Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991 Oct;57(10):2829-33.
doi: 10.1128/aem.57.10.2829-2833.1991.

Osmotically regulated transport of proline by Lactobacillus acidophilus IFO 3532

Affiliations

Osmotically regulated transport of proline by Lactobacillus acidophilus IFO 3532

J B Jewell et al. Appl Environ Microbiol. 1991 Oct.

Erratum in

  • Appl Environ Microbiol 1991 Dec;57(12):3683

Abstract

We reported previously that, when exposed to high osmotic pressure, Lactobacillus acidophilus IFO 3532 cells accumulated N,N,N-trimethylglycine (glycine betaine), which serves as a compatible intracellular solute. When grown in medium with high osmotic pressure, these cells also accumulated one amino acid, proline. The uptake of [3H]proline by resting, glucose-energized cells was stimulated by increasing the osmotic pressure of the assay medium with 0.5 to 1.0 M KCl, 1.0 M NaCl, or 0.5 M sucrose. The accumulated [3H]proline was not metabolized further. In contrast, there was no osmotic stimulation of [3H]leucine uptake. The uptake of proline was activated rather than induced by exposure of the cells to high osmotic pressure. Only one proline transport system could be discerned from kinetics plots. The affinity of the carrier for proline remained constant over a range of osmotic pressures from 650 to 1,910 mosM (Kt, 7.8 to 15.5 mM). The Vmax, however, increased from 15 nmol/min/mg of dry weight in 0.5 M sucrose to 27 and 40 nmol/min/mg of dry weight in 0.5 M KCl and in 1.0 M KCl or NaCl, respectively. The efflux of proline from preloaded cells occurred rapidly when the osmotic pressure of the suspending buffer was lowered.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Bacteriol. 1981 Oct;148(1):64-71 - PubMed
    1. Appl Environ Microbiol. 1987 Oct;53(10):2275-81 - PubMed
    1. J Bacteriol. 1990 Sep;172(9):5286-92 - PubMed
    1. Biochim Biophys Acta. 1977 Aug 15;469(1):1-12 - PubMed
    1. FEMS Microbiol Rev. 1990 Jun;6(2-3):239-46 - PubMed

Publication types

MeSH terms

LinkOut - more resources