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Plant Physiol. 1981 Jun;67(6):1214-9. doi: 10.1104/pp.67.6.1214.

Measurement of Protein Degradation in Leaves of Zea mays Using [H]Acetic Anhydride and Tritiated Water.

Plant physiology

E Simpson

Affiliations

  1. Department of Biology, Washington University, St. Louis, Missouri 63130.

PMID: 16661839 PMCID: PMC425864 DOI: 10.1104/pp.67.6.1214

Abstract

The rate of protein degradation in Zea mays leaves has been estimated by using tritiated water and [(3)H]acetic anhydride as the labeling agents. Both methods circumvent many of the problems usually associated with measuring protein degradation in plants. The half-life of ribulose-1,5-bisphosphate carboxylase protein in second leaves of 13-day-old seedlings under continuous light was found to be 7.8 +/- 0.9 days by the tritiated water technique and 6.5 +/- 0.8 days by the [(3)H]acetic anhydride method. The half-lives determined under a 14-hour-light, 10-hour-dark photoperiod are 6.2 +/- 0.8 days with tritiated water and 5.4 +/- 0.4 days with [(3)H]acetic anhydride. Whereas the values obtained by the two methods do not differ significantly, the use of either method for the determination of protein half-life can be recommended.

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