Winkler J, Eltis L D, Dwyer D F, Rohde M
Department of Microbiology, National Research Center for Biotechnology, Braunschweig, Germany.
Arch Microbiol. 1995 Jan;163(1):65-9. doi: 10.1007/BF00262205.
Catechol 2,3-dioxygenase from the meta-cleavage pathway encoded on the TOL plasmid of Pseudomonas putida (pWWO) was investigated by electron microscopy. Negatively stained samples of the purified catechol 2,3-dioxygenase revealed that the enzyme consists of four subunits arranged in a tetrahedral conformation. Monoclonal antibodies raised against catechol 2,3-dioxygenase showed highly specific reactions and were used to localize the enzyme in Escherichia coli (pAW31) and P. putida (pWWO), using the protein A-gold technique carried out as a post-embedding immunoelectron microscopy procedure. Our in situ labeling studies revealed a cytoplasmic location of the catechol 2,3-dioxygenase in both cell types.
利用电子显微镜对恶臭假单胞菌(pWWO)TOL质粒上编码的间位裂解途径中的儿茶酚2,3-双加氧酶进行了研究。纯化后的儿茶酚2,3-双加氧酶的负染样品显示,该酶由四个以四面体构象排列的亚基组成。针对儿茶酚2,3-双加氧酶产生的单克隆抗体表现出高度特异性反应,并通过作为包埋后免疫电子显微镜程序进行的蛋白A-金技术,用于在大肠杆菌(pAW31)和恶臭假单胞菌(pWWO)中定位该酶。我们的原位标记研究揭示了两种细胞类型中儿茶酚2,3-双加氧酶均位于细胞质中。