Abstract
We have found that Na+ is required for the alkalotolerance of the cyanobacterium Synechococcus leopoliensis. Cell division did not occur at any pH in the absence of Na+, but cells inoculated into Na+-free growth medium at pH 6.8 did continue metabolic activity, and over a period of 48 h, the cells became twice their normal size. Many of these cells remained viable for at least 59 h and formed colonies on Na+ -containing medium. Cells grown in the presence of Na+ and inoculated into Na+ -free growth medium at pH 9.6 rapidly lost viability. An Na+ concentration of ca. 0.5 milliequivalents X liter-1 was required for sustained growth above pH 9.0. The Na+ requirement could be only partially met by Li+ and not at all by K+ or Rb+. Cells incubated in darkness in growth medium at pH 6.8 had an intracellular pH near neutrality in the presence or absence of Na+. When the external pH was shifted to 9.6, only cells in the presence of Na+ were able to maintain an intracellular pH near 7.0. The membrane potential, however, remained high (-120 mV) in the absence or presence of Na+ unless collapsed by the addition of gramicidin. Thus, the inability to maintain a neutral intracellular pH at pH 9.6 in the absence of Na+ was not due to a generalized disruption of membrane integrity.Even cells containing Na+ still required added Na+ to restore photosynthetic rates to normal after the cells had been washed in Na+ -free buffer at pH 9.6. This requirement was only partially met by Li+ and was not met at all by K+, Rb+, Cs+ Mg2+, or Ca2+. The restoration of photosynthesis by added Na+ occurred within 30 s and suggests a role for extracellular Na+. Part of our results can be explained in terms of the operation of an Na+/H+ antiporter activity in the plasma membrane, but some results would seem to require other mechanisms for Na+ action.
Full text
PDF






Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Coleman J. R., Colman B. Inorganic Carbon Accumulation and Photosynthesis in a Blue-green Alga as a Function of External pH. Plant Physiol. 1981 May;67(5):917–921. doi: 10.1104/pp.67.5.917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Falkner G., Horner F. pH Changes in the Cytoplasm of the Blue-Green Alga Anacystis nidulans Caused by Light-dependent Proton Flux into the Thylakoid Space. Plant Physiol. 1976 Dec;58(6):717–718. doi: 10.1104/pp.58.6.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guffanti A. A., Cohn D. E., Kaback H. R., Krulwich T. A. Relationship between the Na+/H+ antiporter and Na+/substrate symport in Bacillus alcalophilus. Proc Natl Acad Sci U S A. 1981 Mar;78(3):1481–1484. doi: 10.1073/pnas.78.3.1481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guffanti A. A., Susman P., Blanco R., Krulwich T. A. The protonmotive force and alpha-aminoisobutyric acid transport in an obligately alkalophilic bacterium. J Biol Chem. 1978 Feb 10;253(3):708–715. [PubMed] [Google Scholar]
- Kallas T., Castenholz R. W. Internal pH and ATP-ADP pools in the cyanobacterium Synechococcus sp. during exposure to growth-inhibiting low pH. J Bacteriol. 1982 Jan;149(1):229–236. doi: 10.1128/jb.149.1.229-236.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kallas T., Dahlquist F. W. Phosphorus-31 nuclear magnetic resonance analysis of internal pH during photosynthesis in the cyanobacterium Synechococcus. Biochemistry. 1981 Sep 29;20(20):5900–5907. doi: 10.1021/bi00523a038. [DOI] [PubMed] [Google Scholar]
- Krulwich T. A., Guffanti A. A., Bornstein R. F., Hoffstein J. A sodium requirement for growth, solute transport, and pH homeostasis in Bacillus firmus RAB. J Biol Chem. 1982 Feb 25;257(4):1885–1889. [PubMed] [Google Scholar]
- Krulwich T. A., Mandel K. G., Bornstein R. F., Guffanti A. A. A non-alkalophilic mutant of Bacillus alcalophilus lacks the Na+/H+ antiporter. Biochem Biophys Res Commun. 1979 Nov 14;91(1):58–62. doi: 10.1016/0006-291x(79)90582-5. [DOI] [PubMed] [Google Scholar]
- Lee-Kaden J., Simonis W. Amino acid uptake and energy coupling dependent on photosynthesis in Anacystis nidulans. J Bacteriol. 1982 Jul;151(1):229–236. doi: 10.1128/jb.151.1.229-236.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mandel K. G., Guffanti A. A., Krulwich T. A. Monovalent cation/proton antiporters in membrane vesicles from Bacillus alcalophilus. J Biol Chem. 1980 Aug 10;255(15):7391–7396. [PubMed] [Google Scholar]
- Miller A. G., Colman B. Active transport and accumulation of bicarbonate by a unicellular cyanobacterium. J Bacteriol. 1980 Sep;143(3):1253–1259. doi: 10.1128/jb.143.3.1253-1259.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Padan E., Zilberstein D., Schuldiner S. pH homeostasis in bacteria. Biochim Biophys Acta. 1981 Dec;650(2-3):151–166. doi: 10.1016/0304-4157(81)90004-6. [DOI] [PubMed] [Google Scholar]
- Paschinger H. DCCD induced sodium uptake by Anacystis nidulans. Arch Microbiol. 1977 Jun 20;113(3):285–291. doi: 10.1007/BF00492037. [DOI] [PubMed] [Google Scholar]
- Wolk C. P. Physiology and cytological chemistry blue-green algae. Bacteriol Rev. 1973 Mar;37(1):32–101. doi: 10.1128/br.37.1.32-101.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
