Delaunay A M, Huault C, Balangé A P
Centre National de la Recherche Scientifique, Unité Associée 203, Faculté des Sciences, Mont Saint Aignan, France.
J Bacteriol. 1991 Apr;173(8):2712-5. doi: 10.1128/jb.173.8.2712-2715.1991.
A hemB mutant of Escherichia coli was used to clone the gene encoding 5-aminolevulinic acid dehydratase from Rhodobacter sphaeroides after physiological complementation of the mutation. A 2.9-kb DNA fragment was obtained and cloned in both orientations into the unique PstI restriction site of pUC19. This recombinant plasmid encodes a protein (Mr 39,000) that is immunoreactive with antibodies raised against the enzyme from higher plants.
利用大肠杆菌的hemB突变体,在对该突变进行生理互补后,克隆来自球形红杆菌的编码5-氨基乙酰丙酸脱水酶的基因。获得了一个2.9 kb的DNA片段,并将其以两种方向克隆到pUC19的唯一PstI限制性酶切位点中。该重组质粒编码一种蛋白质(Mr 39,000),它与针对高等植物中该酶产生的抗体发生免疫反应。