| Literature DB >> 16106753 |
Kimiko Saka1, Maki Tadenuma, Shinsuke Nakade, Noriko Tanaka, Hideaki Sugawara, Ken Nishikawa, Nobuyuki Ichiyoshi, Masanari Kitagawa, Hirotada Mori, Naotake Ogasawara, Akiko Nishimura.
Abstract
To facilitate genetic studies of Escherichia coli, we constructed a complete set of mobile plasmid clones of intact open reading frames (ORFs). Their expression is strictly controlled by Ptac / lacI(q). The plasmids carrying each ORF were introduced into an F+ recA strain and stored in 96-well microtiter plates. In this way, 96 clones can be transferred simultaneously to F- bacteria using the conjugative system. This provides a convenient procedure for systematic identification of ORFs that suppress or complement mutations. We created two types of clone sets: the original set contained individual clones in 45 microtiter plates, and a second set contained pools of 48 clones stored in a single microtiter plate. Using these clone sets, we have identified 403 genes that can correct in trans the temperature-sensitive defect of cell division mutants, which would suggest multiple global regulators for bacterial cell division.Entities:
Mesh:
Year: 2005 PMID: 16106753 DOI: 10.1093/dnares/12.1.63
Source DB: PubMed Journal: DNA Res ISSN: 1340-2838 Impact factor: 4.458