Huang Haomin, Masters Millicent
Institute of Cell Biology, University of Edinburgh, Kings׳ Buildings, Edinburgh EH9 3JR, UK.
Virology. 2014 Nov;468-470:274-282. doi: 10.1016/j.virol.2014.07.029. Epub 2014 Sep 12.
The Escherichia coli bacteriophage P1 packages host chromosome separately from phage DNA, and transfers it to recipient cells at low frequency in a process called generalized transduction. Phage genomes are packaged from concatemers beginning at a specific site, pac. To increase transduction rate, we have inserted pac into the chromosome at up to five equally spaced positions; at least this many are fully tolerated in the absence of P1 infection. A single chromosomal pac greatly increases transduction of downstream markers without decreasing phage yields; 3.5 × as much total chromosomal DNA is packaged. Additional insertions decrease phage yield by > 90% and also decrease phage DNA synthesis, although less dramatically. Packaging of chromosomal markers near to and downstream of each inserted pac site is, at the same time, increased by greater than 10 fold. Transduction of markers near an inserted pac site can be increased by over 1000-fold, potentially allowing identification of such transductants by screening.
大肠杆菌噬菌体P1将宿主染色体与噬菌体DNA分开包装,并在一个称为普遍性转导的过程中以低频率将其转移到受体细胞中。噬菌体基因组从串联体开始,在一个特定的位点pac进行包装。为了提高转导率,我们已将pac插入染色体上多达五个等距位置;在没有P1感染的情况下,至少这么多位置是完全可耐受的。单个染色体pac极大地提高了下游标记的转导效率,而不会降低噬菌体产量;包装的总染色体DNA增加了3.5倍。额外的插入会使噬菌体产量降低>90%,也会降低噬菌体DNA合成,尽管影响较小。同时,每个插入的pac位点附近和下游的染色体标记的包装增加了10倍以上。插入的pac位点附近标记的转导可提高1000倍以上,这有可能通过筛选来鉴定此类转导子。