TY - JOUR
T1 - Glucose-induced production of a Penicillium purpurogenum xylanase by Aspergillus nidulans
AU - Ravanal, María Cristina
AU - Espinosa, Yeison
AU - Rosa, Lorena
AU - Vaca, Inmaculada
AU - Polanco, Rubén
AU - Eyzaguirre, Jaime
AU - Levicán, Gloria
AU - Chávez, Renato
N1 - Funding Information:
Acknowledgments This work was supported by grants from DI-CYT-USACH, FONDECYT 1100084 and UNAB DI-03-10/R. I. Vaca acknowledges support from the ‘‘Programa Bicentenario de Ciencia y Tecnología’’ program (Chile), project PDA13. Technical assistance of Carlos Aguirre is gratefully acknowledged.
PY - 2012/3
Y1 - 2012/3
N2 - The heterologous secretion of xylanase B from Penicillium purpurogenum using glucose as inducer was performed in Aspergillus nidulans. For this purpose, plasmid pEVXB, containing the xylanase B cDNA (including its own signal peptide) under the control of the glyceraldehyde-3-phosphate dehydrogenase promoter, was constructed and used to transform A. nidulans. Analysis of transformed clones showed that several of them secreted extracellular xylanase activity when grown in a medium containing glucose. The clone showing the highest xylanase activity was chosen for further work. When this clone was grown on glucose, xylanase activity (0. 72 U/ml), was detected in the culture supernatant. This was confirmed by a zymogram analysis and by the amplification of xynB cDNA from this clone. To our knowledge, this is the first example of the production of a xylanase from Penicillium in heterologous fungal hosts using glucose as inducer.
AB - The heterologous secretion of xylanase B from Penicillium purpurogenum using glucose as inducer was performed in Aspergillus nidulans. For this purpose, plasmid pEVXB, containing the xylanase B cDNA (including its own signal peptide) under the control of the glyceraldehyde-3-phosphate dehydrogenase promoter, was constructed and used to transform A. nidulans. Analysis of transformed clones showed that several of them secreted extracellular xylanase activity when grown in a medium containing glucose. The clone showing the highest xylanase activity was chosen for further work. When this clone was grown on glucose, xylanase activity (0. 72 U/ml), was detected in the culture supernatant. This was confirmed by a zymogram analysis and by the amplification of xynB cDNA from this clone. To our knowledge, this is the first example of the production of a xylanase from Penicillium in heterologous fungal hosts using glucose as inducer.
KW - Glucose induction
KW - Heterologous expression
KW - Penicillium purpurogenum
KW - Xylanase
UR - http://www.scopus.com/inward/record.url?scp=84858152256&partnerID=8YFLogxK
U2 - 10.1007/s10267-011-0144-1
DO - 10.1007/s10267-011-0144-1
M3 - Article
AN - SCOPUS:84858152256
SN - 1340-3540
VL - 53
SP - 152
EP - 155
JO - Mycoscience
JF - Mycoscience
IS - 2
ER -