American Society for Microbiology, Applied and Environmental Microbiology, 5(74), p. 1649-1652, 2008
DOI: 10.1128/aem.01864-07
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ABSTRACT A rapid protocol was developed for constructing plasmid libraries from small quantities of genomic/metagenomic DNA. The technique utilizes linker amplification with topoisomerase cloning and allows for inducible transcription in Escherichia coli . As proof of principle, several anti- Bacillus lysins were cloned from bacteriophage genomes and an aerolysin was cloned from a metagenomic sample.