Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Plant Physiol. 1985 Jan;77(1):35-42. doi: 10.1104/pp.77.1.35.
Adherence of Agrobacterium tumefaciens to suspension-cultured tomato cells has been characterized using a quantitative binding assay. Saturable binding of radiolabeled A. tumefaciens to plant cells resulted in 100 to 300 bacteria bound per cell. Specificity of A. tumefaciens binding was also inferred from two additional results: (a) an initial incubation of plant cells with A. tumefaciens reduced subsequent binding of radiolabeled A. tumefaciens by 60% to 75%; (b) tomato cells bound less than three E. coli per cell. Protease treatment of plant cells had no effect on subsequent bacterial binding, but prior treatment of plant cells with pectinolytic enzymes increased binding 2- to 3-fold. Pectin-enriched and neutral polymer-enriched fractions were obtained from tomato cell walls. The soluble pectin-enriched fraction inhibited binding of bacteria to plant cells by 85% to 95%, whereas the neutral polymer fraction only partially inhibited binding. Preliminary characterization of the activity showed it is heat stable, partially inactivated by protease treatment, and substantially inactivated by acid hydrolysis.
采用定量结合测定法研究了根癌农杆菌对悬浮培养的番茄细胞的附着情况。放射性标记的根癌农杆菌与植物细胞的可饱和结合导致每个细胞结合 100 至 300 个细菌。根癌农杆菌结合的特异性还可以从以下两个附加结果推断出来:(a)植物细胞与根癌农杆菌的初始孵育减少了后续结合放射性标记的根癌农杆菌的 60%至 75%;(b)番茄细胞结合的大肠杆菌少于三个。蛋白酶处理植物细胞对随后的细菌结合没有影响,但先用果胶酶处理植物细胞可使结合增加 2 至 3 倍。从番茄细胞壁中获得了果胶富集体和中性聚合物富集体。可溶性果胶富集体抑制细菌与植物细胞的结合达 85%至 95%,而中性聚合物部分抑制结合。该活性的初步特征表明其具有热稳定性,蛋白酶处理部分失活,酸水解则基本失活。