Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1968 Oct;109(4):687–691. doi: 10.1042/bj1090687

Studies on halotolerance in a moderately halophilic bacterium. Effect of betaine on salt resistance of the respiratory system

Dvora Rafaeli-Eshkol 1, Y Avi-Dor 1
PMCID: PMC1186956  PMID: 5683517

Abstract

The role of betaine as a factor influencing the salt resistance of the respiratory system in resting cells of the moderately halophilic halotolerant bacterium Ba1 was studied. Betaine accelerated succinate oxidation in cells obtained from low-salt medium, and stimulation of the respiratory rate was stronger the higher the sodium chloride concentration in the assay medium. The stimulatory effect also depended on the ratio of betaine concentration to the amount of bacteria present. Accumulation of labelled betaine by the bacterial cells was demonstrated; like the respiratory stimulation, it was favourably influenced by an increase in the sodium chloride concentration of the medium. In cells harvested from a high-salt medium and washed with 2·0m-sodium chloride, betaine caused no increase in the respiratory rate, nor was the already high salt resistance of the respiratory system further improved by the addition of betaine. When, however, these cells lost their salt resistance as a result of washing in the absence of sodium chloride, betaine was able to restore it to its original level. In contrast with respiration in low-salt-grown bacteria, that in high-salt-grown cells was not affected by betaine, even after they were washed in the absence of sodium chloride, when the sodium chloride concentration was optimum.

Full text

PDF
690

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AVI-DOR Y., KUCZYNSKI M., SCHATZBERG G., MAGER J. Turbidity changes in bacterial suspensions: kinetics and relation to metabolic state. J Gen Microbiol. 1956 Feb;14(1):76–83. doi: 10.1099/00221287-14-1-76. [DOI] [PubMed] [Google Scholar]
  2. BUHLER D. R. A simple scintillation counting technique for assaying C1402 in a Warburg flask. Anal Biochem. 1962 Nov;4:413–417. doi: 10.1016/0003-2697(62)90143-4. [DOI] [PubMed] [Google Scholar]
  3. DURELL J., ANDERSON D. G., CANTONI G. L. The synthesis of methionine by enzymic transmethylation. I. Purification and properties of thetin homocysteine methylpherase. Biochim Biophys Acta. 1957 Nov;26(2):270–281. doi: 10.1016/0006-3002(57)90005-7. [DOI] [PubMed] [Google Scholar]
  4. GOLDSTEIN D. B. Induction of cholinesterase biosynthesis in Pseudomonas fluorescens. J Bacteriol. 1959 Nov;78:695–702. doi: 10.1128/jb.78.5.695-702.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. MILLER S., AVI-DOR Y. The effect of inorganic ions on respiration in Pasteurella tularensis and Escherichia coli. J Gen Microbiol. 1958 Feb;18(1):221–226. doi: 10.1099/00221287-18-1-221. [DOI] [PubMed] [Google Scholar]
  6. Rafaeli-Eshkol D. Studies on halotolerance in a moderately halophilic bacterium. Effect of growth conditions on salt resistance of the respiratory system. Biochem J. 1968 Oct;109(4):679–685. doi: 10.1042/bj1090679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. SHIEH H. S. AEROBIC DEGRADATION OF CHOLINE. I. FERMENTATION OF CHOLINE BY A MARINE BACTERIUM, ACHROMOBACTER CHOLINOPHAGUM N. SP. Can J Microbiol. 1964 Dec;10:837–842. doi: 10.1139/m64-109. [DOI] [PubMed] [Google Scholar]
  8. SHIEH H. S. AEROBIC DEGRADATION OF CHOLINE. II. SOME PROPERTIES OF WHOLE CELLS AND CELL-FREE EXTRACTS OF ACHROMOBACTER CHOLINOPHAGUM. Can J Microbiol. 1965 Apr;11:375–379. doi: 10.1139/m65-045. [DOI] [PubMed] [Google Scholar]
  9. Shieh H. S. Further studies on the oxidation of betaine by a marine bacterium, Achromobacter cholinophagum. Can J Microbiol. 1966 Apr;12(2):299–302. doi: 10.1139/m66-040. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES