Scheme of gene replacement approach for
bcaba1. Physical maps of
bcaba1 from wild-type strain ATCC 58025 (A), the gene replacement fragment pABA1Rep (B), and
bcaba1 from a ΔBccpr1 replacement mutant (C) showing organization of exons (□), introns (

), the hygromycin resistance cassette (▨), and flanking regions of
bcaba1 (heavy lines). Orientations of the genes are indicated by arrowheads. The binding sites of primers 6, 7, and 10 to 16 used for PCR analysis of replacement mutants (see Materials and Methods) and the 5′ flank of pABA1Rep (dotted line) used as a probe for Southern and Northern analysis are indicated.