As part of the Bacillus subtilis genome sequencing project, we have determined a 283 kb contiguous sequence from 210" to 232" of the B. subtilis genome. This region contains the 48 kb skin element which is excised during sporulation by a site-specific recombinase. In this region, 310 complete ORFs and one tRNA gene were identified: 66 ORFs have been sequenced and characterized previously by other workers, e.g. acC ans, bfm8 blt, bmr, corn€, comG, dnaK, POD and sin operons; cwlA, gpr and /FA genes; many sporulation genes and operons, spoOA, spollA, spollM, spo//P# spolllA, spolllC spo/W, Sp0lv-8 spolVCB and *OVA, etc. The products of 84 ORFs were found to display significant similarity to proteins with known function in data banks, e.g., proteins involved in nucleotide metabolism, lipid biosynthesis, amino acid transport (ABC transporter), phosphate-specif ic transport, the glycine cleavage system, the two-component regulatory system, cell wall autolysis, ferric uptake and sporulation. However, the functions of more than half of the ORFs (52%, 160 ORFs) are still unknown. In the skin element containing 60 ORFs, 32 ORFs (53%) encode proteins which have significant homology to gene products of the B. subtilis temperate phage 4105 and/or the defective phage PBSX. The EMBUGenBankDDBJ accession number for the nucleotide sequence reported in this paper is D84432.
Keywordsthe understanding of the function of whole genes, global regulation of gene expression and molecular evolution. As part of the international B. stlbtilis genome sequencing project, we report here the cloning and sequencing of the ~sA-spolllC region (21 Oo-232O, 282 700 bp) containing the skin element (Takemaru e t a/., 1975).A DASH I1 and EMBL3 libraries of the B. szrbtilis JH642 (trpC2pheA I ) chromosome partially digested with MboI, EcoRI and Hind111 were constructed as described previously (Takemaru et al., 1995). Clones used for sequence determination were isolated from these libraries by plaque hybridization (Sambrook e t al., 1987)