| Literature DB >> 6539773 |
C A Borrebaeck, B Mattiasson, B Nordbring-Hertz.
Abstract
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.Entities:
Mesh:
Substances:
Year: 1984 PMID: 6539773 PMCID: PMC215591 DOI: 10.1128/jb.159.1.53-56.1984
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490