Ulijasz A T, Grenader A, Weisblum B
Pharmacology Department, University of Wisconsin Medical School, Madison 53706, USA.
J Bacteriol. 1996 Nov;178(21):6305-9. doi: 10.1128/jb.178.21.6305-6309.1996.
We have constructed a Bacillus subtilis strain in which expression of a vanH::lacZ gene fusion is regulated by VanR and VanS of Enterococcus faecium. This construct allows a nonpathogenic bacterial strain to be used as a model system for studying regulation of vancomycin resistance. Antibiotics and enzymes that affect cell wall biosynthesis and stability were tested for the ability to induce lacZ expression. As a result, fosfomycin and D-cycloserine were added to the group of peptidoglycan synthesis inhibitors shown to induce expression from the vanH promoter. Induction by cell wall hydrolytic enzymes, as well as by antibiotics whose actions may lead to the accumulation of chemically different peptidoglycan precursors, raises the possibility that models that postulate induction by peptidoglycan [correction of peptidodoglycan] precursors are wrong.
我们构建了一种枯草芽孢杆菌菌株,其中vanH::lacZ基因融合体的表达受粪肠球菌的VanR和VanS调控。该构建体使得一种非致病性细菌菌株能够用作研究万古霉素抗性调控的模型系统。测试了影响细胞壁生物合成和稳定性的抗生素及酶诱导lacZ表达的能力。结果,磷霉素和D-环丝氨酸被加入到已证明可诱导vanH启动子表达的肽聚糖合成抑制剂组中。细胞壁水解酶以及其作用可能导致化学性质不同的肽聚糖前体积累的抗生素所引发的诱导作用,增加了假定由肽聚糖[肽聚糖校正]前体诱导的模型有误的可能性。