Publication | Closed Access
HIGH LOCALIZATION OF RIBULOSE‐1,5‐BISPHOSPHATE CARBOXULASE/OXYGENASE IN THE PYRENOIDS OF <i>CHLAMYDOMONAS REINHARDTII</i> (CHLOROPHYTA), AS REVEALED BY CRYOFIXATION AND IMMUNOGOLD ELECTRON MICROSCOPY
54
Citations
19
References
1997
Year
BiosynthesisEngineeringCellular EnzymologyBiochemistryPhotosystemsBioenergeticsNatural SciencesGold ParticlesEnzyme CatalysisCo 2Conventional FixationMicrobiologyCellular BiochemistryPhotosynthesisPlant CytologyPlant PhysiologyUltrastructure
ABSTRACT The distribution of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco) in the chloroplasts of the unicellular green alga Chlamydomonas reinhardtii Dangeard was examined using cryotechnique and conventional fixation for immunogold electron microscopy. Both methods provided essentially identical results, although somewhat higher densities of gold particles indicating Rubisco molecules were recognized in the pyrenoids of cryofixed cells. The gold particles were highly concentrated in the pyrenoid matrix within the chloroplasts. Even when considering the vast difference in volume between the pyrenoid and the rest of the Chloroplast, more than 99% of the total Rubisco labeling in the chloroplast was calculated to be present in the pyrenoid matrix. High localization of Rubisco in the pyrenoid matrix was also recognized regardless of cell age, based on immunofluorescence microscopy of the same en bloc samples. These results are inconsistent with a recent immunocytochemical study employing cryotechnique in which more than 90% of the total Rubisco was recognized in the thylakoid region (thylakoid membranes and stroma) of C. reinhardtii cells. Rubisco highly localized in the pyrenoid matrix may take part in active photosynthetic CO 2 fixation and/or the CO 2 concentrating mechanism .
| Year | Citations | |
|---|---|---|
Page 1
Page 1