• This record comes from PubMed

Characterization of a long-chain α-galactosidase from Papiliotrema flavescens

. 2018 Jan 04 ; 34 (2) : 19. [epub] 20180104

Language English Country Germany Media electronic

Document type Journal Article

Grant support
2/0023/14 the Scientific Grant Agency of Ministry of Education, Science, Research and Sport of Slovak Republic
VEGA 2/0058/16 the Scientific Grant Agency of Ministry of Education, Science, Research and Sport of Slovak Republic

Links

PubMed 29302817
DOI 10.1007/s11274-017-2403-6
PII: 10.1007/s11274-017-2403-6
Knihovny.cz E-resources

α-Galactosidases are assigned to the class of hydrolases and the subclass of glycoside hydrolases (GHs). They belong to six GH families and include the only characterized α-galactosidases from yeasts (GH 27, Saccharomyces cerevisiae). The present study focuses on an investigation of the lactose-inducible α-galactosidase produced by Papiliotrema flavescens. The enzyme was present on the surface of cells and in the cytosol. Its temperature optimum was about 60 °C and the pH optimum was 4.8; the pH stability ranged from 3.2 to 6.6. This α-galactosidase also exhibited transglycosylation activity. The cytosol α-galactosidase with a molecular weight about 110 kDa, was purified using a combination of liquid chromatography techniques. Three intramolecular peptides were determined by the partial structural analysis of the sequences of the protein isolated, using MALDI-TOF/TOF mass spectrometry. The data obtained recognized the first yeast α-galactosidase, which belongs to the GH 36 family. The bioinformatics analysis and homology modeling of a 210 amino acids long C-terminal sequence (derived from cDNA) confirmed the correctness of these findings. The study was also supplemented by the screening of capsular cryptococcal yeasts, which produce the surface lactose-inducible α- and β-galactosidases. The production of the lactose-inducible α-galactosidases was not found to be a general feature within the yeast strains examined and, therefore, the existing hypothesis on the general function of this enzyme in cryptococcal capsule rearrangement cannot be confirmed.

See more in PubMed

Nature. 1970 Aug 15;227(5259):680-5 PubMed

J Biol Chem. 1970 Aug 10;245(15):3945-55 PubMed

Biochem J. 1998 Jun 15;332 ( Pt 3):789-97 PubMed

Nat Protoc. 2006;1(6):2856-60 PubMed

Appl Microbiol Biotechnol. 1999 Nov;52(5):681-8 PubMed

Carbohydr Res. 1997 Dec;305(1):83-91 PubMed

Zentralbl Bakteriol. 1996 Aug;284(4):475-95 PubMed

Biosci Biotechnol Biochem. 1995 Apr;59(4):619-23 PubMed

Biochim Biophys Acta. 2005 Nov 15;1726(2):206-16 PubMed

Carbohydr Res. 1995 Nov 30;278(1):129-42 PubMed

J Basic Microbiol. 2006;46(6):470-9 PubMed

Appl Microbiol Biotechnol. 2009 Jul;83(5):875-84 PubMed

Prep Biochem. 1990;20(3-4):263-96 PubMed

Z Naturforsch C. 2005 Nov-Dec;60(11-12):899-905 PubMed

J Proteomics. 2012 Jul 16;75(13):4027-37 PubMed

Antonie Van Leeuwenhoek. 2007 Jul;92(1):29-36 PubMed

Biochem J. 1999 Apr 1;339 ( Pt 1):43-53 PubMed

Eur J Biochem. 1996 Aug 15;240(1):104-11 PubMed

Anal Chem. 2003 Feb 1;75(3):663-70 PubMed

Carbohydr Res. 2002 Feb 11;337(3):221-8 PubMed

Mol Microbiol. 2007 May;64(3):771-81 PubMed

Proc Natl Acad Sci U S A. 1988 Dec;85(23):8998-9002 PubMed

FEMS Microbiol Lett. 1993 Aug 15;112(1):35-41 PubMed

Nucleic Acids Res. 2009 Jan;37(Database issue):D233-8 PubMed

Appl Environ Microbiol. 1993 May;59(5):1347-53 PubMed

J Biol Chem. 2012 Nov 16;287(47):39642-52 PubMed

Stud Mycol. 2015 Jun;81:85-147 PubMed

Nucleic Acids Res. 2003 Jul 1;31(13):3763-6 PubMed

Biochim Biophys Acta. 1981 Apr 17;674(1):71-7 PubMed

Carbohydr Res. 2000 Oct 20;329(1):65-73 PubMed

Biochim Biophys Acta. 2001 Nov 15;1524(1):27-37 PubMed

Biotechnol Appl Biochem. 1993 Jun;17 ( Pt 3):361-71 PubMed

Biochemistry. 2007 Mar 20;46(11):3319-30 PubMed

Science. 2005 Feb 25;307(5713):1321-4 PubMed

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...