2020 - Fellow of the American Association for the Advancement of Science (AAAS)
Her primary areas of investigation include Escherichia coli, Biochemistry, Transcription factor, Genetics and Operon. Her work deals with themes such as Iron–sulfur cluster, Transcription and Binding site, which intersect with Escherichia coli. Her study in Binding site is interdisciplinary in nature, drawing from both Transcriptional regulation and Regulon.
Her Biochemistry research incorporates elements of Stereochemistry and Bacteria. Her Biosynthesis study in the realm of Genetics interacts with subjects such as Photosynthetic membrane. Her studies in Operon integrate themes in fields like Promoter, Peptide sequence and Genome.
Her main research concerns Escherichia coli, Biochemistry, Transcription factor, Operon and Genetics. Her study in Escherichia coli is interdisciplinary in nature, drawing from both Biogenesis, DNA, Promoter, Iron–sulfur cluster and Stereochemistry. In her study, Dithionite is strongly linked to Redox, which falls under the umbrella field of Biochemistry.
Her Transcription factor study incorporates themes from Regulation of gene expression, Binding site and Cell biology. Her Operon research integrates issues from Anaerobic exercise, Genome and Structural gene. Her work investigates the relationship between Genetics and topics such as Computational biology that intersect with problems in Zymomonas mobilis, Genomics and Phylogenetic tree.
Her scientific interests lie mostly in Escherichia coli, Gene, Zymomonas mobilis, Operon and Computational biology. Escherichia coli is a primary field of her research addressed under Biochemistry. Patricia J. Kiley works mostly in the field of Zymomonas mobilis, limiting it down to topics relating to Metabolic engineering and, in certain cases, Lignocellulosic biomass, Sugar, Xylose and Saccharomyces cerevisiae, as a part of the same area of interest.
The various areas that Patricia J. Kiley examines in her Operon study include Plasmid, Psychological repression, Genome and Homologous recombination. Her study focuses on the intersection of Gene expression and fields such as Bacteria with connections in the field of Microbiology. Her research integrates issues of Ferric, Anaerobic exercise, Repressor and Aerobactin in her study of Regulon.
Her primary scientific interests are in Escherichia coli, Cell biology, Gene expression, Transcription factor and Anaerobic respiration. Her Escherichia coli research is within the category of Biochemistry. Her Cell biology research includes elements of Yersinia, Hemin, Heme and Yersinia pseudotuberculosis.
Patricia J. Kiley has researched Gene expression in several fields, including Bacteriophage, DNA, Bacterial cell structure, Bacteria and Microbiology. Her Transcription factor study combines topics in areas such as Regulation of gene expression, Function and Bioinformatics. Her Anaerobic respiration study integrates concerns from other disciplines, such as Phenotype and Regulator.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
IscR, an Fe-S cluster-containing transcription factor, represses expression of Escherichia coli genes encoding Fe-S cluster assembly proteins.
Christopher J. Schwartz;Jennifer L. Giel;Thomas Patschkowski;Christopher Luther.
Proceedings of the National Academy of Sciences of the United States of America (2001)
The role of Fe–S proteins in sensing and regulation in bacteria
Patricia J Kiley;Helmut Beinert.
Current Opinion in Microbiology (2003)
Iron-sulfur cluster disassembly in the FNR protein of Escherichia coli by O2: [4Fe-4S] to [2Fe-2S] conversion with loss of biological activity
Natalia Khoroshilova;Codrina Popescu;Eckard Münck;Helmut Beinert.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Oxygen sensing by the global regulator, FNR: the role of the iron-sulfur cluster.
Patricia J. Kiley;Helmut Beinert.
Fems Microbiology Reviews (1998)
DNA Binding and Dimerization of the Fe−S-containing FNR Protein from Escherichia coli Are Regulated by Oxygen
Beth A. Lazazzera;Helmut Beinert;Natalia Khoroshilova;Mary Claire Kennedy.
Journal of Biological Chemistry (1996)
The cysteine desulfurase, IscS, has a major role in in vivo Fe-S cluster formation in Escherichia coli.
Christopher J. Schwartz;Ouliana Djaman;James A. Imlay;Patricia J. Kiley.
Proceedings of the National Academy of Sciences of the United States of America (2000)
Genome-Wide Expression Analysis Indicates that FNR of Escherichia coli K-12 Regulates a Large Number of Genes of Unknown Function
Yisheng Kang;K. Derek Weber;Yu Qiu;Patricia J. Kiley.
Journal of Bacteriology (2005)
IscR‐dependent gene expression links iron‐sulphur cluster assembly to the control of O2‐regulated genes in Escherichia coli
Jennifer L. Giel;Dmitry Rodionov;Mingzhu Liu;Frederick R. Blattner.
Molecular Microbiology (2006)
Molecular genetics of photosynthetic membrane biosynthesis in Rhodobacter sphaeroides.
P J Kiley;S Kaplan.
Microbiological Research (1988)
Fe-S proteins in sensing and regulatory functions.
Helmut Beinert;Patricia J Kiley.
Current Opinion in Chemical Biology (1999)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: