Cloning and expression of cDNA coding for bouganin.

Eur J Biochem

Tanox Pharma B.V., Amsterdam, the Netherlands; Dipartimento di Patologia Sperimentale, Università di Bologna, Bologna, Italy.

Published: March 2002

Bouganin is a ribosome-inactivating protein that recently was isolated from Bougainvillea spectabilis Willd. In this work, the cloning and expression of the cDNA encoding for bouganin is described. From the cDNA, the amino-acid sequence was deduced, which correlated with the primary sequence data obtained by amino-acid sequencing on the native protein. Bouganin is synthesized as a pro-peptide consisting of 305 amino acids, the first 26 of which act as a leader signal while the 29 C-terminal amino acids are cleaved during processing of the molecule. The mature protein consists of 250 amino acids. Using the cDNA sequence encoding the mature protein of 250 amino acids, a recombinant protein was expressed, purified and characterized. The recombinant molecule had similar activity in a cell-free protein synthesis assay and had comparable toxicity on living cells as compared to the isolated native bouganin.

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http://dx.doi.org/10.1046/j.1432-1327.2002.02823.xDOI Listing

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