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首页> 外文期刊>Applied and Environmental Microbiology >Alteration of the Trifoliin A-Binding Capsule of Rhizobium trifolii 0403 by Enzymes Released from Clover Roots
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Alteration of the Trifoliin A-Binding Capsule of Rhizobium trifolii 0403 by Enzymes Released from Clover Roots

机译:三叶草根中释放的酶改变三叶草0403的三叶草素A结合胶囊。

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The effect of white clover root exudate on capsules of Rhizobium trifolii 0403 was examined. The clover lectin trifoliin A was detected in root exudate of two clover varieties by indirect immunofluorescence with antibody against this lectin purified from clover seed. Trifoliin A bound uniformly to encapsulated, heat-fixed cells during 1 h of incubation with root exudate. After 4 to 8 h of incubation, trifoliin A was only bound to one pole of the cells. Transmission electron microscopy showed that the capsule itself was altered. The disorganization of the acidic polymers of the capsule began in the equatorial center of the rod-shaped cell and then progressed toward the poles at unequal rates. Trifoliin A could no longer be detected on heat-fixed cells after 12 h of incubation with root exudate. However, trifoliin A was detected in situ on one pole of cells grown for 4 days in the clover root environment of Fahraeus slide cultures. Inhibition studies with the hapten 2-deoxy-d-glucose showed that trifoliin A in root exudate had a higher affinity for one of the cell poles. Immunoelectrophoresis was used to monitor the alteration of the extracellular polysaccharides from R. trifolii 0403 by concentrated root exudate. These polysaccharides were converted into products which eventually lost their ability to immunoprecipitate with homologous antibody. This progressive loss of antigenic reactivity proceeded more rapidly with root exudate from seedlings grown under nitrogen-free conditions than with root exudate from plants grown with 15 mM KNO3. The root exudate, depleted of trifoliin A by immunoaffinity chromatography, was still able to alter the capsule of R. trifolii 0403. Reconstitution experiments showed that the substance(s) in root exudate which induced this alteration of the capsule was of a high molecular weight, heat labile, trypsin sensitive, and antigenically unrelated to trifoliin A. A variety of glycosidase activities were also detected in the fraction depleted of trifoliin A. These results suggest that enzymes in clover root exudate alter the trifoliin A-binding capsule in a way which would favor polar attachment of R. trifolii to clover root hairs.
机译:研究了三叶草根分泌物对三叶草0403胶囊的影响。通过用针对从三叶草种子中纯化的该凝集素的抗体进行间接免疫荧光检测,在两个三叶草变种的根分泌物中检测到三叶草凝集素三叶草素A。 Trifoliin A在与根系分泌液孵育1小时的过程中均匀地结合到封装的热固定细胞上。温育4至8小时后,三叶草素A仅结合至细胞的一个极。透射电子显微镜显示胶囊本身被改变。胶囊中酸性聚合物的分解开始于棒状细胞的赤道中心,然后以不相等的速率向两极发展。与根系分泌液孵育12小时后,在热固定细胞上不再检测到三叶草素A。然而,在Fahraeus玻片培养物的三叶草根环境中,在生长了4天的一极细胞上原位检测到三叶草素A。半抗原2-deoxy-d-glucose的抑制研究表明,根系分泌物中的三叶草素A对其中一个细胞极具有更高的亲和力。免疫电泳被用于监测浓根渗出液对三叶苜蓿0403细胞外多糖的改变。这些多糖被转化为产物,最终使它们失去了用同源抗体免疫沉淀的能力。与在15 mM KNO3上生长的植物的根系分泌物相比,在无氮条件下生长的幼苗的根系分泌物的抗原反应性的逐步丧失进行得更快。通过免疫亲和色谱法去除三叶草素A的根系分泌物仍然能够改变R. trifolii 0403的胶囊。重建实验表明,引起根系改变的根系分泌物中的一种或多种物质具有高分子量,对热不稳定,对胰蛋白酶敏感,并且与三叶草素A无关。在三叶草素A消耗的部分中也检测到多种糖苷酶活性。这些结果表明,三叶草根分泌物中的酶以某种方式改变了三叶草素A结合胶囊。会有利于三叶草对三叶草根毛的极性附着。

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