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猪黏膜器官培养物中大肠杆菌K88肠膜结合位点的恢复

Recovery of intestinal membrane binding sites for K88 E. coli from pig mucosal organ cultures.

作者信息

Wilson I B, Staley T E, Bush L J, Gilliland S E

出版信息

Mol Cell Biochem. 1984 Apr;62(1):57-65. doi: 10.1007/BF00230078.

Abstract

Putative receptors for K88 + E. coli from piglet intestinal epithelium were released into the organ culture medium and were demonstrated by direct binding with K88 + E. coli through the utilization of an in vitro binding procedure or by immunoprecipitation with K88 antigen. Incorporation of 14C-glucosamine by newborn to day old and 3-week to 6-week old piglet jejunal and ileal mucosa, in organ culture, occurred throughout the 24 hr culture period. Uptake in both age groups and both areas of the intestine was similar with a somewhat greater incorporation by the older age group. Secretion of 14C-glucosamine-labeled components into the culture medium was demonstrated by gel filtration of the concentrated medium. Some large molecular weight components eluted in the void volume in excess of 2 X 10(6) daltons. A second peak of activity was spread from approximately 690K to 25K daltons. All eluted fractions demonstrated binding to K88 + E. coli. Antibodies to purified brush borders from susceptible pigs produced prominent precipitation bands following double diffusion with concentrated organ culture media which confirmed that the organ culture media contained labeled proteins of brush border origin. Immunoprecipitation of the intestinal mucosal organ culture media with K88 + pili and pilus antisera, followed by electrophoresis with SDS and reduced conditions, demonstrated a subunit of approximately 35K daltons.

摘要

来自仔猪肠上皮的K88 +大肠杆菌的推定受体被释放到器官培养基中,并通过体外结合程序与K88 +大肠杆菌直接结合或用K88抗原进行免疫沉淀来证明。在器官培养中,新生至日龄以及3周龄至6周龄仔猪空肠和回肠黏膜对14C-葡糖胺的掺入在整个24小时培养期内均有发生。两个年龄组以及肠道的两个区域的摄取情况相似,年龄较大的组掺入量略高。通过对浓缩培养基进行凝胶过滤证明了14C-葡糖胺标记的成分分泌到培养基中。一些大于2×10(6)道尔顿的大分子成分在空体积中洗脱。第二个活性峰从约690K到25K道尔顿分布。所有洗脱级分均显示与K88 +大肠杆菌结合。用来自易感猪的纯化刷状缘抗体与浓缩的器官培养基进行双向扩散后产生明显的沉淀带,这证实器官培养基中含有刷状缘来源的标记蛋白。用K88 +菌毛和菌毛抗血清对肠黏膜器官培养基进行免疫沉淀,然后在SDS和还原条件下进行电泳,显示出一个约35K道尔顿的亚基。

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