Pillidge C J, Cambourn W M, Pearce L E
NZ Dairy Research Institute, Palmerston North, New Zealand.
Plasmid. 1996 Mar;35(2):131-40. doi: 10.1006/plas.1996.0015.
A 2.8-kb cryptic plasmid showing no homology to either pFX3 (rolling circle, pE194-type) or pCI305 (theta-type) lactococcal replicons was identified in Lactococcus lactis subsp. cremoris 2204. The plasmid, pWC1, was compatible with both pCI3340 (a pCI305 derivative) and pFX3 in L. lactis subsp. cremoris 2204. Sequence analysis of pWC1 showed one major ORF encoding a protein with a deduced size of 316 amino acids (aa). Database comparisons showed that the protein was distinct from the pFX- and pCI-type replication proteins (less than 21% aa identity), but shared significant homology (up to 57% aa identity) with the replication proteins from a different group of rolling circle plasmids (pC194-type) commonly found in gram-positive bacteria. A pC194-type rolling circle plasmid has not been previously described in L. lactis. Further sequence analysis showed a conserved double-stranded origin of replication in pWC1 preceded by a large (118-bp) direct repeat. The chloramphenicol-resistance gene from pC194 was inserted into a nonessential region of pWC1 to give pCP12. The host range of pCP12 included Streptococcus thermophilus, Enterococcus faecalis, and Staphylococcus aureus, but not Escherichia coli. Both pCP12 and to a lesser extent pWC1 generated single-stranded DNA (ssDNA) in L. lactis. A possible single-stranded origin of replication was identified by sequence analysis of pWC1 and by comparing levels of ssDNA produced by pCP12 deletion derivatives. The pWC1 replicon may be a useful addition to other replicons currently available for vector construction.
在乳酸乳球菌乳脂亚种2204中鉴定出一个2.8 kb的隐蔽质粒,它与pFX3(滚环,pE194型)或pCI305(θ型)乳球菌复制子均无同源性。该质粒pWC1与乳酸乳球菌乳脂亚种2204中的pCI3340(pCI305衍生物)和pFX3都兼容。pWC1的序列分析显示有一个主要的开放阅读框,编码一个推导大小为316个氨基酸(aa)的蛋白质。数据库比较表明,该蛋白质与pFX型和pCI型复制蛋白不同(氨基酸同一性小于21%),但与革兰氏阳性菌中常见的另一组滚环质粒(pC194型)的复制蛋白具有显著同源性(氨基酸同一性高达57%)。此前尚未在乳酸乳球菌中描述过pC194型滚环质粒。进一步的序列分析显示,pWC1中有一个保守的双链复制起点,其前面有一个大的(118 bp)直接重复序列。将pC194的氯霉素抗性基因插入pWC1的一个非必需区域,得到pCP12。pCP12的宿主范围包括嗜热链球菌、粪肠球菌和金黄色葡萄球菌,但不包括大肠杆菌。pCP12以及程度较轻的pWC1在乳酸乳球菌中产生单链DNA(ssDNA)。通过对pWC1的序列分析以及比较pCP12缺失衍生物产生的ssDNA水平,确定了一个可能的单链复制起点。pWC1复制子可能是目前可用于载体构建的其他复制子的有益补充。