGATATGAGGGACAAT60TGGAGAAGTGAATTATATAAATATAAAGTAGTAAAAATTGAACCATTAGGAGTAGCACCC120ACCAAGGCAAAGAGAAGAGTGGTGCAGAGAGAAAAAAGAGCAGTGGGAATAGGAG CTTTG180TTCCTTGGGTTCTTGGGAGCAGCAGGAAGCACTATGGGCGCAGCGTCAATGACGCTGACG240GTACAGGCCAGACAATTATTGTCTGGTATAGTGCAGCAGCAGAACAATTTGCTGAGGGCT300ATTGAGGGCCAACAGCATCTGTTGCAACTCAC AGTCTGGGGCATCAAGCAGCTCCAGGCA360AGAATCCTGGCTGTGGAAAGATACCTAAAGGATCAACAGCTCCTGGGGATTTGGGGTTGC420TCTGGAAAACTCATTTGCACCACTGCTGTGCCTTGGAATGCTAGTTGGAGTAATAAATCT480CTGGAACAGA TTTGGAATAACATGACCTGGATGGAGTGGGACAGAGAAATTAACAATTAC540ACAAGCTTAATACACTCCTTAATTGAAGAATCGCAAAACCAGCAAGAAAAGAATGAACAA600GAATTATTGGAATTAGATAAATGGGCAAGTTTGTGGAATTGGTTTAACATAACAA ATTGG660CTGTGGTATATAAAATTATTCATAATGATAGTAGGAGGCTTGGTAGGTTTAAGAATAGTT720TTTGCTGTACTTTCTATAGTGAATAGAGTTAGGCAGGGATATTCACCATTATCGTTTCAG780ACCCACCTCCCAAACCCGAGGGGACCCGACAG GCCCGAAGGAATAGAAGAAGAAGGTGGA840GAGAGAGACAGAGACAGATCCATTCGATTAGTGAACGGATCCTTAGCACTTATCTGGGAC900GATCTGCGGAGCCTGTGCCTCTTCAGCTACCACCGCTTGAGAGACTTACTCTTGATTGTA960ACGAGGATTG TGGAACTTCTGGGACGCAGGGGGTGGGAAGCCCTCAAATATTGGTGGAAT1020CTCCTACAGTATTGGAGTCAGGAACTAAAGAATAGTGCTGTTAACTTGCTCAATGCCACA1080GCTATAGCAGTAGCTGAGGGGACAGATAGGGTTATAGAATTAGTACAAGCAGCTT ATAGA1140GCCATTCGCCACATACCTAGAAGAATAAGACAGGGCTTGGAAAGGATTTTGCTATAAGAT1200GGGTGGCAAGTGGTCAAAAAGTAGTGTGGTTGGATGGCCTGCTGTAAGGGAAAGAATGAG1260ACGAGCTGAGCCAGCAGCAGATGGGGTGGGAG CAGTATCTCGAGACCTAGAAAAACATGG1320AGCAATCACAAGTAGCAATACAGCAGCTACCAATGCCGATTGTGCTTGGCTAGAAGCACA1380AGAGGAGGAGGAGGTGGGTTTTCCAGTCACACCTCAGGTACCTTTAAGACCAATGACTTA1440CAAGGCAGCT G1451(2) INFORMATION FOR SEQ ID NO: 2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 525 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2:TCTAGAACTAGTG GATCCATCGAGGGTAGGTCTATGGACCCGTCCAAGGACTCCAAAGCT60CAGGTTTCTGCAGCCGAAGCTGGTATCACTGGCACCTGGTATAACCAACTGGGGTCGACT120TTCATTGTGACCGCTGGTGCGGACGGAGCTCTGACTGGCACCTACGAATCTGCGGTTGGT18 0AACGCAGAATCCCGCTACGTACTGACTGGCCGTTATGACTCTGCACCTGCCACCGATGGC240TCTGGTACCGCTCTGGGCTGGACTGTGGCTTGGAAAAACAACTATCGTAATGCGCACAGC300GCCACTACGTGGTCTGGCCAATACGTTGGCGGTGCTGAGGCTCGT ATCAACACTCAGTGG360CTGTTAACATCCGGCACTACCGAAGCGAATGCATGGAAATCGACACTAGTAGGTCATGAC420ACCTTTACCAAAGTTAAGCCTTCTGCTGCTAGCATTGATGCTGCCAAGAAAGCAGGCGTA480AACAACGGTAACCCTCTAGACGCTGTTC AGCAATAATAAGGATCC525(2) INFORMATION FOR SEQ ID NO: 3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 3152 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3:ATGACCATGATTACGAATTGCTGCAGGTCGACG GATCCCGTCGTTTTACAACGTCGTGAC60TGGGAAAACCCTGGCGTTACCCAACTTAATCGCCTTGCAGCACATCCCCCTTTCGCCAGC120TGGCGTAATAGCGAAGAGGCCCGCACCGATCGCCCTTCCCAACAGTTGCGCAGCCTGAAT180GGCGAATGGCGCT TTGCCTGGTTTCCGGCACCAGAAGCGGTGCCGGAAAGCTGGCTGGAG240TGCGATCTTCCTGAGGCCGATACTGTCGTCGTCCCCTCAAACTGGCAGATGCACGGTTAC300GATGCGCCCATCTACACCAACGTAACCTATCCCATTACGGTCAATCCGCCGTTTGTTCCC 360ACGGAGAATCCGACGGGTTGTTACTCGCTCACATTTAATGTTGATGAAAGCTGGCTACAG420GAAGGCCAGACGCGAATTATTTTTGATGGCGTTAACTCGGCGTTTCATCTGTGGTGCAAC480GGGCGCTGGGTCGGTTACGGCCAGGACAGTCGTTTGCCGT CTGAATTTGACCTGAGCGCA540TTTTTACGCGCCGGAGAAAACCGCCTCGCGGTGATGGTGCTGCGTTGGAGTGACGGCAGT600TATCTGGAAGATCAGGATATGTGGCGGATGAGCGGCATTTTCCGTGACGTCTCGTTGCTG660CATAAACCGACTACACAAAT CAGCGATTTCCATGTTGCCACTCGCTTTAATGATGATTTC720AGCCGCGCTGTACTGGAGGCTGAAGTTCAGATGTGCGGCGAGTTGCGTGACTACCTACGG780GTAACAGTTTCTTTATGGCAGGGTGAAACGCAGGTCGCCAGCGGCACCGCGCCTTTCGGC840 GGTGAAATTATCGATGAGCGTGGTGGTTATGCCGATCGCGTCACACTACGTCTGAACGTC900GAAAACCCGAAACTGTGGAGCGCCGAAATCCCGAATCTCTATCGTGCGGTGGTTGAACTG960CACACCGCCGACGGCACGCTGATTGAAGCAGAAGCCTGCGATGTCGGT TTCCGCGAGGTG1020CGGATTGAAAATGGTCTGCTGCTGCTGAACGGCAAGCCGTTGCTGATTCGAGGCGTTAAC1080CGTCACGAGCATCATCCTCTGCATGGTCAGGTCATGGATGAGCAGACGATGGTGCAGGAT1140ATCCTGCTGATGAAGCAGAACAACTTTA ACGCCGTGCGCTGTTCGCATTATCCGAACCAT1200CCGCTGTGGTACACGCTGTGCGACCGCTACGGCCTGTATGTGGTGGATGAAGCCAATATT1260GAAACCCACGGCATGGTGCCAATGAATCGTCTGACCGATGATCCGCGCTGGCTACCGGCG1320ATGAGCGA ACGCGTAACGCGAATGGTGCAGCGCGATCGTAATCACCCGAGTGTGATCATC1380TGGTCGCTGGGGAATGAATCAGGCCACGGCGCTAATCACGACGCGCTGTATCGCTGGATC1440AAATCTGTCGATCCTTCCCGCCCGGTGCAGTATGAAGGCGGCGGAGCCGACACCA CGGCC1500ACCGATATTATTTGCCCGATGTACGCGCGCGTGGATGAAGACCAGCCCTTCCCGGCTGTG1560CCGAAATGGTCCATCAAAAAATGGCTTTCGCTACCTGGAGAGACGCGCCCGCTGATCCTT1620TGCGAATACGCCCACGCGATGGGTAACAGTCTTGG CGGTTTCGCTAAATACTGGCAGGCG1680TTTCGTCAGTATCCCCGTTTACAGGGCGGCTTCGTCTGGGACTGGGTGGATCAGTCGCTG1740ATTAAATATGATGAAAACGGCAACCCGTGGTCGGCTTACGGCGGTGATTTTGGCGATACG1800CCGAACGATCGCCAG TTCTGTATGAACGGTCTGGTCTTTGCCGACCGCACGCCGCATCCA1860GCGCTGACGGAAGCAAAACACCAGCAGCAGTTTTTCCAGTTCCGTTTATCCGGGCAAACC1920ATCGAAGTGACCAGCGAATACCTGTTCCGTCATAGCGATAACGAGCTCCTGCACTGGATG19 80GTGGCGCTGGATGGTAAGCCGCTGGCAAGCGGTGAAGTGCCTCTGGATGTCGCTCCACAA2040GGTAAACAGTTGATTGAACTGCCTGAACTACCGCAGCCGGAGAGCGCCGGGCAACTCTGG2100CTCACAGTACGCGTAGTGCAACCGAACGCGACCGCATGGTCA GAAGCCGGGCACATCAGC2160GCCTGGCAGCAGTGGCGTCTGGCGGAAAACCTCAGTGTGACGCTCCCCGCCGCGTCCCAC2220GCCATCCCGCATCTGACCACCAGCGAAATGGATTTTTGCATCGAGCTGGGTAATAAGCGT2280TGGCAATTTAACCGCCAGTCAG GCTTTCTTTCACAGATGTGGATTGGCGATAAAAAACAA2340CTGCTGACGCCGCTGCGCGATCAGTTCACCCGTGCACCGCTGGATAACGACATTGGCGTA2400AGTGAAGCGACCCGCATTGACCCTAACGCCTGGGTCGAACGCTGGAAGGCGGCGGGCCAT2460TA CCAGGCCGAAGCAGCGTTGTTGCAGTGCACGGCAGATACACTTGCTGATGCGGTGCTG2520ATTACGACCGCTCACGCGTGGCAGCATCAGGGGAAAACCTTATTTATCAGCCGGAAAACC2580TACCGGATTGATGGTAGTGGTCAAATGGCGATTACCGTTGATGTTGAAGT GGCGAGCGAT2640ACACCGCATCCGGCGCGGATTGGCCTGAACTGCCAGCTGGCGCAGGTAGCAGAGCGGGTA2700AACTGGCTCGGATTAGGGCCGCAAGAAAACTATCCCGACCGCCTTACTGCCGCCTGTTTT2760GACCGCTGGGATCTGCCATTGTCAGACATG TATACCCCGTACGTCTTCCCGAGCGAAAAC2820GGTCTGCGCTGCGGGACGCGCGAATTGAATTATGGCCCACACCAGTGGCGCGGCGACTTC2880CAGTTCAACATCAGCCGCTACAGTCAACAGCAACTGATGGAAACCAGCCATCGCCATCTG2940CTGCACGCGG AAGAAGGCACATGGCTGAATATCGACGGTTTCCATATGGGGATTGGTGGC3000GACGACTCCTGGAGCCCGTCAGTATCGGCGGAATTCCAGCTGAGCGCCGGTCGCTACCAT3060TACCAGTTGGTCTGGTGTCAAAAATAATAATAACCGGGCAGGCCATGTCTGCCCGTA TTT3120CGCGTAAGGAAATCCATTATGTACTATTTAAA3152(2) INFORMATION FOR SEQ ID NO: 4:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 5314 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4:AAATTGTAAACGTTAATATTAGACATAATTTATCCTCAAGTAAGGGGCCGAAGCCCCTGC60AATTAAAATTGTTGACCACCTACATACCAAAGACGAGCGCCTTTACGCTTGCCTTTAGTA120CCTCGCAACGGCTGCGGACGACCAGGGCGAGCGCCAGAACG TTTTTTACCTTTAGACATT180ACATCACTCCTTCCGCACGTAATTTTTGACGCACGTTTTCTTCTGCGTCAGTAAGAACGT240CAGTGTTTCCTGCGCGTACACGCAAGGTAAACGCGAACAATTCAGCGGCTTTAACCGGAC300GCTCGACGCCATTAATAATGT TTTCCGTAAATTCAGCGCCTTCCATGATGAGACAGGCCG360TTTGAATGTTGACGGGATGAACATAATAAGCAATGACGGCAGCAATAAACTCAACAGGAG420CAGGAAAGCGAGGGTATCCCACAAAGTCCAGCGTACCATAAACGCAAGCCTCAACGCAGC480G ACGAGCACGAGAGCGGTCAGTAGCAATCCAAACTTTGTTACTCGTCAGAAAATCGAAAT540CATCTTCGGTTAAATCCAAAACGGCAGAAGCCTGAATTCTAGCTAGAGGATCTTTAGCTG600TCTTGGTTTGCCCAAAGCGCATTGCATAATCTTTCAGGGTTATGCGTTG TTCCATACAAC660CTCCTTAGTACATGCAACCATTATCACCGCCAGAGGTAAAATAGTCAACACGCACGGTGT720TAGATATTTATCCCTTGCGGTGATAGATTTAACGTATGAGCACAAAAAAGAAACCATTAA780CACAAGAGCAGCTTGAGGACGCACGTCGC CTTAAAGCAATTTATGAAAAAAAGAAAAATG840AACTTGGCTTATCCCAGGAATCTGTCGCAGACAAGATGGGGATGGGGCAGTCAGGCGTTG900GTGCTTTATTTAATGGCATCAATGCATTAAATGCTTATAACGCCGCATTGCTTACAAAAA960TTCTCAAAG TTAGCGTTGAAGAATTTAGCCCTTCAATCGCCAGAGAAATCTACGAGATGT1020ATGAAGCGGTTAGTATGCAGCCGTCACTTAGAAGTGAGTATGAGTACCCTGTTTTTTCTC1080ATGTTCAGGCAGGGATGTTCTCACCTAAGCTTAGAACCTTTACCAAAGGTGATGCG GAGA1140GATGGGTAAGCACAACCAAAAAAGCCAGTGATTCTGCATTCTGGCTTGAGGTTGAAGGTA1200ATTCCATGACCGCACCAACAGGCTCCAAGCCAAGCTTTCCTGACGGAATGTTAATTCTCG1260TTGACCCTGAGCAGGCTGTTGAGCCAGGTGATTTCT GCATAGCCAGACTTGGGGGTGATG1320AGTTTACCTTCAAGAAACTGATCAGGGATAGCGGTCAGGTGTTTTTACAACCACTAAACC1380CACAGTACCCAATGATCCCATGCAATGAGAGTTGTTCCGTTGTGGGGAAAGTTATCGCTA1440GTCAGTGGCCTGAAGA GACGTTTGGCTGATCGGCAAGGTGTTCTGGTCGGCGCATAGCTG1500ATAACAATTGAGCAAGAATCTTCATCGAATTAGGGGAATTTTCACTCCCCTCAGAACATA1560ACATAGTAAATGGATTGAATTATGAAGAATGGTTTTTATGCGACTTACCGCAGCAAAAAT162 0AAAGGGAAAGATACTTGAAGACGAAAGGGCATTTTGTTAAAATTCGCGTTAAATTTTTGT1680TAAATCAGCTCATTTTTTAACCAATAGGCCGAAATCGGCAAAATCCCTTATAAATCAAAA1740GAATAGACCGAGATAGGGTTGAGTGTTGTTCCAGTTTGGAACA AGAGTCCACTATTAAAG1800AACGTGGACTCCAACGTCAAAGGGCGAAAAACCGTCTATCAGGGCGATGGCCCACTACGT1860GAACCATCACCCTAATCAAGTTTTTTGGGGTCGAGGTGCCGTAAAGCACTAAATCGGAAC1920CCTAAAGGGAGCCCCCGATTTAG AGCTTGACGGGGAAAGCCGGCGAACGTGGCGAGAAAG1980GAAGGGAAGAAAGCGAAAGGAGCGGGCGCTAGGGCGCTGGCAAGTGTAGCGGTCACGCTG2040CGCGTAACCACCACACCCGCCGCGCTTAATGCGCCGCTACAGGGCGCGTCCCATTCGCCA2100TTC AGGCTACGCAACTGTTGGGAAGGGCGATCGGTGCGGGCCTCTTCGCTATTACGCCAG2160CTGGCGAAGGGGGGATGTGCTGCAAGGCGATTAAGTTGGGTAACGCCAGGGTTTTCCCAG2220TCACGACGTTGTAAAACGACGGCCAGTGAATTGTAATACGACTCACTATA GGGCGAATTG2280GAGCTCCACCGCGGTGGCGGCCGCTCTAGTATGGTGCACTCTCAGTACAATCTGCTCTGA2340TGCCGCATAGTTAAGCCAGTATATACACTCCGCTATCGCTACGTGACTGGGTCATGGCTG2400CGCCCCGACACCCGCCAACACCCGCTGACG CGCCCTGACGGGCTTGTCTGCTCCCGGCAT2460CCGCTTACAGACAAGCTGTGACCGTCTCCGGGAGCTGCATGTGTCAGAGGTTTTCACCGT2520CATCACCGAAACGCGCGAGGCAGTAAGGTCGGATGCTTTGTGAGCAATTCGTCCCTTAAG2580TAAGCAATTG CTGTAAAGTCGTCACTGTGCGGATCACCGCTTCCAGTAGCGACAGAAGCA2640ATTGATTGGTAAATTTCGAGAGAAAGATCGCGAGGAAGATCAATACATAAAGAGTTGAAC2700TTCTTTGTTGTCTTCGACATGGGTAATCCTCATGTTTGAATGGCCCTAGAGGATCCGG CC2760AAGCTTGCATGCCTGCAGGTCGACTCTAGAGGATCCCCGACGCTCGACGCCATTAATAAT2820GTTTTCCGTAAATTCAGCGCCTTCCATGATGAGACAGGCCGTTTGAATGTTGACGGGATG2880AACATAATAAGCAATGACGGCAGCAATAAACTCAACAG GAGCAGGAAAGCGAGGGTATCC2940CACAAAGTCCAGCGTACCATAAACGCAAGCCTCAACGCAGCGACGAGCACGAGAGCGGTC3000AGTAGCAATCCAAACTTTGTTACTCGTCAGAAAATCGAAATCATCTTCGGTTAAATCCAA3060AACGGCAGAAGCCTGAAT GAGAATTCGACCTCGAGGGGGGGCCCGGTACCCAGCTTTTGT3120TCCCTTTAGTGAGGGTTAATTCCGAGCTTGGCGTAATCATGGTCATAGCTGTTTCCTGTG3180TGAAATTGTTATCCGCTCACAATTCCACACAACATAGGAGCCGGAAGCATAAAGTGTAAA3240GCCTGGGGTGCCTAATGAGTGAGGTAACTCACATTAATTGCGTTGCGCTCACTGCCCGCT3300TTCCAGTCGGGAAACCTGTCGTGCCAGCTGCATTAATGAATCGGCCAACGCGCGGGGAGA3360GGCGGTTTGCGTATTGGGCGCTCTTCCGCTTCCTCGCTCACTGAC TCGCTGCGCTCGGTC3420GTTCGGCTGCGGCGAGCGGTATCAGCTCACTCAAAGGCGGTAATACGGTTATCCACAGAA3480TCAGGGGATAACGCAGGAAAGAACATGTGAGCAAAAGGCCAGCAAAAGGCCAGGAACCGT3540AAAAAGGCCGCGTTGCTGGCGTTTT TCCATAGGCTCGGCCCCCCTGACGAGCATCACAAA3600AATCGACGCTCAAGTCAGAGGTGGCGAAACCCGACAGGACTATAAAGATACCAGGCGTTC3660CCCCCTGGAAGCTCCCTCGTGCGCTCTCCTGTTCCGACCCTGCCGCTTACCGGATACCTG3720TCCGC CTTTCTCCCTTCGGGAAGCGTGGCGCTTTCTCAATGCTCACGCTGTAGGTATCTC3780AGTTCGGTGTAGGTCGTTCGCTCCAAGCTGGGCTGTGTGCACGAACCCCCCGTTCAGCCC3840GACCGCTGCGCCTTATCCGGTAACTATCGTCTTGAGTCCAACCCGGTAAGAC ACGACTTA3900TCGCCACTGGCAGCAGCCACTGGTAACAGGATTAGCAGAGCGAGGTATGTAGGCGGTGCT3960ACAGAGTTCTTGAAGTGGTGGCCTAACTACGGCTACACTAGAAGGACAGTATTTGGTATC4020TGCGCTCTGCTGAAGCCAGTTACCTTCGGAAA AAGAGTTGGTAGCTCTTGATCCGGCAAA4080CAAACCACCGCTGGTAGCGGTGGTTTTTTTGTTTGCAAGCAGCAGATTACGCGCAGAAAA4140AAAGGATCTCAAGAAGATCCTTTGATCTTTTCTACGGGGTCTGACGCTCAGTGGAACGAA4200AACTCACGTTAA GGGATTTTGGTCATGAGATTATCAAAAAGGATCTTCACCTAGATCCTT4260TTAAATTAAAAATGAAGTTTTAAATCAATCTAAAGTATATATGAGTAAACTTGGTCTGAC4320AGTTACCAATGCTTAATCAGTGAGGCACCTATCTCAGCGATCTGTCTATTTCGTTCATCC 4380ATAGTTGCCTGACTGCCCGTCGTGTAGATAACTACGATACGGGAGGGCTTACCATCTGGC4440CCCAGTGCTGCAATGATACCGCGAGACCCACGCTCACCGGCTCCAGATTTATCAGCAATA4500AACCAGCCAGCCGGAAGGGCCGAGCGCAGAAGTGGTCCTG CAACTTTATCCGCCTCCATC4560CAGTCTATTAATTGTTGCCGGGAAGCTAGAGTAAGTAGTTCGCCAGTTAATAGTTTGCGC4620AACGTTGTTGCCATTGCTACAGGCATCGTGGTGTCACGCTCGTCGTTTGGTATGGCTTCA4680TTCAGCTCCGGTTCCCAACG ATCAAGGCGAGTTACATGATCCCCCATGTTGTGAAAAAAA4740GCGGTTAGCTCCTTCGGTCCTCCGATCGTTGTCAGAAGTAAGTTGGCCGCAGTGTTATCA4800CTCATGCTTATGGCAGCACTGCATAATTCTCTTACTGTCATGCCATCCGTAAGATGCTTT4860 TCTGTGACTGGTGAGTACTCAACCAAGTCATTCTGAGAATAGTGTATGCGGCGACCGAGT4920TGCTCTTGCCCGGCGTCAATACGGGATAATACCGCGCCACATAGCAGAACTTTAAAAGTG4980CTCATCATTGGAAAACGTTCTTCGGGGCGAAAACTCTCAAGGATCTT ACCGCTGTTGAGA5040TCCAGTTCGATGTAACCCACTCGTGCACCCAACTGATCTTCAGCATCTTTTACTTTCACC5100AGCGTTTCTGGGTGAGCAAAAACAGGAAGGCAAAATGCCGCAAAAAAGGGAATAAGGGCG5160ACACGGAAATGTTGAATACTCATACTC TTCCTTTTTCAATATTATTGAAGCATTTATCAG5220GGTTATTGTCTCATGAGCGGATACATATTTGAATGTATTTAGAAAAATAAACAAATAGGG5280GTTCCGCGCACATTTCCCCGAAAAGTGCCACCTG5314(2) INFORMATION FOR SEQ ID NO: 5:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 7641 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5:GACGCCGGGCAAGAGCAACTCGGTCGCCGCATACACTATTCTCAGAATGACTTGGTTGAG60TACTCACCAGT CACAGAAAAGCATCTTACGGATGGCATGACAGTAAGAGAATTATGCAGT120GCTGCCATAACCATGAGTGATAACACTGCGGCCAACTTACTTCTGACAACGATCGGAGGA180CCGAAGGAGCTAACCGCTTTTTTGCACAACATGGGGGATCATGTAACTCGCCTTGATCG T240TGGGAACCGGAGCTGAATGAAGCCATACCAAACGACGAGCGTGACACCACGATGCCTGCA300GCAATGGCAACAACGTTGCGCAAACTATTAACTGGCGAACTACTTACTCTAGCTTCCCGG360CAACAATTAATAGACTGGATGGAGGCGGATAAAGTTGCA GGACCACTTCTGCGCTCGGCC420CTTCCGGCTGGCTGGTTTATTGCTGATAAATCTGGAGCCGGTGAGCGTGGGTCTCGCGGT480ATCATTGCAGCACTGGGGCCAGATGGTAAGCCCTCCCGTATCGTAGTTATCTACACGACG540GGGAGTCAGGCAACTATGG ATGAACGAAATAGACAGATCGCTGAGATAGGTGCCTCACTG600ATTAAGCATTGGTAACTGTCAGACCAAGTTTACTCATATATACTTTAGATTGATTTAAAA660CTTCATTTTTAATTTAAAAGGATCTAGGTGAAGATCCTTTTTGATAATCTCATGACCAAA720ATCCCTTAACGTGAGTTTTCGTTCCACTGAGCGTCAGACCCCTTAATAAGATGATCTTCT780TGAGATCGTTTTGGTCTGCGCGTAATCTCTTGCTCTGAAAACGAAAAAACCGCCTTGCAG840GGCGGTTTTTCGAAGGTTCTCTGAGCTACCAACTCTTTGAACCGAG GTAACTGGCTTGGA900GGAGCGCAGTCACCAAAACTTGTCCTTTCAGTTTAGCCTTAACCGGCGCATGACTTCAAG960ACTAACTCCTCTAAATCAATTACCAGTGGCTGCTGCCAGTGGTGCTTTTGCATGTCTTTC1020CGGGTTGGACTCAAGACGATAGTTAC CGGATAAGGCGCAGCGGTCGGACTGAACGGGGGG1080TTCGTGCATACAGTCCAGCTTGGAGCGAACTGCCTACCCGGAACTGAGTGTCAGGCGTGG1140AATGAGACAAACGCGGCCATAACAGCGGAATGACACCGGTAAACCGAAAGGCAGGAACAG1200GAGAGC GCACGAGGGAGCCGCCAGGGGAAACGCCTGGTATCTTTATAGTCCTGTCGGGTT1260TCGCCACCACTGATTTGAGCGTCAGATTTCGTGATGCTTGTCAGGGGGGCGGAGCCTATG1320GAAAAACGGCTTTGCCGCGGCCCTCTCACTTCCCTGTTAAGTATCTTCCTGGC ATCTTCC1380AGGAAATCTCCGCCCCGTTCGTAAGCCATTTCCGCTCGCCGCAGTCGAACGACCGAGCGT1440AGCGAGTCAGTGAGCGAGGAAGCGGAATATATCCTGTATCACATATTCTGCTGACGCACC1500GGTGCAGCCTTTTTTCTCCTGCCACATGAAGCA CTTCACTGACACCCTCATCAGTGCCAA1560CATAGTAAGCCAGTATACACTCCGCTAGCGCTGAGGTCTGCCTCGTGAAGAAGGTGTTGC1620TGACTCATACCAGGCCTGAATCGCCCCATCATCCAGCCAGAAAGTGAGGGAGCCACGGTT1680GATGAGAGCTTTG TTGTAGGTGGACCAGTTGGTGATTTTGAACTTTTGCTTTGCCACGGA1740ACGGTCTGCGTTGTCGGGAAGATGCGTGATCTGATCCTTCAACTCAGCAAAAGTTCGATT1800TATTCAACAAAGCCACGTTGTGTCTCAAAATCTCTGATGTTACATTGCACAAGATAAAAA 1860TATATCATCATGAACAATAAAACTGTCTGCTTACATAAACAGTAATACAAGGGGTGTTAT1920GAGCCATATTCAACGGGAAACGTCTTGCTCGAGGCCGCGATTAAATTCCAACATGGATGC1980TGATTTATATGGGTATAAATGGGCTCGCGATAATGTCGGG CAATCAGGTGCGACAATCTA2040TCGATTGTATGGGAAGCCCGATGCGCCAGAGTTGTTTCTGAAACATGGCAAAGGTAGCGT2100TGCCAATGATGTTACAGATGAGATGGTCAGACTAAACTGGCTGACGGAATTTATGCCTCT2160TCCGACCATCAAGCATTTTA TCCGTACTCCTGATGATGCATGGTTACTCACCACTGCGAT2220CCCCGGGAAAACAGCATTCCAGGTATTAGAAGAATATCCTGATTCAGGTGAAAATATTGT2280TGATGCGCTGGCAGTGTTCCTGCGCCGGTTGCATTCGATTCCTGTTTGTAATTGTCCTTT2340 TAACAGCGATCGCGTATTTCGTCTCGCTCAGGCGCAATCACGAATGAATAACGGTTTGGT2400TGATGCGAGTGATTTTGATGACGAGCGTAATGGCTGGCCTGTTGAACAAGTCTGGAAAGA2460AATGCATAAGCTTTTGCCATTCTCACCGGATTCAGTCGTCACTCATGG TGATTTCTCACT2520TGATAACCTTATTTTTGACGAGGGGAAATTAATAGGTTGTATTGATGTTGGACGAGTCGG2580AATCGCAGACCGATACCAGGATCTTGCCATCCTATGGAACTGCCTCGGTGAGTTTTCTCC2640TTCATTACAGAAACGGCTTTTTCAAAAA TATGGTATTGATAATCCTGATATGAATAAATT2700GCAGTTTCATTTGATGCTCGATGAGTTTTTCTAATCAGAATTGGTTAATTGGTTGTAACA2760CTGGCAGAGCATTACGCTGACTTGACGGGACGGCGGCTTTGTTGAATAAATCGAACTTTT2820GCTGAGTT GAAGGATCAGATCACGCATCTTCCCGACAACGCAGACCGTTCCGTGGCAAAG2880CAAAAGTTCAAAATCACCAACTGGTCCACCTACAACAAAGCTCTCATCAACCGTGGCTCC2940CTCACTTTCTGGCTGGATGATGGGGCGATTCAGGCCTGGTATGAGTCAGCAACAC CTTCT3000TCACGAGGCAGACCTCAGCGCTCAAAGATGCAGGGGTAAAAGCTAACCGCATCTTTACCG3060ACAAGGCATCCGGCAGTTCAACAGATCGGGAAGGGCTGGATTTGCTGAGGATGAAGGTGG3120AGGAAGGTGATGTCATTCTGGTGAAGAAGCTCGAC CGTCTTGGCCGCGACACCGCCGACA3180TGATCCAACTGATAAAAGAGTTTGATGCTCAGGGTGTAGCGGTTCGGTTTATTGACGACG3240GGATCAGTACCGACGGTGATATGGGGCAAATGGTGGTCACCATCCTGTCGGCTGTGGCAC3300AGGCTGAACGCCGGA GGATCCAGTTCGATGTAACCCACTCGTGCACCCAACTGATCTTCA3360GCATCTTTTACTTTCACCAGCGTTTCTGGGTGAGCAAAAACAGGAAGGCAAAATGCCGCA3420AAAAAGGGAATAAGGGCGACACGGAAATGTTGAATACTCATACTCTTCCTTTTTCAATAT34 80TATTGAAGCATTTATCAGGGTTATTGTCTCATGAGCGGATACATATTTGAATGTATTTAG3540AAAAATAAACAAATAGGGGTTCCGCGCACATTTCCCCGAAAAGTGCCACCTGACGTCTAA3600GAAACCATTATTATCATGACATTAACCTATAAAAATAGGCGT ATCACGAGGCCCTTTCGT3660CTTCAAGTATCTTTCCCTTTATTTTTGCTGCGGTAAGTCGCATAAAAACCATTCTTCATA3720ATTCAATCCATTTACTATGTTATGTTCTGAGGGGAGTGAAAATTCCCCTAATTCGATGAA3780GATTCTTGCTCAATTGTTATCA GCTATGCGCCGACCAGAACACCTTGCCGATCAGCCAAA3840CGTCTCTTCAGGCCACTGACTAGCGATAACTTTCCCCACAACGGAACAACTCTCATTGCA3900TGGGATCATTGGGTACTGTGGGTTTAGTGGTTGTAAAAACACCTGACCGCTATCCCTGAT3960CA GTTTCTTGAAGGTAAACTCATCACCCCCAAGTCTGGCTATGCAGAAATCACCTGGCTC4020AACAGCCTGCTCAGGGTCAACGAGAATTAACATTCCGTCAGGAAAGCTTGGCTTGGAGCC4080TGTTGGTGCGGTCATGGAATTACCTTCAACCTCAAGCCAGAATGCAGAAT CACTGGCTTT4140TTTGGTTGTGCTTACCCATCTCTCCGCATCACCTTTGGTAAAGGTTCTAAGCTTAGGTGA4200GAACATCCCTGCCTGAACATGAGAAAAAACAGGGTACTCATACTCACTTCTAAGTGACGG4260CTGCATACTAACCGCTTCATACATCTCGTA GATTTCTCTGGCGATTGAAGGGCTAAATTC4320TTCAACGCTAACTTTGAGAATTTTTGTAAGCAATGCGGCGTTATAAGCATTTAATGCATT4380GATGCCATTAAATAAAGCACCAACGCCTGACTGCCCCATCCCCATCTTGTCTGCGACAGA4440TTCCTGGGAT AAGCCAAGTTCATTTTTCTTTTTTTCATAAATTGCTTTAAGGCGACGTGC4500GTCCTCAAGCTGCTCTTGTGTTAATGGTTTCTTTTTTGTGCTCATACGTTAAATCTATCA4560CCGCAAGGGATAAATATCTAACACCGTGCGTGTTGACTATTTTACCTCTGGCGGTGA TAA4620TGGTTGCATGTACTAAGGAGGTTGTATGGAACAACGCATAACCCTGAAAGATTATGCAAT4680GCGCTTTGGGCAAACCAAGACAGCTAAAGATCCTCTAGCTAGAATTCAGGCTTCTGCCGT4740TTTGGATTTAACCGAAGATGATTTCGATTTTCTGACG AGTAACAAAGTTTGGATTGCTAC4800TGACCGCTCTCGTGCTCGTCGCTGCGTTGAGGCTTGCGTTTATGGTACGCTGGACTTTGT4860GGGATACCCTCGCTTTCCTGCTCCTGTTGAGTTTATTGCTGCCGTCATTGCTTATTATGT4920TCATCCCGTCAACATTC AAACGGCCTGTCTCATCATGGAAGGCGCTGAATTTACGGAAAA4980CATTATTAATGGCGTCGAGCGTCCGGTTAAAGCCGCTGAATTGTTCGCGTTTACCTTGCG5040TGTACGCGCAGGAAACACTGACGTTCTTACTGACGCAGAAGAAAACGTGCGTCAAAAATT5100ACGTGCGGAAGGAGTGATGTAATGTCTAAAGGTAAAAAACGTTCTGGCGCTCGCCCTGGT5160CGTCCGCAGCCGTTGCGAGGTACTAAAGGCAAGCGTAAAGGCGCTCGTCTTTGGTATGTA5220GGTGGTCAACAATTTTAATTGCAGGGGCTTCGGCCCCTTACTTG AGGATAAATTATGTCT5280AATATTCAAACTGGCGCCGAGCGTATGCCGCATGACCTTTCCCATCTTGGCTTCCTTGCT5340GGTCAGATTGGTCGTCTTATTACCATTTCAACTACTCCGGTTATCGCTGGCGACTCCTTC5400GAGATGGACGCCGTTGGCGCTCTC CGTCTTTCTCCATTGCGTCGTGGCCTTGCTATTGAC5460TCTACTGTAGACATTTTTACTTTTTATGTCCCTCATCGTCACGTTTATGGTGAACAGTGG5520ATTAAGTTCATGAAGGATGGTGTTAATGCCACTCCTCTCCCGACTGTTAACACTACTGGT5580TATA TTGACCATGCCGCTTTTCTTGGCACGATTAACCCTGATACCAATAAAATCCCTAAG5640CATTTGTTTCAGGGTTATTTGAATATCTATAACAACTATTTTAAAGCGCCGTGGATGCCT5700GACCGTACCGAGGCTAACCCTAATGAGAATTCTCATGTTTGACAGCTTATC ATCGATAAG5760CTTTAATGCGGTAGTTTATCACAGTTAAATTGCTAACGCAGTCAGGCACCGTGTATGAAA5820TCTAACAATGCGCTCATCGTCATCCTCGGCACCGTCACCCTGGATGCTGTAGGCATAGGC5880TTGGTTATGCCGGTACTGCCGGGCCTCTTGC GGGATATCGTCCATTCCGACAGCATCGCC5940AGTCACTATGGCGTGCTGCTAGCGCTATATGCGTTGATGCAATTTCTATGCGCACCCGTT6000CTCGGAGCACTGTCCGACCGCTTTGGCCGCCGCCCAGTCCTGCTCGCTTCGCTACTTGGA6060GCCACTATCGA CTACGCGATCATGGCGACCACACCCGTCCTGTGGATCCGGATCAGCAGG6120TGGAAGAGGGACTGGATTCCAAAGTTCTCAATGCTGCTTGCTGTTCTTGAATGGGGGGTC6180GTTGACGACGACATGGCTCGATTGGCGCGACAAGTTGCTGCGATTCTCACCAATAAAAA A6240CGCCCGGCGGCAACCGAGCGTTCTGAACAAATCCAGATGGAGTTCTGAGGTCATTACTGG6300ATCGCCGGATCTGAATTGCTATGTTTAGTGAGTTGTATCTATTTATTTTTCAATAAATAC6360AATTGGTTATGTGTTTTGGGGGCGATCGTGAGGCAAAGA AAACCCGGCGCTGAGGCCGGA6420AGCATAAAGTGTAAAGCCTGGGGTGCCTAATGAGTGAGCTAACTCACATTAATTGCGTTG6480CGCTCACTGCCCGCTTTCCAGTCGGGAAACCTGTCGTGCCAGCTGCATTAATGAATCGGC6540CAACGCGCGGGGAGAGGCG GTTTGCGTATTGGGCGCCAGGGTGGTTTTTCTTTTCACCAG6600TGAGACGGGCAACAGCTGATTGCCCTTCACCGCCTGGCCCTGAGAGAGTTGCAGCAAGCG6660GTCCACGCTGGTTTGCCCCAGCAGGCGAAAATCCTGTTTGATGGTGGTTGACGGCGGGAT6720ATAACATGAGCTGTCTTCGGTATCGTCGTATCCCACTACCGAGATATCCGCACCAACGCG6780CAGCCCGGACTCGGTAATGGCGCGCATTGCGCCCAGCGCCATCTGATCGTTGGCAACCAG6840CATCGCAGTGGGAACGATGCCCTCATTCAGCATTTGCATGGTTTGT TGAAAACCGGACAT6900GGCACTCCAGTCGCCTTCCCGTTCCGCTATCGGCTGAATTTGATTGCGAGTGAGATATTT6960ATGCCAGCCAGCCAGACGCAGACGCGCCGAGACAGAACTTAATGGGCCCGCTAACAGCGC7020GATTTGCTGGTGACCCAATGCGACCA GATGCTCCACGCCCAGTCGCGTACCGTCTTCATG7080GGAGAAAATAATACTGTTGATGGGTGTCTGGTCAGAGACATCAAGAAATAACGCCGGAAC7140ATTAGTGCAGGCAGCTTCCACAGCAATGGCATCCTGGTCATCCAGCGGATAGTTAATGAT7200CAGCCC ACTGACGCGTTGCGCGAGAAGATTGTGCACCGCCGCTTTACAGGCTTCGACGCC7260GCTTCGTTCTACCATCGACACCACCACGCTGGCACCCAGTTGATCGGCGCGAGATTTAAT7320CGCCGCGACAATTTGCGACGGCGCGTGCAGGGCCAGACTGGAGGTGGCAACGC CAATCAG7380CAACGACTGTTTGCCCGCCAGTTGTTGTGCCACGCGGTTGGGAATGTAATTCAGCTCCGC7440CATCGCCGCTTCCACTTTTTCCCGCGTTTTCGCAGAAACGTGGCTGGCCTGGTTCACCAC7500GCGGGAAACGGTCTGATAAGAGACACCGGCATA CTCTGCGACATCGTATAACGTTACTGG7560TTTCACATTCACCACCCTGAATTGACTCTCTTCCGGCGCTATCATGCCATACCGCGAAAG7620GTTTTGCGCCATTCGATGGTG7641(2) INFORMATION FOR SEQ ID NO: 6: (i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 3681 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 6:AAATTGTAAACGTTAATATTTTGTTAAAATTCGCGTTAAATTTTTGTTAAATCAGCTCAT60TTTTTAACCAATAGGCCG AAATCGGCAAAATCCCTTATAAATCAAAAGAATAGACCGAGA120TAGGGTTGAGTGTTGTTCCAGTTTGGAACAAGAGTCCACTATTAAAGAACGTGGACTCCA180ACGTCAAAGGGCGAAAAACCGTCTATCAGGGCGATGGCCCACTACGTGAACCATCACCCT240AATCAAGTTTTTTGGGGTCGAGGTGCCGTAAAGCACTAAATCGGAACCCTAAAGGGAGCC300CCCGATTTAGAGCTTGACGGGGAAAGCCGGCGAACGTGGCGAGAAAGGAAGGGAAGAAAG360CGAAAGGAGCGGGCGCTAGGGCGCTGGCAAGTGTAGCGGTCACGC TGCGCGTAACCACCA420CACCCGCCGCGCTTAATGCGCCGCTACAGGGCGCGTCCCATTCGCCATTCAGGCTACGCA480ACTGTTGGGAAGGGCGATCGGTGCGGGCCTCTTCGCTATTACGCCAGCTGGCGAAGGGGG540GATGTGCTGCAAGGCGATTAAGTTG GGTAACGCCAGGGTTTTCCCAGTCACGACGTTGTA600AAACGACGGCCAGTGAATTGTAATACGACTCACTATAGGGCGAATTGGAGCTCCACCGCG660GTGGCGGCCGCTCTAGTATGGTGCACTCTCAGTACAATCTGCTCTGATGCCGCATAGTTA720AGCCA GTATATACACTCCGCTATCGCTACGTGACTGGGTCATGGCTGCGCCCCGACACCC780GCCAACACCCGCTGACGCGCCCTGACGGGCTTGTCTGCTCCCGGCATCCGCTTACAGACA840AGCTGTGACCGTCTCCGGGAGCTGCATGTGTCAGAGGTTTTCACCGTCATCA CCGAAACG900CGCGAGGCAGTAAGGTCGGATGCTTTGTGAGCAATTCGTCCCTTAAGTAAGCAATTGCTG960TAAAGTCGTCACTGTGCGGATCACCGCTTCCAGTAGCGACAGAAGCAATTGATTGGTAAA1020TTTCGAGAGAAAGATCGCGAGGAAGATCAATA CATAAAGAGTTGAACTTCTTTGTTGTCT1080TCGACATGGGTAATCCTCATGTTTGAATGGCCCTAGAGGATCCGGCCAAGCTTGCATGCC1140TGCAGGTCGACTCTAGAGGATCCCCGACGCTCGACGCCATTAATAATGTTTTCCGTAAAT1200TCAGCGCCTTCC ATGATGAGACAGGCCGTTTGAATGTTGACGGGATGAACATAATAAGCA1260ATGACGGCAGCAATAAACTCAACAGGAGCAGGAAAGCGAGGGTATCCCACAAAGTCCAGC1320GTACCATAAACGCAAGCCTCAACGCAGCGACGAGCACGAGAGCGGTCAGTAGCAATCCAA 1380ACTTTGTTACTCGTCAGAAAATCGAAATCATCTTCGGTTAAATCCAAAACGGCAGAAGCC1440TGAATGAGAATTCGACCTCGAGGGGGGGCCCGGTACCCAGCTTTTGTTCCCTTTAGTGAG1500GGTTAATTCCGAGCTTGGCGTAATCATGGTCATAGCTGTT TCCTGTGTGAAATTGTTATC1560CGCTCACAATTCCACACAACATAGGAGCCGGAAGCATAAAGTGTAAAGCCTGGGGTGCCT1620AATGAGTGAGGTAACTCACATTAATTGCGTTGCGCTCACTGCCCGCTTTCCAGTCGGGAA1680ACCTGTCGTGCCAGCTGCAT TAATGAATCGGCCAACGCGCGGGGAGAGGCGGTTTGCGTA1740TTGGGCGCTCTTCCGCTTCCTCGCTCACTGACTCGCTGCGCTCGGTCGTTCGGCTGCGGC1800GAGCGGTATCAGCTCACTCAAAGGCGGTAATACGGTTATCCACAGAATCAGGGGATAACG1860 CAGGAAAGAACATGTGAGCAAAAGGCCAGCAAAAGGCCAGGAACCGTAAAAAGGCCGCGT1920TGCTGGCGTTTTTCCATAGGCTCGGCCCCCCTGACGAGCATCACAAAAATCGACGCTCAA1980GTCAGAGGTGGCGAAACCCGACAGGACTATAAAGATACCAGGCGTTC CCCCCTGGAAGCT2040CCCTCGTGCGCTCTCCTGTTCCGACCCTGCCGCTTACCGGATACCTGTCCGCCTTTCTCC2100CTTCGGGAAGCGTGGCGCTTTCTCAATGCTCACGCTGTAGGTATCTCAGTTCGGTGTAGG2160TCGTTCGCTCCAAGCTGGGCTGTGTGC ACGAACCCCCCGTTCAGCCCGACCGCTGCGCCT2220TATCCGGTAACTATCGTCTTGAGTCCAACCCGGTAAGACACGACTTATCGCCACTGGCAG2280CAGCCACTGGTAACAGGATTAGCAGAGCGAGGTATGTAGGCGGTGCTACAGAGTTCTTGA2340AGTGGTG GCCTAACTACGGCTACACTAGAAGGACAGTATTTGGTATCTGCGCTCTGCTGA2400AGCCAGTTACCTTCGGAAAAAGAGTTGGTAGCTCTTGATCCGGCAAACAAACCACCGCTG2460GTAGCGGTGGTTTTTTTGTTTGCAAGCAGCAGATTACGCGCAGAAAAAAAGGAT CTCAAG2520AAGATCCTTTGATCTTTTCTACGGGGTCTGACGCTCAGTGGAACGAAAACTCACGTTAAG2580GGATTTTGGTCATGAGATTATCAAAAAGGATCTTCACCTAGATCCTTTTAAATTAAAAAT2640GAAGTTTTAAATCAATCTAAAGTATATATGAGTA AACTTGGTCTGACAGTTACCAATGCT2700TAATCAGTGAGGCACCTATCTCAGCGATCTGTCTATTTCGTTCATCCATAGTTGCCTGAC2760TGCCCGTCGTGTAGATAACTACGATACGGGAGGGCTTACCATCTGGCCCCAGTGCTGCAA2820TGATACCGCGAGAC CCACGCTCACCGGCTCCAGATTTATCAGCAATAAACCAGCCAGCCG2880GAAGGGCCGAGCGCAGAAGTGGTCCTGCAACTTTATCCGCCTCCATCCAGTCTATTAATT2940GTTGCCGGGAAGCTAGAGTAAGTAGTTCGCCAGTTAATAGTTTGCGCAACGTTGTTGCCA3 000TTGCTACAGGCATCGTGGTGTCACGCTCGTCGTTTGGTATGGCTTCATTCAGCTCCGGTT3060CCCAACGATCAAGGCGAGTTACATGATCCCCCATGTTGTGAAAAAAAGCGGTTAGCTCCT3120TCGGTCCTCCGATCGTTGTCAGAAGTAAGTTGGCCGCAGTG TTATCACTCATGCTTATGG3180CAGCACTGCATAATTCTCTTACTGTCATGCCATCCGTAAGATGCTTTTCTGTGACTGGTG3240AGTACTCAACCAAGTCATTCTGAGAATAGTGTATGCGGCGACCGAGTTGCTCTTGCCCGG3300CGTCAATACGGGATAATACCG CGCCACATAGCAGAACTTTAAAAGTGCTCATCATTGGAA3360AACGTTCTTCGGGGCGAAAACTCTCAAGGATCTTACCGCTGTTGAGATCCAGTTCGATGT3420AACCCACTCGTGCACCCAACTGATCTTCAGCATCTTTTACTTTCACCAGCGTTTCTGGGT3480G AGCAAAAACAGGAAGGCAAAATGCCGCAAAAAAGGGAATAAGGGCGACACGGAAATGTT3540GAATACTCATACTCTTCCTTTTTCAATATTATTGAAGCATTTATCAGGGTTATTGTCTCA3600TGAGCGGATACATATTTGAATGTATTTAGAAAAATAAACAAATAGGGGT TCCGCGCACAT3660TTCCCCGAAAAGTGCCACCTG3681

Claims

1. Immunogen comprising a non-lytic fusion protein bound to a portion of a gram negative bacterial cell membrane, wherein said fusion protein comprises:

(i) one hydrophobic, non-lytically active protein domain capable of integration into a gram negative bacterial cell membrane wherein said hydrophobic, non-lytically active protein domain is selected from the group consisting of: (a) amino acids 1 to 54 of protein E of phage Phix174, and (b) amino acids 21 to 75 of protein L of phage MS2, and

(ii) a protein foreign to a gram negative bacteria in which said fusion protein is expressed.

2. The immunogen of claim 1, wherein said at least one hydrophobic, non-lytically active protein domain and said foreign protein are linked by a hydrophilic amino acid sequence of from 2 to 100 amino acids.

3. The immunogen of claim 1, wherein said hydrophic, non-lytically active protein domain and said protein foreign to said gram negative bacteria are linked to each other via from 10 to 16 amino acids which have a .beta. pleated secondary structure.

4. The immunogen bacteria of claim 1, wherein said protein foreign to said gram negative bacteria is antigenic.

5. The immunogen of claim 1, further comprising a non-covalently bound binding partner bound to said foreign protein.

6. The immunogen of claim 1, further comprising an additional substance bound to said binding partner.

7. The immunogen of claim 5, wherein said protein foreign to said gram negative bacteria comprises the protein portion of streptavidin or avidin.

8. The immunogen of claim 5, wherein said covalently bound binding partner is a biotinylated antigen.