Matsuyama S, Akimaru J, Mizushima S
Institute of Applied Microbiology, University of Tokyo, Japan.
FEBS Lett. 1990 Aug 20;269(1):96-100. doi: 10.1016/0014-5793(90)81128-b.
The secY and secE genes were individually cloned and placed under the control of the tac promoter on plasmids. Induction with isopropyl-beta-D-thiogalactopyranoside resulted in the overproduction of SecE, but not that of SecY. The simultaneous induced expression of both genes in the same cells resulted in the overproduction of SecY together with that of SecE. SecY and SecE thus overproduced were localized in the cytoplasmic membrane as those expressed at the normal levels were. It is suggested that SecY and SecE interact with each other in the cytoplasmic membrane. The numbers of the SecY and SecE molecules per cell were estimated.
secY和secE基因分别被克隆,并置于质粒上tac启动子的控制之下。用异丙基-β-D-硫代半乳糖苷诱导导致SecE过量产生,但SecY没有。在同一细胞中同时诱导这两个基因表达,导致SecY与SecE一起过量产生。如此过量产生的SecY和SecE与正常水平表达时一样定位于细胞质膜。这表明SecY和SecE在细胞质膜中相互作用。估算了每个细胞中SecY和SecE分子的数量。