Effects of varied pH, growth rate and temperature using controlled fermentation and batch culture on Matrix Assisted Laser Desorption/Ionization whole cell protein fingerprints
Rapid identification of microorganisms using matrix assisted laser desorption/ionization (MALDI) is a rapidly growing area of research due to the minimal sample preparation, speed of analysis and broad applicability of the technique. This approach relies on expressed biochemical markers, often prote...
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creator | Wunschel, David S. Hill, Eric A. McLean, Jeffrey S. Jarman, Kristin Gorby, Yuri A. Valentine, Nancy Wahl, Karen |
description | Rapid identification of microorganisms using matrix assisted laser desorption/ionization (MALDI) is a rapidly growing area of research due to the minimal sample preparation, speed of analysis and broad applicability of the technique. This approach relies on expressed biochemical markers, often proteins, to identify microorganisms. Therefore, variations in culture conditions that affect protein expression may limit the ability of MALDI-MS to correctly identify an organism. We have expanded our efforts to investigate the effects of culture conditions on MALDI-MS signatures to specifically examine the effects of pH, growth rate and temperature. Continuous cultures maintained in bioreactors were used to maintain specific growth rates and pH for
E. coli HB 101. Despite measurable morphological differences between growth conditions, the MALDI-MS data associated each culture with the appropriate library entry (
E. coli HB 101 generated using batch culture on a LB media), independent of pH or growth rate. The lone exception was for a biofilm sample collected from one of the reactors which had no appreciable degree of association with the correct library entry. Within the data set for planktonic organisms, variations in growth rate created the largest variation between fingerprints. The effect of varying growth temperature on
Y. enterocolitica was also examined. While the anticipated effects on phenotype were observed, the MALDI-MS technique provided the proper identification. |
doi_str_mv | 10.1016/j.mimet.2005.04.033 |
format | Article |
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E. coli HB 101. Despite measurable morphological differences between growth conditions, the MALDI-MS data associated each culture with the appropriate library entry (
E. coli HB 101 generated using batch culture on a LB media), independent of pH or growth rate. The lone exception was for a biofilm sample collected from one of the reactors which had no appreciable degree of association with the correct library entry. Within the data set for planktonic organisms, variations in growth rate created the largest variation between fingerprints. The effect of varying growth temperature on
Y. enterocolitica was also examined. While the anticipated effects on phenotype were observed, the MALDI-MS technique provided the proper identification.</description><identifier>ISSN: 0167-7012</identifier><identifier>EISSN: 1872-8359</identifier><identifier>DOI: 10.1016/j.mimet.2005.04.033</identifier><identifier>PMID: 15979749</identifier><identifier>CODEN: JMIMDQ</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>09 BIOMASS FUELS ; Bacterial Identification ; Bacterial Proteins - isolation & purification ; Bacteriology ; BATCH CULTURE ; Biological and medical sciences ; BIOREACTORS ; Condensed matter: electronic structure, electrical, magnetic, and optical properties ; CONTINUOUS CULTURE ; controlled cultivation ; Culture condition ; Electron and ion emission by liquids and solids; impact phenomena ; environmental molecular sciences laboratory ; Escherichia coli ; Escherichia coli - chemistry ; Escherichia coli - growth & development ; Escherichia coli Proteins - isolation & purification ; Exact sciences and technology ; FERMENTATION ; Field emission, ionization, evaporation, and desorption ; Fundamental and applied biological sciences. Psychology ; Hydrogen-Ion Concentration ; LASERS ; MALDI ; MALDI-MS ; Mass spectrometry ; Microbiological Techniques ; Microbiology ; MICROORGANISMS ; Miscellaneous ; Peptide Mapping - methods ; PHENOTYPE ; Physics ; Protein signatures ; PROTEINS ; SAMPLE PREPARATION ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Temperature ; VELOCITY ; Yersinia enterocolitica - chemistry ; Yersinia enterocolitica - growth & development</subject><ispartof>Journal of Microbiological Methods, 2005-09, Vol.62 (3), p.259-271</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-b27183de75b61a28f66cb56898164af01cb952b6ecf538598e486ccc8c19995c3</citedby><cites>FETCH-LOGICAL-c512t-b27183de75b61a28f66cb56898164af01cb952b6ecf538598e486ccc8c19995c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mimet.2005.04.033$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,885,3548,23929,23930,25139,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17078279$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15979749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/15020824$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Wunschel, David S.</creatorcontrib><creatorcontrib>Hill, Eric A.</creatorcontrib><creatorcontrib>McLean, Jeffrey S.</creatorcontrib><creatorcontrib>Jarman, Kristin</creatorcontrib><creatorcontrib>Gorby, Yuri A.</creatorcontrib><creatorcontrib>Valentine, Nancy</creatorcontrib><creatorcontrib>Wahl, Karen</creatorcontrib><creatorcontrib>Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)</creatorcontrib><title>Effects of varied pH, growth rate and temperature using controlled fermentation and batch culture on Matrix Assisted Laser Desorption/Ionization whole cell protein fingerprints</title><title>Journal of Microbiological Methods</title><addtitle>J Microbiol Methods</addtitle><description>Rapid identification of microorganisms using matrix assisted laser desorption/ionization (MALDI) is a rapidly growing area of research due to the minimal sample preparation, speed of analysis and broad applicability of the technique. This approach relies on expressed biochemical markers, often proteins, to identify microorganisms. Therefore, variations in culture conditions that affect protein expression may limit the ability of MALDI-MS to correctly identify an organism. We have expanded our efforts to investigate the effects of culture conditions on MALDI-MS signatures to specifically examine the effects of pH, growth rate and temperature. Continuous cultures maintained in bioreactors were used to maintain specific growth rates and pH for
E. coli HB 101. Despite measurable morphological differences between growth conditions, the MALDI-MS data associated each culture with the appropriate library entry (
E. coli HB 101 generated using batch culture on a LB media), independent of pH or growth rate. The lone exception was for a biofilm sample collected from one of the reactors which had no appreciable degree of association with the correct library entry. Within the data set for planktonic organisms, variations in growth rate created the largest variation between fingerprints. The effect of varying growth temperature on
Y. enterocolitica was also examined. While the anticipated effects on phenotype were observed, the MALDI-MS technique provided the proper identification.</description><subject>09 BIOMASS FUELS</subject><subject>Bacterial Identification</subject><subject>Bacterial Proteins - isolation & purification</subject><subject>Bacteriology</subject><subject>BATCH CULTURE</subject><subject>Biological and medical sciences</subject><subject>BIOREACTORS</subject><subject>Condensed matter: electronic structure, electrical, magnetic, and optical properties</subject><subject>CONTINUOUS CULTURE</subject><subject>controlled cultivation</subject><subject>Culture condition</subject><subject>Electron and ion emission by liquids and solids; impact phenomena</subject><subject>environmental molecular sciences laboratory</subject><subject>Escherichia coli</subject><subject>Escherichia coli - chemistry</subject><subject>Escherichia coli - growth & development</subject><subject>Escherichia coli Proteins - isolation & purification</subject><subject>Exact sciences and technology</subject><subject>FERMENTATION</subject><subject>Field emission, ionization, evaporation, and desorption</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hydrogen-Ion Concentration</subject><subject>LASERS</subject><subject>MALDI</subject><subject>MALDI-MS</subject><subject>Mass spectrometry</subject><subject>Microbiological Techniques</subject><subject>Microbiology</subject><subject>MICROORGANISMS</subject><subject>Miscellaneous</subject><subject>Peptide Mapping - methods</subject><subject>PHENOTYPE</subject><subject>Physics</subject><subject>Protein signatures</subject><subject>PROTEINS</subject><subject>SAMPLE PREPARATION</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Temperature</subject><subject>VELOCITY</subject><subject>Yersinia enterocolitica - chemistry</subject><subject>Yersinia enterocolitica - growth & development</subject><issn>0167-7012</issn><issn>1872-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAURSMEokPhC5CQJURXJLWTOHYWXVRtoZUGsYG15TjPHY8SO9hOC3wVn4gzGak7WFm2zn2-990se0twQTBpzvfFaEaIRYkxLXBd4Kp6lm0IZ2XOK9o-zzaJYjnDpDzJXoWwx5jQquYvsxNCW9ayut1kf260BhUDcho9SG-gR9PtR3Tv3WPcIS8jIGl7FGGcIN1mD2gOxt4j5Wz0bhiSQIMfwUYZjbMHupNR7ZCahwOfHr_I6M1PdBmCCTEptjKAR9cQnJ8W1fmds-b3OuBx5wZACoYBTd5FMBbp9CH4yRsbw-vshZZDgDfH8zT7_unm29Vtvv36-e7qcpsrSsqYdyUjvOqB0a4hsuS6aVRHG95y0tRSY6K6lpZdA0rTitOWQ80bpRRXpG1bqqrT7P0614VoRFAmgtql0DZtSxCKS8zLOlFnK5Ws_pghRDGasHiXFtwcRMNrllZO_wsSVvHUY5XAagWVdyF40CLlHqX_JQgWS-9iLw69i6V3gWuRek-qd8fxczdC_6Q5Fp2AD0dABiUH7aVVJjxxDDNesoW7WDlIu30w4JfoYBX0xi_Je2f-aeQvzzPQMA</recordid><startdate>20050901</startdate><enddate>20050901</enddate><creator>Wunschel, David S.</creator><creator>Hill, Eric A.</creator><creator>McLean, Jeffrey S.</creator><creator>Jarman, Kristin</creator><creator>Gorby, Yuri A.</creator><creator>Valentine, Nancy</creator><creator>Wahl, Karen</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>20050901</creationdate><title>Effects of varied pH, growth rate and temperature using controlled fermentation and batch culture on Matrix Assisted Laser Desorption/Ionization whole cell protein fingerprints</title><author>Wunschel, David S. ; Hill, Eric A. ; McLean, Jeffrey S. ; Jarman, Kristin ; Gorby, Yuri A. ; Valentine, Nancy ; Wahl, Karen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-b27183de75b61a28f66cb56898164af01cb952b6ecf538598e486ccc8c19995c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>09 BIOMASS FUELS</topic><topic>Bacterial Identification</topic><topic>Bacterial Proteins - isolation & purification</topic><topic>Bacteriology</topic><topic>BATCH CULTURE</topic><topic>Biological and medical sciences</topic><topic>BIOREACTORS</topic><topic>Condensed matter: electronic structure, electrical, magnetic, and optical properties</topic><topic>CONTINUOUS CULTURE</topic><topic>controlled cultivation</topic><topic>Culture condition</topic><topic>Electron and ion emission by liquids and solids; impact phenomena</topic><topic>environmental molecular sciences laboratory</topic><topic>Escherichia coli</topic><topic>Escherichia coli - chemistry</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli Proteins - isolation & purification</topic><topic>Exact sciences and technology</topic><topic>FERMENTATION</topic><topic>Field emission, ionization, evaporation, and desorption</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hydrogen-Ion Concentration</topic><topic>LASERS</topic><topic>MALDI</topic><topic>MALDI-MS</topic><topic>Mass spectrometry</topic><topic>Microbiological Techniques</topic><topic>Microbiology</topic><topic>MICROORGANISMS</topic><topic>Miscellaneous</topic><topic>Peptide Mapping - methods</topic><topic>PHENOTYPE</topic><topic>Physics</topic><topic>Protein signatures</topic><topic>PROTEINS</topic><topic>SAMPLE PREPARATION</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</topic><topic>Temperature</topic><topic>VELOCITY</topic><topic>Yersinia enterocolitica - chemistry</topic><topic>Yersinia enterocolitica - growth & development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wunschel, David S.</creatorcontrib><creatorcontrib>Hill, Eric A.</creatorcontrib><creatorcontrib>McLean, Jeffrey S.</creatorcontrib><creatorcontrib>Jarman, Kristin</creatorcontrib><creatorcontrib>Gorby, Yuri A.</creatorcontrib><creatorcontrib>Valentine, Nancy</creatorcontrib><creatorcontrib>Wahl, Karen</creatorcontrib><creatorcontrib>Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Journal of Microbiological Methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wunschel, David S.</au><au>Hill, Eric A.</au><au>McLean, Jeffrey S.</au><au>Jarman, Kristin</au><au>Gorby, Yuri A.</au><au>Valentine, Nancy</au><au>Wahl, Karen</au><aucorp>Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of varied pH, growth rate and temperature using controlled fermentation and batch culture on Matrix Assisted Laser Desorption/Ionization whole cell protein fingerprints</atitle><jtitle>Journal of Microbiological Methods</jtitle><addtitle>J Microbiol Methods</addtitle><date>2005-09-01</date><risdate>2005</risdate><volume>62</volume><issue>3</issue><spage>259</spage><epage>271</epage><pages>259-271</pages><issn>0167-7012</issn><eissn>1872-8359</eissn><coden>JMIMDQ</coden><abstract>Rapid identification of microorganisms using matrix assisted laser desorption/ionization (MALDI) is a rapidly growing area of research due to the minimal sample preparation, speed of analysis and broad applicability of the technique. This approach relies on expressed biochemical markers, often proteins, to identify microorganisms. Therefore, variations in culture conditions that affect protein expression may limit the ability of MALDI-MS to correctly identify an organism. We have expanded our efforts to investigate the effects of culture conditions on MALDI-MS signatures to specifically examine the effects of pH, growth rate and temperature. Continuous cultures maintained in bioreactors were used to maintain specific growth rates and pH for
E. coli HB 101. Despite measurable morphological differences between growth conditions, the MALDI-MS data associated each culture with the appropriate library entry (
E. coli HB 101 generated using batch culture on a LB media), independent of pH or growth rate. The lone exception was for a biofilm sample collected from one of the reactors which had no appreciable degree of association with the correct library entry. Within the data set for planktonic organisms, variations in growth rate created the largest variation between fingerprints. The effect of varying growth temperature on
Y. enterocolitica was also examined. While the anticipated effects on phenotype were observed, the MALDI-MS technique provided the proper identification.</abstract><cop>Shannon</cop><pub>Elsevier B.V</pub><pmid>15979749</pmid><doi>10.1016/j.mimet.2005.04.033</doi><tpages>13</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | 09 BIOMASS FUELS Bacterial Identification Bacterial Proteins - isolation & purification Bacteriology BATCH CULTURE Biological and medical sciences BIOREACTORS Condensed matter: electronic structure, electrical, magnetic, and optical properties CONTINUOUS CULTURE controlled cultivation Culture condition Electron and ion emission by liquids and solids impact phenomena environmental molecular sciences laboratory Escherichia coli Escherichia coli - chemistry Escherichia coli - growth & development Escherichia coli Proteins - isolation & purification Exact sciences and technology FERMENTATION Field emission, ionization, evaporation, and desorption Fundamental and applied biological sciences. Psychology Hydrogen-Ion Concentration LASERS MALDI MALDI-MS Mass spectrometry Microbiological Techniques Microbiology MICROORGANISMS Miscellaneous Peptide Mapping - methods PHENOTYPE Physics Protein signatures PROTEINS SAMPLE PREPARATION Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Temperature VELOCITY Yersinia enterocolitica - chemistry Yersinia enterocolitica - growth & development |
title | Effects of varied pH, growth rate and temperature using controlled fermentation and batch culture on Matrix Assisted Laser Desorption/Ionization whole cell protein fingerprints |
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