Trautwetter A, Blanco C
Laboratoire de Génétique et Physiologie Microbienne, CNRS UA 256, Université de Rennes I, France.
J Gen Microbiol. 1991 Sep;137(9):2093-101. doi: 10.1099/00221287-137-9-2093.
pCG100, a 3 kb cryptic plasmid of Corynebacterium glutamicum ATCC 13058, probably identical with pSR1 from C. glutamicum ATCC 19223, was characterized. The minimum region for autonomous replication was shown to be contained on a 1.9 kb BglII-NcoI fragment; a 380 bp HindIII-SphI fragment can replicate in the presence of the parental plasmid, which presumably provides a trans-acting replication factor. Derivatives of pCG100 are able to replicate in several Corynebacterium, Brevibacterium and Arthrobacter strains. pCG100 is compatible with pBL1, a cryptic plasmid of Brevibacterium lactofermentum. Shuttle plasmid vectors, containing the kanamycin-resistance gene from Tn903 or from Streptococcus faecalis as selectable markers and the AmpR, TetR or lacZ alpha genes for insertional inactivation, were constructed using the minimum replication fragment of pCG100.
pCG100是谷氨酸棒杆菌ATCC 13058的一个3 kb隐蔽质粒,可能与谷氨酸棒杆菌ATCC 19223的pSR1相同,已对其进行了表征。自主复制的最小区域位于一个1.9 kb的BglII - NcoI片段上;一个380 bp的HindIII - SphI片段在亲本质粒存在的情况下能够复制,推测亲本质粒提供了一个反式作用复制因子。pCG100的衍生物能够在几种棒杆菌、短杆菌和节杆菌菌株中复制。pCG100与乳糖发酵短杆菌的一个隐蔽质粒pBL1兼容。利用pCG100的最小复制片段构建了穿梭质粒载体,这些载体含有来自Tn903或粪链球菌的卡那霉素抗性基因作为选择标记,以及用于插入失活的AmpR、TetR或lacZα基因。