Characterization of transgenic poplar with ectopic expression of pine cytosolic glutamine synthetase under conditions of varying nitrogen availability

$\bullet$ The present study addresses the hypothesis that enhanced expression of glutamine synthetase (GS) in transgenic poplar, characterized by the ectopic expression of pine cytosolic GS, results in an enhanced efficiency of nitrogen (N) assimilation and enhanced growth. $\bullet$ Transgenic and...

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Published inThe New phytologist Vol. 167; no. 1; pp. 31 - 39
Main Authors Man, H, Boriel, R, El-Khatib, R, Kirby, E.G
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science 01.07.2005
Blackwell Science Ltd
Blackwell
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Summary:$\bullet$ The present study addresses the hypothesis that enhanced expression of glutamine synthetase (GS) in transgenic poplar, characterized by the ectopic expression of pine cytosolic GS, results in an enhanced efficiency of nitrogen (N) assimilation and enhanced growth. $\bullet$ Transgenic and control poplar were supplied with low and high N levels and the role of ectopic expression of the pine GS in growth and N assimilation was assessed by using amino acid analysis, 15N enrichment, biochemical analyses, and growth measurements. $\bullet$ While leaves of transgenic poplar contained 85% less (P < 0.01) free ammonium than leaves of nontransgenic control plants, leaves of transgenics showed increases in the levels of free glutamine and total free amino acids. Transgenic poplar lines also displayed significant increases in growth parameters when compared with controls grown under both low (0.3 mM) and high (10 mM) nitrate conditions. Furthermore, $^{15}N-enrichment$ experiments showed that 27% more (P < 0.05) 15N was incorporated into structural compounds in transgenic lines than in nontransgenic controls. $\bullet$ Using the methods described here, we present direct evidence for increased N assimilation efficiency and growth in GS transgenic lines.
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content type line 23
ISSN:0028-646X
1469-8137
DOI:10.1111/j.1469-8137.2005.01461.x