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. 1994 Mar;104(3):865–871. doi: 10.1104/pp.104.3.865

The Synthesis of [gamma]-Aminobutyric Acid in Response to Treatments Reducing Cytosolic pH.

L A Crawford 1, A W Bown 1, K E Breitkreuz 1, F C Guinel 1
PMCID: PMC160683  PMID: 12232132

Abstract

[gamma]-Aminobutyric acid (GABA) synthesis (L-glutamic acid + H+ -> GABA + CO2) is rapidly stimulated by a variety of stress conditions including hypoxia. Recent literature suggests that GABA production and concomitant H+ consumption ameliorates the cytosolic acidification associated with hypoxia or other stresses. This proposal was investigated using isolated asparagus (Asparagus sprengeri Regel) mesophyll cells. Cell acidification was promoted using hypoxia, H+/L-glutamic acid symport, and addition of butyrate or other permeant weak acids. Sixty minutes of all three treatments stimulated the levels of both intracellular and extracellular GABA by values ranging from 100 to 1800%. At an external pH of 5.0, addition of 5 mM butyrate stimulated an increase in overall GABA level from 3.86 (0.56 [plus or minus] SE) to 20.4 (2.16 [plus or minus] SE) nmol of GABA/106 cell. Butyrate stimulated GABA levels by 200 to 300% within 15 s, and extracellular GABA was observed after 10 min. The acid load due to butyrate addition was assayed by measuring [14C]butyrate uptake. After 45 s of butyrate treatment, H+-consuming GABA production accounted for 45% of the imposed acid load. The cytosolic location of a fluorescent pH probe was confirmed using fluorescent microscopy. Spectrofluorimetry indicated that butyrate addition reduced cytosolic pH by 0.60 units with a half-time of approximately 2 s. The proposal that GABA synthesis ameliorates cytosolic acidification is supported by the data. The possible roles of H+ and Ca2+ in stimulating GABA synthesis are discussed.

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Selected References

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  1. Baum G., Chen Y., Arazi T., Takatsuji H., Fromm H. A plant glutamate decarboxylase containing a calmodulin binding domain. Cloning, sequence, and functional analysis. J Biol Chem. 1993 Sep 15;268(26):19610–19617. [PubMed] [Google Scholar]
  2. Gehring C. A., Irving H. R., Parish R. W. Effects of auxin and abscisic acid on cytosolic calcium and pH in plant cells. Proc Natl Acad Sci U S A. 1990 Dec 15;87(24):9645–9649. doi: 10.1073/pnas.87.24.9645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Knight M. R., Campbell A. K., Smith S. M., Trewavas A. J. Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium. Nature. 1991 Aug 8;352(6335):524–526. doi: 10.1038/352524a0. [DOI] [PubMed] [Google Scholar]
  4. Mathieu Y., Guern J., Pean M., Pasquier C., Beloeil J. C., Lallemand J. Y. Cytoplasmic pH Regulation in Acer pseudoplatanus Cells: II. Possible Mechanisms Involved in pH Regulation during Acid-Load. Plant Physiol. 1986 Nov;82(3):846–852. doi: 10.1104/pp.82.3.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. McCutcheon S. L., Ciccarelli B. W., Chung I., Shelp B., Bown A. W. l-Glutamate-Dependent Medium Alkalinization by Asparagus Mesophyll Cells : Cotransport or Metabolism? Plant Physiol. 1988 Dec;88(4):1042–1047. doi: 10.1104/pp.88.4.1042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Menegus F., Cattaruzza L., Chersi A., Fronza G. Differences in the Anaerobic Lactate-Succinate Production and in the Changes of Cell Sap pH for Plants with High and Low Resistance to Anoxia. Plant Physiol. 1989 May;90(1):29–32. doi: 10.1104/pp.90.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Satyanarayan V., Nair P. M. Purification and characterization of glutamate decarboxylase from Solanum tuberosum. Eur J Biochem. 1985 Jul 1;150(1):53–60. doi: 10.1111/j.1432-1033.1985.tb08987.x. [DOI] [PubMed] [Google Scholar]
  8. Snedden W. A., Chung I., Pauls R. H., Bown A. W. Proton/l-Glutamate Symport and the Regulation of Intracellular pH in Isolated Mesophyll Cells. Plant Physiol. 1992 Jun;99(2):665–671. doi: 10.1104/pp.99.2.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Thomas J. A., Buchsbaum R. N., Zimniak A., Racker E. Intracellular pH measurements in Ehrlich ascites tumor cells utilizing spectroscopic probes generated in situ. Biochemistry. 1979 May 29;18(11):2210–2218. doi: 10.1021/bi00578a012. [DOI] [PubMed] [Google Scholar]
  10. Wagner G. J. Content and vacuole/extravacuole distribution of neutral sugars, free amino acids, and anthocyanin in protoplasts. Plant Physiol. 1979 Jul;64(1):88–93. doi: 10.1104/pp.64.1.88. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Walker K. A., Givan C. V., Keys A. J. Glutamic Acid metabolism and the photorespiratory nitrogen cycle in wheat leaves: metabolic consequences of elevated ammonia concentrations and of blocking ammonia assimilation. Plant Physiol. 1984 May;75(1):60–66. doi: 10.1104/pp.75.1.60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Wallace W., Secor J., Schrader L. E. Rapid Accumulation of gamma-Aminobutyric Acid and Alanine in Soybean Leaves in Response to an Abrupt Transfer to Lower Temperature, Darkness, or Mechanical Manipulation. Plant Physiol. 1984 May;75(1):170–175. doi: 10.1104/pp.75.1.170. [DOI] [PMC free article] [PubMed] [Google Scholar]

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