Covarrubias L, Bolivar F
Gene. 1982 Jan;17(1):79-89. doi: 10.1016/0378-1119(82)90103-2.
The 4150-bp plasmid pBR329 was constructed by the the insertion into pBR327 of an 877-bp DNA fragment carrying the Cmr gene from pBR328. This new cloning vector does not contain the 482-bp inverted duplication that has been reported to be present in pBR325 and pBR328 (Prentki et al., 1981). In pBR329 the Cmr gene lacks its original promoter but is transcribed counterclockwise toward the Apr gene by a promoter located to the right of the HindIII site in the Tcr gene.
4150碱基对的质粒pBR329是通过将携带来自pBR328的Cmr基因的877碱基对DNA片段插入pBR327构建而成。这个新的克隆载体不包含据报道存在于pBR325和pBR328中的482碱基对反向重复序列(普伦蒂基等人,1981年)。在pBR329中,Cmr基因缺乏其原始启动子,但由位于Tcr基因中HindIII位点右侧的启动子逆时针转录朝向Apr基因。