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. 1994 Jul;105(3):921–926. doi: 10.1104/pp.105.3.921

Putrescine Channels in the Plasma Membrane of Arabidopsis thaliana.

L Giromini 1, A Paina 1, R Cerana 1, R Colombo 1
PMCID: PMC160741  PMID: 12232254

Abstract

The patch-clamp technique was used in the whole-cell configuration to study plasma membrane channels permeable to the diamine putrescine in protoplasts isolated from cultured cells of Arabidopsis thaliana L. Under our experimental conditions, no channels selectively mediating putrescine influx were observed. Inward K+ channels showed a low permeability to putrescine, the permeability ratio of putrescine relative to K+ being around 0.1. Further characterization of the previously identified outward channels mediating putrescine efflux (R. Colombo, R. Cerana, N. Bagni [1992] Biochem Biophys Res Commun 182: 1187-1192) indicated that their activity was regulated by the overall ion concentration of the external medium.

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Selected References

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  1. Colombo R., Cerana R., Bagni N. Evidence for polyamine channels in protoplasts and vacuoles of Arabidopsis thaliana cells. Biochem Biophys Res Commun. 1992 Feb 14;182(3):1187–1192. doi: 10.1016/0006-291x(92)91857-m. [DOI] [PubMed] [Google Scholar]
  2. Ditomaso J. M., Hart J. J., Kochian L. V. Transport kinetics and metabolism of exogenously applied putrescine in roots of intact maize seedlings. Plant Physiol. 1992 Feb;98(2):611–620. doi: 10.1104/pp.98.2.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fairley-Grenot K. A., Assmann S. M. Permeation of Ca2+ through K+ channels in the plasma membrane of Vicia faba guard cells. J Membr Biol. 1992 Jun;128(2):103–113. doi: 10.1007/BF00231883. [DOI] [PubMed] [Google Scholar]
  4. Hedrich R., Marten I. Malate-induced feedback regulation of plasma membrane anion channels could provide a CO2 sensor to guard cells. EMBO J. 1993 Mar;12(3):897–901. doi: 10.1002/j.1460-2075.1993.tb05730.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Inoue I. Activation-inactivation of potassium channels and development of the potassium-channel spike in internally perfused squid giant axons. J Gen Physiol. 1981 Jul;78(1):43–61. doi: 10.1085/jgp.78.1.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Pardo L. A., Heinemann S. H., Terlau H., Ludewig U., Lorra C., Pongs O., Stühmer W. Extracellular K+ specifically modulates a rat brain K+ channel. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2466–2470. doi: 10.1073/pnas.89.6.2466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Seiler N., Dezeure F. Polyamine transport in mammalian cells. Int J Biochem. 1990;22(3):211–218. doi: 10.1016/0020-711x(90)90332-w. [DOI] [PubMed] [Google Scholar]
  8. Slocum R. D., Kaur-Sawhney R., Galston A. W. The physiology and biochemistry of polyamines in plants. Arch Biochem Biophys. 1984 Dec;235(2):283–303. doi: 10.1016/0003-9861(84)90201-7. [DOI] [PubMed] [Google Scholar]

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