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Enhanced levels of methionine and cysteine in transgenic alfalfa (Medicago sativa L.) plants over-expressing the Arabidopsis cystathionine γ-synthase gene

Summary With the aim of increasing the methionine level in alfalfa (Medicago sativa L.) and thus improving its nutritional quality, we produced transgenic alfalfa plants that expressed the Arabidopsis cystathionine γ‐synthase (AtCGS), the enzyme that controls the synthesis of the first intermediate...

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Published in:Plant biotechnology journal 2005-01, Vol.3 (1), p.71-79
Main Authors: Avraham, Tal, Badani, Hanna, Galili, Shmuel, Amir, Rachel
Format: Article
Language:English
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Summary:Summary With the aim of increasing the methionine level in alfalfa (Medicago sativa L.) and thus improving its nutritional quality, we produced transgenic alfalfa plants that expressed the Arabidopsis cystathionine γ‐synthase (AtCGS), the enzyme that controls the synthesis of the first intermediate metabolite in the methionine pathway. The AtCGS cDNA was driven by the Arabidopsis rubisco small subunit promoter to obtain expression in leaves. Thirty transgenic plants were examined for the transgene protein expression, and four lines with a high expression level were selected for further work. In these lines, the contents of methionine, S‐methylmethionine (SMM), and methionine incorporated into the water‐soluble protein fraction increased up to 32‐fold, 19‐fold, and 2.2‐fold, respectively, compared with that in wild‐type plants. Notably, in these four transgenic lines, the levels of free cysteine (the sulphur donor for methionine synthesis), glutathione (the cysteine storage and transport form), and protein‐bound cysteine increased up to 2.6‐fold, 5.5‐fold, and 2.3‐fold, respectively, relative to that in wild‐type plants. As the transgenic alfalfa plants over‐expressing AtCGS had significantly higher levels of both soluble and protein‐bound methionine and cysteine, they may represent a model and target system for improving the nutritional quality of forage crops.
ISSN:1467-7644
1467-7652
DOI:10.1111/j.1467-7652.2004.00102.x