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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Veröffentlicht in:Microbial biotechnology 2010-09, Vol.3 (5), p.564-575
Hauptverfasser: Joint, Ian, Mühling, Martin, Querellou, Joël
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Querellou, Joël
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.
doi_str_mv 10.1111/j.1751-7915.2010.00188.x
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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 &amp; development ; Bacteria - isolation &amp; 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 &amp; Sons, Inc. Sep 2010</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2010 The Author. 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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. 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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. 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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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