Loading…
Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5
Alternative strategies to antibiotic treatment are required to inhibit pathogens, including Staphylococcus aureus . Bacteriocins, such as the lantibiotic bovicin HC5, have shown potential to control pathogens. This study aims to evaluate the stress response of S. aureus to bovicin HC5 using a proteo...
Saved in:
Published in: | Applied microbiology and biotechnology 2021-10, Vol.105 (20), p.7857-7869 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03 |
---|---|
cites | cdi_FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03 |
container_end_page | 7869 |
container_issue | 20 |
container_start_page | 7857 |
container_title | Applied microbiology and biotechnology |
container_volume | 105 |
creator | Pimentel-Filho, Natan de Jesus Fuchs, Stephan Baracat-Pereira, Maria Cristina Mantovani, Hilário Cuquetto Riedel, Katharina Vanetti, Maria Cristina Dantas |
description | Alternative strategies to antibiotic treatment are required to inhibit pathogens, including
Staphylococcus aureus
. Bacteriocins, such as the lantibiotic bovicin HC5, have shown potential to control pathogens. This study aims to evaluate the stress response of
S. aureus
to bovicin HC5 using a proteomic approach. Sublethal concentrations of the bacteriocin repressed the synthesis of 62 cytoplasmic proteins, whereas 42 proteins were induced in
S. aureus
COL. Specifically, synthesis of several proteins involved in amino acid biosynthesis, mainly products of
ilv-leu
operon, and DNA metabolism, such as DNA polymerase I, decreased following bovicin treatment while proteins involved in catabolism, mainly tricarboxylic acid cycle metabolism, and chaperones were over-expressed. The levels of CodY and CcpA, important regulators involved in the stationary phase adaptation and catabolite repression, respectively, also increased in the presence of the bacteriocin. These results indicate that stress caused by the sublethal concentration of bovicin HC5 in the cell membrane results in growth reduction, reduced protein synthesis, and, at the same time, enhanced the levels of chaperones and enzymes involved in energy-efficient catabolism in an attempt to restore energy and cell homeostasis. These results bring relevant information to amplify the knowledge concerning the bacterial physiological changes in response to the stress caused by the cell exposition to bovicin HC5. New potential targets for controlling this pathogen can also be determined from the new protein expression pattern presented.
Key points
•
Bovicin HC5 changed the synthesis of cytoplasmic proteins of S. aureus
.
•
Bovicin HC5 interfered in the synthesis of proteins of amino acids biosynthesis
.
•
Synthesis of chaperones enhanced in the presence of sublethal dosage of bovicin HC5
.
Graphical abstract |
doi_str_mv | 10.1007/s00253-021-11594-3 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2575828349</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A678578304</galeid><sourcerecordid>A678578304</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03</originalsourceid><addsrcrecordid>eNp9kUFv1DAQhSMEEkvpH-AUiQsc0o7t2HGO1QpopUpUbe-u40y2rrJxsJ2q_ffMskiwCFU-zGG-N34zryg-MDhhAM1pAuBSVMBZxZhs60q8KlasFrwCxerXxQpYI6tGtvpt8S6lBwDGtVKr4u4qhox-KvFpjpiSD1M5xzD40U-bMgzlTbbz_fMYXHBuSaVdIlIhAdFzmBKWOZT5HsvOuozRB0e9Ljz6XT1fy_fFm8GOCY9_16Pi9uuX2_V5dfn928X67LJytRS5csC1ACUH7HUPUg-8rfuOWlrIVva6Vko3XAGzrO2cFR1HResAxxraHsRR8Wk_lsz_WDBls_XJ4TjaCcOSDJeN1PRF3RL68R_0ISxxInNEaRBNo9hf1MaOaPw0hByt2w01Z6rRsiG7NVEn_6Ho9bj1LkxIh8RDwecDATEZn_LGLimZi5vrQ5bvWRdDShEHM0e_tfHZMDC72M0-dkOxm1-xG0EisRclgqcNxj_bvaD6CaMtrJg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2580377619</pqid></control><display><type>article</type><title>Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5</title><source>ABI/INFORM Global</source><source>Springer Nature</source><creator>Pimentel-Filho, Natan de Jesus ; Fuchs, Stephan ; Baracat-Pereira, Maria Cristina ; Mantovani, Hilário Cuquetto ; Riedel, Katharina ; Vanetti, Maria Cristina Dantas</creator><creatorcontrib>Pimentel-Filho, Natan de Jesus ; Fuchs, Stephan ; Baracat-Pereira, Maria Cristina ; Mantovani, Hilário Cuquetto ; Riedel, Katharina ; Vanetti, Maria Cristina Dantas</creatorcontrib><description>Alternative strategies to antibiotic treatment are required to inhibit pathogens, including
Staphylococcus aureus
. Bacteriocins, such as the lantibiotic bovicin HC5, have shown potential to control pathogens. This study aims to evaluate the stress response of
S. aureus
to bovicin HC5 using a proteomic approach. Sublethal concentrations of the bacteriocin repressed the synthesis of 62 cytoplasmic proteins, whereas 42 proteins were induced in
S. aureus
COL. Specifically, synthesis of several proteins involved in amino acid biosynthesis, mainly products of
ilv-leu
operon, and DNA metabolism, such as DNA polymerase I, decreased following bovicin treatment while proteins involved in catabolism, mainly tricarboxylic acid cycle metabolism, and chaperones were over-expressed. The levels of CodY and CcpA, important regulators involved in the stationary phase adaptation and catabolite repression, respectively, also increased in the presence of the bacteriocin. These results indicate that stress caused by the sublethal concentration of bovicin HC5 in the cell membrane results in growth reduction, reduced protein synthesis, and, at the same time, enhanced the levels of chaperones and enzymes involved in energy-efficient catabolism in an attempt to restore energy and cell homeostasis. These results bring relevant information to amplify the knowledge concerning the bacterial physiological changes in response to the stress caused by the cell exposition to bovicin HC5. New potential targets for controlling this pathogen can also be determined from the new protein expression pattern presented.
Key points
•
Bovicin HC5 changed the synthesis of cytoplasmic proteins of S. aureus
.
•
Bovicin HC5 interfered in the synthesis of proteins of amino acids biosynthesis
.
•
Synthesis of chaperones enhanced in the presence of sublethal dosage of bovicin HC5
.
Graphical abstract</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-021-11594-3</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amino acids ; Analysis ; Antibiotics ; Bacteriocins ; Biomedical and Life Sciences ; Biosynthesis ; Biotechnology ; Catabolism ; Catabolite repression ; Cell membranes ; Chaperones ; Deoxyribonucleic acid ; DNA ; DNA polymerase ; DNA-directed DNA polymerase ; Energy efficiency ; Genetic aspects ; Genomics ; Homeostasis ; Identification and classification ; Life Sciences ; Metabolism ; Microbial Genetics and Genomics ; Microbiology ; Pathogens ; Physiological aspects ; Properties ; Protein biosynthesis ; Protein expression ; Protein synthesis ; Proteins ; Proteomics ; Staphylococcus aureus ; Stationary phase ; Stress (Physiology) ; Stress response ; Sublethal dosage ; Transcriptomics ; Tricarboxylic acid cycle</subject><ispartof>Applied microbiology and biotechnology, 2021-10, Vol.105 (20), p.7857-7869</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03</citedby><cites>FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2580377619/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2580377619?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml></links><search><creatorcontrib>Pimentel-Filho, Natan de Jesus</creatorcontrib><creatorcontrib>Fuchs, Stephan</creatorcontrib><creatorcontrib>Baracat-Pereira, Maria Cristina</creatorcontrib><creatorcontrib>Mantovani, Hilário Cuquetto</creatorcontrib><creatorcontrib>Riedel, Katharina</creatorcontrib><creatorcontrib>Vanetti, Maria Cristina Dantas</creatorcontrib><title>Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><description>Alternative strategies to antibiotic treatment are required to inhibit pathogens, including
Staphylococcus aureus
. Bacteriocins, such as the lantibiotic bovicin HC5, have shown potential to control pathogens. This study aims to evaluate the stress response of
S. aureus
to bovicin HC5 using a proteomic approach. Sublethal concentrations of the bacteriocin repressed the synthesis of 62 cytoplasmic proteins, whereas 42 proteins were induced in
S. aureus
COL. Specifically, synthesis of several proteins involved in amino acid biosynthesis, mainly products of
ilv-leu
operon, and DNA metabolism, such as DNA polymerase I, decreased following bovicin treatment while proteins involved in catabolism, mainly tricarboxylic acid cycle metabolism, and chaperones were over-expressed. The levels of CodY and CcpA, important regulators involved in the stationary phase adaptation and catabolite repression, respectively, also increased in the presence of the bacteriocin. These results indicate that stress caused by the sublethal concentration of bovicin HC5 in the cell membrane results in growth reduction, reduced protein synthesis, and, at the same time, enhanced the levels of chaperones and enzymes involved in energy-efficient catabolism in an attempt to restore energy and cell homeostasis. These results bring relevant information to amplify the knowledge concerning the bacterial physiological changes in response to the stress caused by the cell exposition to bovicin HC5. New potential targets for controlling this pathogen can also be determined from the new protein expression pattern presented.
Key points
•
Bovicin HC5 changed the synthesis of cytoplasmic proteins of S. aureus
.
•
Bovicin HC5 interfered in the synthesis of proteins of amino acids biosynthesis
.
•
Synthesis of chaperones enhanced in the presence of sublethal dosage of bovicin HC5
.
Graphical abstract</description><subject>Amino acids</subject><subject>Analysis</subject><subject>Antibiotics</subject><subject>Bacteriocins</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Biotechnology</subject><subject>Catabolism</subject><subject>Catabolite repression</subject><subject>Cell membranes</subject><subject>Chaperones</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA polymerase</subject><subject>DNA-directed DNA polymerase</subject><subject>Energy efficiency</subject><subject>Genetic aspects</subject><subject>Genomics</subject><subject>Homeostasis</subject><subject>Identification and classification</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Pathogens</subject><subject>Physiological aspects</subject><subject>Properties</subject><subject>Protein biosynthesis</subject><subject>Protein expression</subject><subject>Protein synthesis</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Staphylococcus aureus</subject><subject>Stationary phase</subject><subject>Stress (Physiology)</subject><subject>Stress response</subject><subject>Sublethal dosage</subject><subject>Transcriptomics</subject><subject>Tricarboxylic acid cycle</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><recordid>eNp9kUFv1DAQhSMEEkvpH-AUiQsc0o7t2HGO1QpopUpUbe-u40y2rrJxsJ2q_ffMskiwCFU-zGG-N34zryg-MDhhAM1pAuBSVMBZxZhs60q8KlasFrwCxerXxQpYI6tGtvpt8S6lBwDGtVKr4u4qhox-KvFpjpiSD1M5xzD40U-bMgzlTbbz_fMYXHBuSaVdIlIhAdFzmBKWOZT5HsvOuozRB0e9Ljz6XT1fy_fFm8GOCY9_16Pi9uuX2_V5dfn928X67LJytRS5csC1ACUH7HUPUg-8rfuOWlrIVva6Vko3XAGzrO2cFR1HResAxxraHsRR8Wk_lsz_WDBls_XJ4TjaCcOSDJeN1PRF3RL68R_0ISxxInNEaRBNo9hf1MaOaPw0hByt2w01Z6rRsiG7NVEn_6Ho9bj1LkxIh8RDwecDATEZn_LGLimZi5vrQ5bvWRdDShEHM0e_tfHZMDC72M0-dkOxm1-xG0EisRclgqcNxj_bvaD6CaMtrJg</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Pimentel-Filho, Natan de Jesus</creator><creator>Fuchs, Stephan</creator><creator>Baracat-Pereira, Maria Cristina</creator><creator>Mantovani, Hilário Cuquetto</creator><creator>Riedel, Katharina</creator><creator>Vanetti, Maria Cristina Dantas</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>LK8</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>202110</creationdate><title>Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5</title><author>Pimentel-Filho, Natan de Jesus ; Fuchs, Stephan ; Baracat-Pereira, Maria Cristina ; Mantovani, Hilário Cuquetto ; Riedel, Katharina ; Vanetti, Maria Cristina Dantas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amino acids</topic><topic>Analysis</topic><topic>Antibiotics</topic><topic>Bacteriocins</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Biotechnology</topic><topic>Catabolism</topic><topic>Catabolite repression</topic><topic>Cell membranes</topic><topic>Chaperones</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA polymerase</topic><topic>DNA-directed DNA polymerase</topic><topic>Energy efficiency</topic><topic>Genetic aspects</topic><topic>Genomics</topic><topic>Homeostasis</topic><topic>Identification and classification</topic><topic>Life Sciences</topic><topic>Metabolism</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>Pathogens</topic><topic>Physiological aspects</topic><topic>Properties</topic><topic>Protein biosynthesis</topic><topic>Protein expression</topic><topic>Protein synthesis</topic><topic>Proteins</topic><topic>Proteomics</topic><topic>Staphylococcus aureus</topic><topic>Stationary phase</topic><topic>Stress (Physiology)</topic><topic>Stress response</topic><topic>Sublethal dosage</topic><topic>Transcriptomics</topic><topic>Tricarboxylic acid cycle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pimentel-Filho, Natan de Jesus</creatorcontrib><creatorcontrib>Fuchs, Stephan</creatorcontrib><creatorcontrib>Baracat-Pereira, Maria Cristina</creatorcontrib><creatorcontrib>Mantovani, Hilário Cuquetto</creatorcontrib><creatorcontrib>Riedel, Katharina</creatorcontrib><creatorcontrib>Vanetti, Maria Cristina Dantas</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Hospital Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central - New (Subscription)</collection><collection>Business Premium Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>ProQuest Biological Science Collection</collection><collection>ABI/INFORM Global</collection><collection>ProQuest Health & Medical Collection</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Business (UW System Shared)</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pimentel-Filho, Natan de Jesus</au><au>Fuchs, Stephan</au><au>Baracat-Pereira, Maria Cristina</au><au>Mantovani, Hilário Cuquetto</au><au>Riedel, Katharina</au><au>Vanetti, Maria Cristina Dantas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5</atitle><jtitle>Applied microbiology and biotechnology</jtitle><stitle>Appl Microbiol Biotechnol</stitle><date>2021-10</date><risdate>2021</risdate><volume>105</volume><issue>20</issue><spage>7857</spage><epage>7869</epage><pages>7857-7869</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><abstract>Alternative strategies to antibiotic treatment are required to inhibit pathogens, including
Staphylococcus aureus
. Bacteriocins, such as the lantibiotic bovicin HC5, have shown potential to control pathogens. This study aims to evaluate the stress response of
S. aureus
to bovicin HC5 using a proteomic approach. Sublethal concentrations of the bacteriocin repressed the synthesis of 62 cytoplasmic proteins, whereas 42 proteins were induced in
S. aureus
COL. Specifically, synthesis of several proteins involved in amino acid biosynthesis, mainly products of
ilv-leu
operon, and DNA metabolism, such as DNA polymerase I, decreased following bovicin treatment while proteins involved in catabolism, mainly tricarboxylic acid cycle metabolism, and chaperones were over-expressed. The levels of CodY and CcpA, important regulators involved in the stationary phase adaptation and catabolite repression, respectively, also increased in the presence of the bacteriocin. These results indicate that stress caused by the sublethal concentration of bovicin HC5 in the cell membrane results in growth reduction, reduced protein synthesis, and, at the same time, enhanced the levels of chaperones and enzymes involved in energy-efficient catabolism in an attempt to restore energy and cell homeostasis. These results bring relevant information to amplify the knowledge concerning the bacterial physiological changes in response to the stress caused by the cell exposition to bovicin HC5. New potential targets for controlling this pathogen can also be determined from the new protein expression pattern presented.
Key points
•
Bovicin HC5 changed the synthesis of cytoplasmic proteins of S. aureus
.
•
Bovicin HC5 interfered in the synthesis of proteins of amino acids biosynthesis
.
•
Synthesis of chaperones enhanced in the presence of sublethal dosage of bovicin HC5
.
Graphical abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00253-021-11594-3</doi><tpages>13</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0175-7598 |
ispartof | Applied microbiology and biotechnology, 2021-10, Vol.105 (20), p.7857-7869 |
issn | 0175-7598 1432-0614 |
language | eng |
recordid | cdi_proquest_miscellaneous_2575828349 |
source | ABI/INFORM Global; Springer Nature |
subjects | Amino acids Analysis Antibiotics Bacteriocins Biomedical and Life Sciences Biosynthesis Biotechnology Catabolism Catabolite repression Cell membranes Chaperones Deoxyribonucleic acid DNA DNA polymerase DNA-directed DNA polymerase Energy efficiency Genetic aspects Genomics Homeostasis Identification and classification Life Sciences Metabolism Microbial Genetics and Genomics Microbiology Pathogens Physiological aspects Properties Protein biosynthesis Protein expression Protein synthesis Proteins Proteomics Staphylococcus aureus Stationary phase Stress (Physiology) Stress response Sublethal dosage Transcriptomics Tricarboxylic acid cycle |
title | Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-03-06T22%3A23%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Protein%20expression%20profiling%20of%20Staphylococcus%20aureus%20in%20response%20to%20the%20bacteriocin%20bovicin%20HC5&rft.jtitle=Applied%20microbiology%20and%20biotechnology&rft.au=Pimentel-Filho,%20Natan%20de%20Jesus&rft.date=2021-10&rft.volume=105&rft.issue=20&rft.spage=7857&rft.epage=7869&rft.pages=7857-7869&rft.issn=0175-7598&rft.eissn=1432-0614&rft_id=info:doi/10.1007/s00253-021-11594-3&rft_dat=%3Cgale_proqu%3EA678578304%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c453t-c0283065fed8d058f294db45383595d8466872601a19bca3b2e675902e409d03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2580377619&rft_id=info:pmid/&rft_galeid=A678578304&rfr_iscdi=true |