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. 1978 Mar;61(3):342–347. doi: 10.1104/pp.61.3.342

Regulation of Sulfate Assimilation in Plants

7. Cysteine Inactivation of Adenosine 5′-Phosphosulfate Sulfotransferase in Lemna minor L. 1

Christian Brunold 1,2, Ahlert Schmidt 1,2
PMCID: PMC1091864  PMID: 16660289

Abstract

When 0.5 mm cysteine is added to cultures of Lemna minor L. growing with sulfate as the sole sulfur source, there is a rapid 80% loss of extractable adenosine 5′-phosphosulfate sulfotransferase. This loss is accompanied by an inhibition of sulfate uptake; however, lack of sulfate is not responsible for the decreasing adenosine 5′-phosphosulfate sulfotransferase activity.

Cultivation with cysteine causes an increase in the cyst(e)ine pool of L. minor. This fact taken together with the observed inactivation of adenosine 5′-phosphosulfate sulfotransferase in crude extracts by cysteine suggests that the cysteine pool is involved in the in vivo regulation of the enzyme.

The activity of adenosine 5′-phosphosulfate sulfotransferase is restored within 24 hours after transfer to a culture medium without cysteine. This restoration is partially blocked by 6-methyl purine and actinomycin D and completely by cycloheximide.

Cycloheximide added to cultures of L. minor L. causes a loss of extractable APSTase comparable to the one obtained with cysteine. This loss may be in part due to cysteine, since cycloheximide causes a pronounced increase in the cysteine pool of L. minor.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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