Speciation of coagulase negative staphylococci, isolated from indoor air, using SDS page gel bands of expressed proteins followed by MALDI TOF MS and MALDI TOF-TOF MS-MS analysis of tryptic peptides

A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. Afte...

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Published inJournal of microbiological methods Vol. 84; no. 2; pp. 243 - 250
Main Authors Fox, Karen, Fox, Alvin, Rose, John, Walla, Michael
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.02.2011
Elsevier
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Abstract A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100 kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/ z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins. ► One of the first mass spectrometry works defining peptide markers for bacteria. ► May have widespread application in speciation of isolates of diverse origin. ► Profiling of tryptic peptides from gel bands allowed ready speciation. ► Cross-correlation of data from unknown and reference organisms aids identification. ► Proteins from species with sequenced or un-sequenced genomes can be compared.
AbstractList A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins.
A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100 kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/ z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins. ► One of the first mass spectrometry works defining peptide markers for bacteria. ► May have widespread application in speciation of isolates of diverse origin. ► Profiling of tryptic peptides from gel bands allowed ready speciation. ► Cross-correlation of data from unknown and reference organisms aids identification. ► Proteins from species with sequenced or un-sequenced genomes can be compared.
A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100 kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins.
A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100 kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins.A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF MS profiling of cellular extracts and physiological tests (including API STAPH) provided incomplete identification of the set of strains. After separation of a 100 kDa band using 1D gel electrophoresis, profiling of peptides (released with tryptic digestion) using MALDI TOF MS allowed improved bacterial speciation in addition to determination of the identity of the protein of origin (aconitate hydratase). This was performed by Mascot search, empirical observation and computer-generated cross-correlation analysis of environmental isolates versus reference strains. The species studied included some with sequenced genomes and others with un-sequenced genomes. Peptide sequences were confirmed to originate from aconitate hydratase using MALDI TOF-TOF MS-MS analysis of a diverse set of m/z values representing variable and conserved sequences. The methodological approach described here might have widespread application in speciation of environmental isolates of diverse origin and in identification of their expressed proteins.
Author Fox, Karen
Walla, Michael
Rose, John
Fox, Alvin
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Issue 2
Keywords MALDI-TOFTOF MS-MS
Tandem mass spectrometry
MALDI-TOF MS
Mass spectrometry
Proteomics
Peptides
Protein
Staphylococcus
Mass spectrometry MS/MS
Bacteria
Micrococcales
Micrococcaceae
Speciation
Language English
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SSID ssj0015348
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Snippet A group of coagulase negative staphylococcal strains isolated from indoor air of occupied school rooms were the subject of this study. Conventional MALDI TOF...
SourceID proquest
pubmed
pascalfrancis
crossref
fao
elsevier
SourceType Aggregation Database
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Enrichment Source
Publisher
StartPage 243
SubjectTerms aconitate hydratase
air
Air Microbiology
Bacterial Proteins - analysis
Bacteriological methods and techniques used in bacteriology
Bacteriological Techniques - methods
Bacteriology
Biological and medical sciences
coagulase negative staphylococci
conserved sequences
digestion
Electrophoresis, Polyacrylamide Gel - methods
environmental assessment
Fundamental and applied biological sciences. Psychology
genome
MALDI-TOF MS
MALDI-TOFTOF MS-MS
Mass spectrometry
Microbiology
peptides
polyacrylamide gel electrophoresis
protein synthesis
Proteome - analysis
Proteomics
Schools
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods
Staphylococcus - chemistry
Staphylococcus - classification
Staphylococcus - isolation & purification
Tandem mass spectrometry
Title Speciation of coagulase negative staphylococci, isolated from indoor air, using SDS page gel bands of expressed proteins followed by MALDI TOF MS and MALDI TOF-TOF MS-MS analysis of tryptic peptides
URI https://dx.doi.org/10.1016/j.mimet.2010.12.007
https://www.ncbi.nlm.nih.gov/pubmed/21167877
https://www.proquest.com/docview/2000055288
https://www.proquest.com/docview/850561988
https://www.proquest.com/docview/860383767
Volume 84
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