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Study of a factor produced by suspension-cultured Pinus radiata cells which enhances cell growth at low inoculum densities

Low inoculum growth factor from Pinus radiata

  • Conifer Biotechnology Working Group
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Abstract

Pinus radiata cells in suspension culture abruptly lose their growth capacity when diluted below a critical inoculum density. This threshold density can be lowered by adding the supernatant (conditioned medium) from healthy cultures which have been grown separately at high densities. Fresh medium is conditioned rapidly indicating that the factor responsible is either potent or produced rapidly. Activity-response curves increase progressively with concentration indicating that still greater effect may be obtained if the factor can be concentrated following separation from other medium components. The effect is not mimicked by a number of candidate compounds (including auxins, cytokinins, polyamines and vitamins). Partial characterisation studies indicate that the factor is relatively small (<1 000 dalton) and possibly an oligosaccharide. It is considered that the factor is an essential structural component of the walls of expanding cells where it is reversibly-bound.

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Abbreviations

2,4-D:

dichlorophenoxyacetic acid

LIGF:

Low Inoculum Growth Factor

NAA:

naphthalene acetic acid

References

  • Birnberg PR, Somers DA & Brenner ML (1988) Characterisation of conditioning factors that increase colony formation from ‘black mexican sweet’ corn protoplasts. J. Plant Physiol. 132: 316–321

    Google Scholar 

  • Flory PJ (1953) Principles of Polymer Chemistry. Cornell University Press, Ithaca, New York

    Google Scholar 

  • Fry SC (1989) The structure and functions of xyloglucan. J. Exp. Bot. 40: 1–11

    Google Scholar 

  • Gilmour DM, Davey MR, Cocking EC & Pental D (1987) Culture of low numbers of forage legume protoplasts in membrane chambers. J. Plant Physiol. 126: 457–465

    Google Scholar 

  • Hayashi T (1989) Xyloglucans in the primary cell wall. Ann. Rev. Plant Physiol. Plant Molec. Bio. 40: 139–168

    Google Scholar 

  • Jeffrey PD, Nichol LW & Teasdale RD (1979) Studies of macromolecular heterogeneous associations involving cross-linking: A re-examination of the ovalbumin-lysozyme system. Bioph. Chem. 10: 379–387

    Google Scholar 

  • Kao KN (1977) Chromosomal behaviour in somatic hybrids of soybean-nicotiana glauca. Molec. Gen. Genet. 150: 225–230

    Google Scholar 

  • Kohler F & Wenzel G (1985) Regeneration of isolated barley microspores in conditioned media and trials to characterise the responsible factor. J. Plant Physiol. 121: 181–191

    Google Scholar 

  • Ludwig SR, Somers DA, Petersen L, Pohlman RF, Zarowitz MA, Gengenba BG & Messing J (1985) High frequency callus formation from maize zea-mays protoplasts. Theor. Appl. Genet. 71: 344–350

    Google Scholar 

  • Nichol LW, Scully MJ, Jeffrey PD & Teasdale RD (1981) Cross-linking interactions in systems of three reactants: theory pertaining to their experimental elucidation. J. Theor. Biol. 91: 215–230

    Google Scholar 

  • Smith JA, Green CE & Gengenbach BG (1984) Feeder layer support of low density populations of Zea mays L suspension cells. Plant Sci. Lett. 36: 67–72

    Google Scholar 

  • Somers DA, Birnberg PR, Petersen WL & Brenner ML (1987) The effect of conditioned medium on colony formation from ‘black mexican sweet’ corn protoplasts. Plant Sci. 53: 249–256

    Google Scholar 

  • Stockmayer WH (1943) Theory of molecular size distribution and gel formation in branched-chain polymers. J. Chem. Phys. 11: 45–55

    Google Scholar 

  • Stuart R & Street HE (1971) Studies on the growth in culture of plant cells X. Further studies on the conditioning of culture media by suspensions of Acer pseudoplatanus L. cells. J. Exp. Bot. 22: 96–106

    Google Scholar 

  • Teasdale RD (1984) Application of growth analysis to trace element nutrition: study of copper uptake with a loblolly pine (Pinus taeda) cell suspension culture. J. Exp. Bot. 35: 1495–1506

    Google Scholar 

  • Teasdale RD (1986) Generation of a sustainable Pinus radiata cell suspension culture and studies of cellular nitrogen nutrition. New Zealand Journal of Forest Science 17: 377–386

    Google Scholar 

  • Teasdale RD, Carr AR & Read RSD (1985) Substrate aggregation and cooperative enzyme kinetics: consideration of enzyme access with large aggregates. J. Theor. Biol. 114: 375–382

    Google Scholar 

  • Teasdale RD, Dawson PA & Woolhouse HW (1986) Mineral nutrient requirements of a loblolly pine (Pinus taeda) cell suspension culture Plant Physiol. 82: 942–945

    Google Scholar 

  • Teasdale RD & Richards DK (1987) Culture of Pinus radiata cells: study of a cell viability factor. In: Hanover JW & Keathley DE (Eds) Genetic Manipulation of Woody Plants (p 489) Plenum Press, New York, London

    Google Scholar 

  • Teasdale RD & Richards DK (1990) Boron deficiency in cultured pine cells: Quantitative studies of the intraction with Ca and Mg. Plant Physiol. 93: 1071–1077

    Google Scholar 

  • Xu ZH, Huang B & Sunderland N (1981) Culture of barley anthers in conditioned media. J. Exp. Bot. 32: 767–778

    Google Scholar 

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Teasdale, R.D., Richards, D.K. Study of a factor produced by suspension-cultured Pinus radiata cells which enhances cell growth at low inoculum densities. Plant Cell Tiss Organ Cult 26, 53–59 (1991). https://doi.org/10.1007/BF00116610

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  • DOI: https://doi.org/10.1007/BF00116610

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