Process for the microbiological preparation of human serum albumin

The present invention relates to protein synthesis.
More especially, the invention provides a process for the synthesis of human serum albumin by a bacterium, which has been subjected to in vitro genetic manipulation techniques to obtain a concerted rearrangement of deoxyribonucleic acid sequences.
Human serum albumin is a protein consisting of 585 amino acids which does not contain associated glycoside residues and has a molecular weight of the order of 66,000 daltons.
Genetically, human serum albumin is encoded in man by two codominant autosomal allelic genes. The genes for human serum albumin are notoriously polymorphic, and at least twenty-four variants of serum albumin are known, differentiated by their electrophoretic behaviour (Shell and Blumberg, "The genetics of human serum albumin", in "Albumin Structure, Function and Uses", Rosenoer, Oratz and Rothschild eds., Pergamon Press, 1977).
Serum albumin is synthesized in the hepatocytes, and then excreted into the serum in which it constitutes the most abundant protein, with mean concentrations of the order of 4 g/100 ml of serum. It performs a major physiological role in the maintenance of the oncotic pressure of the plasma, and thus contributes to the stability of the balance between the internal (cellular) environment and the external (circulating) environment, which balance provides, among other functions, for the maintenance of a level of cell hydration which is compatible with the normal physiological functioning of the body.
Human serum albumin also performs a role in the transport of "natural" hydrophobic molecules (steroids and bile salts, for example) and drug molecules to their sites of action.
This explains why human serum albumin is used both in the therapy of blood volume disorders, for example posthaemorrhagic acute hypovolaemia or extensive burns, and in supportive therapy in so-called volume expansion solutions in general surgery, and in the treatment of dehydration states (for example nephrotic syndromes), all these uses demanding the supply of considerable amounts of serum albumin (several tens of grammes per day per patient).
Human serum albumin is at present extracted from serum by techniques derived from that of E. J. Cohn et al., J. Am. Chem. Soc. (1946), 68, p. 459 et seq., or from placenta by the technique of J. Liautaud et al., 13th Internat. Congress of IABS, Budapest; A: Purification of Proteins, Development of Biological Standard (1973) Karger, ed., Bale, 27, p. 107 et seq. These sources, which hardly meet the requirements of the world market, suffer from several defects, inter alia their uncertain nature. Moreover, they are not devoid of the risk of contamination (hepatitis, for example, and more recently acquired immunodeficiency syndrome), and this would have dramatic consequences when the protein was used in therapy.
In vitro genetic recombination techniques now offer the possibility of making a micro-organism, for example the Escherichia coli bacterium, synthesize any protein or any polypeptide and, in theory, doing this in unlimited quantities (see for example F. Gros et al., Sciences de La Vie et Societe, Documentation Francaise ed., 1979).
Since the classical experiments of F. Jacob et al., it is known that DNA contains, on the one hand a group of so-called "structural" genes, that is to say genes which code for a given protein, and on the other hand so-called "regulator" genes, that is to say genes capable of modulating the expression of the structural genes, the combination of the two types forming an entity known as an "operon".
Research in molecular biology and the development of DNA sequencing techniques [F. Sanger and A. R. Coulson, J. Mol. Biol. (1975), 94, p. 441 et seq., A. M. Maxam and W. Gilbert, Proc. Natl. Acad. Sci. (USA) (1977), 74, p. 560 et seq.] have made it possible to specify the organization of the operon as it had been conceived by F. Jacob and J. Monod [F. Jacob and J. Monod, Cold Spring Harbor Symp. Quant. Biol. (1961), 26, p. 193 et seq.; F. Jacob and J. Monod, J. Mol. Biol. (1961), 26 p. 318 et seq.], and to identify the special features of the primary structure of the two types of gene.
Thus, all structural genes are enclosed by a so-called "translation initiation" codon (ATG) and a "stop" codon. The function of the initiation codon is to bind a transfer RNA bearing a formylmethionine. The protein chain will elongate from this formylmethionine by successive attachment of amino acids encoded by the structural gene; the "stop" codon will finally cause the elongation to stop and bring about the release of the newly formed protein.
As regards the regulating genes (promoters, repressors), a promoter, for example, being defined as a DNA fragment to which RNA polymerase is bound, it has been possible to identify the most highly conserved sequences [D. Pribnow, Proc. Natl. Acad. Sci. (USA) (1975), 72, p. 784 et seq.]; similarly, it has been possible to define the most highly conserved DNA sequences at the level of the ribosome binding sites (RBS) [J. Shine and L. Dalgarno, Nature (1975), 254, p. 34 et seq.], which sites perform a role in the translation of the transcribed RNA to protein.
Thus, the bacterial regulator genes can hence be defined by their functional properties and also by their primary sequence, and in vitro genetic recombination techniques turn this to good account to place any structural gene under their control, this being possible as a result of the existence of "restriction enzymes" which cut the DNA at specific points [H. O. Smith and K. W. Wilcox, J. Mol. Biol. (1970), 51, p. 379 et seq., M. Meselson and R. Yuan, Nature (1968), 217, p. 1110 et seq., R. J. Roberts, Nucleic Acids Res. (1982), 1, p. 135 et seq.].
The techniques used, which are in other respects known, employ the concerted use of these enzymes to cut the DNA at predetermined points, and enzymes known as "ligases" to link the fragments together [P. E. Loban and A. D. Kaiser, J. Mol. Biol. (1973), 78, p. 453 et seq.] The assembly is carried by "vectors" (plasmids or bacteriophages) capable of being introduced into a bacterium such as E. coli by processes which are in other respects known, and of being maintained there during the growth of the host bacterium [M. Mandel and A. Higa, J. Mol. Biol. (1970), 53, p. 154 et seq.].
Thus, the present invention provides a process for the biosynthesis of human serum albumin in a microorganism.
To achieve this objective the structural gene for human serum albumin is modified in such a manner that it possesses an initiation codon, and the modified structural gene is then linked to an inducible regulator gene.
Culture of a host bacterium, such as E. coli, containing the modified gene produces a useful amount of albumin after induction under defined conditions.
In that which follows, the technical terms of molecular biology are used in their normal sense [see, for example, "Molecular Biology of the Gene" by J. Watson (French edition, Intereditions 1978)]. In that which follows, the construction and the processes used for expression of the human serum albumin gene are described successively.

A. CONSTRUCTION OF THE HUMAN SERUM ALBUMIN GENE
1. Preparation of Liver messenger RNA
Liver cells are used, obtained, for example, by biopsy, and the messenger RNA is extracted therefrom according to the method described, for example, by V. Glisin et al., Biochemistry (1974), 13, p. 2633 et seq.; and by R. Deeley et al., J. Biol. Chem. (1977), 252, p. 8310 et seq. The biopsy is treated with 6M guanidine thiocyanate solution and the total RNA is purified by several cycles of precipitation in ethanol at -20.degree. C., centrifugation and redissolution of the centrifugation pellets.
The preparation is enriched in messenger RNA by several cycles of affinity chromatography on columns of oligo(dT)-cellulose according to the technique described by H. Aviv and P. Leder, Proc. Natl. Acad. Sci. (USA) (1972), 69, p. 1408 et seq. The messenger RNA thus isolated, containing 1 to 2% of total RNA, is stored in aqueous solution at -70.degree. C.
It is possible to determine the proportion of messenger RNA specific for human serum albumin within the total population (for example by in vitro translation of an aliquot of the RNA solution in rabbit reticulocyte lysates). One method consists in using the reticulocyte lysate supplied by Amersham, following the procedure recommended by this supplier. Thus, it is possible to determine the fraction of newly formed protein which is immunoprecipitable by anti-albumin antibodies within the whole group of newly formed proteins. A fraction, for example, of the order of 6% is obtained.
2. Synthesis of cDNA and cloning in E. coli.
a. Synthesis of the first strand
Starting with a modification of the technique of G. N. Buell et al., J. Biol. Chem. (1978), 253, p. 2471 et seq., 5 .mu.g of total messenger RNA, for example, are used in a final volume of 50 microliters of a solution containing: 100 mM Tris.HCl pH 8.3, 10 mM MgCl.sub.2, 0.4 mM DTT, 20 mM KCl, 0.4 mM Na pyrophosphate, 1 mM with respect to each nucleotide triphosphate (dNTP), 100 .mu.g/ml of oligo(dt).sub.12-18, 0.5 U/ml of ribonuclease inhibitor, 50 picomoles of radioactive tracer and 40 units of reverse transcriptase (Life Sciences, Inc.).
The reaction of reverse transcription of the messenger RNA to the complementary DNA (cDNA) takes place for 1 hour at 42.degree. C.
The extent of synthesis of cDNA is calculated by measuring the level of incorporation of the radioactive tracer into acid-precipitable molecules, according to a known technique.
After 1 hour, the reaction is stopped by adding EDTA (20 mM), and the messenger RNA is destroyed by alkaline digestion in 50 mM NaOH at 42.degree. C. for 3 hours.
The newly formed cDNA is separated from the nonincorporated dNTPs and the alkaline degradation products of the RNAs by chromatography, for example, on a column of Sephadex G100 (Pharmacia Fine Chemicals). 1.5 .mu.g of single-stranded cDNA is obtained from 5 .mu.g of total messenger RNA.
b. Synthesis of the second strand
The single-stranded cDNA is converted to double-stranded DNA by the action of the "Klenow" fragment of DNA polymerase I.
The reaction conditions are: 100 mM Hepes pH 7, 10 mM MgCl.sub.2, 2.5 mM DTT, 70 mM KCl, 0.5 mM with respect to each dNTP and 50 units of DNA polymerase I "Klenow" fragment (marketed, for example, by New England Biolabs Inc.).
The reaction is carried out for 15 hours at 15.degree. C., and the double-stranded DNA is separated from the nonincorporated dNTPs again by chromatography on a column of Sephadex G100.
c. Cloning of the double-stranded DNA
To eliminate the single-stranded DNA molecules and obtain a blunt-ended double-stranded DNA, the unpaired sequences are treated with S.sub.1 nuclease according to the technique described by A. Efstradiatis et al., Cell (1976), 7, p. 279 et seq. The double-stranded newly formed DNAs are separated according to their size by centrifugation in a sucrose gradient. In general, a gradient of 5%-20% of sucrose in 50 mM Tris.HCl pH 8.5, 10 mM EDTA, 800 mM NaCl is used, centrifuged at 210,000 g for 15 hours at 20.degree. C., and the gradient is fractionated into aliquots after centrifugation.
The size of the molecules in each fraction is monitored by electrophoresis of samples carried out in parallel with DNA standards of known sizes, and the fractions containing a DNA consisting of a chain of more than 500 base pairs are combined.
For the purpose of cloning this DNA, its 3' ends are first elongated with oligo(dC) and, in parallel, the 3' ends of the PstI site of the plasmid vector pBR322 are elongated with oligo(dG) according to the technique of F. Rougeon et al., J. Biol. Chem. (1977), 252, p. 2209 et seq.
The double-stranded DNA described above is then hybridized with the plasmid vector, for example according to the technique of L. Villa-Komaroff et al., Proc. Natl. Acad. Sci. (USA) (1978), 75, p. 3727 et seq.
A "library" of liver cDNA clones is created by transformation of E. coli bacteria with this hybridized DNA, according to the method described by M. Mandel and A. Higa, J. Mol. Biol. (1970), 53, p: 154 et seq., and M. Dagert and S. D. Erlich, Gene (1979), 6, p. 23 et seq.
d. Identification of the albumin cDNA clones
A colony hybridization technique is employed, using synthetic oligonucleotides the sequences of which are deduced from the protein sequence of human albumin [B. Meloun et al., FEBS Letters (1975), 58, p. 134 et seq.; M. Grunstein and D. Hogness, Proc. Natl. Acad. Sci. (USA) (1975), 72, p. 3961 et seq.; R. B. Wallace et al., Nucleic Acids Res. (1981), 9, p. 879 et seq.].
The clones are cultured in square dishes directly on nitrocellulose filters in series of 96 in Luria medium containing 25 .mu.g/ml of tetracycline. After growth at 37.degree. C. followed by amplification in the presence of 250 .mu.g/ml of chloramphenicol, the colonies are lysed with sodium hydroxide and then hybridized with oligonucleotides which have been radioactively labelled at position 5' by kinase treatment, in a solution containing: 5.times.SSC, 0.5% NP 40, 100 .mu.g/ml of salmon sperm DNA denatured by boiling and cooled rapidly in ice, and 0.5 ng/ml of kinase-treated oligonucleotide. The hybridization is performed at 37.degree. C. for 18 hours. The filters are then washed in 5.times.SSC at 25.degree. C., then at 37.degree. C. and then at 45.degree. C., this being done four times for 15 minutes at each stage.
The filters are then exposed at -70.degree. C. to Kodak X-OMAT film with an enhancing screen for 15 to 24 hours. The clones which hybridize with the probes are re-isolated and then lysed. The plasma DNA is purified by centrifugation in caesium chloride/ethidium bromide medium according to a known technique.
The DNA of the insertion is sequenced by the Maxam-Gilbert technique [A. Maxam and W. Gilbert, Methods Enzymol. (1980), 65, p. 499 et seq.] to compare the protein sequence derived from the nucleotide sequence with that of human serum albumin.
In this manner a series of clones is identified in which the insertions correspond to the whole human serum albumin gene.
FIG. 1 shows the restriction map of the serum albumin gene, as well as the position of three of the most representative insertions, designated "pT1B11", "pAA38" and "p6D8".
e. Incorporation of an initiation codon into the structural gene (FIG. 2)
(a) The DNA of plasmid "pT1B11" is digested with the enzymes PstI and PvuII, and a 125 base-pair DNA fragment is isolated corresponding to the sequence of the 5' end of the serum albumin gene (amino acids Nos. 1 to 62). At the PvuII end, a junction sequence is attached consisting of the site for recognition of the enzyme BamHI. A PstI-BamHI fragment is thereby obtained.
A synthetic oligonucleotide 21 bases long is prepared separately, the oligonucleotide possessing an "ATG" triplet in front of the nucleotides which code for the amino acids of human serum albumin and also an NcoI restriction site, and its sequence being as follows: 5'GAATCCATGGATGCACACAAG 3'.
The PstI-BamHI DNA fragment is denatured and hybridized with the synthetic oligonucleotide. The hybridization is accomplished through the sequence 5' . . . GATGCACACAAG 3', the 3' end of the complementary DNA strand being unpaired. The unpaired ends are digested and polymerization is then carried out in the 5' . . . 3' direction with DNA polymerase I Klenow fragment, according to the techniques of H. Jacobsen et al., Eur. J. Biochem. (1974), 45, p. 623 et seq.
A fragment is thereby obtained containing an NcoI site followed by the ATG triplet at the 5' end and a BamHI site at the 3' end.
(b) The ligation is carried out of three DNA fragments:
(1) an EcoRI-BamHI fragment of plasmid "pLG200" [L. Guarente et al., Cell (1980) 20p. 543 et seq.] carrying a gene for resistance to antibiotics, the origin of replication and the 3' end of the .beta.-galactosidase gene,
(2) an EcoRI-PvuII fragment of plasmid "pGL101" [G. Lauer et al., J. Mol. Appl. Genet. (1981), 1, p. 139 et seq.] carrying the P.sub.lac promoter and the ribosome binding site (RBS) of the E. coli LacZ gene,
(3) the mutagenized DNA fragment described above which codes for the first 62 amino acids of human albumin.
A plasmid (pXL52) is isolated in which fusion of the 5' end of the human serum albumin gene with the E. coli .beta.-galactosidase gene has been accomplished.
f. Construction of the complete gene (FIG. 2)
The DNA of plasmid "p6D8" is digested with EcoRI, and partially with BglII, according to a technique already described. The large EcoRI-BglII fragment, containing the sequence which codes for the last 405 amino acids of human serum albumin followed by the origin of replication of the plasmid and the gene for resistance to tetracycline, is isolated.
The DNA of plasmid "pXL52" described above is digested with EcoRI and Sau3A, and a fragment containing 200 base pairs is isolated.
The DNA of plasmid "pAA38" is digested with Sau3A and a fragment containing 540 base pairs is isolated.
The three fragments are ligated (in the order [pXL52 EcoRI-Sau3A]--[pAA38 Sau3A]--[p6D8 Bg1II-EcoRI]), turning to advantage the compatibility between the Sau3A and BglII sites. A plasmid known as "pXL53" is obtained, the quality of the construction of which is monitored by complete sequencing of the fragment between the EcoRI site and the PstI site corresponding to the junction between the insertion and the plasmid vector.
The complete nucleotide sequence, together with the derived protein sequence, are shown in FIGS. 3 and 4.
The observed variations between this sequence and the published protein sequence [B. Meloun et al., FEBS Letters (1975), 58, p. 134 et seq.; M. Dayhoff, Atlas of Protein sequence and structure (1978), 5, supplement 3, p. 306] are as follows:
______________________________________ Human serum albumin deducedPosition Meloun et al. from the sequence of "pXL53"______________________________________131 Glutamine Glutamic acid364 Histidine Alanine367 Tyrosine Histidine370 Alanine Tyrosine381 Valine Methionine464 Glutamic acid Histidine465 Histidine Glutamic acid501 Glutamine Glutamic acid______________________________________
B. CONSTRUCTION OF SYSTEMS FOR THE EXPRESSION OF HUMAN SERUM ALBUMIN
1. Use of bacteriophage lambda "P.sub.L " promoter
(a) Plasmid "pXL53" is linearized by partial digestion with the enzyme NcoI, with respect only to the NcoI site at the 5' end of the initiation codon, and blunt ends are formed by filling-in according to the technique of R. M. Wartell and W. S. Reznikoff, Gene (1980), 9, p. 307 et seq.
An "adaptor" is synthesized containing at the 5' end a sequence corresponding to the recognition site for a restriction enzyme such as BamHI, followed by a sequence corresponding to a ribosome binding site ("consensus" or "theoretical" RBS). The adaptor sequence is 5'GGATCCTAGGAGGAAC 3'.
The ligation of the adaptor at the 5' end of a blunt-ended DNA has been described, for example, by C. P. Bahl et al., Gene (1976), 1, p. 81 et seq.
The method consists in performing the reaction on 20 microliters of a solution containing 50 mM Tris.HCl pH 7.5, 10 mM MgCl.sub.2, 15 mM DTT, 1 mM ATP, 50 .mu.g/ml of adaptor, 20 .mu.g/ml of DNA and 1 unit of DNA ligase (New England Biolabs Inc.). The reaction is carried out for 10 hours at 15.degree. C. This ligation creates a BamHI site without eliminating the NcoI site.
The ligation product is digested with BamHI and with HinDIII. As a result of the presence of a HinDIII site at the 3' end of the human serum albumin gene, a DNA fragment containing the entire coding sequence is obtained.
The HinDIII-BamHI fragment thereby obtained is subcloned, for example, in plasmid "pBR322" by transforming E. coli according to the method described above to obtain plasmid "pXL61".
Plasmid "pXL61" does not contain any promoter.
Bacteriophage lambda "P.sub.L " promoter is situated on the bacteriophage chromosome between a BglII site and a BamHI site [see E. Szybalski and W. Szybalski, Gene (1979), 7, p. 217 et seq.], and its nucleotide sequence is known [F. Sanger et al., J. Mol. Biol. (1982), 162, p. 279 et seq.]. This fragment can be cloned and its restriction sites modified according to known methods.
It is noted that plasmids carrying P.sub.L have to be propagated in E. coli strains carrying the repressor gene cI, in order to prevent this promoter from being expressed constitutively.
In a first construction, P.sub.L is available in the form of a BamHI fragment from plasmid "pP.sub.L -lambda" (Pharmacia P. L. Biochemicals). By insertion of this BamHI fragment into the BamHI site of plasmid "pXL61", plasmid "pXL65" may be obtained, in which plasmid it has been verified that the orientation of promoter with respect to the structural gene for human serum albumin is correct.
Other constructions can be carried out from available plasmids. For example, it is possible to excise from plasmid "pP.sub.L -lambda" an HaeIII-HaeIII fragment containing the P.sub.L promoter and insert it into the SmaI site of a multi-site cloning sequence carried by a plasmid, such as plasmid "pUC8" [J. Vieira and J. Messing, Gene (1982), 79, p. 259 et seq.], to obtain "pUC8-P.sub.L " in which the EcoRI site is on the 5' side of the promoter.
Starting with plasmid "pPS1" [P. Sarmientos et al., Cell (1983), 32, p. 1337 et seq.], the HinDIII site closest to the NdeI site (FIG. 2) can first be destroyed and the small EcoRI-HinDIII fragment then replaced by, on the one hand the EcoRI-BamHI fragment of plasmid "pUC8-P.sub.L " containing the P.sub.L promoter, and on the other hand the BamHI-HinDIII fragment of plasmid "pXL61" containing the serum albumin gene. Plasmid "pXL70" is thereby obtained, in which the assembly [P.sub.L -"consensus" RBS-ATG-human serum albumin gene] is carried on an EcoRI-HinDIII DNA fragment.
(b) Replacement of the "consensus" RBS by that of the CII gene of bacteriophage lambda
The CII gene of bacteriophage lambda, the sequence and the initiation site of which are known, can be efficiently translated [E. Schwarz et al., Nature (1978), 272, p. 410 et seq. ].
A plasmid is constructed containing the expression system ["P.sub.L " promoter-CII RBS-ATG-serum albumin gene].
For example, after the BamHI site of "pUC8-P.sub.L " has been destroyed by the action of SI enzyme [A. J. Berck and P. A. Sharp, Cell (1977), 12, p. 721] an EcoRI-HinDIII fragment can be isolated containing the P.sub.L promoter, and the fragment can then be linked with an EcoRI-HinDIII fragment of plasmid "pDS20" [G. Duester et al., Cell (1982), 30, p. 855 et seq.] to obtain plasmid "pXL73".
The CII gene RBS is extracted from plasmid "pPS1". This plasmid is digested with NdeI and a BamHI adaptor is inserted after the formation of blunt ends. The RBS is then excised in the form of a HinDIII-BamHI fragment.
A plasmid "pXL88" in which this HinDIII-BamHI fragment is linked with the large HinDIII-BamHI fragment of plasmid "pXL73" is constructed first. In the new plasmid "pXL88", the CII RBS is inserted in the correct orientation with respect to the P.sub.L promoter, and the whole combination is present in a multi-site system in such a way that the P.sub.L -CIII RBS assembly is carried on a 578 base-pair EcoRI-BamHI DNA fragment.
The 578 base-pair EcoRI-BamHI fragment is sub-cloned between the EcoRI and BamHI sites of plasmid "pMC1403" [M. J. Casadaban et al., J. Bacteriol. (1980), 143, p. 971 et seq.] which carries the .beta.-galactosidase gene (lacZ) after the BamHi site. This construction leads to plasmid "pXL91" in which the .beta.-galactosidase gene is expressed under the control of the [P.sub.L -CII RBS] system.
The BamHI-BglII fragment of plasmid "pXL61" described above is sub-cloned in the BamHI site of plasmid "pMC1403". (The ligation of a BglII site in a BamHI site is possible, but excision by BamHI at BglII is no longer possible; there consequently remains only one BamHI site).
This construction ("pXL71") leads to the insertion of a 700 base-pair DNA fragment containing the sequence [BamHI-"consensus" RBS-ATG-NcoI-partial gene for serum albumin (coding for amino acids 1 to 218)-.beta.-galactosidase gene].
This plasmid is cut with BamHI and SacI (the SacI site is present in the .beta.-galactosidase gene) and inserted in plasmid "pXL91" described above in place of the preexisting BamHI-SacI fragment.
This then leads to plasmid "pXL97" in which the insertion has the following structure:
[EcoRI site-P.sub.L -CII RBS-BamHI site-"consensus" RBS-NcoI site-ATG-partial gene for serum albumin-.beta.-galactosidase gene].
Plasmid "pXL97" is digested with BamHI, and partially with NcoI with respect only to the NcoI site near to the initiation codon, and blunt ends are formed by the action of S.sub.1 nuclease, and the plasmid is then closed up again. This manipulation on the one hand eliminates the "consensus" RBS DNA sequence, and on the other hand brings an ATG of the CII RBS into phase with the serum albumin sequence.
Plasmid "pXL136" is thereby obtained, which contains the sequence [EcoRI site-P.sub.L -CII RBS-ATG-partial gene for serum albumin-.beta.-galactosidase gene].
Since the partial gene for serum albumin possesses a PvuII site, plasmid "pXL136" is digested with EcoRI and PvuII, and a 760 base-pair fragment is extracted and inserted between the EcoRI and PvuII sites of plasmid "pXL70" described above. Plasmid "pXL139" is thereby obtained, which carries the structure [P.sub.L -CII RBS-complete serum albumin gene] on an EcoRI-HinDIII fragment, like plasmid "pXL70", and which carries the substitution of the "consensus" RBS by that of the CII gene.
(c) Expression of serum albumin after induction of the "P.sub.L " promoter
Inoculation is carried out of an isolated E. coli colony carrying the temperature-sensitive repressor gene of the "P.sub.L " promoter (cI.sup.ts gene) and transformed by one of the plasmids "pXL65", "pXL70" and "pXL139".
When the bacterium is in exponential phase, the "P.sub.L " promoter of the plasmid is induced by raising the incubation temperature very rapidly to 42.degree. C. Incubation is continued for 90 minutes. A sample of the culture is withdrawn and the bacteria are lysed in a suspension containing 60 mM Tris.HCl pH 6.8, 2% SDS, 100 mM .beta.-mercaptoethanol, 10% of glycerol and 0.1% of bromophenol blue for 5 minutes.
The proteins are separated by polyacrylamide gel electrophoresis according to the method of U. K. Laemli, Nature (1970), 227, p. 680 et seq. or that of K. Weber and M. Osborne, J. Biol. Chem. (1969), 244, p. 4406 et seq.
The proteins are transferred to a nitrocellulose filter [M. Bittner et al., Anal. Biochem. (1980) 102, p. 459 et seq.; E. J. Stellwsag and A. E. Dahlberg, Nucleic Acid Res. (1980), 8, p. 229 et seq.). The presence of human albumin is detected by immunology, either with antibodies to human albumin followed by binding of labelled protein A, or with biotin-labelled anti-albumin antibodies visualized by means of avidin-peroxydase complexes.
In this manner, the presence is demonstrated of a protein which reacts with antibodies to human albumin, which co-migrates with authentic albumin and which is only present in lysates of E. coli after induction of this bacterium at 42.degree. C. in the presence of plasmid "pXL65", "pXL70" or "pXL139".
The level of human serum albumin produced under these conditions can be determined. The proportion of albumin reproducibly produced is of the order of 0.1% of the total proteins demonstrated in an E. coli lysate under denaturing conditions.
2. Use of the promoter of the trytophan operon (P.sub.trp) in tandem with the penicillin amidase promoter of E. coli
The introduction of the structural gene for human serum albumin behind an inducible bacterial promoter enables this protein to be expressed in E. coli. The levels of expression of the different systems described above are close to each other, and of the order of 1000 molecules of serum albumin per cell. These results are close to those obtained with similar systems such as those described in European Patent Applications EP 73,646 and EP 91,527. In particular, in European Patent Application EP 91,527, a maximum yield of 8,000 molecules per cell of a "polypeptide resembling human serum albumin" is noted. The protein obtained is not strictly identical to human serum albumin, and the levels produced are incompatible with the demands of industrial productivity. Moreover, the production of serum albumin is accompanied by a lethal effect of the producing bacterium.
It has now been found, and this forms the subject of the present invention, that the production of human serum albumin can be considerably improved by using a plasmid containing, after the gene for the pre-peptide of E. coli penicillin amidase, the structural gene for human serum albumin, the expression of which is controlled by two regulator genes in tandem.
More especially, the invention provides a process for preparing human serum albumin by culturing a bacterium such as E. coli containing a plasmid comprising, after the gene for the pre-peptide (signal peptide) of E. coli penicillin amidase, the structural gene for human serum albumin, the expression of which is controlled by the penicillin amidase promoter in tandem with an inducible promoter such as the promoter of the tryptophan operon "P.sub.trp ".
The promoter of the tryptophan operon of E. coli enables the expression of a gene to be induced when the strain of E. coli is cultured in the absence of tryptophan or in the presence of an analogue such as 3-indolylacrylic acid [C. Yanofsky et al., Nucleic Acids Res. (1981), 9, p. 6647 et seq.]. Such a promoter is available in plasmids such as "pDR720" (Pharmacia PL Biochemicals) [also see D. Russel and G. Bennett, Gene (1982), 20, p. 231 et seq.].
E. coli penicillin G amidase (PAM) (EC 3.5.11; penicillin aminohydrolase), which converts penicillin G to 6-aminopenicillanic acid, is produced by strains of E. coli such as E. coli ATCC 11105 [C. Kutzbach and E. Rauenbusch, Hoppe-Seyler's Z. Physiol. Chem. (1974), 354p. 45 et seq.; E. J. Vandamme, Economic Microbiology (1980), 5, p. 467 et. seq.]. This enzyme possesses a signal peptide which is normally excised by E. coli. The gene has been cloned and its primary structure defined by sequencing [H. Mayer et al., in "Plasmids of Medical, Environmental and Commercial Importance" (1979), K. N. Timmis and A. Puhler, editors, Elsevier/North-Holland Biomedical Press, p. 459 et seq. and W. Bruns et al., in "Third European Congress of Biotechnology", (1984) vol. III, Verlag Chemie, p. 371 et seq.]. The sequence of the signal peptide consists of an "ATG" translation initiation codon followed by 75 nucleotides which code for the 25 amino acids of the signal peptide. The gene for human serum albumin is fused to it in such a way that the translation phase is conserved. Thus, after translation, the first amino acid of the albumin (aspartic acid) is present at the junction of the site of excision of the signal peptide.
This construction can be carried out in the following manner:
A EcoRI-PstI fragment of the E. coli ATCC 11105 chromosome containing the PAM gene is inserted between the EcoRI and PstI sites of plasmid pBR 322. Plasmid "pXL20" is thereby obtained.
The HinDIII-HinDIII fragment of plasmid "pXL20" containing the PAM gene is then inserted in the same orientation as the P.sub.L promoter in the HinDIII site of plasmid "pXL73". Plasmid "pXL125" is thereby obtained, containing the sequence [P.sub.L promoter-PAM gene]. Plasmid "pXL125" is digested with NruI (blunt-ended site) and a BamHI synthetic restriction site is inserted into the site situated at the beginning of the PAM gene at 170 nucleotides from the HinDIII site. The BamHI-BamHI [NruI] fragment containing P.sub.L gives plasmid "pXL134" by ligation with itself.
The EcoRI-BamHI fragment of plasmid "pXL70" is then replaced by the EcoRI-BamHI fragment of plasmid "pXL134" containing the P.sub.L promoter, the PAM RBS and the beginning of the PAM gene. Plasmid "pXL137" is thereby obtained, containing the following sequence: EcoRI-P.sub.L -PAM[promoter-RBS-nucleotides coding for the signal peptide]-BamHI-"consensus" RBS-ATG-serum albumin gene.
The EcoRI-SalI fragment of plasmid "pXL137" is replaced by that of plasmid "pDR720". Plasmid "pXL194" is obtained, which contains the following construction: EcoRI-P.sub.trp -SalI-PAM[promoter-RBS-signal peptide nucleotides]-BamHI-"consensus" RBS-ATG-serum albumin gene.
The signal peptide/serum albumin fusion is carried out by in vitro mutagenesis after sub-cloning in bacteriophage M13mp10 [J. Messing, Methods Enzymol. (1984), 101, p. 20 et seq.] according to known techniques [J. P. Adelmar et al., DNA (1983), 2, p. 183). The quality of the fusion is verified by sequencing and the fused fragment is reinserted into plasmid "pXL194". Plasmid "pXL288" is thereby obtained, which possesses the following structure: EcoRI-P.sub.trp -SalI-PAM[promoter-RBS-ATG-signal peptide nucleotides]-serum albumin gene.
E. coli strains such as E. coli E 103S or E. coli B are transformed with plasmid "pXL288".
A 16-hour culture of E. coli (pXL288) in rich medium is cultured at a dilution of 1/100 in enriched M9 minimal medium (0.1% casamino acids) without tryptophan, incubating at 37.degree. C. with constant agitation. Growth is stopped at the end of the exponential phase and the bacteria are lysed ultrasonically and then centrifuged. The proteins in the supernatant and the pellet are analysed by electrophoresis under denaturing conditions. The level of human serum albumin obtained is of the order of 10% of the proteins observed under denaturing conditions.
Under these conditions, the production of human serum albumin is in the region of 10 mg per liter of medium, for an absorbence of 1 at 610 nm. Under these conditions, no lethal effect is observed on the bacterial strain.
In addition, conditions can be found such that the PAM/human serum albumin fusion, not matured in vivo, is digested with a peptidase specific for the "leader" sequences of E. coli [P. B. Wolf et al., J. Biol. Chem. (1982), 257, p. 7098 et seq.] to yield a protein identical to authentic human serum albumin.

Number	Name	Date
4382028	Paget	May 1983
4551433	Deboer	Nov 1985
4666836	Inouye et al.	May 1987

Process for the microbiological preparation of human serum albumin

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Nishi et al, Agric. Biol. Chem., vol. 48, pp. 669-675 (1984).
Lawn et al, Nucleic Acids Research, vol. 9, pp. 6103-6114 (1981).