Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2000-4-3
pubmed:databankReference
pubmed:abstractText
The ampC and ampR genes of Enterobacter cloacae GN7471 were cloned into pMW218 to yield pKU403. Four mutant plasmids derived from pKU403 (pKU404, pKU405, pKU406, and pKU407) were isolated in an AmpD mutant of Escherichia coli ML4953 by selection with ceftazidime or aztreonam. The beta-lactamase activities expressed by pKU404, pKU405, pKU406, and pKU407 were about 450, 75, 160, and 160 times higher, respectively, than that expressed by the original plasmid, pKU403. These mutant plasmids all carried point mutations in the ampR gene. In pKU404 and pKU405, Asp-135 was changed to Asn and Val, respectively. In both pKU406 and pKU407, Arg-86 was changed to Cys. The ease of selection of AmpR mutations at a frequency of about 10(-6) in this study strongly suggests that derepressed strains, such as AmpD or AmpR mutants, could frequently emerge in the clinical setting.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-149110, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-1943705, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-2448875, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-2692514, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-271968, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-2786868, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-2829250, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-2991883, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-3027046, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-3030737, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-3032901, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-314270, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-3260487, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-4559594, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-6096829, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-6300947, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-6333871, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-6968541, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-6972193, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-7574506, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-7783625, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-7925310, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-7958768, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-7968533, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8231804, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8383940, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8559061, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8585732, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8665470, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8723487, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8843314, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-8913462, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-9118225, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-9158742, http://linkedlifedata.com/resource/pubmed/commentcorrection/10681318-9333034
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0066-4804
pubmed:author
pubmed:issnType
Print
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
561-7
pubmed:dateRevised
2010-9-10
pubmed:meshHeading
pubmed-meshheading:10681318-Amino Acid Sequence, pubmed-meshheading:10681318-Aztreonam, pubmed-meshheading:10681318-Bacterial Proteins, pubmed-meshheading:10681318-Ceftazidime, pubmed-meshheading:10681318-Cephalosporin Resistance, pubmed-meshheading:10681318-Cephalosporins, pubmed-meshheading:10681318-DNA, Bacterial, pubmed-meshheading:10681318-Enterobacter cloacae, pubmed-meshheading:10681318-Enterobacteriaceae Infections, pubmed-meshheading:10681318-Humans, pubmed-meshheading:10681318-Microbial Sensitivity Tests, pubmed-meshheading:10681318-Molecular Sequence Data, pubmed-meshheading:10681318-Monobactams, pubmed-meshheading:10681318-Mutation, pubmed-meshheading:10681318-Plasmids, pubmed-meshheading:10681318-Sequence Analysis, DNA, pubmed-meshheading:10681318-beta-Lactam Resistance, pubmed-meshheading:10681318-beta-Lactamases
pubmed:year
2000
pubmed:articleTitle
ampR gene mutations that greatly increase class C beta-lactamase activity in Enterobacter cloacae.
pubmed:affiliation
Department of Microbiology, Kitasato University School of Medicine, 1-15-1 Kitasato, Sagamihara, Kanagawa 228-8555, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't