Skip to main content
Log in

Recombinant expression systems in the pharmaceutical industry

  • Mini-Review
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

In terms of downstream processing efficiency, secretory expression systems offer potential advantages for the production of recombinant proteins, compared with inclusion body forming cytosolic systems. However, for high-volume therapeutics like insulin, the product yields of the majority of the potentially available secretory systems is not yet fully competitive. Current strategies to improve productivity and secretion efficiency comprise: (1) enhancement of gene expression rates, (2) optimization of secretion signal sequences, (3) coexpression of chaperones and foldases, (4) creation of protease deficient mutants to avoid premature product degradation and (5) subsequent breeding and mutagenesis. For the production of non-glycosylated proteins and proteins, which are natively glycosylated but are also pharmacologically active without glycosylation, prokaryotes, which usually lack metabolic pathways for glycosylation, are theoretically the most suitable organisms and offer two alternatives: either Escherichia coli strains are conditioned to be efficient secreters or efficient native secreters like Bacillus species are accordingly developed. To fully exploit the secretory capacity of fungal species, a deeper understanding of their posttranslational modification physiology will be necessary to steer the degree and pattern of glycosylation, which influences both folding and secretion efficiency. Insect and mammalian cells display posttranslational modification patterns very similar or identical to humans, but in view of the entailed expenditures, their employment can only be justified if their modification machinery is required to ensure a desired pharmacological activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Anné J, Mellaert L van (1993) Streptomyces lividans as host for heterologous protein production. FEMS Microbiol Lett 114:121–128

    Article  PubMed  Google Scholar 

  • Bassford PJ, Silhavy TJ, Beckwith JR (1979) Use of gene fusion to study secretion of maltose-binding protein into Escherichia coli periplasm. J Bacteriol 139:19–31

    CAS  PubMed  Google Scholar 

  • Benz I, Schmidt A (2002) Never say never again: protein glycosylation in pathogenic bacteria. Mol Microbiol 45:267–276

    Article  CAS  PubMed  Google Scholar 

  • Berg JA van der, Laken KJ van den, Ooyen AJJ van, Renniers TCHM, Rietveld K, Schaap A, Brake AJ, Bishop RJ, Schultz K, Moyer D, Richman M, Shuster JR (1990) Kluyveromyces as a host for heterologous gene expression: expression and secretion of prochymosin. Bio/technology 8:135–142

    Google Scholar 

  • Berks BC, Sargent F, Palmer T (2000) The tat protein export pathway. Mol Microbiol 35:260–274

    Article  CAS  PubMed  Google Scholar 

  • Betenbaugh MJ, Ailor E, Whiteley E, Hinderliter P, Hsu TA (1996) Chaperone and foldase coexpression in the baculovirus-insect cell expression system. Cytotechnology 20:149–159

    CAS  Google Scholar 

  • Birch JR, Froud SJ (1994) Mammalian cell culture system for recombinant protein production. Biologicals 22:127–133

    Article  CAS  PubMed  Google Scholar 

  • Buckholz RG, Gleeson MA (1991) Yeast systems for the commcercial production of heterologous proteins. Bio/technology 9:1067–1072

    Google Scholar 

  • Carter P, Kelley RF, Rodrigues ML, Snedecor B, Covarrubias M, Velligan MD, Wong WL, Rowland AM, Kotts CE, Carver ME (1992) High level Escherichia coli expression and production of a bivalent humanized antibody fragment. Bio/technology 10:163–167

    Google Scholar 

  • Choi JH, Lee SY (2004) Secretory and extracellular production of recombinant proteins using Escherichia coli. Appl Microbiol Biotechnol (online)dodo

  • Chow TY, Ash JJ, Dignard D, Thomas DY (1992) Screening and identification of a gene, PSE-1, that affects protein secretion in Saccharomyces cerevisiae. J Cell Sci 101:709–719

    CAS  PubMed  Google Scholar 

  • Clare JJ, Rayment FB, Ballantine SP, Sreekrishna K, Romanos MA (1991) High-level expression of tetanus toxin fragment C in Pichia pastoris strains containing multiple tandem integrations of the gene. Bio/technology 9:455–460

    Google Scholar 

  • Collier DN (1993) SecB: a molecular chaperone of Escherichia coli protein secretion pathway. Adv Protein Chem 44:151–193

    CAS  PubMed  Google Scholar 

  • Conesa A, Punt PJ, Luijk N van, Hondel C van den (2001) The secretion pathway in fimanetous fungi: a biotechnological view. Fungal Genet Biol 33:155–171

    Article  CAS  PubMed  Google Scholar 

  • Cregg JM, Lin Cereghino JL, Shi J, Higgins DR (2000) Recombinant protein expression in Pichia pastoris. Mol Biotechnol 16:23–52

    Article  CAS  PubMed  Google Scholar 

  • De Taxis du Poet P, Scacheri E, Benatti E, Nitti G, Valsasina B, Sarmientos P (1991) Production of HV1 variant of hirudin by recombinant DNA methodology. Blood Coagul Fibrinolysis 2:113

    PubMed  Google Scholar 

  • Dilsen S, Paul W, Sandgathe A, Tippe D, Freudl R, Thömmes J, Kula MR, Takors R, Wandrey C, Weuster-Botz D (2000) Fed-batch production of recombinant human calcitonin precursor fusion protein using Staphylococcus carnosus as an expression–secretion system. Appl Microbiol Biotechnol 54:361–369

    Article  CAS  PubMed  Google Scholar 

  • Fleer R (1992) Engineering yeast for high level expression. Curr Opin Biotechnol 3:486–496

    CAS  PubMed  Google Scholar 

  • Fleer R, Chen XJ, Amellal N, Yeh P, Fournier A, Guinet F, Gault N, Faucher D, Folliard F, Fukuhara H, Mayaux JF (1991a) High-level secretion of correctly processed recombinant human interleukin-1β in Kluyveromyces lactis. Gene 107:285–295

    Article  CAS  PubMed  Google Scholar 

  • Fleer R, Yeh P, Amellal N, Maury I, Fournier A, Bacchetta F, Baduel P, Jung G, L’Hôte H, Becquart J (1991b) Stable multicopy vectors for high level secretion of recombinant human serum albumin by Kluyveromyces lactis. Bio/technology 9:968–975

  • Forsberg G, Forsgren M, Jaki M, Norin M, Sterky C, Enhörning A, Larsson K, Ericsson M, Björk P (1997) Identification of framework residues in a secreted recombinant antibody fragment that control production level and localization in Escherichia coli. J Biol Chem 272:12430–12450

    Article  CAS  PubMed  Google Scholar 

  • Gellissen G (2000) Heterologous protein production in methylotrophic yeasts. Appl Microbiol Biotechnol 54:741–750

    Article  CAS  PubMed  Google Scholar 

  • Gellissen G, Hollenberg CP (1997) Application of yeasts in gene expression studies: a comparison of Saccharomyces cerevisiae, Hansenula polymorpha and Kluyveromyces lactis—a review. Gene 190:87–97

    Article  CAS  PubMed  Google Scholar 

  • Gellissen G, Weydemann U, Strasser AWM, Piontek M, Janowicz ZA, Hollenberg CP (1992) Progress in developing methylotrophic yeasts as expression systems. Trends Biotechnol 10:413–417

    Article  CAS  PubMed  Google Scholar 

  • Gentschev I, Dietrich G, Goebel W (2002) The E. coli alpha-hemolysin secretion system and its use in vaccine development. Trends Microbiol 10:39–45

    Article  CAS  PubMed  Google Scholar 

  • George HJ, Marchand P, Murphy K, Wiwall BH, Dowling R, Giannara J, Hollis GF, Trzaskos JM, Copeland RA (1997) Recombinant human 92-kDa type IV collagenase/gelatinase from baculovirus-infected insect cells: expression, purification, and characterization. Protein Expr Purif 10:154–161

    Article  CAS  PubMed  Google Scholar 

  • Gervais A, Hammel YA, Pelloux S, Lepage P, Baer G, Carte N, Sorokine O, Strub JM, Koerner R, Leize E, Van Dorsselaer A (2003) Glycosylation of human recombinant gonadotropins: characterization and batch-to-batch consistency. Glycobiology 13:179–189

    Article  CAS  PubMed  Google Scholar 

  • Gouka RJ, Punt PJ, Hondel C van den (1997) Efficient production of secreted proteins by Aspergillus: progress limitations and prospects. Appl Microbiol Biotechnol 47:1–11

    Article  CAS  PubMed  Google Scholar 

  • Grampp GE, Sambanis A, Stephanopoulos GN (1992) Use of regulated secretion in protein production from animal cells: an overview. Adv Biochem Eng Biotechnol 46:35–62

    CAS  PubMed  Google Scholar 

  • Gregory G, Heyneker HL (1988) Secretion of correctly processed human growth hormone in E. coli and Pseudomonas. US patent 4755465

  • Guisez Y, Tison B, Vandekerckhove J, Demolder J, Bauw G, Haegeman G, Fiers W, Contreras R (1991) Production and purification of recombinant human interleukin-6 secreted by the yeast Saccharomyces cerevisiae. Eur J Biochem 198:217–222

    CAS  PubMed  Google Scholar 

  • Habermann P, Bender R (2001) Signal sequences for the production of leu-hirudin via secretion by E. coli in a culture medium. Int patent WO 01/21662

  • Hartl FU (1996) Molecular chaperones in cellular protein folding. Nature 381:571–580

    Article  CAS  PubMed  Google Scholar 

  • Hesse F, Wagner R (2000) Developments and improvements in the manufacturing of human therapeutics with mammalian cell cultures. Trends Biotechnol 18:173–180

    Article  CAS  PubMed  Google Scholar 

  • Ikonomou L, Schneider YJ, Agathos SN (2003) Insect culture for industrial production of recombinant proteins. Appl Microbiol Biotechnol 62:1–20

    Article  CAS  PubMed  Google Scholar 

  • Jeenes DJ, Mackenzie DA, Roberts IN, Archer DB (1991) Heterologous protein production by filamentous fungi. Biotechnol Genet Eng Rev 90:327–367

    Google Scholar 

  • Kariya Y, Ishida K, Tsubota Y, Nakashima Y, Hirosaki T, Ogawa T, Miyazaki K (2002) Efficient expression system of human recombinant laminin-5. J Biochem 132:607–612

    CAS  PubMed  Google Scholar 

  • Kirk N, Piper PW (1991) The determination of heat-shock element directed lacZ expression in Saccharomyces cerevisiae. Yeast 7:539–546

    CAS  PubMed  Google Scholar 

  • Kjeldsen T (2000) Yeast secretory expression of insulin precursors. Appl Microbiol Biotechnol 54:277–286

    Article  CAS  PubMed  Google Scholar 

  • Kjeldsen T, FrostPettersson A, Hach M (1999) Secretory expression and characterization of insulin in Pichia pastoris. Biotechnol Appl Biochem 29:79–86

    CAS  PubMed  Google Scholar 

  • Kobayashi K, Kuwae S, Ohya T, Ohda T, Ohyama M, Ohi H, Tomomitsu K, Ohmura T (2000) High-level expression of recombinant human serum albumin from the methylotrophic yeast Pichia pastoris with minimal protease production and activation. J Biosci Bioeng 89:55–61

    Article  CAS  Google Scholar 

  • Kujau MJ, Hoischen C, Riesenberg D, Gumpert J (1998) Expression and secretion of functional miniantibodies McPC603scFvDhlx in cell-wall-less l-form strains of Proteus mirabilis and Escherichia coli: a comparison of the synthesis capacities of l-form strains with an E. coli producer strain. Appl Microbiol Biotechnol 49:51–58

    Article  CAS  PubMed  Google Scholar 

  • Lin Cereghino JL, Cregg JM (2000) Heterologous protein expression in the methylotrophic yeast Pichia pastoris. FEMS Microbiol Rev 24:45–66

    Article  PubMed  Google Scholar 

  • Lin Cereghino GP, Lin Cereghino J, Ilgen C, Cregg JM (2002) Production of recombinant proteins in fermenter cultures of the yeast Pichia pastoris. Curr Opin Biotechnol 13:329–332

    Article  PubMed  Google Scholar 

  • Lund PA (2001) Microbial molecular chaperones. Adv Microb Physiol 44:93–140

    Article  CAS  PubMed  Google Scholar 

  • Makrides SC (1996) Strategies for achieving high-level expression of genes in Escherichia coli. Microbiol Rev 60:512–538

    CAS  PubMed  Google Scholar 

  • Mayer AF, Hellmuth K, Schlieker H, Lopez-Ulibarri R, Oertel S, Dahlems U, Strasser AWM, Loon APGM van (1999) An expression system matures: a highly efficient and cost-effective process for phytase production by recombinant strains of Hansenula polymorpha. Biotechnol Bioeng 63:373–381

    Article  CAS  PubMed  Google Scholar 

  • McCarroll L, King LA (1997) Stable insect cultures for recombinant protein production. Curr Opin Biotechnol 8:590–594

    Article  CAS  PubMed  Google Scholar 

  • Morita S, Kuriyama M, Nakatsu M, Kitano K (1994) High level expression of Fusarium alkaline protease gene in Acremonium chrysogenum. Biosci Biotechnol Biochem 58:627–630

    CAS  PubMed  Google Scholar 

  • Müller R, Glaser S, Geipel F, Thalhofer JP, Rexer B, Schneider C, Ratka M, Ronning S Eckstein H, Giessel C (2002) Method for producing recombinant trypsin. Int patent WO 02/061064 A2

  • Okabayashi K, Nakagawa Y, Hayasuke N, Ohi H, Miura M, Ishida Y, Shimizu M, Murakami K, Hirabayashi K, Minamino H (1991) Secretory expression of the human serum albumin gene in the yeast, Saccharomyces cerevisiae. J Biochem 110:103–110

    CAS  PubMed  Google Scholar 

  • Olmos-Soto J, Contreras-Flores R (2003) Genetic system to overproduce and secrete proinsulin in Bacillus subtilis. Appl Microbiol Biotechnol 62:369–373

    Article  CAS  PubMed  Google Scholar 

  • Paradkar A, Trefzer A, Chakraburtty R, Stassi D (2003) Streptomyces genetics: a genomic perspective. Crit Rev Biotechnol 23:1–27

    CAS  PubMed  Google Scholar 

  • Park EH, Shin YM, Lim YY, Kwon TH, Kim DH, Yang MS (2000) Expression of glucose oxidase by using recombinant yeast. J Biotechnol 81:35–44

    Article  CAS  PubMed  Google Scholar 

  • Pierce JJ, Robinson SC, Ward JM, Keshavarz-Moore E, Dunnill P (2002) A comparison of the process issues in expressing the same recombinant enzyme periplasmatically in Escherichia coli and extracellularly in Streptomyces lividans. J Biotechnol 92:205–215

    Article  CAS  PubMed  Google Scholar 

  • Pines O, Inouye M (1999) Expression and secretion of proteins in E. coli. Mol Biotechnol 12:25–34

    Article  CAS  PubMed  Google Scholar 

  • Poletti A, Weigel NL, McDonnell DP, Schrader WT, O’Malley BW, Conneely OM (1992) A novel, highly regulated, rapidly inducible system for the expression of chicken progesterone receptor, cPRA, in Saccharomyces cerevisiae. Gene 114:51–58

    Article  CAS  PubMed  Google Scholar 

  • Prevatt WD, Dost W (1992) Expression of human serum albumin in Pichia pastoris. Eur patent 00510678

  • Punt PJ, van Biezen N, Conesa A, Albers A, Mangnus J, van den Hondel C (2002) Filamentous fungi as cell factories for heterologous protein production. Trends Biotechnol 20:200–206

    Article  CAS  PubMed  Google Scholar 

  • Purvis IJ, Chotai D, Dykes CW, Lubahn DB, French FS, Wilson EM, Hobden AN (1991) An androgen-inducible expression system for Saccharomyces cerevisiae. Gene 106:35–42

    Article  CAS  PubMed  Google Scholar 

  • Pyle LE, Barton P, Fujiwara Y, Mitchell A, Fidge N (1995) Secretion of biologically active human proapolipoprotein A–I in a baculovirus-insect cell system: protection from degradation by protease inhibitors. J Lipid Res 36:2355–2361

    CAS  PubMed  Google Scholar 

  • Radzio R, Kück U (1997) Synthesis of biotechnologically relevant heterologous proteins in filamentous fungi. Proc Biochem 32:529–539

    Article  CAS  Google Scholar 

  • Reiter M, Blüml G (1994) Large-scale mammalian cell culture. Curr Opin Biotechnol 5:175–179

    CAS  PubMed  Google Scholar 

  • Rippmann JF, Klein M, Hoischen C, Brocks B, Rettig WJ, Gumpert J, Pfizenmaier K, Mattes R, Moosmayer D (1998) Procaryotic expression of single-chain variable-fragment (scFv) antibodies: secretion in l-form cells of Proteus mirabilis leads to active product and overcomes the limitations of periplasmic expression in Escherichia coli. Appl Environ Microbiol 64:4862–4869

    CAS  PubMed  Google Scholar 

  • Romanos MA, Makoff AJ, Fairweather NF, Beesley KM, Slater DE, Rayment FB, Payne MM, Clare JJ (1991) Expression of tetanus toxin fragment C in yeast: gene synthesis is required to eliminate fortuitous polyadenylation sites in AT-rich DNA. Nucleic Acids Res 19:1461–1467

    CAS  PubMed  Google Scholar 

  • Russel C, Mawson J, Yu PL (1991) Production of recombinant products in yeasts: a review. Aust J Biotechnol 5:48–55

    PubMed  Google Scholar 

  • Schaerlaekens K, Mellaert L van, Lammertyn E, Geukens N, Anne J (2004) The importance of the Tat-dependent protein secretion pathway in Streptomyces as revealed by phenotypic changes in tat deletion mutants and genome analysis. Microbiology 150:21–31

    Article  CAS  PubMed  Google Scholar 

  • Schaffrath R, Breuning KD (2000) Genetics and molecular physiology of the yeast Kluyveromyces lactis. Fungal Genet Biol 30:173–190

    Article  CAS  PubMed  Google Scholar 

  • Schmidt HHJ, Genschel J, Haas R, Büttner C, Manns MP (1997) Expression and purification of recombinant human apolipoprotein A–I in chinese hamster ovary cells. Protein Expr Purif 10:226–236

    Article  CAS  PubMed  Google Scholar 

  • Schult-Linkholt S, Jenzelewski V, Weißeis F (2002) Kooperation von Phrma-Anlagenbau und Biotechnologie-Unternehmen bei der Optimierung eines Produktionsverfahrens für Hepatitis B-Impfstoff. Ber Tech Wiss (Linde Magazine) 81:3–8

    Google Scholar 

  • Sivakesava S, Xu ZN, Chen YH, Hackett J, Huang RC, Lam E, Lam TL, Siu KL, Wong RSC, Wong WKR (1999) Production of excreted human epidermal growth factor (hEGF) by an efficient recombinant Escherichia coli system. Proc Biochem 34:893–900

    Article  Google Scholar 

  • Sleep D, Belfield GP, Ballance DJ, Steven J, Jones S, Evans LR, Moir PD, Goodey AR (1991) Saccharomyces cerevisiae strains that overexpress heterologous proteins. Bio/technology 9:183–187

  • Sodoyer R (2004) Expression systems for the production of recombinant pharmaceuticals. BioDrugs 18:51–62

    CAS  PubMed  Google Scholar 

  • Srinivasan S, Barnard GC, Gerngross TU (2002) A novel high-cell-density protein expression system based on Ralstonia eutropha. Appl Environ Microbiol 68:5925–5932

    Article  CAS  PubMed  Google Scholar 

  • Swartz JR (2001) Advances in Escherichia coli production of therapeutic proteins. Curr Opin Biotechnol 12:195–201

    Article  CAS  PubMed  Google Scholar 

  • Swinkels BW, Ooyen AJJ van, Bonekamp FL (1993) The yeast Kluyveromyces lactis as an efficient host for heterologous gene expression. Antonie van Leeuwenhoek 64:187–201

    PubMed  Google Scholar 

  • Tate CG, Haase J, Baker C, Boorsma M, Magnani F, Vallis Y, Williams DC (2003) Comparison of seven different heterologous protein expression systems for the production of the serotonin transporter. Biochim Biophys Acta 1610:141–153

    Article  CAS  PubMed  Google Scholar 

  • Teter SA, Klionsky DJ (1999) How to get a folded protein across a membrane. Trends Cell Biol 9:428–431

    Article  CAS  PubMed  Google Scholar 

  • Turner BG, Avgerinos GC, Melnick LM, Moir DT (1991) Optimization of pro-urokinase secretion from recombinant Saccharomyces cerevisiae. Biotechnol Bioeng 37:869–875

    CAS  Google Scholar 

  • Upreti RK, Kumar M, Shankar V (2003) Bacterial glycoproteins: functions, biosynthesis and applications. Proteomics 3:363–379

    Article  CAS  PubMed  Google Scholar 

  • Vapnek P (1991) Choosing a production system for recombinant proteins. Biol Rec Microorg Anim Cells 34:1–14

    Google Scholar 

  • Wadensten H, Ekebacke A, Hammarberg B, Holmgren E, Kalderen C, Tally M, Moks T, Uhlen M, Josephson S, Hartmanis M (1991) Purification and characterization of recombinant human insulin-like growth factor II (IGF II) expressed as a secreted fusion protein in Escherichia coli. Biotechnol Appl Biochem 13:412–421

    CAS  PubMed  Google Scholar 

  • Ward A, Hoyle C, Palmer S, O’Reilly J, Griffith J, Pos M, Morrison S, Poolman B, Gwynne M, Henderson P (2001) Prokaryote multidrug efflux proteins of the major facilitator superfamily: amplified expression, purification and characterisation. J Mol Biotechnol 3:193–200

    CAS  Google Scholar 

  • Weickert MJ, Doherty DH, Best EA, Olins PO (1996) Optimization of heterologous protein production in Escherichia coli. Curr Opin Biotechnol 7:494–499

    Article  CAS  PubMed  Google Scholar 

  • Werten MW, Bosch TJ van den, Wind RD, Mooibroek H, Wolf FA de (1999) High-yield secretion of recombinant gelatins by Pichia pastoris. Yeast 15:1087–1096

    Article  CAS  PubMed  Google Scholar 

  • Werten MW, Wisselink WH, Jansen-van den Bosch TJ, Bruin EC de, Wolf FA de (2001) Secreted production of a custom-designed, highly hydrophilic gelatin in Pichia pastoris. Protein Eng 14:447–454

    Article  CAS  PubMed  Google Scholar 

  • Weydemann U, Keup P, Pionetk M, Strasser AW, Schweden J, Gellissen G, Janowicz ZA (1995) High-level secretion of hirudin by Hansenula polymorpha—authentic processing of three different preprohirudins. Appl Microbiol Biotechnol 44:377–385

    Article  CAS  PubMed  Google Scholar 

  • Wurm F, Bernard A (1999) Large scale transient expression in mammalian cells for recombinant protein production. Curr Opin Biotechnol 10:156–159

    Article  CAS  PubMed  Google Scholar 

  • Yamanaka H, Nomura T, Fujii Y, Okamoto K (1998) Need for TolC, an Escherichia coli outer membrane protein, in the secretion of heat-stable enterotoxin I across the outer membrane. Microb Pathog 25:111–120

    Article  CAS  PubMed  Google Scholar 

  • Ye R, Kim JH, Kim BG, Szarka S, Sihota E, Wong SL (1999) High-level secretory production of intact, biologically active staphylokinase from Bacillus subtilis. Biotechnol Bioeng 62:87–96

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to F. R. Schmidt.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schmidt, F.R. Recombinant expression systems in the pharmaceutical industry. Appl Microbiol Biotechnol 65, 363–372 (2004). https://doi.org/10.1007/s00253-004-1656-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-004-1656-9

Keywords

Navigation