Hogg R W
J Bacteriol. 1971 Feb;105(2):604-8. doi: 10.1128/jb.105.2.604-608.1971.
An "in vivo" assay for the detection of mutants negative to CRM (cross-reacting material) is described. l-Arabinose-negative mutants of Escherichia coli B/r were grown on Casamino Acids-l-arabinose plates to which a 3-ml agar layer, containing antiserum to the l-arabinose-binding protein (ABP), had been applied. After incubation and partial lysis of the clones "in situ," the plates were refrigerated for 36 hr, rinsed of colonial growth with water, and observed for the presence or absence of an immune precipitation. ABP-minus and l-arabinose regulator (araC)-minus mutants do not produce a precipitin reaction. l-Arabinose isomeraseless (EC 5.3.1.4; araA), kinaseless (EC 2.7.1.16; araB), and epimeraseless (EC 5.1.3.a; araD) mutants produce precipitin reactions. Mutants of E. coli B/r generated by treatment of the wild type with ethyl methane sulfonate or ultraviolet irradiation were isolated, tested for l-arabinose uptake, and screened for the presence or absence of ABP by the described assay. The applications of such an assay are discussed.
本文描述了一种用于检测对CRM(交叉反应物质)呈阴性的突变体的“体内”测定法。将大肠杆菌B/r的L-阿拉伯糖阴性突变体接种在酪蛋白氨基酸-L-阿拉伯糖平板上,平板上已铺有一层3毫升含有抗L-阿拉伯糖结合蛋白(ABP)抗血清的琼脂层。在克隆“原位”孵育并部分裂解后,将平板冷藏36小时,用水冲洗掉菌落生长物,然后观察是否存在免疫沉淀。ABP缺陷型和L-阿拉伯糖调节子(araC)缺陷型突变体不产生沉淀素反应。无L-阿拉伯糖异构酶(EC 5.3.1.4;araA)、无激酶(EC 2.7.1.16;araB)和无表异构酶(EC 5.1.3.a;araD)的突变体产生沉淀素反应。分离出通过用甲磺酸乙酯或紫外线照射野生型产生的大肠杆菌B/r突变体,检测其对L-阿拉伯糖的摄取,并通过所述测定法筛选ABP的存在与否。讨论了这种测定法的应用。