Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
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Plant Physiology 70:1347-1352 (1982)
© 1982 American Society of Plant Biologists

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Articles

Methionine Synthesis in Lemna1

Inhibition of Cystathionine {gamma}-Synthase by Propargylglycine

Gregory A. Thompson, Anne H. Datko and S. Harvey Mudd

National Institute of Mental Health, Bethesda, Maryland 20205, Laboratory of General and Comparative Biochemistry, Bethesda, Maryland 20205

Propargylglycine, vinylglycine, and cysteine each cause irreversible inactivations of cystathionine {gamma}-synthase (and, in parallel, of O-phosphohomoserine sulfhydrylase) activities in crude extracts of Lemna paucicostata. Inactivation by propargylglycine or vinylglycine is completely prevented by 40 millimolar O-phospho- or O-succinyl-L-homoserine; that by cysteine is only partially prevented. Propargylglycine (PAG), the most potent of these inhibitors, causes rapid and drastic inactivation of both activities in intact Lemna. Studies of plants growing in steady states in the presence of various concentrations (0-150 nanomolar) of PAG showed that 16% of control activity is necessary and sufficient to maintain normal rates of growth and methionine biosynthesis, and that 10% of control activity is essential for viability. Addition of either 2 micromolar methionine or 31 micromolar cystine to growth medium containing 150 nanomolar PAG permits growth at 75 to 100% of control rates when enzyme activity is less than 10% of control. Whereas methionine presumably rescues by directly providing the missing metabolite, cystine may rescue by enhancing substrate accumulation and thereby promoting flux through residual cystathionine {gamma}-synthase. The results indicate that the down-regulation of cystathionine {gamma}-synthase to 15% of control which occurs when plants are grown in 2 micromolar methionine (Thompson, Datko, Mudd, Giovanelli Plant Physiol 69: 1077-1083), by itself, is not sufficient to reduce the rate of methionine biosynthesis.


1 Reprint requests should be addressed to the authors at Building 32, Room 101, National Institute of Mental Health, Bethesda, MD 20205.




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