Literature DB >> 9063971

Purification and some properties of a beta-xylosidase and an alpha-fucosidase from apple snails (Pomacea canaliculata).

K Hirata1, Y Nakahara, Y Kimura, G Funatsu.   

Abstract

beta-Xylosidase and alpha-fucosidase were purified from the viscera of apple snails (Pomacea canaliculata) using ammonium sulfate precipitation, hydrophobic chromatography on Butyl-Toyopearl, gel filtration on Sephacryl S-300, and Q-Sepharose column chromatography. beta-Xylosidase and alpha-fucosidase are glycoproteins and their molecular masses were estimated to be approximately 85 kDa and 54 kDa by SDS-polyacrylamide gel electrophoresis, and assumed to be about 96 kDa and 230 kDa from their sedimentation coefficients, respectively, indicating that the former is a monomer and the latter has a tetrameric structure. beta-Xylosidase is stable at pH 4-10 and its optimum pH toward pNP-beta-D-xyloside is around 3.6, while alpha-fucosidase is fairly stable at 65 degrees C and pH 4-10, and its optimum pHs toward pNP-alpha-L-fucoside are around 3.2 and 5.2. beta-Xylosidase released a xylose residue from Xylbeta1->2Manbeta1->4GlcNAcbeta1->4(Fucalpha1-> 3)GlcNAc-PA and Manalpha1->6(Manalpha1->3)(Xylbeta1->2)Manbeta1- >4GlcNAcbeta1->4(Fucalpha1->3)GlcNAc-PA, but not from GlcNAcbeta1->2Manalpha1->6(GlcNAcbeta1->2Manalpha1+ ++->3)(Xylbeta1->2)Manbeta1->4GlcNAcbeta1-> 4(Fucalpha1->3)GlcNAc-PA, while alpha-fucosidase released a fucose residue from these three PA-oligosaccharides.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9063971     DOI: 10.1271/bbb.60.249

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  3 in total

1.  AtFXG1, an Arabidopsis gene encoding alpha-L-fucosidase active against fucosylated xyloglucan oligosaccharides.

Authors:  Francisco de La Torre; Javier Sampedro; Ignacio Zarra; Gloria Revilla
Journal:  Plant Physiol       Date:  2002-01       Impact factor: 8.340

2.  Purification and characterization of β-xylosidase that is active for plant complex type N-glycans from tomato (Solanum lycopersicum): removal of core α1-3 mannosyl residue is prerequisite for hydrolysis of β1-2 xylosyl residue.

Authors:  Daisuke Yokouchi; Natsuko Ono; Kosuke Nakamura; Megumi Maeda; Yoshinobu Kimura
Journal:  Glycoconj J       Date:  2012-08-30       Impact factor: 2.916

3.  PROTEIN N-GLYCOSYLATION OF GASTROPODS.

Authors:  Erika Staudacher; Herwig Stepan; Martin Gutternigg
Journal:  Curr Top Biochem Res       Date:  2009-12
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.