Dewar S J, Kagan-Zur V, Begg K J, Donachie W D
Department of Molecular Biology, University of Edinburgh, UK.
Mol Microbiol. 1989 Oct;3(10):1371-7. doi: 10.1111/j.1365-2958.1989.tb00118.x.
The complete Escherichia coli ftsQ coding sequence, together with part of the ftsA coding sequence, has been cloned upstream of the lacZ open reading frame in a lambda-vector (lambda JFL100). Cells which are lysogenic for lambda JFL100 transcribe the cloned lacZ from promoter(s) within the ftsQ and ftsA sequences. The level of beta-galactosidase produced is dependent on growth rate (and/or cell size) and is derepressed in an ftsA-deficient mutant. Transcription during the cell cycle is restricted to the time of cell division.
完整的大肠杆菌ftsQ编码序列,连同ftsA编码序列的一部分,已被克隆到λ载体(λJFL100)中lacZ开放阅读框的上游。对λJFL100溶源化的细胞从ftsQ和ftsA序列内的启动子转录克隆的lacZ。产生的β-半乳糖苷酶水平取决于生长速率(和/或细胞大小),并且在ftsA缺陷型突变体中去阻遏。细胞周期中的转录限于细胞分裂时间。