Amino Acid Metabolism of Lemna minor L. : III. Responses to Aminooxyacetate.
Journal: 2010/June - Plant Physiology
ISSN: 0032-0889
PUBMED: 16666162
Abstract:
Aminooxyacetate, a known inhibitor of transaminase reactions and glycine decarboxylase, promotes rapid depletion of the free pools of serine and aspartate in nitrate grown Lemna minor L. This compound markedly inhibits the methionine sulfoximine-induced accumulation of free ammonium ions and greatly restricts the methionine sulfoximine-induced depletion of amino acids such as glutamate, alanine, and asparagine. These results suggest that glutamate, alanine, and asparagine are normally catabolized to ammonia by transaminase-dependent pathways rather than via dehydrogenase or amidohydrolase reactions. Aminooxyacetate does not inhibit the methionine sulfoximine-induced irreversible deactivation of glutamine synthetase in vivo, indicating that these effects cannot be simply ascribed to inhibition of methionine sulfoximine uptake by amino-oxyacetate. This transaminase inhibitor promotes extensive accumulation of several amino acids including valine, leucine, isoleucine, alanine, glycine, threonine, proline, phenylalanine, lysine, and tyrosine. Since the aminooxyacetate induced accumulations of valine, leucine, and isoleucine are not inhibited by the branched-chain amino acid biosynthesis inhibitor, chlorsulfuron, these amino acid accumulations most probably involve protein turnover. Depletions of soluble protein bound amino acids are shown to be approximately stoichiometric with the free amino acid pool accumulations induced by aminooxyacetate. Aminooxyacetate is demonstrated to inhibit the chlorsulfuron-induced accumulation of alpha-amino-n-butyrate in L. minor, supporting the notion that this amino acid is derived from transamination of 2-oxobutyrate.
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Plant Physiol 87(2): 447-453

Amino Acid Metabolism of <em>Lemna minor</em> L. <sup><a href="#fn1" rid="fn1" class=" fn">1</a></sup>

Abstract

Aminooxyacetate, a known inhibitor of transaminase reactions and glycine decarboxylase, promotes rapid depletion of the free pools of serine and aspartate in nitrate grown Lemna minor L. This compound markedly inhibits the methionine sulfoximine-induced accumulation of free ammonium ions and greatly restricts the methionine sulfoximine-induced depletion of amino acids such as glutamate, alanine, and asparagine. These results suggest that glutamate, alanine, and asparagine are normally catabolized to ammonia by transaminase-dependent pathways rather than via dehydrogenase or amidohydrolase reactions. Aminooxyacetate does not inhibit the methionine sulfoximine-induced irreversible deactivation of glutamine synthetase in vivo, indicating that these effects cannot be simply ascribed to inhibition of methionine sulfoximine uptake by amino-oxyacetate. This transaminase inhibitor promotes extensive accumulation of several amino acids including valine, leucine, isoleucine, alanine, glycine, threonine, proline, phenylalanine, lysine, and tyrosine. Since the aminooxyacetate induced accumulations of valine, leucine, and isoleucine are not inhibited by the branched-chain amino acid biosynthesis inhibitor, chlorsulfuron, these amino acid accumulations most probably involve protein turnover. Depletions of soluble protein bound amino acids are shown to be approximately stoichiometric with the free amino acid pool accumulations induced by aminooxyacetate. Aminooxyacetate is demonstrated to inhibit the chlorsulfuron-induced accumulation of α-amino-n-butyrate in L. minor, supporting the notion that this amino acid is derived from transamination of 2-oxobutyrate.

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  • Davies DD, Humphrey TJ. Amino Acid recycling in relation to protein turnover. Plant Physiol. 1978 Jan;61(1):54–58.[PMC free article] [PubMed] [Google Scholar]
  • Ferreira RB, Davies DD. Protein degradation in lemna with particular reference to ribulose bisphosphate carboxylase: I. The effect of light and dark. Plant Physiol. 1987 Apr;83(4):869–877.[PMC free article] [PubMed] [Google Scholar]
  • Ferreira RB, Davies DD. Protein Degradation in Lemna with Particular Reference to Ribulose Bisphosphate Carboxylase: II. The Effect of Nutrient Starvation. Plant Physiol. 1987 Apr;83(4):878–883.[PMC free article] [PubMed] [Google Scholar]
  • Havir EA. Inactivation of serine:glyoxylate and glutamate:glyoxylate aminotransferases from tobacco leaves by glyoxylate in the presence of ammonium ion. Plant Physiol. 1986 Feb;80(2):473–478.[PMC free article] [PubMed] [Google Scholar]
  • Ireland RJ, Joy KW. Purification and properties of an asparagine aminotransferase from Pisum sativum leaves. Arch Biochem Biophys. 1983 May;223(1):291–296. [PubMed] [Google Scholar]
  • John RA, Charteris A. The reaction of amino-oxyacetate with pyridoxal phosphate-dependent enzymes. Biochem J. 1978 Jun 1;171(3):771–779.[PMC free article] [PubMed] [Google Scholar]
  • Joy KW, Prabha C. The role of transamination in the synthesis of homoserine in peas. Plant Physiol. 1986 Sep;82(1):99–102.[PMC free article] [PubMed] [Google Scholar]
  • Kinney AJ, Moore TS. Phosphatidylcholine Synthesis in Castor Bean Endosperm : I. Metabolism of l-Serine. Plant Physiol. 1987 May;84(1):78–81.[PMC free article] [PubMed] [Google Scholar]
  • LaRossa RA, Van Dyk TK, Smulski DR. Toxic accumulation of alpha-ketobutyrate caused by inhibition of the branched-chain amino acid biosynthetic enzyme acetolactate synthase in Salmonella typhimurium. J Bacteriol. 1987 Apr;169(4):1372–1378.[PMC free article] [PubMed] [Google Scholar]
  • Martin F, Winspear MJ, Macfarlane JD, Oaks A. Effect of Methionine Sulfoximine on the Accumulation of Ammonia in C(3) and C(4) Leaves : The Relationship between NH(3) Accumulation and Photorespiratory Activity. Plant Physiol. 1983 Jan;71(1):177–181.[PMC free article] [PubMed] [Google Scholar]
  • Nakamura Y, Tolbert NE. Serine: glyoxylate, alanine:glyoxylate, and glutamate:glyoxylate aminotransferase reactions in peroxisomes from spinach leaves. J Biol Chem. 1983 Jun 25;258(12):7631–7638. [PubMed] [Google Scholar]
  • Ray TB. Site of action of chlorsulfuron: inhibition of valine and isoleucine biosynthesis in plants. Plant Physiol. 1984 Jul;75(3):827–831.[PMC free article] [PubMed] [Google Scholar]
  • Rhodes D, Deal L, Haworth P, Jamieson GC, Reuter CC, Ericson MC. Amino Acid Metabolism of Lemna minor L. : I. Responses to Methionine Sulfoximine. Plant Physiol. 1986 Dec;82(4):1057–1062.[PMC free article] [PubMed] [Google Scholar]
  • Rhodes D, Hogan AL, Deal L, Jamieson GC, Haworth P. Amino Acid Metabolism of Lemna minor L. : II. Responses to Chlorsulfuron. Plant Physiol. 1987 Jul;84(3):775–780.[PMC free article] [PubMed] [Google Scholar]
  • Rhodes D, Myers AC, Jamieson G. Gas Chromatography-Mass Spectrometry of N- Heptafluorobutyryl Isobutyl Esters of Amino Acids in the Analysis of the Kinetics of [N]H(4) Assimilation in Lemna minor L. Plant Physiol. 1981 Nov;68(5):1197–1205.[PMC free article] [PubMed] [Google Scholar]
  • Sarojini G, Oliver DJ. Inhibition of glycine oxidation by carboxymethoxylamine, methoxylamine, and acethydrazide. Plant Physiol. 1985 Mar;77(3):786–789.[PMC free article] [PubMed] [Google Scholar]
  • Ta TC, Joy KW, Ireland RJ. Amino Acid metabolism in pea leaves : utilization of nitrogen from amide and amino groups of [N]asparagine. Plant Physiol. 1984 Apr;74(4):822–826.[PMC free article] [PubMed] [Google Scholar]
  • Ta TC, Joy KW, Ireland RJ. Role of asparagine in the photorespiratory nitrogen metabolism of pea leaves. Plant Physiol. 1985 Jun;78(2):334–337.[PMC free article] [PubMed] [Google Scholar]
  • Yamaya T, Oaks A, Rhodes D, Matsumoto H. Synthesis of [N]glutamate from [N]h(4) and [N]glycine by mitochondria isolated from pea and corn shoots. Plant Physiol. 1986 Jul;81(3):754–757.[PMC free article] [PubMed] [Google Scholar]
Center for Plant Environmental Stress Physiology, Purdue University, West Lafayette, Indiana 47907
Department of Horticulture, Purdue University, West Lafayette, Indiana 47907
Supported by Purdue University Agricultural Experiment Station funds via a David Ross assistantship awarded to D.G.B.
Abstract
Aminooxyacetate, a known inhibitor of transaminase reactions and glycine decarboxylase, promotes rapid depletion of the free pools of serine and aspartate in nitrate grown Lemna minor L. This compound markedly inhibits the methionine sulfoximine-induced accumulation of free ammonium ions and greatly restricts the methionine sulfoximine-induced depletion of amino acids such as glutamate, alanine, and asparagine. These results suggest that glutamate, alanine, and asparagine are normally catabolized to ammonia by transaminase-dependent pathways rather than via dehydrogenase or amidohydrolase reactions. Aminooxyacetate does not inhibit the methionine sulfoximine-induced irreversible deactivation of glutamine synthetase in vivo, indicating that these effects cannot be simply ascribed to inhibition of methionine sulfoximine uptake by amino-oxyacetate. This transaminase inhibitor promotes extensive accumulation of several amino acids including valine, leucine, isoleucine, alanine, glycine, threonine, proline, phenylalanine, lysine, and tyrosine. Since the aminooxyacetate induced accumulations of valine, leucine, and isoleucine are not inhibited by the branched-chain amino acid biosynthesis inhibitor, chlorsulfuron, these amino acid accumulations most probably involve protein turnover. Depletions of soluble protein bound amino acids are shown to be approximately stoichiometric with the free amino acid pool accumulations induced by aminooxyacetate. Aminooxyacetate is demonstrated to inhibit the chlorsulfuron-induced accumulation of α-amino-n-butyrate in L. minor, supporting the notion that this amino acid is derived from transamination of 2-oxobutyrate.
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