Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Research Paper
  • Published:

Controlled Expression and Secretion of Bovine Chymosin in Aspergillus Nidulans

Abstract

To test the ability of the filamentous fungus Aspergillus nidulans to secrete bovine prochymosin, four plasmids were constructed in which the transcriptional, translational, and secretory control regions of the A. niger glucoamylase gene were functionally coupled to either prochymosin or preprochymosin cDNA. Three plasmid constructions involved the in–frame fusion of prochymosin coding sequences to glucoamylase sequences at 1) the glucoamylase signal peptide cleavage site, 2) the glucoamylase propeptide cleavage site, or 3) after 11 codons of the mature glucoamylase. In a fourth construction, preprochymosin was directly fused to the glucoamylase promoter. In all four constructions, the glucoamylase terminator was fused to the 3′ end of the prochymosin coding sequence. Secretion of polypeptides enzymatically and immunologically indistinguishable from bovine chymosin was achieved following transformation of A. nidulans with each of these plasmids. In all cases the primary translation product was partially processed to a polypeptide having a molecular weight similar to bovine chymosin. Synthesis of the chymosin polypeptides was induced in a medium that contained starch as the sole carbon source, whereas little or no expression was detected when xylose was the sole carbon source. Immunological assays indicated that the majority (>90%) of chymosin was extracellular. Hybridization analysis of genomic DNA from chymosin transformants showed chromosomal integration of prochymosin sequences, and for some transformants, multiple copies were observed.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Queener, S.W., Ingolia, T.D., Skatrud, P.L., Chapman, J.L. and Kaster, K.R. 1984. Recombinant DNA studies in Cephalosporium acremonium. ASM Conference on Genetics and Molecular Biology of Industrial Microorganisms. Abstr. p. 29.

  2. Bull, J.H. and Wooton, J.C. 1984. Heavily methylated amplified DNA in transformants of Neurospora crassa. Nature 310: 701–704.

    Article  CAS  Google Scholar 

  3. Buxton, F.P., Gwynne, D.I., and Davies, R.W. 1985. Transformation of Aspergillus niger using the argB gene of Aspergillus nidulans. Gene 37: 207–214.

    Article  CAS  Google Scholar 

  4. Kelly, J.M. and Hynes, M.J. 1985. Transformation of Aspergillus niger by the amdS gene of Aspergillus nidulans. EMBO J. 4: 475–479.

    Article  CAS  Google Scholar 

  5. Ballance, D.J., Buxton, F.P. and Turner, G. 1983. Transformation of Aspergillis nidulans by the orotidine-5′-phosphate decarboxylase gene of Neurospora crassa. Biochem. Biophys. Res. Commun. 112: 284–289.

    Article  CAS  Google Scholar 

  6. Cullen, D., Gray, G.L. and Berka, R.M. 1986. Molecular cloning vectors for Aspergillus and Neurospora. In: Vectors: A Survey of Molecular Cloning Vectors and Their Uses. Rodriguez, R. L. and Denhardt, D. T. (eds.). Butterworth Publishers, Stoneham, MA.

  7. Foltmann, B. 1970. Prochymosin and chymosin (prorennin and rennin). Methods Enzymol. 19: 421–436.

    Article  Google Scholar 

  8. Harris, T.J.R., Lowe, P.A., Thomas, P.G., Eaton, M.A.W., Millican, T.A., Patel, T.P., Bose, C.C., Carey, N.H. and Doel, M.T. 1982. Molecular cloning and nucleotide sequence of cDNA coding for calf preprochymosin. Nucl. Acids Res. 10: 2177–2187.

    Article  CAS  Google Scholar 

  9. Emtage, J.S., Angal, S., Doel, M.T., Harris, T.J.R., Jenkins, B., Lilley, G. and Lowe, P.A. 1983. Synthesis of calf prochymosin (prorennin) in Escherichia coli. Proc. Nat. Acad. Sci. USA 80: 3671–3675.

    Article  CAS  Google Scholar 

  10. Mellor, J., Dobson, M.J., Roberts, N.A., Tuite, M.F., Emtage, J.S., White, S., Lowe, P.A., Patel, T., Kingsman, A.J. and Kingsman, S.M. 1983. Efficient synthesis of enzymatically active calf chymosin in Saccharomyces cerevisiae. Gene 24: 1–14.

    Article  CAS  Google Scholar 

  11. Marston, F.A.O., Lowe, P.A., Doel, M.T., Shoemaker, J.M., White, S. and Angal, S. 1984. Purification of calf-prochymosin (prorennin) synthesized in Escherichia coli. Bio/Technology 2: 800–804.

    CAS  Google Scholar 

  12. Moir, D.T., Mao, J., Duncan, M.J., Smith, R.A. and Kohno, T. 1985. Production of calf chymosin by the yeast Saccharomyces cerevisiae. p. 75–85 In: Developments in Industrial Microbiology. Vol. 26. Society for Industrial Microbiology, Arlington, VA.

    Google Scholar 

  13. Smith, R.A., Duncan, M.J. and Moir, D.T. 1985. Heterologous protein secretion from yeast. Science 229: 1219–1224.

    Article  CAS  Google Scholar 

  14. Foltmann, B., Pedersen, V.B., Jacobson, H., Kaufmann, D. and Wybrandt, D. 1977. The complete amino acid sequence of prochymosin. Proc. Nat. Acad. Sci. USA 74: 2321–2324.

    Article  CAS  Google Scholar 

  15. Bech, A.M. and Foltmann, B. 1981. Partial primary structure of Mucor miehei protease. Neth. Milk Dairy J. 35: 275–200.

    CAS  Google Scholar 

  16. Graham, J.E.S., Sodek, J. and Hofmann, T. 1973. Rhizopus acid proteinases (rhizopus-pepsins): Properties and homology with other acid proteinases. Can. J. Biochem. 51: 789–796.

    Article  CAS  Google Scholar 

  17. Nunberg, J.H., Meade, J.H., Cole, G., Lawyer, F.C., McCabe, P., Schweickart, V., Tal, R., Wittman, V.P., Flatgaard, J.E. and Innis, M.A. 1984. Molecular cloning and characterization of the glucoamylase gene of Aspergillus awamori. Mol. Cell. Biol. 4: 2306–2315.

    Article  CAS  Google Scholar 

  18. Boel, E., Hansen, M.T., Hjort, I., Hoegh, I. and Fiil, N.P. 1984. Two different types of intervening sequences in the glucoamylase gene from Aspergillus niger. EMBO J. 3: 1581–1585.

    Article  CAS  Google Scholar 

  19. Barton, L.L., Lineback, D.R. and Georgi, C.E. 1969. The influence of nitrogen and carbon sources on the production of glucoamylase by Aspergilli. J. Gen. Appl. Microbiol. 15: 327–344.

    Article  CAS  Google Scholar 

  20. Turner, G. and Ballance, D.J. 1985. Cloning and Transformation in Aspergillus. p. 259–278. In: Gene Manipulations in Fungi. J. W.Bennett and L. A.Lasure (eds.) Academic Press, New York, NY.

    Chapter  Google Scholar 

  21. Ballance, D.J. and Turner, G. 1985. Development of a high-frequency transforming vector for Aspergillus nidulans. Gene 36: 321–331.

    Article  CAS  Google Scholar 

  22. Pedersen, V.B., Christensen, K.A. and Foltmann, B. 1979. Investigations on the activation of bovine prochymosin. Eur. J. Biochem. 94: 573–580.

    Article  CAS  Google Scholar 

  23. Messing, J., Crea, R. and Seeburg, P.H. 1981. A system for shotgun DNA sequencing. Nucl. Acids Res. 9: 309–321.

    Article  CAS  Google Scholar 

  24. Yanisch-Perron, C., Vieira, J. and Messing, J. 1985. Improved M13 phage cloning vectors and host strains: Nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33: 103–119.

    Article  CAS  Google Scholar 

  25. Bolivar, F., Rodriguez, R.L., Greene, P.J., Betlach, M.C. and Heyneker, H.L. 1977. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene 2: 95–113.

    Article  CAS  Google Scholar 

  26. Adelman, J.P., Hayflick, J.S., Vasser, M. and Seeburg, P.H. 1983. In vitro deletional mutagenesis for bacterial production of the 20,000-dalton form of pituitary growth hormone. DNA 2: 183–193.

    Article  CAS  Google Scholar 

  27. Messing, J. 1983. New M13 vectors for cloning. Methods Enzymol. 101: 20–79.

    Article  CAS  Google Scholar 

  28. Maniatis, T., Fritsch, E.F. and Sambrook, J. 1982. Molecular Cloning, A Laboratory Manual, p.164–169. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.

  29. Timberlake, W.E. and Barnard, E.C. 1981. Organization of a gene cluster expressed specifically in the asexual spores of Aspergillus nidulans. Cell 26: 29–37.

    Article  CAS  Google Scholar 

  30. Southern, E. 1975. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 98: 503–517.

    Article  CAS  Google Scholar 

  31. Thomas, P.S. 1980. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc. Nat. Acad. Sci. USA 77: 5201–5205.

    Article  CAS  Google Scholar 

  32. Maniatis, T., Fritsch, E.F. and Sambrook, J. 1982. A Molecular Cloning, A Laboratory Manual. p 109–112. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.

  33. Engvall, E. 1980. Immunoassay: ELISA and EMIT. Methods Enzymol. 70: 419–439.

    Article  CAS  Google Scholar 

  34. DeMan, J.M. and Batra, S.C. 1964. Measurement of the rennet clotting time of milk with an automatic clot-timer. Dairy Industries 29: 32.

    Google Scholar 

  35. Towbin, H., Staehlin, T. and Gordon, J. 1979. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and applications. Proc. Nat. Acad. Sci. USA 76: 4350–4354.

    Article  CAS  Google Scholar 

  36. Morrissey, J.H. 1981. Silver stain for proteins in polyacrylamide gels. Anal. Biochem. 117: 307–310.

    Article  CAS  Google Scholar 

  37. Berse, B., Dmochowska, A., Skryzpek, M., Weglenski, P., Bates, M.A. and Weiss, from Aspergillus nidulans. Gene 25: 109–117.

  38. Singh, I. and Jones, K.W. 1984. The use of heparin as a simple cost-effective means of controlling background in nucleic acid hybridiza°tion procedures. Nucl. Acids Res. 12: 5627–5638.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cullen, D., Gray, G., Wilson, L. et al. Controlled Expression and Secretion of Bovine Chymosin in Aspergillus Nidulans. Nat Biotechnol 5, 369–376 (1987). https://doi.org/10.1038/nbt0487-369

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nbt0487-369

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing