Bakhiet N, Stahly D P
Appl Environ Microbiol. 1985 Mar;49(3):577-81. doi: 10.1128/aem.49.3.577-581.1985.
Protoplasts of Bacillus larvae NRRL b-3555 and Bacillus subtilis RM125 (restrictionless, modificationless mutant) were transfected with DNA from the B. larvae bacteriophage PBL1c in the presence of polyethylene glycol. B. subtilis 168 and Bacillus popilliae NRRL B-2309M protoplasts could not be transfected with PBL1c DNA. Protoplasts of B larvae NRRL B-3555 were transformed with plasmids pC194 and pHV33 in the presence of polyethylene glycol. The frequency of transformation was much higher when the plasmids were isolated from B. larvae NRRL B-3555 transformants than when they were isolated from B. subtilis 168. These results indicate that the restriction-modification systems found in B. larvae NRRL B-3555 and B. subtilis 168 may be different. Conditions for protoplast formation and cell wall regeneration were developed for B. popilliae NRRL B-2309S. However, no transformation occurred with plasmids pC194 and pHV33 (isolated from B. subtilis 168).
在聚乙二醇存在的情况下,用来自幼虫芽孢杆菌噬菌体PBL1c的DNA转染幼虫芽孢杆菌NRRL b - 3555和枯草芽孢杆菌RM125(无限制、无修饰突变体)的原生质体。枯草芽孢杆菌168和日本金龟子芽孢杆菌NRRL B - 2309M的原生质体不能用PBL1c DNA进行转染。在聚乙二醇存在的情况下,用质粒pC194和pHV33转染幼虫芽孢杆菌NRRL B - 3555的原生质体。当从幼虫芽孢杆菌NRRL B - 3555转化体中分离质粒时,转化频率比从枯草芽孢杆菌168中分离质粒时高得多。这些结果表明,在幼虫芽孢杆菌NRRL B - 3555和枯草芽孢杆菌168中发现的限制 - 修饰系统可能不同。已为日本金龟子芽孢杆菌NRRL B - 2309S建立了原生质体形成和细胞壁再生的条件。然而,用质粒pC194和pHV33(从枯草芽孢杆菌168中分离)未发生转化。