Diverse effects of a biosurfactant from Rhodococcus ruber IEGM 231 on the adhesion of resting and growing bacteria to polystyrene
This study evaluated the effects of a trehalolipid biosurfactant produced by Rhodococcus ruber IEGM 231 on the bacterial adhesion and biofilm formation on the surface of polystyrene microplates. The adhesion of Gram-positive ( Arthrobacter simplex , Bacillus subtilis , Brevibacterium linens , Coryne...
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description | This study evaluated the effects of a trehalolipid biosurfactant produced by
Rhodococcus ruber
IEGM 231 on the bacterial adhesion and biofilm formation on the surface of polystyrene microplates. The adhesion of Gram-positive (
Arthrobacter simplex
,
Bacillus subtilis
,
Brevibacterium linens
,
Corynebacterium glutamicum
,
Micrococcus luteus
) and Gram-negative (
Escherichia coli
,
Pseudomonas fluorescencens
) bacteria correlated differently with the cell hydrophobicity and surface charge. In particular, exponentially growing bacterial cells with increased hydrophobicities adhered stronger to polystyrene compared to more hydrophilic stationary phase cells. Also, a moderate correlation (0.56) was found between zeta potential and adhesion values of actively growing bacteria, suggesting that less negatively charged cells adhered stronger to polystyrene. Efficient biosurfactant concentrations (10–100 mg/L) were determined, which selectively inhibited (up to 76 %) the adhesion of tested bacterial cultures, however without inhibiting their growth. The biosurfactant was more active against growing bacteria rather than resting cells, thus showing high biofilm-preventing properties. Contact angle measurements revealed more hydrophilic surface of the biosurfactant-covered polystyrene compared to bare polystyrene, which allowed less adhesion of hydrophobic bacteria. Furthermore, surface free-energy calculations showed a decrease in the Wan der Waals (γ
LW
) component and an increase in the acid-based (γ
AB
) component caused by the biosurfactant coating of polysterene. However, our results suggested that the biosurfactant inhibited the adhesion of bacteria independently on their surface charges. AFM scanning revealed three-type biosurfactant structures (micelles, cord-like assemblies and large vesicles) formed on glass, depending on concentrations used, that could lead to diverse anti-adhesive effects against different bacterial species. |
doi_str_mv | 10.1186/s13568-016-0186-z |
format | Article |
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Rhodococcus ruber
IEGM 231 on the bacterial adhesion and biofilm formation on the surface of polystyrene microplates. The adhesion of Gram-positive (
Arthrobacter simplex
,
Bacillus subtilis
,
Brevibacterium linens
,
Corynebacterium glutamicum
,
Micrococcus luteus
) and Gram-negative (
Escherichia coli
,
Pseudomonas fluorescencens
) bacteria correlated differently with the cell hydrophobicity and surface charge. In particular, exponentially growing bacterial cells with increased hydrophobicities adhered stronger to polystyrene compared to more hydrophilic stationary phase cells. Also, a moderate correlation (0.56) was found between zeta potential and adhesion values of actively growing bacteria, suggesting that less negatively charged cells adhered stronger to polystyrene. Efficient biosurfactant concentrations (10–100 mg/L) were determined, which selectively inhibited (up to 76 %) the adhesion of tested bacterial cultures, however without inhibiting their growth. The biosurfactant was more active against growing bacteria rather than resting cells, thus showing high biofilm-preventing properties. Contact angle measurements revealed more hydrophilic surface of the biosurfactant-covered polystyrene compared to bare polystyrene, which allowed less adhesion of hydrophobic bacteria. Furthermore, surface free-energy calculations showed a decrease in the Wan der Waals (γ
LW
) component and an increase in the acid-based (γ
AB
) component caused by the biosurfactant coating of polysterene. However, our results suggested that the biosurfactant inhibited the adhesion of bacteria independently on their surface charges. AFM scanning revealed three-type biosurfactant structures (micelles, cord-like assemblies and large vesicles) formed on glass, depending on concentrations used, that could lead to diverse anti-adhesive effects against different bacterial species.</description><identifier>ISSN: 2191-0855</identifier><identifier>EISSN: 2191-0855</identifier><identifier>DOI: 10.1186/s13568-016-0186-z</identifier><identifier>PMID: 26888203</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Arthrobacter simplex ; Bacillus subtilis ; Biomedical and Life Sciences ; Biotechnology ; Brevibacterium linens ; Corynebacterium glutamicum ; Escherichia coli ; Life Sciences ; Microbial Genetics and Genomics ; Microbiology ; Micrococcus luteus ; Original ; Original Article ; Pseudomonas ; Rhodococcus ruber</subject><ispartof>AMB Express, 2016-02, Vol.6 (1), p.14-14, Article 14</ispartof><rights>Kuyukina et al. 2016</rights><rights>The Author(s) 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-8b3eb248e5e62b2ccca9d6960d74c254e3d80eb3a064a81e00acae1bf19df9b33</citedby><cites>FETCH-LOGICAL-c503t-8b3eb248e5e62b2ccca9d6960d74c254e3d80eb3a064a81e00acae1bf19df9b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759446/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759446/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,41464,42165,42533,51294,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26888203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuyukina, Maria S.</creatorcontrib><creatorcontrib>Ivshina, Irena B.</creatorcontrib><creatorcontrib>Korshunova, Irina O.</creatorcontrib><creatorcontrib>Stukova, Galina I.</creatorcontrib><creatorcontrib>Krivoruchko, Anastasiya V.</creatorcontrib><title>Diverse effects of a biosurfactant from Rhodococcus ruber IEGM 231 on the adhesion of resting and growing bacteria to polystyrene</title><title>AMB Express</title><addtitle>AMB Expr</addtitle><addtitle>AMB Express</addtitle><description>This study evaluated the effects of a trehalolipid biosurfactant produced by
Rhodococcus ruber
IEGM 231 on the bacterial adhesion and biofilm formation on the surface of polystyrene microplates. The adhesion of Gram-positive (
Arthrobacter simplex
,
Bacillus subtilis
,
Brevibacterium linens
,
Corynebacterium glutamicum
,
Micrococcus luteus
) and Gram-negative (
Escherichia coli
,
Pseudomonas fluorescencens
) bacteria correlated differently with the cell hydrophobicity and surface charge. In particular, exponentially growing bacterial cells with increased hydrophobicities adhered stronger to polystyrene compared to more hydrophilic stationary phase cells. Also, a moderate correlation (0.56) was found between zeta potential and adhesion values of actively growing bacteria, suggesting that less negatively charged cells adhered stronger to polystyrene. Efficient biosurfactant concentrations (10–100 mg/L) were determined, which selectively inhibited (up to 76 %) the adhesion of tested bacterial cultures, however without inhibiting their growth. The biosurfactant was more active against growing bacteria rather than resting cells, thus showing high biofilm-preventing properties. Contact angle measurements revealed more hydrophilic surface of the biosurfactant-covered polystyrene compared to bare polystyrene, which allowed less adhesion of hydrophobic bacteria. Furthermore, surface free-energy calculations showed a decrease in the Wan der Waals (γ
LW
) component and an increase in the acid-based (γ
AB
) component caused by the biosurfactant coating of polysterene. However, our results suggested that the biosurfactant inhibited the adhesion of bacteria independently on their surface charges. AFM scanning revealed three-type biosurfactant structures (micelles, cord-like assemblies and large vesicles) formed on glass, depending on concentrations used, that could lead to diverse anti-adhesive effects against different bacterial species.</description><subject>Arthrobacter simplex</subject><subject>Bacillus subtilis</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Brevibacterium linens</subject><subject>Corynebacterium glutamicum</subject><subject>Escherichia coli</subject><subject>Life Sciences</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Micrococcus luteus</subject><subject>Original</subject><subject>Original Article</subject><subject>Pseudomonas</subject><subject>Rhodococcus ruber</subject><issn>2191-0855</issn><issn>2191-0855</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkl1rFDEUhgdRbGn7A7yRgDfeTM33ZG4EqbUWWoRSr0OSOdmdMpusSaayvfOfN8vWsgqCgZATznPefJy3ad4QfEqIkh8yYUKqFhNZp5Ltw4vmkJKetFgJ8XIvPmhOcr7DdQiMeyleNwdUKqUoZofNr8_jPaQMCLwHVzKKHhlkx5jn5I0rJhTkU1yhm2UcoovOzRml2UJCl-cX14gygmJAZQnIDEvIY91UiQS5jGGBTBjQIsWf29hWOUijQSWidZw2uWwSBDhuXnkzZTh5Wo-a71_Ob8--tlffLi7PPl21TmBWWmUZWMoVCJDUUuec6QfZSzx03FHBgQ0Kg2UGS24UAYyNM0CsJ_3ge8vYUfNxp7ue7QoGB6EkM-l1GlcmbXQ0o_4zE8alXsR7zTvRcy6rwPsngRR_zPWBejVmB9NkAsQ5a9IpLKjABP8HKjvcUdXxir77C72Lcwr1JzRRhFPe1Z5Viuwol2LOCfzzvQnWWzvonR10tYPe2kE_1Jq3-w9-rvjd_ArQHZBrKiwg7R39T9VHGKnCZA</recordid><startdate>20160218</startdate><enddate>20160218</enddate><creator>Kuyukina, Maria S.</creator><creator>Ivshina, Irena B.</creator><creator>Korshunova, Irina O.</creator><creator>Stukova, Galina I.</creator><creator>Krivoruchko, Anastasiya V.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>LK8</scope><scope>M7P</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20160218</creationdate><title>Diverse effects of a biosurfactant from Rhodococcus ruber IEGM 231 on the adhesion of resting and growing bacteria to polystyrene</title><author>Kuyukina, Maria S. ; Ivshina, Irena B. ; Korshunova, Irina O. ; Stukova, Galina I. ; Krivoruchko, Anastasiya V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-8b3eb248e5e62b2ccca9d6960d74c254e3d80eb3a064a81e00acae1bf19df9b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Arthrobacter simplex</topic><topic>Bacillus subtilis</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Brevibacterium linens</topic><topic>Corynebacterium glutamicum</topic><topic>Escherichia coli</topic><topic>Life Sciences</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>Micrococcus luteus</topic><topic>Original</topic><topic>Original Article</topic><topic>Pseudomonas</topic><topic>Rhodococcus ruber</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuyukina, Maria S.</creatorcontrib><creatorcontrib>Ivshina, Irena B.</creatorcontrib><creatorcontrib>Korshunova, Irina O.</creatorcontrib><creatorcontrib>Stukova, Galina I.</creatorcontrib><creatorcontrib>Krivoruchko, Anastasiya V.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>MEDLINE - Academic</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>PubMed Central (Full Participant titles)</collection><jtitle>AMB Express</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuyukina, Maria S.</au><au>Ivshina, Irena B.</au><au>Korshunova, Irina O.</au><au>Stukova, Galina I.</au><au>Krivoruchko, Anastasiya V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diverse effects of a biosurfactant from Rhodococcus ruber IEGM 231 on the adhesion of resting and growing bacteria to polystyrene</atitle><jtitle>AMB Express</jtitle><stitle>AMB Expr</stitle><addtitle>AMB Express</addtitle><date>2016-02-18</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>14</spage><epage>14</epage><pages>14-14</pages><artnum>14</artnum><issn>2191-0855</issn><eissn>2191-0855</eissn><abstract>This study evaluated the effects of a trehalolipid biosurfactant produced by
Rhodococcus ruber
IEGM 231 on the bacterial adhesion and biofilm formation on the surface of polystyrene microplates. The adhesion of Gram-positive (
Arthrobacter simplex
,
Bacillus subtilis
,
Brevibacterium linens
,
Corynebacterium glutamicum
,
Micrococcus luteus
) and Gram-negative (
Escherichia coli
,
Pseudomonas fluorescencens
) bacteria correlated differently with the cell hydrophobicity and surface charge. In particular, exponentially growing bacterial cells with increased hydrophobicities adhered stronger to polystyrene compared to more hydrophilic stationary phase cells. Also, a moderate correlation (0.56) was found between zeta potential and adhesion values of actively growing bacteria, suggesting that less negatively charged cells adhered stronger to polystyrene. Efficient biosurfactant concentrations (10–100 mg/L) were determined, which selectively inhibited (up to 76 %) the adhesion of tested bacterial cultures, however without inhibiting their growth. The biosurfactant was more active against growing bacteria rather than resting cells, thus showing high biofilm-preventing properties. Contact angle measurements revealed more hydrophilic surface of the biosurfactant-covered polystyrene compared to bare polystyrene, which allowed less adhesion of hydrophobic bacteria. Furthermore, surface free-energy calculations showed a decrease in the Wan der Waals (γ
LW
) component and an increase in the acid-based (γ
AB
) component caused by the biosurfactant coating of polysterene. However, our results suggested that the biosurfactant inhibited the adhesion of bacteria independently on their surface charges. AFM scanning revealed three-type biosurfactant structures (micelles, cord-like assemblies and large vesicles) formed on glass, depending on concentrations used, that could lead to diverse anti-adhesive effects against different bacterial species.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26888203</pmid><doi>10.1186/s13568-016-0186-z</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arthrobacter simplex Bacillus subtilis Biomedical and Life Sciences Biotechnology Brevibacterium linens Corynebacterium glutamicum Escherichia coli Life Sciences Microbial Genetics and Genomics Microbiology Micrococcus luteus Original Original Article Pseudomonas Rhodococcus ruber |
title | Diverse effects of a biosurfactant from Rhodococcus ruber IEGM 231 on the adhesion of resting and growing bacteria to polystyrene |
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