Abstract
The electrophoretic mobility of mature spinach (Spinacia oleracea L. var. Americana) chloroplasts sampled over a 7-month period was between −2.03 and −2.45 micrometers per second per volt per centimeter when suspended in a solution containing 1 millimolar CaCl2. The surface charge density of EDTA-treated chloroplasts was calculated to be −7,400 electrostatic units per square centimeter representing, on the average, one electronic charge per 645 square Angstroms. Electrophoretic mobility increases during plastid maturation. Calcium, but not magnesium, generally stabilized the envelope of isolated plastids against small increases in surface charge that occur with time in the absence of calcium. Pronase caused a sharp, but temporary, decrease in the electrophoretic mobility of chloroplasts. This was interpreted as representing a transient binding of pronase to the envelope surface during proteolysis. No −SH groups were detected on the surface of the plastid envelope. Inasmuch as the isoelectric point of intact chloroplasts was found to be at pH 4.5, it is likely that the major part of the total surface charge results from the presence of exposed carboxyl groups of intrinsic envelope proteins that are not readily hydrolyzed by mild pronase treatment.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BANGHAM A. D., HEARD D. H., FLEMANS R., SEAMAN G. V. An apparatus for microelectrophoresis of small particles. Nature. 1958 Sep 6;182(4636):642–644. doi: 10.1038/182642a0. [DOI] [PubMed] [Google Scholar]
- Barber J., Mills J., Love A. Electrical diffuse layers and their influence on photosynthetic processes. FEBS Lett. 1977 Mar 1;74(2):174–181. doi: 10.1016/0014-5793(77)80841-7. [DOI] [PubMed] [Google Scholar]
- Fish L., Franceschi V. R., Stocking C. R. Effects of pronase on isolated chloroplasts. Plant Physiol. 1979 Dec;64(6):1012–1014. doi: 10.1104/pp.64.6.1012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grassetti D. R., Murray J. F., Jr, Ruan H. T. The interaction of 6,6'-dithiodinicotinic acid with thiols and with ehrlich ascites tumor cells. Biochem Pharmacol. 1969 Mar;18(3):603–611. doi: 10.1016/0006-2952(69)90085-9. [DOI] [PubMed] [Google Scholar]
- Gross J. A., Becker M. J., Shefner A. M. Electrophoretic fractionation of chloroplast fragments in a pH gradient. Experientia. 1964 May 15;20(5):261–262. doi: 10.1007/BF02151793. [DOI] [PubMed] [Google Scholar]
- Mehrishi J. N., Grassetti D. R. Sulphydryl groups on the surface of intact Ehrlich ascites tumour cells, human blood platelets and lymphocytes. Nature. 1969 Nov 8;224(5219):563–564. doi: 10.1038/224563a0. [DOI] [PubMed] [Google Scholar]
- Mehrishi J. N. Molecular aspects of the mammalian cell surface. Prog Biophys Mol Biol. 1972;25:1–70. doi: 10.1016/0079-6107(72)90013-2. [DOI] [PubMed] [Google Scholar]
- Nakatani H. Y., Barber J., Forrester J. A. Surface charges on chloroplast membranes as studied by particle electrophoresis. Biochim Biophys Acta. 1978 Oct 11;504(1):215–225. doi: 10.1016/0005-2728(78)90019-1. [DOI] [PubMed] [Google Scholar]
- Nakatani H. Y., Barber J., Minski M. J. The influence of the thylakoid membrane surface properties on the distribution of ions in chloroplasts. Biochim Biophys Acta. 1979 Jan 11;545(1):24–35. doi: 10.1016/0005-2728(79)90110-5. [DOI] [PubMed] [Google Scholar]
- Nobel P. S., Mel H. C. Electrophoretic studies of light-induced charge in spinach chloroplasts. Arch Biochem Biophys. 1966 Mar;113(3):695–702. doi: 10.1016/0003-9861(66)90250-5. [DOI] [PubMed] [Google Scholar]
