Identification of an Operon Involved in the Production of Lactacin B, a bacteriocin Produced by Lactobacillus acidophilus

dc.contributor.advisorDr. Todd R. Klaenhammer, Committee Chairen_US
dc.contributor.advisorDr. Robert Kelly, Committee Memberen_US
dc.contributor.advisorDr. Fred Breidt, Committee Memberen_US
dc.contributor.authorDobson, Alleson Een_US
dc.date.accessioned2010-04-02T18:11:16Z
dc.date.available2010-04-02T18:11:16Z
dc.date.issued2007-05-12en_US
dc.degree.disciplineFood Scienceen_US
dc.degree.levelthesisen_US
dc.degree.nameMSen_US
dc.description.abstractLactacin B is a class II bacteriocin produced by Lactobacillus acidophilus NCFM (Barefoot and Klaenhammer 1983). Mutational, nucleotide sequence, and transcriptional analyses revealed that the genetic determinants responsible for lactacin B regulation and production are located on a 9.5 kb polycistronic region (LBA1803-LBA1791) of the L. acidophilus NCFM chromosome. The lab operon comprised 12 putative open reading frames (ORFs) organized into three clusters: a production and regulation cluster encoding putative proteins that resemble two component signal transduction systems of the AgrC-AgrA type; an export cluster encoding putative proteins that resemble ATP-binding cassette (ABC) transporters and accessory proteins, and the final cluster composed of three putative proteins of unknown functionality. Each cluster was separated by an intrinsic terminator, the strongest terminators flanked the entire lactacin B region (ΔG = -13.4kcal⁄mol and ΔG = -17.0kcal/mol respectively). A total of 7 genes with unknown functionality were situated in this region, each containing a double-glycine leader motif characteristic of bacteriocin structural genes and their precursors. Insertional inactivation of the gene believed to encode an ABC transporter (labT) completely abolished bacteriocin activity, implicating this region in lactacin B production. Cloning of the first four genes within this region (LBA1803-LBA1800) onto a high copy number plasmid resulted in markedly higher levels of lactacin B activity compared to the control. These ORFs encoded proteins typical to bacteriocin peptides; small, cationic peptides, each with an N-terminal double glycine leader motif. Experiments with chemically synthesized peptides revealed that LBA1800 was not inhibitory, but induced lactacin B production in broth cultures. The genetic organization of the region indicates that lactacin B production is regulated through the three component regulatory system common to many class II bacteriocin systems.en_US
dc.identifier.otheretd-04282006-173216en_US
dc.identifier.urihttp://www.lib.ncsu.edu/resolver/1840.16/2209
dc.rightsI hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.en_US
dc.subjectABC transporteren_US
dc.subjectLactobacillus acidophilusen_US
dc.subjectbacteriocinen_US
dc.subjectoperonen_US
dc.subjectinducibleen_US
dc.subjectantimicrobial peptidesen_US
dc.titleIdentification of an Operon Involved in the Production of Lactacin B, a bacteriocin Produced by Lactobacillus acidophilusen_US

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