Optimization of an Immunofluorescent Assay of the Internal Enzyme Ribulose‐1,5‐bisphosphate Carboxylase (Rubisco) in Single Phytoplankton Cells¹

Immunochemical probes are widely used to identih different species and to quantify and understand the role that different antigens play within cells. We optimized a single‐cell immunofluorescent assay for the carbon fixation enzyme ribulose‐1,5‐bisphosphate carboxylase (Rubisco) in order to quantify the enzyme by flow cytometry in phytoplankton cells. The criteria for optimization of the immunofluorescent assay for Rubisco in single cells included maximization of Rubisco immunogenicity, minimization of Rubisco diffusion out of the cells, minimization of cell breakage, and maximization of the cell labeling. Several fixatives (cross‐linkers and denaturing) and permeabilizing agents were tested on 26 species of phytoplankton. The only fixative / permeabilizing agent that fulfilled the criteria established for the assay was 96% ethanol. Phytoplankton cells collected from the field needed further treatment with a strong oxidant to permeabilize ethanolfixed cells and thus allow the antibody probe to access the Rubisco antigen. This study should have a general applicability to the study of other soluble photosynthetic antigens in single phytoplankton cells .