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Plant Physiology 89:192-196 (1989)
© 1989 American Society of Plant Biologists

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Metabolism and Enzymology

Effect of Methionine Sulfoximine on Asparaginase Activity and Ammonium Levels in Pea Leaves 1

Konrad A. Sieciechowicz2, Kenneth W. Joy and Robert J. Ireland

Department of Biology, Carleton University, Ottawa, Ontario K1S 5B6, Canada, Department of Biology, Mount Allison University, Sackville, New Brunswick E0A 3C0, Canada

In developing leaves of Pisum sativum the levels of ammonium did not change during the light-dark photoperiod even though asparaginase (EC 3.5.1.1) did; asparaginase activity in detached leaves doubled during the first 2.5 hours in the light. When these leaves were supplied with 1 millimolar methionine sulfoximine (MSX, an inhibitor of glutamine synthetase, GS, activity) at the beginning of the photoperiod, levels of ammonium increased 8-to 10-fold, GS activity was inhibited 95%, and the light-stimulated increase in asparaginase activity was completely prevented, and declined to less than initial levels. When high concentrations of ammonium were supplied to leaves, the light-stimulated increase of asparaginase was partially prevented. However, it was also possible to prevent asparaginase increase, in the absence of ammonium accumulation, by the addition of MSX together with aminooxyacetate (AOA, which inhibits transamination and some other reactions of photorespiratory nitrogen cycling). AOA alone did not prevent light-stimulated asparaginase increase; neither MSX, AOA, or elevated ammonium levels inhibited the activity of asparaginase in vitro. These results suggest that the effect of MSX on asparaginase increase is not due solely to interference with photorespiratory cycling (since AOA also prevents cycling, but has no effect alone), nor to the production of high ammonium concentration or its subsequent effect on photosynthetic mechanisms. MSX must have further inhibitory effects on metabolism. It is concluded that accumulation of ammonium in the presence of MSX may underestimate rates of ammonium turnover, since liberation of ammonium from systems such as asparaginase is reduced by the effects of MSX.


2 Current address: Department of Biological Sciences, Simon Fraser University, Burnaby, B. C. Canada, V6A 1S6.

1 Supported by grants to K. W. J. and R. J. I. from Natural Sciences and Engineering Research Council of Canada.







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