Lee I W, Gambill B D, Summers A O
Department of Microbiology, University of Georgia, Athens 30602.
J Bacteriol. 1989 Apr;171(4):2222-5. doi: 10.1128/jb.171.4.2222-2225.1989.
All four sequenced examples of the mercury resistance (mer) operon of gram-negative bacteria have a promoter-distal reading frame, merD, whose removal has little effect on the resistance phenotype and whose translation has not previously been observed. Using merD-lacZ protein fusions, we show that merD is translated. However, Hg(II)-induced merD expression, as measured by beta-galactosidase activity and immunoblotting, is 10- to 15-fold lower than that of fusions to the gene immediately preceding it, merA.
革兰氏阴性菌汞抗性(mer)操纵子的所有四个测序示例都有一个启动子远端阅读框merD,去除该阅读框对抗性表型影响不大,且此前未观察到其翻译情况。通过merD-lacZ蛋白融合,我们证明merD是可翻译的。然而,通过β-半乳糖苷酶活性和免疫印迹测量,汞(II)诱导的merD表达比与它前面紧邻的基因merA的融合表达低10至15倍。