Utilization of glycine and serine as nitrogen sources in the roots of Zea mays and Chamaegigas intrepidus
- PMID: 12432023
- DOI: 10.1093/jxb/erf092
Utilization of glycine and serine as nitrogen sources in the roots of Zea mays and Chamaegigas intrepidus
Abstract
Glycine and serine are potential sources of nitrogen for the aquatic resurrection plant Chamaegigas intrepidus Dinter in the rock pools that provide its natural habitat. The pathways by which these amino acids might be utilized were investigated by incubating C. intrepidus roots and maize (Zea mays) root tips with [(15)N]glycine, [(15)N]serine and [2-(13)C]glycine. The metabolic fate of the label was followed using in vivo NMR spectroscopy, and the results were consistent with the involvement of the glycine decarboxylase complex (GDC) and serine hydroxymethyltransferase (SHMT) in the utilization of glycine. In contrast, the labelling patterns provided no evidence for the involvement of serine:glyoxylate aminotransferase in the metabolism of glycine by the root tissues. The key observations were: (i) the release of [(15)N]ammonium during [(15)N]-labelling experiments; and (ii) the detection of a characteristic set of serine isotopomers in the [2-(13)C]glycine experiments. The effects of aminoacetonitrile, amino-oxyacetate, and isonicotinic acid hydrazide, all of which inhibit GDC and SHMT to some extent, and of methionine sulphoximine, which inhibited the reassimilation of the ammonium, supported the conclusion that GDC and SHMT were essential for the metabolism of glycine. C. intrepidus was observed to metabolize serine more readily than the maize root tips and this may be an adaptation to its nitrogen-deficient habitat. Overall, the results support the emerging view that GDC is an essential component of glycine catabolism in non-photosynthetic tissues.
Similar articles
-
Uptake of amino acids by the aquatic resurrection plant Chamaegigas intrepidus and its implication for N nutrition.Oecologia. 1998 Nov;117(1-2):63-69. doi: 10.1007/s004420050632. Oecologia. 1998. PMID: 28308507
-
Urea: a nitrogen source for the aquatic resurrection plant Chamaegigas intrepidus Dinter.Oecologia. 2000 Apr;123(1):9-14. doi: 10.1007/s004420050984. Oecologia. 2000. PMID: 28308748
-
Abscisic acid (ABA) relations in the aquatic resurrection plant Chamaegigas intrepidus under naturally fluctuating environmental conditions.New Phytol. 1997 Aug;136(4):603-611. doi: 10.1046/j.1469-8137.1997.00789.x. New Phytol. 1997. PMID: 33863103
-
Genetic manipulation of glycine decarboxylation.J Exp Bot. 2003 Jun;54(387):1523-35. doi: 10.1093/jxb/erg171. Epub 2003 Apr 28. J Exp Bot. 2003. PMID: 12730263 Review.
-
Ideotype root architecture for efficient nitrogen acquisition by maize in intensive cropping systems.Sci China Life Sci. 2010 Dec;53(12):1369-73. doi: 10.1007/s11427-010-4097-y. Epub 2010 Dec 23. Sci China Life Sci. 2010. PMID: 21181338 Review.
Cited by
-
Nitrogen Source and External Medium pH Interaction Differentially Affects Root and Shoot Metabolism in Arabidopsis.Front Plant Sci. 2016 Feb 1;7:29. doi: 10.3389/fpls.2016.00029. eCollection 2016. Front Plant Sci. 2016. PMID: 26870054 Free PMC article.
-
Comparative analysis of tissue-specific transcriptomic responses to nitrogen stress in spinach (Spinacia oleracea).PLoS One. 2020 May 6;15(5):e0232011. doi: 10.1371/journal.pone.0232011. eCollection 2020. PLoS One. 2020. PMID: 32374731 Free PMC article.
-
Oak protein profile alterations upon root colonization by an ectomycorrhizal fungus.Mycorrhiza. 2017 Feb;27(2):109-128. doi: 10.1007/s00572-016-0734-z. Epub 2016 Oct 7. Mycorrhiza. 2017. PMID: 27714470
-
NMR analysis of plant nitrogen metabolism.Photosynth Res. 2005;83(2):163-80. doi: 10.1007/s11120-004-2081-8. Photosynth Res. 2005. PMID: 16143850 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources