RT Journal Article SR Electronic(1) A1 Avanzo, Petra A1 Sabotič, Jerica A1 Anžlovar, Sabina A1 Popovič, Tatjana A1 Leonardi, Adrijana A1 Pain, Roger H. A1 Kos, Janko A1 Brzin, JožeYR 2009 T1 Trypsin-specific inhibitors from the basidiomycete Clitocybe nebularis with regulatory and defensive functions JF Microbiology, VO 155 IS 12 SP 3971 OP 3981 DO https://doi.org/10.1099/mic.0.032805-0 PB Microbiology Society, SN 1465-2080, AB We have isolated serine protease inhibitors from the basidiomycete Clitocybe nebularis, CnSPIs, using trypsin affinity chromatography. Full-length gene and cDNA sequences were determined for one of them, named cnispin, and the recombinant protein was expressed in Escherichia coli at high yield. The primary structure and biochemical properties of cnispin are very similar to those of the Lentinus edodes serine protease inhibitor, until now the only member of the I66 family of protease inhibitors in the MEROPS classification. Cnispin is highly specific towards trypsin, with K i in the nanomolar range. It also exhibited weaker inhibition of chymotrypsin and very weak inhibition of subtilisin and kallikrein; other proteases were not inhibited. Inhibitory activity against endogenous proteases from C. nebularis revealed a possible regulatory role for CnSPIs in the endogenous proteolytic system. Another possible biological function in defence against predatory insects was indicated by the deleterious effect of CnSPIs on the development of larvae of Drosophila melanogaster. These findings, together with the biochemical and genetic characterization of cnispin, suggest a dual physiological role for this serine protease inhibitor of the I66 MEROPS family., UL https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.032805-0