Fig. 6From: Mob/oriT, a mobilizable site-specific recombination system for unmarked genetic manipulation in Bacillus thuringiensis and Bacillus cereus Construction of crystal protein gene insertion mutants BMB0261 and BMB0262. Depiction of cry5Ba (a) and cry2Aa (b) insertion. PCR detection with primers amyE-wS and amyE-wA (c) and 5B-S and 5B-A (lanes 1–4) or 2A-S and 2A-A (lanes 5–8) (d); DNA templates were from: 1, pBMB0261 (negative control); 2 and 6, BMB171; 3–4, mutant BMB0261; 5, pBMB0262 (negative control); 7–8, mutant BMB0262; M Trans2 K Plus II DNA marker. e Scanning electron microscopy image of parasporal crystals in unmarked cry integrate mutants. 1, BMB171/cry5Ba-pHT304; 2–3, BMB0261; 4, YBT-1518; 5, BMB171/cry2Aa-pHT304; 6–7, BMB0262; 8, CT-43; 9, BMB171. The arrows indicate the diamond-shaped crystals encoded by cry5Ba and the round-shaped crystals encoded by cry2Aa. Bar indicates 1 μmBack to article page