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[Primers for (1,3)-β-glucan synthase gene amplification and partial characterization of the enzyme in Ganoderma lucidum].

Authors :
Guerrero-Torres JV
Mata G
Martínez-Carrera D
Garibay-Orijel C
Garibay-Orijel R
Source :
Revista iberoamericana de micologia [Rev Iberoam Micol] 2013 Oct-Dec; Vol. 30 (4), pp. 267-70. Date of Electronic Publication: 2013 Feb 09.
Publication Year :
2013

Abstract

Background: β-(1,3)(1,6)-D-glucan is fungal cell wall component that has demonstrated immunomodulatory and anti-cancer effects. The (1,3)-β-glucan synthase is one of the main enzymes involved in its biosynthesis.<br />Aims: To design primers to partially amplify and characterize the (1,3)-β-glucan synthase gene and to determine them in Ganoderma lucidum (G. Lucidum) strain CP-132.<br />Methods: The primers were designed on the basis of homologous genes in other fungi. Then, using the PCR technique, primers were tested using DNA extracted from the G. lucidum strain CP-382. Amplified sequences were compared with those from the GenBank.<br />Results: Three primer pairs were designed; all of them produced amplicons of the expected size. The sequences obtained with primer pairs BGS2113UmF and BGS3097UmR, and BGS547UmF and BGS2113UmR matched with 2 sections of the (1,3)-β-glucan synthase gene. The deduced amino acid sequences showed high similarity with homologous genes from other fungi, particularly with those of the Agaricomycetes class.<br />Conclusions: The primer design to partially amplify the (1,3)-β-glucan synthase gene of G. lucidum using sequences from homologous genes was successful. These primers will allow to characterize this important enzyme in a wide group of fungi.<br /> (Copyright © 2012 Revista Iberoamericana de Micología. Published by Elsevier Espana. All rights reserved.)

Details

Language :
Spanish; Castilian
ISSN :
2173-9188
Volume :
30
Issue :
4
Database :
MEDLINE
Journal :
Revista iberoamericana de micologia
Publication Type :
Academic Journal
Accession number :
23402832
Full Text :
https://doi.org/10.1016/j.riam.2012.12.006