Essential residues in the chromate transporter ChrA of<i>Pseudomonas aeruginosa</i>

Aguilera, Selene; Aguilar, Ma.Esther; Chávez, Martha P; López‐Meza, Joel E.; Pedraza-Reyes, Mario; Campos-Garcı́a, Jesús; Cervantes, Carlos

doi:10.1016/s0378-1097(04)00068-0

Cited by 30 publications

(31 citation statements)

References 22 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Random mutagenesis of the P. aeruginosa chrA gene showed that most essential amino acid residues are located in the amino terminal end of ChrA (Aguilera et al 2004). In agreement with this finding, phylogenetic analysis of ChrA homologs revealed that the amino terminal halves are more conserved than the carboxyl terminal halves (Díaz-Pérez et al submitted).…”

Section: Transmembrane Efflux Of Chromatementioning

confidence: 99%

Mechanisms of bacterial resistance to chromium compounds

et al. 2007

Self Cite

View full text Add to dashboard Cite

Chromium is a non-essential and well-known toxic metal for microorganisms and plants. The widespread industrial use of this heavy metal has caused it to be considered as a serious environmental pollutant. Chromium exists in nature as two main species, the trivalent form, Cr(III), which is relatively innocuous, and the hexavalent form, Cr(VI), considered a more toxic species. At the intracellular level, however, Cr(III) seems to be responsible for most toxic effects of chromium. Cr(VI) is usually present as the oxyanion chromate. Inhibition of sulfate membrane transport and oxidative damage to biomolecules are associated with the toxic effects of chromate in bacteria. Several bacterial mechanisms of resistance to chromate have been reported. The best characterized mechanisms comprise efflux of chromate ions from the cell cytoplasm and reduction of Cr(VI) to Cr(III). Chromate efflux by the ChrA transporter has been established in Pseudomonas aeruginosa and Cupriavidus metallidurans (formerly Alcaligenes eutrophus) and consists of an energy-dependent process driven by the membrane potential. The CHR protein family, which includes putative ChrA orthologs, currently contains about 135 sequences from all three domains of life. Chromate reduction is carried out by chromate reductases from diverse bacterial species generating Cr(III) that may be detoxified by other mechanisms. Most characterized enzymes belong to the widespread NAD(P)H-dependent flavoprotein family of reductases. Several examples of bacterial systems protecting from the oxidative stress caused by chromate have been described. Other mechanisms of bacterial resistance to chromate involve the expression of components of the machinery for repair of DNA damage, and systems related to the homeostasis of iron and sulfur.

show abstract

Section: Transmembrane Efflux Of Chromatementioning

confidence: 99%

Mechanisms of bacterial resistance to chromium compounds

et al. 2007

Self Cite

View full text Add to dashboard Cite

show abstract

“…Recently, a series of random mutant strains isolated as chromate sensitive identified 14 residue positions (of the 416 amino acids in ChrA) that are needed for chromate resistance. The positions affected seemed mostly in the N-terminal half of the protein and occurred both in the membrane segments and cytoplasmic loop regions [1].…”

Section: Other Metal Resistancesmentioning

confidence: 99%

A bacterial view of the periodic table: genes and proteins for toxic inorganic ions

Silver

Phung

2005

J IND MICROBIOL BIOTECHNOL

421

287

View full text Add to dashboard Cite

Essentially all bacteria have genes for toxic metal ion resistances and these include those for Ag+, AsO2-, AsO4(3-), Cd2+ Co2+, CrO4(2-), Cu2+, Hg2+, Ni2+, Pb2+, TeO3(2-), Tl+ and Zn2+. The largest group of resistance systems functions by energy-dependent efflux of toxic ions. Fewer involve enzymatic transformations (oxidation, reduction, methylation, and demethylation) or metal-binding proteins (for example, metallothionein SmtA, chaperone CopZ and periplasmic silver binding protein SilE). Some of the efflux resistance systems are ATPases and others are chemiosmotic ion/proton exchangers. For example, Cd2+-efflux pumps of bacteria are either inner membrane P-type ATPases or three polypeptide RND chemiosmotic complexes consisting of an inner membrane pump, a periplasmic-bridging protein and an outer membrane channel. In addition to the best studied three-polypeptide chemiosmotic system, Czc (Cd2+, Zn2+, and Co2), others are known that efflux Ag+, Cu+, Ni2+, and Zn2+. Resistance to inorganic mercury, Hg2+ (and to organomercurials, such as CH3Hg+ and phenylmercury) involve a series of metal-binding and membrane transport proteins as well as the enzymes mercuric reductase and organomercurial lyase, which overall convert more toxic to less toxic forms. Arsenic resistance and metabolizing systems occur in three patterns, the widely-found ars operon that is present in most bacterial genomes and many plasmids, the more recently recognized arr genes for the periplasmic arsenate reductase that functions in anaerobic respiration as a terminal electron acceptor, and the aso genes for the periplasmic arsenite oxidase that functions as an initial electron donor in aerobic resistance to arsenite.

show abstract

“…However, there is little sequence similarity (35% similarity across 106 of 225 amino acids) between the amino and carboxy halves of Arth_4248; hence, it does not appear to have arisen by direct tandem duplication of the same CHR domain-containing open reading frame. Because of the topological diversity of the CHR superfamily proteins [22,25] and the observed preponderance of conserved residues in the N-terminal half of the P. aeruginosa ChrA protein [26], it is expected that the amino and carboxy termini may carry out different functional roles in chromate efflux. Alignment of the amino acid sequence of Arth_4248 with that of P. aeruginosa ChrA indicated that residues which resulted in Cr(VI) sensitivity following mutation in P. aeruginosa [26] are also conserved in Arth_4248.…”

Section: Resultsmentioning

confidence: 99%

High-level chromate resistance in Arthrobacter sp. strain FB24 requires previously uncharacterized accessory genes

et al. 2009

View full text Add to dashboard Cite

BackgroundThe genome of Arthrobacter sp. strain FB24 contains a chromate resistance determinant (CRD), consisting of a cluster of 8 genes located on a 10.6 kb fragment of a 96 kb plasmid. The CRD includes chrA, which encodes a putative chromate efflux protein, and three genes with amino acid similarities to the amino and carboxy termini of ChrB, a putative regulatory protein. There are also three novel genes that have not been previously associated with chromate resistance in other bacteria; they encode an oxidoreductase (most similar to malate:quinone oxidoreductase), a functionally unknown protein with a WD40 repeat domain and a lipoprotein. To delineate the contribution of the CRD genes to the FB24 chromate [Cr(VI)] response, we evaluated the growth of mutant strains bearing regions of the CRD and transcript expression levels in response to Cr(VI) challenge.ResultsA chromate-sensitive mutant (strain D11) was generated by curing FB24 of its 96-kb plasmid. Elemental analysis indicated that chromate-exposed cells of strain D11 accumulated three times more chromium than strain FB24. Introduction of the CRD into strain D11 conferred chromate resistance comparable to wild-type levels, whereas deletion of specific regions of the CRD led to decreased resistance. Using real-time reverse transcriptase PCR, we show that expression of each gene within the CRD is specifically induced in response to chromate but not by lead, hydrogen peroxide or arsenate. Higher levels of chrA expression were achieved when the chrB orthologs and the WD40 repeat domain genes were present, suggesting their possible regulatory roles.ConclusionOur findings indicate that chromate resistance in Arthrobacter sp. strain FB24 is due to chromate efflux through the ChrA transport protein. More importantly, new genes have been identified as having significant roles in chromate resistance. Collectively, the functional predictions of these additional genes suggest the involvement of a signal transduction system in the regulation of chromate efflux and warrants further study.

show abstract

Essential residues in the chromate transporter ChrA ofPseudomonas aeruginosa

Cited by 30 publications

References 22 publications

Mechanisms of bacterial resistance to chromium compounds

Mechanisms of bacterial resistance to chromium compounds

A bacterial view of the periodic table: genes and proteins for toxic inorganic ions

High-level chromate resistance in Arthrobacter sp. strain FB24 requires previously uncharacterized accessory genes

Contact Info

Product

Resources

About