A ribonuclease from the wild mushroom Boletus griseus

Appl Microbiol Biotechnol. 2006 Oct;72(5):912-6. doi: 10.1007/s00253-006-0385-7. Epub 2006 Mar 17.

Abstract

A ribonuclease (RNase) with a molecular mass of 29 kDa and cospecific for poly A and poly U was isolated from fruiting bodies of the mushroom Boletus griseus. Its N-terminal sequence exhibited some similarity to those of RNases from the mushrooms Irpex lacteus and Lentinus edodes. The RNase was adsorbed on diethylaminoethyl-cellulose, Q-Sepharose, and Affi-gel blue gel and was unadsorbed on CM-cellulose. The enzyme exhibited a temperature optimum between 60 and 70 degrees C and a pH optimum at 3.5.

MeSH terms

  • Agaricales / enzymology*
  • Enzyme Stability
  • Hydrogen-Ion Concentration
  • RNA, Transfer / metabolism
  • Ribonucleases / metabolism*
  • Temperature

Substances

  • RNA, Transfer
  • Ribonucleases