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dc.contributor.authorHobson, David Richard
dc.date.accessioned2014-03-04T18:56:11Z
dc.date.available2014-03-04T18:56:11Z
dc.date.issued2010-08
dc.identifier.otherhobson_david_r_201008_ms
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/hobson_david_r_201008_ms
dc.identifier.urihttp://hdl.handle.net/10724/26653
dc.description.abstractCurrent gene annotation methods based on sequence similarity have greatly expanded the ability to search growing databases of genomic information. This system of identification falls short when novel genes are involved or when large protein families show significant homology across an array of protein functions. Such is the case with the bacterial oxygen-independent coproporphyrinogen III oxidase (CPO) HemN. Its association with the radical-SAM protein superfamily has led to incorrect annotation of non-HemN proteins. Radical-SAM family proteins are highly conserved and traditional sequence comparison proves near impossible for accurate identification of HemN proteins. An in vivo system was developed in the naturally transformable bacteria Acinetobacter ADP1. The wild-type CPO was knocked out using basic PCR cloning techniques utilizing this organism’s high competency for natural transformation and recombination. The resulting CPO knockout is presented as an in vivo system for identification of bacterial CPOs.
dc.languageeng
dc.publisheruga
dc.rightspublic
dc.subjectHeme biosynthesis
dc.subjectCoproporphyrinogen III oxidase
dc.subjectAcinetobacter ADP1
dc.subjectRadical-SAM superfamily
dc.subjectGene knockout
dc.titleAcinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases
dc.typeThesis
dc.description.degreeMS
dc.description.departmentBiochemistry and Molecular Biology
dc.description.majorBiochemistry and Molecular Biology
dc.description.advisorHarry Dailey
dc.description.committeeHarry Dailey
dc.description.committeeEllen L. Neidle
dc.description.committeeWilliam Lanzilotta


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