“…Unfortunately, a feasible transformation technique for T. halophilus has not been established thus far ( 6 ), which did not allow us to use a general gene deletion-and-complementation strategy for the analysis of gene function. However, intrinsic ISs of T. halophilus jump within the genomes quite actively, and the transposition of ISs can be detected by comparing the lengths of the PCR-amplified DNA fragments covering the targeted genes between the derivative and parental strains ( 6 , 22 ). Supposing that a deletion or structural alteration of CPSs is responsible for the altered phage susceptibility in the derivatives, other additional phage-resistant derivatives with ISs transposed into the cps loci are expected to be found easily.…”