Borrebaeck C A, Mattiasson B, Nordbring-Hertz B
J Bacteriol. 1984 Jul;159(1):53-6. doi: 10.1128/jb.159.1.53-56.1984.
A developmentally regulated carbohydrate-binding protein from the capture organs of Arthrobotrys oligospora, not present on hyphae, was isolated and partially characterized. Surface structures of A. oligospora were radiolabeled with [125I]iodosulfanilic acid. The fungus was homogenized, and the homogenate was passed over an affinity column containing N-acetyl-D-galactosamine immobilized to Sepharose 6B. The bound radiolabeled protein was eluted from the affinity column with a glycine-hydrochloride buffer (pH 3.0), concentrated, and chromatographed on a metal chelate affinity gel containing Ca2+. EDTA was used as an eluant for the radiolabeled protein. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis in combination with autoradiography revealed a molecular weight for the carbohydrate- and cation-binding polypeptide of ca. 20,000.
从少孢节丛孢菌的捕食器官中分离出一种在菌丝上不存在的、发育调控的碳水化合物结合蛋白,并对其进行了部分特性鉴定。少孢节丛孢菌的表面结构用[125I]碘磺胺酸进行放射性标记。将真菌匀浆,匀浆液通过含有固定在琼脂糖6B上的N-乙酰-D-半乳糖胺的亲和柱。用甘氨酸-盐酸缓冲液(pH 3.0)从亲和柱上洗脱结合的放射性标记蛋白,浓缩后在含有Ca2+的金属螯合亲和凝胶上进行色谱分析。用EDTA作为放射性标记蛋白的洗脱剂。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳结合放射自显影显示,碳水化合物和阳离子结合多肽的分子量约为20,000。