Gharyal P K, Ho S C, Wang J L, Schindler M
Department of Biochemistry, Michigan State University, East Lansing 48824.
J Biol Chem. 1989 Jul 25;264(21):12119-21.
The technique of fluorescence redistribution after photobleaching was utilized to measure intercellular movement of low molecular weight fluorescent hydrophilic substances across the cell wall/membrane interface between contiguous soybean (Glycine max (L.) Merr. cv. Mandarin) root cells (SB-1 cell line) in tissue culture. Lipopolysaccharide (LPS) purified from Bradyrhizobium japonicum R110d, a Gram-negative bacterium that normally infects and induces nodulation in soybean roots in vivo, inhibits intercellular communication between the soybean cells in a dose-dependent manner. In contrast, LPS from noninfecting strains failed to yield the same effect. The inhibitory activity of the LPS was localized to the O-antigen region of the LPS.
利用光漂白后的荧光重新分布技术,来测量低分子量荧光亲水性物质在组织培养中相邻大豆(Glycine max (L.) Merr. cv. Mandarin)根细胞(SB - 1细胞系)之间跨细胞壁/细胞膜界面的细胞间移动。从日本慢生根瘤菌R110d(一种革兰氏阴性细菌,通常在体内感染大豆根并诱导结瘤)纯化得到的脂多糖(LPS),以剂量依赖的方式抑制大豆细胞间的细胞通讯。相比之下,来自非感染菌株的LPS未能产生相同的效果。LPS的抑制活性定位于LPS的O抗原区域。