Bourne N, Dancer B N
J Gen Microbiol. 1986 Feb;132(2):251-5. doi: 10.1099/00221287-132-2-251.
Regeneration of protoplasts to bacilli was attempted in several strains of Bacillus closely related to Bacillus subtilis 168. On DM3 and similar media using succinate as osmotic support, only B. subtilis 168 and Bacillus natto ATCC 15245 were able to regenerate. Media containing mannitol as osmotic support, and agar as gelling agent gave rise to L-form colonies with Bacillus licheniformis NCTC 6346. Many of the L-form colonies were able to regenerate to the bacillary form when plated on the mannitol medium solidified with gelatin. All of the Bacillus species tested were able to regenerate on the latter medium at rates sufficient to allow protoplast transformation and fusion experiments.
在与枯草芽孢杆菌168密切相关的几株芽孢杆菌中尝试了原生质体向杆菌的再生。在以琥珀酸盐作为渗透支持物的DM3和类似培养基上,只有枯草芽孢杆菌168和纳豆芽孢杆菌ATCC 15245能够再生。以甘露醇作为渗透支持物且以琼脂作为胶凝剂的培养基,可使地衣芽孢杆菌NCTC 6346形成L型菌落。当接种在以明胶固化的甘露醇培养基上时,许多L型菌落能够再生为杆菌形态。所有测试的芽孢杆菌物种都能够在后者培养基上以足以进行原生质体转化和融合实验的速率再生。