Nanolitre‐scale assays to determine the activities of enzymes in individual plant cells

• Published in: The Plant journal : for cell and molecular biology 2003-05, Vol.34 (4), p.555-564
• Main Authors: Roy, Stuart J., Cuin, Tracey A., Leigh, Roger A.
• Format: Article
• Language: English
• Subjects: acid phosphatase; Acid Phosphatase - metabolism; Arabidopsis; Arabidopsis - cytology; Arabidopsis - enzymology; Arabidopsis thaliana; barley (Hordeum vulgare); Biological and medical sciences; Cells - cytology; Cells - enzymology; Cysteine Endopeptidases - metabolism; cysteine protease; Enzymes; Fundamental and applied biological sciences. Psychology; Hordeum - cytology; Hordeum - enzymology; Hordeum vulgare; Hydrogen-Ion Concentration; Metabolism; Microchemistry - methods; Nitrate Reductase; Nitrate Reductases - metabolism; Plant Leaves - cytology; Plant Leaves - enzymology; Plant physiology and development; single‐cell sampling; Substrate Specificity
• ISSN: 0960-7412; 1365-313X
• DOI: 10.1046/j.1365-313X.2003.01744.x

Summary There are a variety of methods for characterising gene expression at the level of individual cells and for demonstrating that the cells also contain the encoded proteins. However, measuring the activity of enzymes at the resolution of single cells in complex tissues, such as leaves, is problematic. We have addressed this by using single‐cell sampling to extract 10–100 pl droplets of sap from individual plant cells and then measuring enzyme activities in these droplets with nanolitre‐scale fluorescence‐based assays. We have optimised these assays and used them to measure and characterise the activities of acid phosphatase, cysteine protease and nitrate reductase in sap samples from epidermal and mesophyll cells of barley (Hordeum vulgare L.) and Arabidopsis thaliana leaves exposed to different developmental and environmental conditions. During leaf senescence in barley, we found that the dynamics with which acid phosphatase and protease activities changed were different in each cell type and did not mirror the changes occurring at the whole‐leaf level. Increases in nitrate reductase activities after exposure of barley plants to nitrate were large in mesophyll cells but small in epidermal cells. The technique was applied successfully to Arabidopsis and, as in barley, revealed cell‐specific differences in the activities of both acid phosphatase and nitrate reductase. The assays add to the spectrum of techniques available for characterising cells within complex plant tissues, thus extending the opportunity to relate gene expression to biochemical activities at the single‐cell level.