Proceedings of the National Academy of Sciences · 1999 · 124 citations · 34 references
Life SciencesBiotechnologyMicrobiologyBacteriologyGenomicsMicrobial BiotechnologyAntibiotic Resistance GeneticsBacterial GeneticsBacterial Artificial Chromosome LibrariesBacterial Artificial Chromosome VectorsBacterial Expression VectorsEscherichia ColiFunctional Genomics ApplicationsGenomic Dna Library ConstructionHeterologous Expression SystemsHeterologous Gene Expression
Functional genomics of microbes demands molecular tools, yet many prokaryotes lack adequate genetic tools. The study applies a BAC vector to prokaryotic biology and screens the library for heterologous expression of B. cereus genes in E. coli.
As the study of microbes moves into the era of functional genomics, there is an increasing need for molecular tools for analysis of a wide diversity of microorganisms. Currently, biological study of many prokaryotes of agricultural, medical, and fundamental scientific interest is limited by the lack of adequate genetic tools. We report the application of the bacterial artificial chromosome (BAC) vector to prokaryotic biology as a powerful approach to address this need. We constructed a BAC library in Escherichia coli from genomic DNA of the Gram-positive bacterium Bacillus cereus . This library provides 5.75-fold coverage of the B. cereus genome, with an average insert size of 98 kb. To determine the extent of heterologous expression of B. cereus genes in the library, we screened it for expression of several B. cereus activities in the E. coli host. Clones expressing 6 of 10 activities tested were identified in the library, namely, ampicillin resistance, zwittermicin A resistance, esculin hydrolysis, hemolysis, orange pigment production, and lecithinase activity. We analyzed selected BAC clones genetically to identify rapidly specific B. cereus loci. These results suggest that BAC libraries will provide a powerful approach for studying gene expression from diverse prokaryotes.
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Molecular cloning: A laboratory manual
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