Uptake, accumulation and metabolism of auxins in tobacco leaf protoplasts

Uptake and metabolism of exogenous naphthalene-1-acetic acid (NAA) and indole-3-acetic acid (IAA) have been studied in tobacco (Nicotiana tabacum L. cv. Xanthi) mesophyll protoplasts. Both auxins entered protoplasts by diffusion under the action of the transmembrane pH gradient without any detectable participation of an influx carrier. Molecules were accumulated by an anion-trapping mechanism and most of them were metabolized within hours, essentially as glucose-ester and amino-acid conjugates. Protoplasts were equipped with a functional auxin-efflux carrier as evidenced by the inhibitory effect of naphthylphtalamic acid on IAA efflux. Basically, similar mechanisms of NAA and IAA uptake occurred in protoplasts. However, the two auxins differed in their levels of accumulation, due to different membrane-transport characteristics, and the nature of the metabolites produced. This shows the need to estimate the accumulation and the metabolism of auxins when analyzing their effects in a given cell system. The internal auxin concentration could be modulated by changing the transmembrane pH gradient, giving an interesting perspective for discriminating between the effects of intra- and extracellular auxin on physiological processes.

[1]  M. Sussman,et al.  Auxin uptake and action of N-1-naphthylphthalamic acid in corn coleoptiles , 2004, Planta.

[2]  C. Maurel,et al.  Antibodies to a peptide from the maize auxin-binding protein have auxin agonist activity. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  D. Inzé,et al.  A new bioassay for auxins and cytokinins. , 1992, Plant physiology.

[4]  C. Pearce,et al.  Specifically deuterated and tritiated auxins , 1980 .

[5]  John Gutknecht,et al.  Transport of auxin (indoleacetic acid) through lipid bilayer membranes , 1980, The Journal of Membrane Biology.

[6]  A. D. Paolis,et al.  Different promoter regions control level and tissue specificity of expression of Agrobacterium rhizogenes rolB gene in plants , 1991, Plant Molecular Biology.

[7]  M. Caboche,et al.  Auxin Conjugation by Tobacco Mesophyll Protoplasts : Correlations between Auxin Cytotoxicity under Low Density Growth Conditions and Induction of Conjugation Processes at High Density. , 1984, Plant physiology.

[8]  Y. Ogata,et al.  The Chemistry of 1-Naphthaleneacetic Acid Derivatives , 1951 .

[9]  R. Bandurski,et al.  Chemistry and Physiology of the Bound Auxins , 1982 .

[10]  W. Pengelly,et al.  Bound auxin metabolism in cultured crown-gall tissues of tobacco. , 1986, Plant physiology.

[11]  P. Rubery The Mechanism of Transmembrane Auxin Transport and Its Relation to the Chemiosmotic Hypothesis of the Polar Transport of Auxin , 1980 .

[12]  T. Schmülling,et al.  Rol genes alter hormonal requirements for protoplast growth and modify the expression of an auxin responsive promoter , 1993, Plant Cell Reports.

[13]  C. Maurel,et al.  The rolB Gene of Agrobacterium rhizogenes Does Not Increase the Auxin Sensitivity of Tobacco Protoplasts by Modifying the Intracellular Auxin Concentration , 1994, Plant physiology.

[14]  C. Maurel,et al.  Auxin regulates the promoter of the root-inducing rolB gene of Agrobacterium rhizogenes in transgenic tobacco , 1990, Molecular and General Genetics MGG.

[15]  N. A. Walker,et al.  Measurement of Fluxes across Membranes , 1976 .

[16]  T. Nagata,et al.  Differential Expression of an Auxin-Regulated Gene, parC, and a Novel Related Gene, C-7, from Tobacco Mesophyll Protoplasts in Response to External Stimuli and in Plant Tissues , 1992 .

[17]  Ross C. Bean,et al.  Permeability of Lipid Bilayer Membranes to Organic Solutes , 1968, The Journal of general physiology.

[18]  R. Hedrich,et al.  Plant growth hormones control voltage-dependent activity of anion channels in plasma membrane of guard cells , 1991, Nature.

[19]  Y. Takahashi,et al.  parB: an auxin-regulated gene encoding glutathione S-transferase. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[20]  Y. Hiraoka,et al.  Characterization of the auxin-regulated par gene from tobacco mesophyll protoplasts. , 1991, The Plant journal : for cell and molecular biology.

[21]  M. Caboche,et al.  Isolation in vitro of naphthaleneacetic acid-tolerant mutants of Nicotiana tabacum, which are impaired in root morphogenesis , 1985, Molecular and General Genetics MGG.

[22]  G. Sandberg,et al.  Metabolism of indole-3-acetic acid in Arabidopsis. , 1998, Plant physiology.

[23]  Y. Niwa,et al.  Location of the cis-acting auxin-responsive region in the promoter of the par gene from tobacco mesophyll protoplasts. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[24]  G. Ephritikhine,et al.  Impermeant auxin analogues have auxin activity , 1990, Planta.

[25]  T. Schmülling,et al.  Indole-3-acetic acid homeostasis in transgenic tobacco plants expressing the Agrobacterium rhizogenes rolB gene , 1993 .

[26]  C. Maurel,et al.  Alterations of Auxin Perception in rolB-Transformed Tobacco Protoplasts (Time Course of rolB mRNA Expression and Increase in Auxin Sensitivity Reveal Multiple Control by Auxin) , 1994, Plant physiology.

[27]  M. Smulders,et al.  Metabolism of 1-naphthaleneacetic acid in explants of tobacco: Evidence for release of free hormone from conjugates , 1990, Journal of Plant Growth Regulation.

[28]  K. Palme,et al.  Patch-clamp analysis establishes a role for an auxin binding protein in the auxin stimulation of plasma membrane current in Zea mays protoplasts , 1993 .

[29]  B. Sundberg,et al.  Conjugation of Indole-3-Acetic Acid (IAA) in Wild-Type and IAA-Overprodcing Transgenic Tobacco Plants, and Identification of the Main Conjugates by Frit-Fast Atom Bombardment Liquid Chromatography-Mass Spectrometry , 1993, Plant physiology.

[30]  Y. Machida,et al.  Isolation of an auxin-regulated gene cDNA expressed during the transition from G0 to S phase in tobacco mesophyll protoplasts. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[31]  John A. Raven,et al.  TRANSPORT OF INDOLEACETIC ACID IN PLANT CELLS IN RELATION TO pH AND ELECTRICAL POTENTIAL GRADIENTS, AND ITS SIGNIFICANCE FOR POLAR IAA TRANSPORT , 1975 .

[32]  J. Bacon,et al.  The carbohydrates of the Jerusalem artichoke and other Compositae. , 1951, The Biochemical journal.

[33]  C. Maurel,et al.  Perception of the auxin signal at the plasma membrane of tobacco mesophyll protoplasts. , 1991, Biochemical Society transactions.

[34]  W. Hartung,et al.  The Permeability Coefficients of the Plasmalemma and the Chloroplast Envelope of Spinach Mesophyll Cells for Phytohormones , 1981 .

[35]  G. Ephritikhine,et al.  Functional evidence for an auxin receptor at the plasmalemma of tobacco mesophyll protoplasts. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[36]  A. Murphy,et al.  Auxin transport. , 2005, Current opinion in plant biology.

[37]  W. Michalke,et al.  Phytotropin-binding sites and auxin transport in Cucurbita pepo: evidence for two recognition sites , 1992, Planta.

[38]  Alan M. Jones,et al.  Auxin‐binding proteins and their possible roles in auxin‐mediated plant cell growth , 1992 .

[39]  P. Nobel,et al.  Introduction to biophysical plant physiology , 1974 .

[40]  J. Guern,et al.  Regulation of intracellular pH in plant cells , 1991 .

[41]  P. Pilet The Physiological Properties of Plant Protoplasts , 1985, Proceedings in Life Sciences.

[42]  M. Goldsmith,et al.  The Polar Transport of Auxin , 1977 .

[43]  M. Caboche Nutritional requirements of protoplast-derived, haploid tobacco cells grown at low cell densities in liquid medium , 1980, Planta.

[44]  G. Sandberg,et al.  Presence of indole-3-acetic acid in chloroplasts ofNicotiana tabacum andPinus sylvestris , 1990, Planta.

[45]  W. Bartley,et al.  The study of steady-state concentrations of internal solutes of mitochondria by rapid centrifugal transfer to a fixation medium. , 1957, The Biochemical journal.