Isolation and characterization of a cDNA clone encoding the pokeweed antiviral protein II from Phytolacca americana and its expression in E. coli

• Published in: FEBS letters 1994-06, Vol.347 (2), p.268-272
• Main Authors: Poyet, Jean-Luc, Radom, Jean, Hoeveler, Arnd
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Base Sequence; cDNA; Cloning, Molecular; DNA, Complementary - chemistry; DNA, Complementary - genetics; DNA, Complementary - isolation & purification; Escherichia coli - genetics; Expression in E. coli; Gene Expression; Inhibition of in vitro translation; Molecular Sequence Data; N-Glycosyl Hydrolases; Phytolacca americana; Plant Proteins - chemistry; Plant Proteins - genetics; Plant Proteins - pharmacology; Plants - chemistry; Plants - genetics; Pokeweed antiviral protein from summer leaves; Poly A - metabolism; Protein Synthesis Inhibitors; Ribosome Inactivating Proteins, Type 1; Ribosome-inactivating protein; Ribosomes - drug effects; Sequence Alignment
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/0014-5793(94)00565-6

Three distinct ribosome-inactivating proteins (RIPs) were isolated from pokeweed Phytolacca americana We identified and sequenced for the first time a complete cDNA encoding the pokeweed antiviral protein II (PAP II), which is expressed in the late summer leaves of pokeweed. The cDNA of PAP II consists of 1, 187 nucleotides and encodes a mature protein of 285 amino acids. Its predicted amino acid sequence is only 33% similar to PAP and PAP-S. The NH 2 terminal extrapeptide (25 amino acid residues) was similar but not identical to that of PAP's extrapeptide. The cDNA of PAP II was expressed in E. coli. The growth of the transformants was strongly inhibited after induction of the gene. Furthermore, PAP II, which was produced in E. coli, inhibited protein synthesis in a rabbit reticulocyte translation system. Thus, recombinant PAP II would appear to be as functional as native PAP in inhibiting protein synthesis in both prokaryotes and eukaryotes.