MOVEMENT AND CONTAINMENT OF MICROBIAL CONTAMINATION IN THE NUTRIENT MIST BIOREACTOR
In vitro plant cultures tend to get contaminated easily with bacteria and fungi because they are grown for long times in sugar-rich media. Contamination of bioreactors is particularly problematic as larger volumes entail larger losses. To study the movement and develop subsequent control of contamin...
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Veröffentlicht in: | In vitro cellular & developmental biology. Plant 2006-11, Vol.42 (6), p.553-557 |
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description | In vitro plant cultures tend to get contaminated easily with bacteria and fungi because they are grown for long times in sugar-rich media. Contamination of bioreactors is particularly problematic as larger volumes entail larger losses. To study the movement and develop subsequent control of contaminants in the mist bioreactor, the spore-forming microbes Penicillium chrysogenum and Bacillus subtilis were deliberately inoculated into three possible locations in the reactor: the growth chamber (GC), the medium reservoir (R), or the mist-generating chamber (MG). Compared to inoculation into either R or MG regions, the growth of P. chrysogenum inoculated into the GC required 3 more days (c. 60% more time) to move throughout the rest of the reactor. In contrast, regardless of where B. subtilis was inoculated (GC, R, or MG), it took 7 d to contaminate the entire system. The movement of filamentous fungi and bacteria seems to follow the same route of contamination throughout this reactor. Once visibly present in the reactor, neither contaminant was controllable by addition of the biocide, Plant Preservative Mixture (PPM). Both microbes were completely inhibited if PPM was added to the MG at the time of inoculation and then again 2-d post-inoculation of plants. Reactors were run for 3 wk. Plants remained free of contamination. These results will prove useful in the implementation of large-scale in vitro culture systems. |
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E.</contributor><creatorcontrib>SHARAF-ELDIN, MAHMOUD A. ; WEATHERS, PAMELA J. ; Horn, M. E.</creatorcontrib><description>In vitro plant cultures tend to get contaminated easily with bacteria and fungi because they are grown for long times in sugar-rich media. Contamination of bioreactors is particularly problematic as larger volumes entail larger losses. To study the movement and develop subsequent control of contaminants in the mist bioreactor, the spore-forming microbes Penicillium chrysogenum and Bacillus subtilis were deliberately inoculated into three possible locations in the reactor: the growth chamber (GC), the medium reservoir (R), or the mist-generating chamber (MG). Compared to inoculation into either R or MG regions, the growth of P. chrysogenum inoculated into the GC required 3 more days (c. 60% more time) to move throughout the rest of the reactor. In contrast, regardless of where B. subtilis was inoculated (GC, R, or MG), it took 7 d to contaminate the entire system. The movement of filamentous fungi and bacteria seems to follow the same route of contamination throughout this reactor. Once visibly present in the reactor, neither contaminant was controllable by addition of the biocide, Plant Preservative Mixture (PPM). Both microbes were completely inhibited if PPM was added to the MG at the time of inoculation and then again 2-d post-inoculation of plants. Reactors were run for 3 wk. Plants remained free of contamination. These results will prove useful in the implementation of large-scale in vitro culture systems.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1079/IVP2006817</identifier><language>eng</language><publisher>Heidelberg: Tissue Culture Association</publisher><subject>aeroponics ; Air flow ; Antibiotics ; Artemisia annua ; Bacillus subtilis ; Bacteria ; Biocides ; Bioreactors ; Contaminants ; Contamination ; Fungi ; Growth chambers ; Immunization ; in vitro culture ; Inoculation ; Microbial contamination ; Microbial growth ; Microorganisms ; MICROPROPAGATION ; Mist ; mist reactor ; Nutrients ; Pathogens ; Penicillium chrysogeneum ; Penicillium chrysogenum ; Plant culture ; Plant Preservative Mixture ; Plant propagation ; Plant tissues ; Plants ; Pollution control ; Preservatives ; Reactors ; Tissues ; Ventilation</subject><ispartof>In vitro cellular & developmental biology. 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E.</contributor><creatorcontrib>SHARAF-ELDIN, MAHMOUD A.</creatorcontrib><creatorcontrib>WEATHERS, PAMELA J.</creatorcontrib><title>MOVEMENT AND CONTAINMENT OF MICROBIAL CONTAMINATION IN THE NUTRIENT MIST BIOREACTOR</title><title>In vitro cellular & developmental biology. Plant</title><description>In vitro plant cultures tend to get contaminated easily with bacteria and fungi because they are grown for long times in sugar-rich media. Contamination of bioreactors is particularly problematic as larger volumes entail larger losses. To study the movement and develop subsequent control of contaminants in the mist bioreactor, the spore-forming microbes Penicillium chrysogenum and Bacillus subtilis were deliberately inoculated into three possible locations in the reactor: the growth chamber (GC), the medium reservoir (R), or the mist-generating chamber (MG). Compared to inoculation into either R or MG regions, the growth of P. chrysogenum inoculated into the GC required 3 more days (c. 60% more time) to move throughout the rest of the reactor. In contrast, regardless of where B. subtilis was inoculated (GC, R, or MG), it took 7 d to contaminate the entire system. The movement of filamentous fungi and bacteria seems to follow the same route of contamination throughout this reactor. Once visibly present in the reactor, neither contaminant was controllable by addition of the biocide, Plant Preservative Mixture (PPM). Both microbes were completely inhibited if PPM was added to the MG at the time of inoculation and then again 2-d post-inoculation of plants. Reactors were run for 3 wk. Plants remained free of contamination. These results will prove useful in the implementation of large-scale in vitro culture systems.</description><subject>aeroponics</subject><subject>Air flow</subject><subject>Antibiotics</subject><subject>Artemisia annua</subject><subject>Bacillus subtilis</subject><subject>Bacteria</subject><subject>Biocides</subject><subject>Bioreactors</subject><subject>Contaminants</subject><subject>Contamination</subject><subject>Fungi</subject><subject>Growth chambers</subject><subject>Immunization</subject><subject>in vitro culture</subject><subject>Inoculation</subject><subject>Microbial contamination</subject><subject>Microbial growth</subject><subject>Microorganisms</subject><subject>MICROPROPAGATION</subject><subject>Mist</subject><subject>mist reactor</subject><subject>Nutrients</subject><subject>Pathogens</subject><subject>Penicillium chrysogeneum</subject><subject>Penicillium chrysogenum</subject><subject>Plant culture</subject><subject>Plant Preservative Mixture</subject><subject>Plant propagation</subject><subject>Plant tissues</subject><subject>Plants</subject><subject>Pollution control</subject><subject>Preservatives</subject><subject>Reactors</subject><subject>Tissues</subject><subject>Ventilation</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE1Lw0AQhoMoWKsX72LwJEJ0djf7dUxjqgtNVtK015C0G2nRpu62B_-9qRG9eZoZ3od54PW8SwT3CLh8UPMXDMAE4kfeAIWcBpgJedztQMOAhpydemfOrQEAAeIDb5rqeZImWeFH2aMf66yIVPZ967GfqjjXIxVN-iBVWVQonfkq84vnxM9mRa4OaKqmhT9SOk-iuND5uXfSVG_OXPzMoTcbJ0X8HEz0k4qjSVATwncBZUZSxDiiBIREeEmEwCIUEgxpDGeiggaMrBdUCFqHS9zQxVLSpaBMhLUBMvRu-r9b237sjduV63ZvN52yRJITibkQHXTXQwvbOmdNU27t6r2ynyWC8tBZ-ddZB1_18NrtWvtLYggZYhh3-XWfN1VbVq925crZFAOiABgI4wfdbU_Uq7bdmP9kXwVmdFs</recordid><startdate>20061101</startdate><enddate>20061101</enddate><creator>SHARAF-ELDIN, MAHMOUD A.</creator><creator>WEATHERS, PAMELA J.</creator><general>Tissue Culture Association</general><general>CABI Publishing</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20061101</creationdate><title>MOVEMENT AND CONTAINMENT OF MICROBIAL CONTAMINATION IN THE NUTRIENT MIST BIOREACTOR</title><author>SHARAF-ELDIN, MAHMOUD A. ; WEATHERS, PAMELA J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b337t-56e9516715308912d388284890e3fe768a0f0e9bc5885b4d2f5cd95d85684be03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>aeroponics</topic><topic>Air flow</topic><topic>Antibiotics</topic><topic>Artemisia annua</topic><topic>Bacillus subtilis</topic><topic>Bacteria</topic><topic>Biocides</topic><topic>Bioreactors</topic><topic>Contaminants</topic><topic>Contamination</topic><topic>Fungi</topic><topic>Growth chambers</topic><topic>Immunization</topic><topic>in vitro culture</topic><topic>Inoculation</topic><topic>Microbial contamination</topic><topic>Microbial growth</topic><topic>Microorganisms</topic><topic>MICROPROPAGATION</topic><topic>Mist</topic><topic>mist reactor</topic><topic>Nutrients</topic><topic>Pathogens</topic><topic>Penicillium chrysogeneum</topic><topic>Penicillium chrysogenum</topic><topic>Plant culture</topic><topic>Plant Preservative Mixture</topic><topic>Plant propagation</topic><topic>Plant tissues</topic><topic>Plants</topic><topic>Pollution control</topic><topic>Preservatives</topic><topic>Reactors</topic><topic>Tissues</topic><topic>Ventilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHARAF-ELDIN, MAHMOUD A.</creatorcontrib><creatorcontrib>WEATHERS, PAMELA J.</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science 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 Basic</collection><collection>SIRS Editorial</collection><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SHARAF-ELDIN, MAHMOUD A.</au><au>WEATHERS, PAMELA J.</au><au>Horn, M. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MOVEMENT AND CONTAINMENT OF MICROBIAL CONTAMINATION IN THE NUTRIENT MIST BIOREACTOR</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><date>2006-11-01</date><risdate>2006</risdate><volume>42</volume><issue>6</issue><spage>553</spage><epage>557</epage><pages>553-557</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>In vitro plant cultures tend to get contaminated easily with bacteria and fungi because they are grown for long times in sugar-rich media. Contamination of bioreactors is particularly problematic as larger volumes entail larger losses. To study the movement and develop subsequent control of contaminants in the mist bioreactor, the spore-forming microbes Penicillium chrysogenum and Bacillus subtilis were deliberately inoculated into three possible locations in the reactor: the growth chamber (GC), the medium reservoir (R), or the mist-generating chamber (MG). Compared to inoculation into either R or MG regions, the growth of P. chrysogenum inoculated into the GC required 3 more days (c. 60% more time) to move throughout the rest of the reactor. In contrast, regardless of where B. subtilis was inoculated (GC, R, or MG), it took 7 d to contaminate the entire system. The movement of filamentous fungi and bacteria seems to follow the same route of contamination throughout this reactor. Once visibly present in the reactor, neither contaminant was controllable by addition of the biocide, Plant Preservative Mixture (PPM). Both microbes were completely inhibited if PPM was added to the MG at the time of inoculation and then again 2-d post-inoculation of plants. Reactors were run for 3 wk. Plants remained free of contamination. These results will prove useful in the implementation of large-scale in vitro culture systems.</abstract><cop>Heidelberg</cop><pub>Tissue Culture Association</pub><doi>10.1079/IVP2006817</doi><tpages>5</tpages></addata></record> |
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subjects | aeroponics Air flow Antibiotics Artemisia annua Bacillus subtilis Bacteria Biocides Bioreactors Contaminants Contamination Fungi Growth chambers Immunization in vitro culture Inoculation Microbial contamination Microbial growth Microorganisms MICROPROPAGATION Mist mist reactor Nutrients Pathogens Penicillium chrysogeneum Penicillium chrysogenum Plant culture Plant Preservative Mixture Plant propagation Plant tissues Plants Pollution control Preservatives Reactors Tissues Ventilation |
title | MOVEMENT AND CONTAINMENT OF MICROBIAL CONTAMINATION IN THE NUTRIENT MIST BIOREACTOR |
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