AN ATP-DEPENDENT L-CARNITINE TRANSPORTER IN LISTERIA-MONOCYTOGENES SCOTT-A IS INVOLVED IN OSMOPROTECTION

Citation
A. Verheul et al., AN ATP-DEPENDENT L-CARNITINE TRANSPORTER IN LISTERIA-MONOCYTOGENES SCOTT-A IS INVOLVED IN OSMOPROTECTION, Journal of bacteriology, 177(11), 1995, pp. 3205-3212
Citations number
51
Categorie Soggetti
Microbiology
Journal title
ISSN journal
00219193
Volume
177
Issue
11
Year of publication
1995
Pages
3205 - 3212
Database
ISI
SICI code
0021-9193(1995)177:11<3205:AALTIL>2.0.ZU;2-2
Abstract
Listeria monocytogenes is a gram-positive, psychrotrophic, food-borne pathogen which is able to grow in osmotically stressful environments. Carnitine (beta-hydroxy-L-tau-N-trimethyl aminobutyrate) can contribut e significantly to growth of L. monocytogenes at high osmolarity (R. R Beumer, M. C. te Giffel, L. J. Cox, F. M. Rombouts, and T. Abee, Appl , Environ, Microbiol. 60:1359-1363, 1994). Transport of L-[N-methyl-C- 14] carnitine in L. monocytogenes was shown to be energy dependent. An alysis of cell extracts revealed that L-carnitine was not further meta bolized, which supplies evidence for its role as an osmoprotectant in L. monocytogenes. Uptake of L-carnitine proceeds in the absence of a p roton motive force and is strongly inhibited in the presence of the ph osphate analogs vanadate and arsenate. The L-carnitine permease is the refore most likely driven by ATP. Kinetic analysis of L-carnitine tran sport in glucose-energized cells revealed the presence of a high-affin ity uptake system with a K-m of 10 mu M and a maximum rate of transpor t (V-max) of 48 nmol min(-1) mg of protein(-1), L-[C-14]carnitine tran sport in L. monocytogenes is significantly inhibited by a 10-fold exce ss of unlabelled L-carnitine, acetylcarnitine, and tau-butyrobetaine, whereas L-proline and betaine display, even at a 100-fold excess, only a weak inhibitory effect, In conclusion, an ATP-dependent L-carnitine transport system in L. monocytogenes is described, and its possible r oles in cold adaptation and intracellular growth in mammalian cells ar e discussed.