Skip to main content
Log in

Dramatic effects of truncation and sub-cellular targeting on the accumulation of recombinant microbial cellulase in tobacco

  • Published:
Molecular Breeding Aims and scope Submit manuscript

Abstract

The economical bioconversion of lignocellulosic biomass to ethanol is dependent on the availability of large quantities of inexpensive cellulase enzymes. One way to reduce the cost of such enzymes is to produce them in crop plants at high levels. In order to assess factors that limit recombinant cellulase expression in plants, we have introduced the gene encoding E1 endo-1,4-β-glucanase (cellulase) of Acidothermus cellulolyticus into tobacco (Nicotiana tabacum) plants. Both the holoenzyme (E1) and catalytic domain (E1cd) were targeted to three sub-cellular compartments; the cytosol, chloroplast and apoplast. Accumulation of both E1 and E1cd was greatest in the apoplast, with levels more than 100-fold higher than observed for cytosolic accumulation. In all three compartments, E1cd accumulated to higher levels than the full-length enzyme. By combining truncation and apoplastic localization, an increase in expression of more than 500-fold was achieved, compared to cytosolic full-length E1. This effect is primarily post-transcriptional, since E1cd mRNA levels are very similar despite the range of E1cd accumulation observed. Recombinant E1cd, expressed at up to 1.6% total soluble protein, is extremely stable in both crude leaf extracts and dried leaf material.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Austin S., Bingham E.T., Mathews D.E., Shahan M.N., Will J. and Burgess R.R. 1995. Production and field performance of transgenic alfalfa (Medicago sativa L.) expressing α-amylase andmanganese-dependent lignin peroxidase. Euphytica 85: 381–393.

    Google Scholar 

  • Austin-Phillips S., Koegel R., Straub R. and Cook M. 1998. Animal feed compositions containing phytase derived from transgenic alfalfa and methods of use thereof. US patent 5,900,525.

  • Austin-Phillips S., Burgess R., Ziegelhoffer T. and German T.L. 1999. Transgenic plants as an alternative source of lignocellulosic degrading enzymes. US patent 5,981,835.

  • Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A. and Struhl K. 1989. Short Protocols in Molecular Biology. John Wiley, New York.

    Google Scholar 

  • Baker J.O., Adney W.S., Nieves R.A., Thomas S.R., Wilson D.B. and Himmel M.E. 1994. A new thermostable endoglucanase, Acidothermus cellulolyticus E1. Synergism with Trichoderma reesei CBH I and comparison to Thermomonospora fusca E5. Appl Biochem. Biotechnol. 45/46: 245–256.

    Google Scholar 

  • Berry-Lowe S.L., McKnight T.D., Shah D.M. and Meagher R.B. 1982. The nucleotide sequence, expression, and evolution of one member of a multigene family encoding the small subunit of rubulose-1,5-bisphophate carboxylase in soybean. J. Mol. Appl. Genet. 1: 483–498.

    Google Scholar 

  • Boston R.S., Viitanen P.V. and Vierling E. 1996. Molecular chaperones and protein folding in plants. Plant Mol. Biol. 32: 191–222.

    Google Scholar 

  • Cheung W.Y., Nathalie H. and Landry B.S. 1993. A simple and rapid DNA microextraction method for plant, animal and insect suitable for RAPD and other PCR analyses. PCR Meth. Appl. 3: 69–70.

    Google Scholar 

  • Conrad U. and Fiedler U. 1998. Compartment-specific accumulation of recombinant immuno-globulins in plant cells: an essential tool for antibody production and immunomodulation of physiological functions and pathogen activity. Plant Mol. Biol. 38: 101–109.

    Google Scholar 

  • Creissen G., Reynolds H., Xue Y. and Mullineaux P. 1995. Simultaneous targeting of pea glutathione reductase and of a bacterial fusion protein to chloroplasts and mitochondria in transgenic tobacco. Plant J. 8: 167–175.

    Google Scholar 

  • Dai Z., Hooker B.S., Quesenberry R.D. and Gao J. 1999. Expression of Trichoderma reesei exo-cellobiohydrolase I in transgenic tobacco leaves and calli. Appl. Biochem. Biotechnol. 77-79: 689–699.

    Google Scholar 

  • Dai Z., Hooker B.S., Anderson D.B. and Thomas S.R. 2000a. Expression of Acidothermus cellulolyticus endoglucanase E1 in transgenic tobcco: biochemical characteristics and physiological effects. Transgenic Res. 9: 43–54.

    Google Scholar 

  • Dai Z., Hooker B.S., Anderson D.B. and Thomas S.R. 2000b. Improved plant-based production of E1 endoglucanase using potato: expression optimization and tissue targeting. Mol. Breed. 6: 277–285.

    Google Scholar 

  • Deragon J.M. and Landry B.S. 1992. RAPD and other PCR-based analyses of plant genomes. PCR Meth. Appl. 1: 175–180.

    Google Scholar 

  • Halliwell N. and Halliwell G. 1995. Biotechnological aspects of lignocellulose and biomass degradation. Outlook Agric. 24: 219–225.

    Google Scholar 

  • Haseloff J., Siemering K.R., Prasher D.C. and Hodge S. 1997. Removal of a cryptic intron and sub-cellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly. Proc. Natl. Acad. Sci. USA 94: 2122–2127.

    Google Scholar 

  • Heber U., Pon N.G. and Heber M. 1963. Localization of carboxydismutase & triosephosphate dehydrogenases in chloroplasts. Plant Physiol. 38: 355–360.

    Google Scholar 

  • Hendriks T., van den Berg B.M. and Schram A.W. 1985. Cellular location of peroxidase isoenzymes in leaf tissue of Petunia and their affinity for concanavalin A-Sepharose. Planta 164: 89–95.

    Google Scholar 

  • Jefferson R.A., Kavanagh T.A. and Bevan M.W. 1987. GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 6: 3901–3907.

    Google Scholar 

  • Koegel R., Straub R. and Austin-Phillips S. 1998. Phytase-proteinpigmenting concentrate derived from green plant juice. [Author: please mention source].

  • Koegel R.G., Straub R.J., Austin-Phillips S., Cook M.E. and Crenshaw T.D. 1999. Alfalfa-produced phytase for supplementation of poultry and swine rations. In: International Summer Meeting of the American Society of Agricultural Engineers.

  • Koziel M.G., Carozzi N.B. and Desai N. 1996. Optimizing expression of transgenes with an emphasis on post-transcriptional events. Plant Mol. Biol. 32: 393–405.

    Google Scholar 

  • Levy M. and Adam Z. 1995. Mutations in the processing site of the precursor of rubulose-1,5-carboxylase/oxygenase small subunit: effects on import, processing, assembly and stability. Plant Mol. Biol. 29: 53–61.

    Google Scholar 

  • Lynd L.R., Cushman J.H., Nichols R.J. and Wyman C.E. 1991. Fuel ethanol from cellulosic biomass. Science 251: 1318–1323.

    Google Scholar 

  • Nishimura M., Graham D. and Akazawa T. 1976. Isolation of intact chloroplasts and other cell organelles from spinach leaf protoplasts. Plant Physiol. 58: 309–314.

    Google Scholar 

  • Parvathi K., Bhagwat A.S. and Raghavendra A.S. 1998. Modulation by bicarbonate of catalytic and regulatory properties of C4 phosphoenolphyruvate carboxylase from Amaranthus hypochondriacus: desensitization to malate and glucose 6-phosphate and sensitization of Mg2+. Plant Cell Physiol. 39: 1294–1298.

    Google Scholar 

  • Rathmell W.G. and Sequeira L. 1974. Soluble peroxidases in fluid from intercellular spaces in tobacco leaves. Plant Physiol. 53: 317–318.

    Google Scholar 

  • Sakon J., Adney W.S., Himmel M.E., Thomas S.R. and Karplus P.A. 1996. Crystal structure of thermostable family 5 endocellulase E1 from Acidothermus cellulolyticus in complex with cellotetraose. Biochemistry 35: 10648–10660.

    Google Scholar 

  • Sheehan J. and Himmel M. 1999. Enzymes, energy, and the environment: a strategic perspective on the U.S. Department of Energy's research and development activities for bioethanol. Biotech. Prog. 15: 817–827.

    Google Scholar 

  • Shepard J.F. and Totten R.E. 1975. Isolation and regeneration of tobacco mesophyll cell protoplasts under low osmotic conditions. Plant Physiol. 55: 689–694.

    Google Scholar 

  • Sullivan M.L. and Green P.J. 1993. Post-transcriptional regulation of nuclear-encoded genes in higher plants: the roles of mRNA stability and translation. Plant Mol. Biol. 23: 1091–1104.

    Google Scholar 

  • Teeri T.T. 1997. Crystalline cellulose degradation: new insight into the function of cellobiohydrolases. Trends Biotechnol. 15: 160–167.

    Google Scholar 

  • Tucker M.P., Mohegheghi A., Grohmann K. and Himmel M.E. 1989. Ultra-thermostable cellulases from Acidothermus cellulolyticus: comparison of temperature optima with previously reported cellulases. Bio/technology 7: 817–820.

    Google Scholar 

  • Wong E.Y., Hironaka C.M. and Fischhoff D.A. 1992. Arabidopsis thaliana small subunit leader and transit peptide enhance the expression of Bacillus thuringiensis proteins in transgenic plants. Plant Mol. Biol. 20: 81–93.

    Google Scholar 

  • Ziegelhoffer T., Will J. and Austin-Phillips S. 1999. Expression of bacterial cellulase genes in transgenic alfalfa (Medicago sativa L.), potato (Solanum tuberosum L.) and tobacco (Nicotiana tabacum L.). Mol. Breed. 5: 309–318.

    Google Scholar 

  • Ziegler M.T., Thomas S.R. and Danna K.J. 2000. Accumulation of a thermostable endo-1,4-β-D-glucanase in the apoplast of Arabidopsis thaliana leaves. Mol. Breed. 6: 37–46.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ziegelhoffer, T., Raasch, J.A. & Austin-Phillips, S. Dramatic effects of truncation and sub-cellular targeting on the accumulation of recombinant microbial cellulase in tobacco. Molecular Breeding 8, 147–158 (2001). https://doi.org/10.1023/A:1013338312948

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1013338312948

Navigation