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   <subfield code="a">Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Akin Delbarre, Philippe Muller, Viviane Imhoff, Jean Guern]</subfield>
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   <subfield code="a">Accumulation of radiolabelled naphthalene-1-acetic acid (1-NAA), 2,4-dichlorophenoxyacetic acid (2,4-D), and indole-3-acetic acid (IAA) has been measured in suspension-cultured tobacco (Nicotiana tabacum) cells. In this paper is presented a simple methodology allowing activities of the auxin influx and efflux carriers to be monitored independently by measuring the cellular accumulation of [3H]NAA and [14C]2,4-D. We have shown that 1-NAA enters cells by passive diffusion and has its accumulation level controlled by the efflux carrier. By contrast, 2,4-D uptake is mostly ensured by the influx carrier and this auxin is not secreted by the efflux carrier. Both auxin carriers contribute to IAA accumulation. The kinetic parameters and specificity of each carrier have been determined and new information concerning interactions with naphthylphthalamic acid, pyrenoylbenzoic acid, and naphthalene-2-acetic acid are provided. The relative contributions of diffusion and carrier-mediated influx and efflux to the membrane transport of 2,4-D, 1-NAA, and IAA have been quantified, and the data indicate that plant cells are able to modulate over a large range their auxin content by modifying the activity of each carrier.</subfield>
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   <subfield code="a">Auxin carriers</subfield>
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   <subfield code="a">Auxin membrane transport</subfield>
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   <subfield code="a">NPA : N-1-naphthylphthalamic acid</subfield>
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   <subfield code="a">PBA : 2-(1-pyrenoyl)benzoic acid</subfield>
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   <subfield code="a">Vm : maximum transport capacity of the carrier</subfield>
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