- Name: pgsA10
- Type: Base Pair Substitution
- Mutation of Gene: pgsA
- Approx. Map Location: 42.90
- Ref. below shows mutation substitutes a T for the C in an ACA (Thr) codon of pgsA10, substituting Ile in hydrophob.reg. Lowers in vitro PGP synthase act. but not acidic-phospholipid synthesis in vivo.
- 1 Strains Carrying This Mutation
Name Mutations Genotype R477-100 14 F-, thr-1, araC14, leuB6(Am), fhuA1, lacY1, tsx-78, Δ(galK-attLAM)99, pgsA10, hisG4(Oc), rfbC1, rpsL136(strR), xylA5, mtl-1, thiE1