PMID:16392005: Difference between revisions

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<span style = 'font-size: large'> '''Friedman, SM, Hossain, M, Hasson, TH and Kawamura, A'''  (2006) Gene expression profiling of intrinsic thermotolerance in Escherichia coli.''Curr. Microbiol.'' '''52''':50-4</span>
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|{{TableHeadingColor}} |'''Abstract''' || DNA microarrays were employed to compare gene expression in a thermotolerant, nalidixic acid-resistant mutant of Escherichia coli with that of the parental strain. When grown at 37 degrees C, up-regulated genes in the mutant included those coding for multiple antibiotic resistance proteins and enzymes for the degradation of small molecules, whereas among the down-regulated genes were those coding for fimbrial, flagellar, and outer membrane proteins as well as sigma 38. When the mutant grown at 42 degrees C was compared to the mutant grown at 37 degrees C, enhanced expression of several genes coding for flagellar proteins was detected. Reverse transcriptase-polymerase chain reaction analysis of selected genes confirmed results obtained with microarrays.
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'''Friedman, SM, Hossain, M, Hasson, TH and Kawamura, A'''  (2006) Gene expression profiling of intrinsic thermotolerance in Escherichia coli. ''Curr. Microbiol.'' '''52''':50-4
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!align=left  |Abstract
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DNA microarrays were employed to compare gene expression in a thermotolerant, nalidixic acid-resistant mutant of Escherichia coli with that of the parental strain. When grown at 37 degrees C, up-regulated genes in the mutant included those coding for multiple antibiotic resistance proteins and enzymes for the degradation of small molecules, whereas among the down-regulated genes were those coding for fimbrial, flagellar, and outer membrane proteins as well as sigma 38. When the mutant grown at 42 degrees C was compared to the mutant grown at 37 degrees C, enhanced expression of several genes coding for flagellar proteins was detected. Reverse transcriptase-polymerase chain reaction analysis of selected genes confirmed results obtained with microarrays.
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16392005 PubMed]
Online version:[http://dx.doi.org/10.1007/s00284-005-4578-6 10.1007/s00284-005-4578-6]
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|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16392005 PubMed]
!align=left  |Keywords
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Adaptation, Physiological; Anti-Bacterial Agents/pharmacology; Drug Resistance, Bacterial; Escherichia coli/genetics; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Gene Expression Profiling; Gene Expression Regulation, Bacterial; Hot Temperature; Mutation; Nalidixic Acid/pharmacology; Oligonucleotide Array Sequence Analysis; RNA, Bacterial/analysis; RNA, Messenger/analysis; Reverse Transcriptase Polymerase Chain Reaction
 
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==EcoliWiki Links {{HelpIcon|Help:Literature}} ==
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Latest revision as of 04:29, 15 September 2013

Citation

Friedman, SM, Hossain, M, Hasson, TH and Kawamura, A (2006) Gene expression profiling of intrinsic thermotolerance in Escherichia coli. Curr. Microbiol. 52:50-4

Abstract

DNA microarrays were employed to compare gene expression in a thermotolerant, nalidixic acid-resistant mutant of Escherichia coli with that of the parental strain. When grown at 37 degrees C, up-regulated genes in the mutant included those coding for multiple antibiotic resistance proteins and enzymes for the degradation of small molecules, whereas among the down-regulated genes were those coding for fimbrial, flagellar, and outer membrane proteins as well as sigma 38. When the mutant grown at 42 degrees C was compared to the mutant grown at 37 degrees C, enhanced expression of several genes coding for flagellar proteins was detected. Reverse transcriptase-polymerase chain reaction analysis of selected genes confirmed results obtained with microarrays.

Links

PubMed Online version:10.1007/s00284-005-4578-6

Keywords

Adaptation, Physiological; Anti-Bacterial Agents/pharmacology; Drug Resistance, Bacterial; Escherichia coli/genetics; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Gene Expression Profiling; Gene Expression Regulation, Bacterial; Hot Temperature; Mutation; Nalidixic Acid/pharmacology; Oligonucleotide Array Sequence Analysis; RNA, Bacterial/analysis; RNA, Messenger/analysis; Reverse Transcriptase Polymerase Chain Reaction

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