File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Identification of catabolite control protein A from Staphylococcus aureus as a target of silver ions

TitleIdentification of catabolite control protein A from Staphylococcus aureus as a target of silver ions
Authors
Issue Date2017
PublisherRoyal Society of Chemistry: Open Access. The Journal's web site is located at http://www.rsc.org/publishing/journals/sc/About.asp
Citation
Chemical Science, 2017, v. 8, p. 8061-8066 How to Cite?
AbstractStaphylococcus aureus is one of the most common pathogenic bacteria that causes human infectious diseases. The emergence of antibiotic-resistant strains of S. aureus promotes the development of new anti-bacterial strategies. Silver ions (Ag+) have attracted profound attention due to their broad-spectrum antimicrobial activities. Although the antibacterial properties of silver have been well known for many centuries, its mechanism of action remains unclear and its protein targets are rarely reported. Herein, we identify the catabolite control protein A (CcpA) of S. aureus as a putative target for Ag+. CcpA binds 2 molar equivalents of Ag+ via its two cysteine residues (Cys216 and Cys242). Importantly, Ag+ binding induces CcpA oligomerization and abolishes its DNA binding capability, which further attenuates S. aureus growth and suppresses a-hemolysin toxicity. This study extends our understanding of the bactericidal effects of silver.
Persistent Identifierhttp://hdl.handle.net/10722/250534
ISSN
2021 Impact Factor: 9.969
2020 SCImago Journal Rankings: 3.687
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiao, XW-
dc.contributor.authorYang, F-
dc.contributor.authorWANG, R-
dc.contributor.authorHe, XJ-
dc.contributor.authorLi, H-
dc.contributor.authorKao, RYT-
dc.contributor.authorXia, W-
dc.contributor.authorSun, H-
dc.date.accessioned2018-01-18T04:28:37Z-
dc.date.available2018-01-18T04:28:37Z-
dc.date.issued2017-
dc.identifier.citationChemical Science, 2017, v. 8, p. 8061-8066-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/10722/250534-
dc.description.abstractStaphylococcus aureus is one of the most common pathogenic bacteria that causes human infectious diseases. The emergence of antibiotic-resistant strains of S. aureus promotes the development of new anti-bacterial strategies. Silver ions (Ag+) have attracted profound attention due to their broad-spectrum antimicrobial activities. Although the antibacterial properties of silver have been well known for many centuries, its mechanism of action remains unclear and its protein targets are rarely reported. Herein, we identify the catabolite control protein A (CcpA) of S. aureus as a putative target for Ag+. CcpA binds 2 molar equivalents of Ag+ via its two cysteine residues (Cys216 and Cys242). Importantly, Ag+ binding induces CcpA oligomerization and abolishes its DNA binding capability, which further attenuates S. aureus growth and suppresses a-hemolysin toxicity. This study extends our understanding of the bactericidal effects of silver.-
dc.languageeng-
dc.publisherRoyal Society of Chemistry: Open Access. The Journal's web site is located at http://www.rsc.org/publishing/journals/sc/About.asp-
dc.relation.ispartofChemical Science-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleIdentification of catabolite control protein A from Staphylococcus aureus as a target of silver ions-
dc.typeArticle-
dc.identifier.emailLi, H: hylichem@hku.hk-
dc.identifier.emailKao, RYT: rytkao@hkucc.hku.hk-
dc.identifier.emailSun, H: hsun@hku.hk-
dc.identifier.authorityKao, RYT=rp00481-
dc.identifier.authoritySun, H=rp00777-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1039/C7SC02251D-
dc.identifier.scopuseid_2-s2.0-85034779786-
dc.identifier.hkuros284030-
dc.identifier.volume8-
dc.identifier.spage8061-
dc.identifier.epage8066-
dc.identifier.isiWOS:000415877000022-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl2041-6520-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats