Applications of flow cytometry in environmental microbiology and biotechnology

Show simple item record

dc.contributor.author Bergquist, Peter en
dc.contributor.author Sowden, Elizabeth en
dc.contributor.author Ferrari, BC en
dc.contributor.author Winsley, T en
dc.date.accessioned 2011-07-24T21:41:41Z en
dc.date.issued 2009-05 en
dc.identifier.citation Extremophiles 13(3):389-401 May 2009 en
dc.identifier.issn 1431-0651 en
dc.identifier.uri http://hdl.handle.net/2292/7038 en
dc.description.abstract Flow cytometry (FCM) is a technique for counting, examining and sorting microscopic particles suspended in a stream of fluid. It uses the principles of light scattering, light excitation and the emission from fluorescent molecules to generate specific multiparameter data from particles and cells. The cells are hydrodynamically focussed in a sheath solution before being intercepted by a focused light source provided by a laser. FCM has been used primarily in medical applications but is being used increasingly for the examination of individual cells from environmental samples. It has found uses in the isolation of both culturable and hitherto non-culturable bacteria present infrequently in environmental samples using appropriate growth conditions. FCM lends itself to high-throughput applications in directed evolution for the analysis of single cells or cell populations carrying mutant genes. It is also suitable for encapsulation studies where individual bacteria are compartmentalised with substrate in water-in-oil-inwater emulsions or with individual genes in transcriptional/ translational mixtures for the production of mutant enzymes. The sensitivity of the technique has allowed the examination of gene optimisation by a procedure known as random or neutral drift where screening and selection is based on the retention of some predetermined level of activity through multiple rounds of mutagenesis. en
dc.language EN en
dc.publisher SPRINGER TOKYO en
dc.relation.ispartofseries EXTREMOPHILES en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/1431-0651/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Fluorescence-activated cell sorting en
dc.subject Directed evolution en
dc.subject In vitro compartmentalisation en
dc.subject Non-culturable bacteria en
dc.subject Single cell analysis en
dc.subject Random (neutral) drift en
dc.subject Random mutagenesis en
dc.subject Protein optimisation en
dc.subject IN-VITRO COMPARTMENTALIZATION en
dc.subject WHOLE-CELL BIOSENSOR en
dc.subject DIRECTED EVOLUTION en
dc.subject MOLECULAR ANALYSIS en
dc.subject ENZYME EVOLUTION en
dc.subject DOUBLE EMULSIONS en
dc.subject QUANTUM DOTS en
dc.subject FLUORESCENCE en
dc.subject LIBRARIES en
dc.subject BACTERIA en
dc.title Applications of flow cytometry in environmental microbiology and biotechnology en
dc.type Journal Article en
dc.identifier.doi 10.1007/s00792-009-0236-4 en
pubs.issue 3 en
pubs.begin-page 389 en
pubs.volume 13 en
dc.rights.holder Copyright: 2009 Springer en
dc.identifier.pmid 19301090 en
pubs.end-page 401 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Review en
pubs.elements-id 197348 en
pubs.org-id Libraries & Learning Services en
pubs.org-id Libraries & Learning Services en
pubs.org-id Research and Collections en
pubs.org-id Research and Collections en
pubs.org-id Research Services en
pubs.org-id Research Services en
pubs.record-created-at-source-date 2011-11-02 en
pubs.dimensions-id 19301090 en


Files in this item

There are no files associated with this item.

Find Full text

This item appears in the following Collection(s)

Show simple item record

Share

Search ResearchSpace


Browse

Statistics