Efficient Bacillus subtilis cloning system using bacteriophage vector phi 105J9.

Abstract

An efficient system for cloning in Bacillus subtilis is described which uses a newly constructed bacteriophage vector, phi 105J9. The phage genome contains cloning sites for the enzymes BamH1, XbaI and SalI, and can accommodate inserts of passenger DNA of at least 4 kbp. Recombinant phages, which can both plaque and lysogenize normally, are recovered after… (More)

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