Culturing marine bacteria - an essential prerequisite for biodiscovery
Summary The potential for using marine microbes for biodiscovery is severely limited by the lack of laboratory cultures. It is a long‐standing observation that standard microbiological techniques only isolate a very small proportion of the wide diversity of microbes that are known in natural environ...
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description | Summary
The potential for using marine microbes for biodiscovery is severely limited by the lack of laboratory cultures. It is a long‐standing observation that standard microbiological techniques only isolate a very small proportion of the wide diversity of microbes that are known in natural environments from DNA sequences. A number of explanations are reviewed. The process of establishing laboratory cultures may destroy any cell‐to‐cell communication that occurs between organisms in the natural environment and that are vital for growth. Bacteria probably grow as consortia in the sea and reliance on other bacteria for essential nutrients and substrates is not possible with standard microbiological approaches. Such interactions should be considered when designing programmes for the isolation of marine microbes. The benefits of novel technologies for manipulating cells are reviewed, including single cell encapsulation in gel micro‐droplets. Although novel technologies offer benefits for bringing previously uncultured microbes into laboratory culture, many useful bacteria can still be isolated using variations of plating techniques. Results are summarized for a study to culture bacteria from a long‐term observatory station in the English Channel. Bacterial biodiversity in this assemblage has recently been characterized using high‐throughput sequencing techniques. Although Alphaproteobacteria dominated the natural bacterial assemblage throughout the year, Gammaproteobacteria were the most frequent group isolated by plating techniques. The use of different gelling agents and the addition of ammonium to seawater‐based agar did lead to the isolation of a higher proportion of Alphaproteobacteria. Variation in medium composition was also able to increase the recovery of other groups of particular interest for biodiscovery, such as Actinobacteria. |
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The potential for using marine microbes for biodiscovery is severely limited by the lack of laboratory cultures. It is a long‐standing observation that standard microbiological techniques only isolate a very small proportion of the wide diversity of microbes that are known in natural environments from DNA sequences. A number of explanations are reviewed. The process of establishing laboratory cultures may destroy any cell‐to‐cell communication that occurs between organisms in the natural environment and that are vital for growth. Bacteria probably grow as consortia in the sea and reliance on other bacteria for essential nutrients and substrates is not possible with standard microbiological approaches. Such interactions should be considered when designing programmes for the isolation of marine microbes. The benefits of novel technologies for manipulating cells are reviewed, including single cell encapsulation in gel micro‐droplets. Although novel technologies offer benefits for bringing previously uncultured microbes into laboratory culture, many useful bacteria can still be isolated using variations of plating techniques. Results are summarized for a study to culture bacteria from a long‐term observatory station in the English Channel. Bacterial biodiversity in this assemblage has recently been characterized using high‐throughput sequencing techniques. Although Alphaproteobacteria dominated the natural bacterial assemblage throughout the year, Gammaproteobacteria were the most frequent group isolated by plating techniques. The use of different gelling agents and the addition of ammonium to seawater‐based agar did lead to the isolation of a higher proportion of Alphaproteobacteria. Variation in medium composition was also able to increase the recovery of other groups of particular interest for biodiscovery, such as Actinobacteria.</description><identifier>ISSN: 1751-7915</identifier><identifier>EISSN: 1751-7915</identifier><identifier>DOI: 10.1111/j.1751-7915.2010.00188.x</identifier><identifier>PMID: 21255353</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Alphaproteobacteria ; Ammonium ; Bacteria ; Bacteria - classification ; Bacteria - genetics ; Bacteria - growth & development ; Bacteria - isolation & purification ; Bacteriological Techniques - methods ; Biodiversity ; Cell culture ; Cell interactions ; Chemical analysis ; Cloning ; Consortia ; Deoxyribonucleic acid ; DNA ; Ecologists ; Essential nutrients ; Gelation ; Gene sequencing ; Genomics ; Laboratories ; Laboratory culture ; Life Sciences ; Marine technology ; Microbiology and Parasitology ; Microorganisms ; Microscopy ; Minireviews ; Nucleotide sequence ; Nutrients ; Organisms ; Phylogenetics ; Plating ; Reagents ; Reviews ; Seawater ; Seawater - microbiology ; Substrates ; Taxonomy ; Water analysis</subject><ispartof>Microbial biotechnology, 2010-09, Vol.3 (5), p.564-575</ispartof><rights>2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd</rights><rights>2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd.</rights><rights>Copyright John Wiley & Sons, Inc. Sep 2010</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2010 The Author. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5688-5b76d41b80f2a9670f57f3d3172d7a9d75b49c96ceaec2654f38b586c26da1e73</citedby><cites>FETCH-LOGICAL-c5688-5b76d41b80f2a9670f57f3d3172d7a9d75b49c96ceaec2654f38b586c26da1e73</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/PMC3815769/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815769/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,1418,11567,27929,27930,45579,45580,46057,46481,53796,53798</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1751-7915.2010.00188.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21255353$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-brest.fr/hal-00616940$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Joint, Ian</creatorcontrib><creatorcontrib>Mühling, Martin</creatorcontrib><creatorcontrib>Querellou, Joël</creatorcontrib><title>Culturing marine bacteria - an essential prerequisite for biodiscovery</title><title>Microbial biotechnology</title><addtitle>Microbial Biotechnology</addtitle><description>Summary
The potential for using marine microbes for biodiscovery is severely limited by the lack of laboratory cultures. It is a long‐standing observation that standard microbiological techniques only isolate a very small proportion of the wide diversity of microbes that are known in natural environments from DNA sequences. A number of explanations are reviewed. The process of establishing laboratory cultures may destroy any cell‐to‐cell communication that occurs between organisms in the natural environment and that are vital for growth. Bacteria probably grow as consortia in the sea and reliance on other bacteria for essential nutrients and substrates is not possible with standard microbiological approaches. Such interactions should be considered when designing programmes for the isolation of marine microbes. The benefits of novel technologies for manipulating cells are reviewed, including single cell encapsulation in gel micro‐droplets. Although novel technologies offer benefits for bringing previously uncultured microbes into laboratory culture, many useful bacteria can still be isolated using variations of plating techniques. Results are summarized for a study to culture bacteria from a long‐term observatory station in the English Channel. Bacterial biodiversity in this assemblage has recently been characterized using high‐throughput sequencing techniques. Although Alphaproteobacteria dominated the natural bacterial assemblage throughout the year, Gammaproteobacteria were the most frequent group isolated by plating techniques. The use of different gelling agents and the addition of ammonium to seawater‐based agar did lead to the isolation of a higher proportion of Alphaproteobacteria. Variation in medium composition was also able to increase the recovery of other groups of particular interest for biodiscovery, such as Actinobacteria.</description><subject>Alphaproteobacteria</subject><subject>Ammonium</subject><subject>Bacteria</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - growth & development</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteriological Techniques - methods</subject><subject>Biodiversity</subject><subject>Cell culture</subject><subject>Cell interactions</subject><subject>Chemical analysis</subject><subject>Cloning</subject><subject>Consortia</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Ecologists</subject><subject>Essential nutrients</subject><subject>Gelation</subject><subject>Gene sequencing</subject><subject>Genomics</subject><subject>Laboratories</subject><subject>Laboratory culture</subject><subject>Life Sciences</subject><subject>Marine technology</subject><subject>Microbiology and Parasitology</subject><subject>Microorganisms</subject><subject>Microscopy</subject><subject>Minireviews</subject><subject>Nucleotide sequence</subject><subject>Nutrients</subject><subject>Organisms</subject><subject>Phylogenetics</subject><subject>Plating</subject><subject>Reagents</subject><subject>Reviews</subject><subject>Seawater</subject><subject>Seawater - microbiology</subject><subject>Substrates</subject><subject>Taxonomy</subject><subject>Water analysis</subject><issn>1751-7915</issn><issn>1751-7915</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNUU1v00AQXSEQLYW_gCxxQBwc9sP7JSGkEuoGEUBIQRxHa3vdbnDsdNdOk3_PGpeo9MReZjTz3tuZeQglBM9IfG_XMyI5SaUmfEZxrGJMlJrtH6HTY-PxvfwEPQthjbHAmNOn6IQSyjnj7BTl86HpB-_aq2RjYrBJYcreemeSNDFtYkOwbe9Mk2y99fZmcMH1Nqk7nxSuq1wou531h-foSW2aYF_cxTP0I79YzRfp8tvlp_n5Mi25UCrlhRRVRgqFa2q0kLjmsmYVI5JW0uhK8iLTpRalNbakgmc1UwVXIuaVIVayM_R-0t0OxcZWZZzNmwa23sXpD9AZB_92WncNV90OmCJcCh0F3kwC1w9oi_MljLV4JCJ0hnckYl_ffea7m8GGHjZxX9s0prXdEEBlkipM6Kj66gFy3Q2-jZcASrUmmVB6HF5NqNJ3IXhbHwcgGEZfYQ2jZTBaBqOv8MdX2Efqy_t7H4l_jYyAdxPg1jX28N_C8OXDKiaRnk50F3q7P9KN_wVCMsnh59dL-J5_znO2-Agr9ht4ob_X</recordid><startdate>201009</startdate><enddate>201009</enddate><creator>Joint, Ian</creator><creator>Mühling, Martin</creator><creator>Querellou, Joël</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>BSCLL</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>3V.</scope><scope>7QO</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope></search><sort><creationdate>201009</creationdate><title>Culturing marine bacteria - an essential prerequisite for biodiscovery</title><author>Joint, Ian ; Mühling, Martin ; Querellou, Joël</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5688-5b76d41b80f2a9670f57f3d3172d7a9d75b49c96ceaec2654f38b586c26da1e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alphaproteobacteria</topic><topic>Ammonium</topic><topic>Bacteria</topic><topic>Bacteria - classification</topic><topic>Bacteria - genetics</topic><topic>Bacteria - growth & development</topic><topic>Bacteria - isolation & purification</topic><topic>Bacteriological Techniques - methods</topic><topic>Biodiversity</topic><topic>Cell culture</topic><topic>Cell interactions</topic><topic>Chemical analysis</topic><topic>Cloning</topic><topic>Consortia</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Ecologists</topic><topic>Essential nutrients</topic><topic>Gelation</topic><topic>Gene sequencing</topic><topic>Genomics</topic><topic>Laboratories</topic><topic>Laboratory culture</topic><topic>Life Sciences</topic><topic>Marine technology</topic><topic>Microbiology and Parasitology</topic><topic>Microorganisms</topic><topic>Microscopy</topic><topic>Minireviews</topic><topic>Nucleotide sequence</topic><topic>Nutrients</topic><topic>Organisms</topic><topic>Phylogenetics</topic><topic>Plating</topic><topic>Reagents</topic><topic>Reviews</topic><topic>Seawater</topic><topic>Seawater - microbiology</topic><topic>Substrates</topic><topic>Taxonomy</topic><topic>Water analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joint, Ian</creatorcontrib><creatorcontrib>Mühling, Martin</creatorcontrib><creatorcontrib>Querellou, Joël</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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 Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Microbial biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Joint, Ian</au><au>Mühling, Martin</au><au>Querellou, Joël</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Culturing marine bacteria - an essential prerequisite for biodiscovery</atitle><jtitle>Microbial biotechnology</jtitle><addtitle>Microbial Biotechnology</addtitle><date>2010-09</date><risdate>2010</risdate><volume>3</volume><issue>5</issue><spage>564</spage><epage>575</epage><pages>564-575</pages><issn>1751-7915</issn><eissn>1751-7915</eissn><abstract>Summary
The potential for using marine microbes for biodiscovery is severely limited by the lack of laboratory cultures. It is a long‐standing observation that standard microbiological techniques only isolate a very small proportion of the wide diversity of microbes that are known in natural environments from DNA sequences. A number of explanations are reviewed. The process of establishing laboratory cultures may destroy any cell‐to‐cell communication that occurs between organisms in the natural environment and that are vital for growth. Bacteria probably grow as consortia in the sea and reliance on other bacteria for essential nutrients and substrates is not possible with standard microbiological approaches. Such interactions should be considered when designing programmes for the isolation of marine microbes. The benefits of novel technologies for manipulating cells are reviewed, including single cell encapsulation in gel micro‐droplets. Although novel technologies offer benefits for bringing previously uncultured microbes into laboratory culture, many useful bacteria can still be isolated using variations of plating techniques. Results are summarized for a study to culture bacteria from a long‐term observatory station in the English Channel. Bacterial biodiversity in this assemblage has recently been characterized using high‐throughput sequencing techniques. Although Alphaproteobacteria dominated the natural bacterial assemblage throughout the year, Gammaproteobacteria were the most frequent group isolated by plating techniques. The use of different gelling agents and the addition of ammonium to seawater‐based agar did lead to the isolation of a higher proportion of Alphaproteobacteria. Variation in medium composition was also able to increase the recovery of other groups of particular interest for biodiscovery, such as Actinobacteria.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21255353</pmid><doi>10.1111/j.1751-7915.2010.00188.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alphaproteobacteria Ammonium Bacteria Bacteria - classification Bacteria - genetics Bacteria - growth & development Bacteria - isolation & purification Bacteriological Techniques - methods Biodiversity Cell culture Cell interactions Chemical analysis Cloning Consortia Deoxyribonucleic acid DNA Ecologists Essential nutrients Gelation Gene sequencing Genomics Laboratories Laboratory culture Life Sciences Marine technology Microbiology and Parasitology Microorganisms Microscopy Minireviews Nucleotide sequence Nutrients Organisms Phylogenetics Plating Reagents Reviews Seawater Seawater - microbiology Substrates Taxonomy Water analysis |
title | Culturing marine bacteria - an essential prerequisite for biodiscovery |
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