Abstract
When cells of a marine pseudomonad were washed with a solution consisting of 0.3 m NaCl, 0.05 m MgSO4, and 0.01 m KCl (complete salts), they maintained their normal morphology. When washed with a solution of 0.05 m MgSO4, they became plasmolyzed as indicated by both phase and electron microscopy. Suspensions of cells washed with 0.05 m MgSO4 showed an increase in optical density (OD) when 0.3 m NaCl was added, and this was followed by a decrease in OD upon the further addition of 0.01 m KCl. Salts of other monovalent cations were not effective in replacing K+ in producing the OD decrease. Phase-contrast microscopy revealed that the increase in OD was accompanied by a decrease in cell size, and the decrease in OD, by an increase in the cell size. Both phase and electron microscopy showed that the K+-dependent decrease in OD was accompanied by deplasmolysis of the cells. Na+ was required in the suspending medium in addition to K+ to obtain deplasmolysis. The intracellular K+ concentration in cells which had been washed with complete salts and which had retained their normal morphology was found to be 0.290 m. In cells plasmolyzed by washing with 0.05 m MgSO4, the intracellular K+ concentration was 0.004 m. Deplasmolyzed cells contained 0.330 m K+. The membrane profile of plasmolyzed cells was retained when protoplasts were formed. The protoplasts became spherical if incubated in a solution permitting the deplasmolysis of the parent cells. The evidence obtained indicates that plasmolysis and deplasmolysis under the conditions described was due to the loss and gain, respectively, of K+ by the cells. The effect of Na+ could be ascribed to its capacity to control the porosity of the cytoplasmic membrane of this organism.
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- Bayer M. E. Areas of adhesion between wall and membrane of Escherichia coli. J Gen Microbiol. 1968 Oct;53(3):395–404. doi: 10.1099/00221287-53-3-395. [DOI] [PubMed] [Google Scholar]
- CHRISTIAN J. H., WALTHO J. A. The sodium and potassium content of non-halophilic bacteria in relation to salt tolerance. J Gen Microbiol. 1961 May;25:97–102. doi: 10.1099/00221287-25-1-97. [DOI] [PubMed] [Google Scholar]
- COTA-ROBLES E. H. ELECTRON MICROSCOPY OF PLASMOLYSIS IN ESCHERICHIA COLI. J Bacteriol. 1963 Mar;85:499–503. doi: 10.1128/jb.85.3.499-503.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Costerton J. W., Forsberg C., Matula T. I., Buckmire F. L., MacLeod R. A. Nutrition and metabolism of marine bacteria. XVI. Formation of protoplasts, spheroplasts, and related forms from a gram-negative marine bacterium. J Bacteriol. 1967 Nov;94(5):1764–1777. doi: 10.1128/jb.94.5.1764-1777.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Voe I. W., Thompson J., Costerton J. W., MacLeod R. A. Stability and comparative transport capacity of cells, mureinoplasts, and true protoplasts of a gram-negative bacterium. J Bacteriol. 1970 Mar;101(3):1014–1026. doi: 10.1128/jb.101.3.1014-1026.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KOCH A. L. Some calculations on the turbidity of mitochondria and bacteria. Biochim Biophys Acta. 1961 Aug 19;51:429–441. doi: 10.1016/0006-3002(61)90599-6. [DOI] [PubMed] [Google Scholar]
- MURRAY R. G., STEED P., ELSON H. E. THE LOCATION OF THE MUCOPEPTIDE IN SECTIONS OF THE CELL WALL OF ESCHERICHIA COLI AND OTHER GRAM-NEGATIVE BACTERIA. Can J Microbiol. 1965 Jun;11:547–560. doi: 10.1139/m65-072. [DOI] [PubMed] [Google Scholar]
- Matula T. I., MacLeod R. A. Mechanism of optical effects in suspensions of a marine pseudomonad. J Bacteriol. 1969 Oct;100(1):403–410. doi: 10.1128/jb.100.1.403-410.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matula T. I., Srivastava V. S., Wong P., MacLeod R. A. Transport and retention of K+ and other metabolites in a marine pseudomonad and their relation to the mechanism of optical effects. J Bacteriol. 1970 Jun;102(3):790–796. doi: 10.1128/jb.102.3.790-796.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scheie P. O. Plasmolysis of Escherichia coli B-r with sucrose. J Bacteriol. 1969 May;98(2):335–340. doi: 10.1128/jb.98.2.335-340.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scholander P. F. Osmotic mechanism and negative pressure. Science. 1967 Apr 7;156(3771):67–69. doi: 10.1126/science.156.3771.67. [DOI] [PubMed] [Google Scholar]
- Stevenson I. L. The cytological effects of myxin on Escherichia coli. Can J Microbiol. 1969 Jul;15(7):707–711. doi: 10.1139/m69-125. [DOI] [PubMed] [Google Scholar]
- Wong P. T., Thompson J., MacLeod R. A. Nutrition and metabolism of marine bacteria. XVII. Ion-dependent retention of alpha-aminoisobutyric acid and its relation to Na+ dependent transport in a marine pseudomonad. J Biol Chem. 1969 Feb 10;244(3):1016–1025. [PubMed] [Google Scholar]