Cysteine Metabolism in Legionella pneumophila : Characterization of an l -Cystine-Utilizing Mutant
- 1 June 2006
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 72 (6) , 3993-4000
- https://doi.org/10.1128/aem.00684-06
Abstract
Growth of Legionella pneumophila on buffered charcoal-yeast extract (BCYE) medium is dependent on l -cysteine (but not l -cystine), which is added in excess over what is required for nutrition. We investigated the biochemical and genetic bases for this unusual requirement and determined that much of the l -cysteine in BCYE medium is rapidly oxidized to l -cystine and is unavailable to the bacteria. Analysis of cysteine consumption during bacterial growth indicated that of the 11% consumed, 3.85% (∼0.1 mM) was incorporated into biomass. The activities of two key cysteine biosynthetic enzymes (serine acetyltransferase and cysteine synthase) were not detected in cell extracts of L. pneumophila , and the respective genes were not present in the genome sequences, confirming cysteine auxotrophy. Kinetic studies identified two energy-dependent cysteine transporters, one with high affinity (apparent K m , 3.29 μM) and the other with low affinity (apparent K m , 93 μM), each of which was inhibited by the uncoupling agent carbonyl cyanide m -chlorophenylhydrazone. Cystine was not transported by L. pneumophila ; however, a mutant strain capable of growth on l -cystine (CYS1 mutant) transported l -cystine with similar kinetics ( K m , 4.4 μM and 90 μM). Based on the bipartite kinetics, requirement for proton motive force, and inhibitor studies, we suggest that a high-affinity periplasmic binding protein and a major facilitator/symporter (low affinity) mediate uptake. The latter most likely is functional at high cysteine concentrations and most likely displays altered substrate specificity in the CYS-1 mutant. Our studies provide biochemical evidence to support a general view that L. pneumophila is restricted to an intracellular lifestyle in natural environments by an inability to utilize cystine, which most likely ensures that the dormant cyst-like transmissible forms do not germinate outside suitable protozoan hosts.Keywords
This publication has 27 references indexed in Scilit:
- Novel ligands for the extracellular solute receptors of two bacterial TRAP transportersMicrobiology, 2006
- Evidence in the Legionella pneumophila genome for exploitation of host cell functions and high genome plasticityNature Genetics, 2004
- Three Different Systems Participate in l -Cystine Uptake in Bacillus subtilisJournal of Bacteriology, 2004
- Phagosomal Acidification Is Not a Prerequisite for Intracellular Multiplication ofLegionella pneumophilain Human MonocytesThe Journal of Infectious Diseases, 2004
- Ultrastructural Analysis of Differentiation in Legionella pneumophilaJournal of Bacteriology, 2002
- Intracellular Growth of Legionella pneumophila Gives Rise to a Differentiated Form Dissimilar to Stationary-Phase FormsInfection and Immunity, 2002
- A point mutation in the active site of O-acetyltransferase results in modified lipopolysaccharide but does not influence virulenceInternational Journal of Medical Microbiology, 2001
- The Escherichia coli ABC transporters: an updateMolecular Microbiology, 1999
- Microbial genome analyses: global comparisons of transport capabilities based on phylogenies, bioenergetics and substrate specificities 1 1Edited by G. Von HeijneJournal of Molecular Biology, 1998
- A Simple Chemically Defined Medium for the Production of Phase I Bordetella pertussisJournal of General Microbiology, 1970