2026-04-26T21:57:43Zhttps://uvadoc.uva.es/oai/request

oai:uvadoc.uva.es:10324/741972025-03-26T19:10:03Zcom_10324_1134com_10324_931com_10324_894col_10324_1213

Antolín, Pilar Girotti ., Alessandra Arias Vallejo, Francisco Javier Barriuso, Begoña Jiménez López, María del Pilar Rojo, María Ángeles Girbés Juan, Tomás 2004 Musarmins are type 1 ribosome-inactivating proteins with N-glycosidase activity on the 28 S rRNA that are present in bulbs of Muscari armeniacum L. and Miller at rather low concentrations. In the present work, a cDNA fragment coding for musarmin 1 was sub-cloned and expressed in Escherichia coli. The recombinant protein (rMU1) was synthesised as a polypeptide of 295 amino acids that was delivered to the periplasm and processed. Recombinant musarmin 1 present in the periplam has two forms: insoluble with a molecular mass of 29,423 and soluble with a molecular mass of 29,117 because of a small proteolytic shortening with respect to the insoluble one, presumably in the C-terminal. The yield of protein homogeneous by polyacrylamide gel electrophoresis was 23 mg l−1 of bacterial culture. The recombinant musarmin 1 forms isolated from both the soluble and the insoluble (upon refolding) fractions retained full translational inhibitory and 28 S rRNA N-glycosidase activities as compared with the native protein. The recombinant protein displayed great stability towards trypsin, collagenase, rat plasma and rat liver protein extract, butwas sensitive to the action of papain and proteinase K. The easy availability and full activity of the recombinant musarmin 1 makes it a good candidate for the preparation of immunotoxins for targeted therapy and for the construction of transgenic plants expressing it as antipathogenic agent. application/pdf https://uvadoc.uva.es/handle/10324/74197 eng Elsevier Bacterial expression of biologically active recombinant musarmin 1 from bulbs of Muscari armeniacum L. and Miller info:eu-repo/semantics/article TEXT UVaDOC. Repositorio Documental de la Universidad de Valladolid Hispana