Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells

Early and mature biofilm formation in the extremely halophilic euryarchaeon Halobacterium salinarum strain R1 was characterized by SWATH‐LC/MS/MS. Using a simple surfactant‐assisted protein solubilization protocol and one‐dimensional ultra‐high performance nanoflow chromatography on the front end, 6...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proteomics (Weinheim) 2017-04, Vol.17 (7), p.np-n/a
Hauptverfasser: Losensky, Gerald, Jung, Klaus, Urlaub, Henning, Pfeifer, Felicitas, Fröls, Sabrina, Lenz, Christof
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 7
container_start_page np
container_title Proteomics (Weinheim)
container_volume 17
creator Losensky, Gerald
Jung, Klaus
Urlaub, Henning
Pfeifer, Felicitas
Fröls, Sabrina
Lenz, Christof
description Early and mature biofilm formation in the extremely halophilic euryarchaeon Halobacterium salinarum strain R1 was characterized by SWATH‐LC/MS/MS. Using a simple surfactant‐assisted protein solubilization protocol and one‐dimensional ultra‐high performance nanoflow chromatography on the front end, 63.2 and 58.6% of the predicted H. salinarum R1 proteome could be detected and quantified, respectively. Analysis of biophysical protein properties, functional analysis and pathway mapping indicated comprehensive characterization of the proteome. Sixty point eight percent of the quantified proteins (or 34.5% of the predicted proteome) exhibited significant abundance changes between planktonic and sessile states, demonstrating that haloarchaeal biofilm formation represents a profound “lifestyle change” on the molecular level. Our results and analysis constitute the first comprehensive study to track molecular changes from planktonic cultures to initial and mature archaeal biofilms on the proteome level. Data are available via ProteomeXchange, identifier PXD003667. Proteins exemplifying different protein expression level profiles were selected, and their corresponding gene transcripts targeted by qRT‐PCR to test the feasibility of establishing rapid PCR‐based assays for archaeal biofilm formation.
doi_str_mv 10.1002/pmic.201600111
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1891871204</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1895026757</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4029-6832e84739f04c035650f898f1926640cb59cfda3462e29f5bcd3f1fe62fbeff3</originalsourceid><addsrcrecordid>eNqNkcFOGzEQhq2qqFDotcfKUi-9JHi8tnd9RBE0SEEgAupx5fXaYPCug72rKpeqj9Bn7JPUaWgOvYA00oxG3_yamR-hj0CmQAg9XnVOTykBQQgAvEEHIIBPZCXg7a7mxT56n9JDRspKlu_QPi0FYVyKA_RjeW_a1vV32Lu7-wGHHjcuWOc7bEPs1OByJ1g8Vz40Sg8murHDSXnXq5ira8DNGi-_ndzMf__8tZgdXyxzYNUrv04ubUZXXvWPQ-idzu0WJ5OS8wZr4306QntW-WQ-POdDdHt2ejObTxaXX89nJ4uJZoTKiagKaipWFtISpknBBSe2kpUFSYVgRDdcatuqgglqqLS80W1hwRpBbWOsLQ7Rl63uKoan0aSh7lzabKB6E8ZUQyWhKoES9gq04IzxUsqMfv4PfQhjzKf_FeSEipKXmZpuKR1DStHYehVdp-K6BlJvTKw3JtY7E_PAp2fZselMu8P_uZYBvgW-50euX5Crry7OZ0BZ3vcPd8yn8w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1895026757</pqid></control><display><type>article</type><title>Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Losensky, Gerald ; Jung, Klaus ; Urlaub, Henning ; Pfeifer, Felicitas ; Fröls, Sabrina ; Lenz, Christof</creator><creatorcontrib>Losensky, Gerald ; Jung, Klaus ; Urlaub, Henning ; Pfeifer, Felicitas ; Fröls, Sabrina ; Lenz, Christof</creatorcontrib><description>Early and mature biofilm formation in the extremely halophilic euryarchaeon Halobacterium salinarum strain R1 was characterized by SWATH‐LC/MS/MS. Using a simple surfactant‐assisted protein solubilization protocol and one‐dimensional ultra‐high performance nanoflow chromatography on the front end, 63.2 and 58.6% of the predicted H. salinarum R1 proteome could be detected and quantified, respectively. Analysis of biophysical protein properties, functional analysis and pathway mapping indicated comprehensive characterization of the proteome. Sixty point eight percent of the quantified proteins (or 34.5% of the predicted proteome) exhibited significant abundance changes between planktonic and sessile states, demonstrating that haloarchaeal biofilm formation represents a profound “lifestyle change” on the molecular level. Our results and analysis constitute the first comprehensive study to track molecular changes from planktonic cultures to initial and mature archaeal biofilms on the proteome level. Data are available via ProteomeXchange, identifier PXD003667. Proteins exemplifying different protein expression level profiles were selected, and their corresponding gene transcripts targeted by qRT‐PCR to test the feasibility of establishing rapid PCR‐based assays for archaeal biofilm formation.</description><identifier>ISSN: 1615-9853</identifier><identifier>EISSN: 1615-9861</identifier><identifier>DOI: 10.1002/pmic.201600111</identifier><identifier>PMID: 27604596</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Archaea ; Archaeal Proteins - analysis ; Archaeal Proteins - genetics ; Archaeal Proteins - metabolism ; Biofilm ; Biofilms ; Biofilms - growth &amp; development ; Chromatography, Liquid ; Functional analysis ; Gene Expression Regulation, Archaeal ; Haloarchaea ; Halobacterium salinarum ; Halobacterium salinarum - chemistry ; Halobacterium salinarum - genetics ; Halobacterium salinarum - metabolism ; Microbiology ; Peptide mapping ; Plankton - chemistry ; Plankton - growth &amp; development ; Plankton - metabolism ; Polymerase chain reaction ; Proteins ; Proteome - analysis ; Proteomes ; Solubilization ; Strain analysis ; SWATH ; Tandem Mass Spectrometry</subject><ispartof>Proteomics (Weinheim), 2017-04, Vol.17 (7), p.np-n/a</ispartof><rights>2016 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2016 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><rights>2017 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4029-6832e84739f04c035650f898f1926640cb59cfda3462e29f5bcd3f1fe62fbeff3</citedby><cites>FETCH-LOGICAL-c4029-6832e84739f04c035650f898f1926640cb59cfda3462e29f5bcd3f1fe62fbeff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpmic.201600111$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpmic.201600111$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27604596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Losensky, Gerald</creatorcontrib><creatorcontrib>Jung, Klaus</creatorcontrib><creatorcontrib>Urlaub, Henning</creatorcontrib><creatorcontrib>Pfeifer, Felicitas</creatorcontrib><creatorcontrib>Fröls, Sabrina</creatorcontrib><creatorcontrib>Lenz, Christof</creatorcontrib><title>Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells</title><title>Proteomics (Weinheim)</title><addtitle>Proteomics</addtitle><description>Early and mature biofilm formation in the extremely halophilic euryarchaeon Halobacterium salinarum strain R1 was characterized by SWATH‐LC/MS/MS. Using a simple surfactant‐assisted protein solubilization protocol and one‐dimensional ultra‐high performance nanoflow chromatography on the front end, 63.2 and 58.6% of the predicted H. salinarum R1 proteome could be detected and quantified, respectively. Analysis of biophysical protein properties, functional analysis and pathway mapping indicated comprehensive characterization of the proteome. Sixty point eight percent of the quantified proteins (or 34.5% of the predicted proteome) exhibited significant abundance changes between planktonic and sessile states, demonstrating that haloarchaeal biofilm formation represents a profound “lifestyle change” on the molecular level. Our results and analysis constitute the first comprehensive study to track molecular changes from planktonic cultures to initial and mature archaeal biofilms on the proteome level. Data are available via ProteomeXchange, identifier PXD003667. Proteins exemplifying different protein expression level profiles were selected, and their corresponding gene transcripts targeted by qRT‐PCR to test the feasibility of establishing rapid PCR‐based assays for archaeal biofilm formation.</description><subject>Archaea</subject><subject>Archaeal Proteins - analysis</subject><subject>Archaeal Proteins - genetics</subject><subject>Archaeal Proteins - metabolism</subject><subject>Biofilm</subject><subject>Biofilms</subject><subject>Biofilms - growth &amp; development</subject><subject>Chromatography, Liquid</subject><subject>Functional analysis</subject><subject>Gene Expression Regulation, Archaeal</subject><subject>Haloarchaea</subject><subject>Halobacterium salinarum</subject><subject>Halobacterium salinarum - chemistry</subject><subject>Halobacterium salinarum - genetics</subject><subject>Halobacterium salinarum - metabolism</subject><subject>Microbiology</subject><subject>Peptide mapping</subject><subject>Plankton - chemistry</subject><subject>Plankton - growth &amp; development</subject><subject>Plankton - metabolism</subject><subject>Polymerase chain reaction</subject><subject>Proteins</subject><subject>Proteome - analysis</subject><subject>Proteomes</subject><subject>Solubilization</subject><subject>Strain analysis</subject><subject>SWATH</subject><subject>Tandem Mass Spectrometry</subject><issn>1615-9853</issn><issn>1615-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFOGzEQhq2qqFDotcfKUi-9JHi8tnd9RBE0SEEgAupx5fXaYPCug72rKpeqj9Bn7JPUaWgOvYA00oxG3_yamR-hj0CmQAg9XnVOTykBQQgAvEEHIIBPZCXg7a7mxT56n9JDRspKlu_QPi0FYVyKA_RjeW_a1vV32Lu7-wGHHjcuWOc7bEPs1OByJ1g8Vz40Sg8murHDSXnXq5ira8DNGi-_ndzMf__8tZgdXyxzYNUrv04ubUZXXvWPQ-idzu0WJ5OS8wZr4306QntW-WQ-POdDdHt2ejObTxaXX89nJ4uJZoTKiagKaipWFtISpknBBSe2kpUFSYVgRDdcatuqgglqqLS80W1hwRpBbWOsLQ7Rl63uKoan0aSh7lzabKB6E8ZUQyWhKoES9gq04IzxUsqMfv4PfQhjzKf_FeSEipKXmZpuKR1DStHYehVdp-K6BlJvTKw3JtY7E_PAp2fZselMu8P_uZYBvgW-50euX5Crry7OZ0BZ3vcPd8yn8w</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Losensky, Gerald</creator><creator>Jung, Klaus</creator><creator>Urlaub, Henning</creator><creator>Pfeifer, Felicitas</creator><creator>Fröls, Sabrina</creator><creator>Lenz, Christof</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201704</creationdate><title>Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells</title><author>Losensky, Gerald ; Jung, Klaus ; Urlaub, Henning ; Pfeifer, Felicitas ; Fröls, Sabrina ; Lenz, Christof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4029-6832e84739f04c035650f898f1926640cb59cfda3462e29f5bcd3f1fe62fbeff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Archaea</topic><topic>Archaeal Proteins - analysis</topic><topic>Archaeal Proteins - genetics</topic><topic>Archaeal Proteins - metabolism</topic><topic>Biofilm</topic><topic>Biofilms</topic><topic>Biofilms - growth &amp; development</topic><topic>Chromatography, Liquid</topic><topic>Functional analysis</topic><topic>Gene Expression Regulation, Archaeal</topic><topic>Haloarchaea</topic><topic>Halobacterium salinarum</topic><topic>Halobacterium salinarum - chemistry</topic><topic>Halobacterium salinarum - genetics</topic><topic>Halobacterium salinarum - metabolism</topic><topic>Microbiology</topic><topic>Peptide mapping</topic><topic>Plankton - chemistry</topic><topic>Plankton - growth &amp; development</topic><topic>Plankton - metabolism</topic><topic>Polymerase chain reaction</topic><topic>Proteins</topic><topic>Proteome - analysis</topic><topic>Proteomes</topic><topic>Solubilization</topic><topic>Strain analysis</topic><topic>SWATH</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Losensky, Gerald</creatorcontrib><creatorcontrib>Jung, Klaus</creatorcontrib><creatorcontrib>Urlaub, Henning</creatorcontrib><creatorcontrib>Pfeifer, Felicitas</creatorcontrib><creatorcontrib>Fröls, Sabrina</creatorcontrib><creatorcontrib>Lenz, Christof</creatorcontrib><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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Proteomics (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Losensky, Gerald</au><au>Jung, Klaus</au><au>Urlaub, Henning</au><au>Pfeifer, Felicitas</au><au>Fröls, Sabrina</au><au>Lenz, Christof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells</atitle><jtitle>Proteomics (Weinheim)</jtitle><addtitle>Proteomics</addtitle><date>2017-04</date><risdate>2017</risdate><volume>17</volume><issue>7</issue><spage>np</spage><epage>n/a</epage><pages>np-n/a</pages><issn>1615-9853</issn><eissn>1615-9861</eissn><abstract>Early and mature biofilm formation in the extremely halophilic euryarchaeon Halobacterium salinarum strain R1 was characterized by SWATH‐LC/MS/MS. Using a simple surfactant‐assisted protein solubilization protocol and one‐dimensional ultra‐high performance nanoflow chromatography on the front end, 63.2 and 58.6% of the predicted H. salinarum R1 proteome could be detected and quantified, respectively. Analysis of biophysical protein properties, functional analysis and pathway mapping indicated comprehensive characterization of the proteome. Sixty point eight percent of the quantified proteins (or 34.5% of the predicted proteome) exhibited significant abundance changes between planktonic and sessile states, demonstrating that haloarchaeal biofilm formation represents a profound “lifestyle change” on the molecular level. Our results and analysis constitute the first comprehensive study to track molecular changes from planktonic cultures to initial and mature archaeal biofilms on the proteome level. Data are available via ProteomeXchange, identifier PXD003667. Proteins exemplifying different protein expression level profiles were selected, and their corresponding gene transcripts targeted by qRT‐PCR to test the feasibility of establishing rapid PCR‐based assays for archaeal biofilm formation.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27604596</pmid><doi>10.1002/pmic.201600111</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1615-9853
ispartof Proteomics (Weinheim), 2017-04, Vol.17 (7), p.np-n/a
issn 1615-9853
1615-9861
language eng
recordid cdi_proquest_miscellaneous_1891871204
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Archaea
Archaeal Proteins - analysis
Archaeal Proteins - genetics
Archaeal Proteins - metabolism
Biofilm
Biofilms
Biofilms - growth & development
Chromatography, Liquid
Functional analysis
Gene Expression Regulation, Archaeal
Haloarchaea
Halobacterium salinarum
Halobacterium salinarum - chemistry
Halobacterium salinarum - genetics
Halobacterium salinarum - metabolism
Microbiology
Peptide mapping
Plankton - chemistry
Plankton - growth & development
Plankton - metabolism
Polymerase chain reaction
Proteins
Proteome - analysis
Proteomes
Solubilization
Strain analysis
SWATH
Tandem Mass Spectrometry
title Shedding light on biofilm formation of Halobacterium salinarum R1 by SWATH‐LC/MS/MS analysis of planktonic and sessile cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T07%3A11%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Shedding%20light%20on%20biofilm%20formation%20of%20Halobacterium%20salinarum%20R1%20by%20SWATH%E2%80%90LC/MS/MS%20analysis%20of%20planktonic%20and%20sessile%20cells&rft.jtitle=Proteomics%20(Weinheim)&rft.au=Losensky,%20Gerald&rft.date=2017-04&rft.volume=17&rft.issue=7&rft.spage=np&rft.epage=n/a&rft.pages=np-n/a&rft.issn=1615-9853&rft.eissn=1615-9861&rft_id=info:doi/10.1002/pmic.201600111&rft_dat=%3Cproquest_cross%3E1895026757%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1895026757&rft_id=info:pmid/27604596&rfr_iscdi=true