Show simple item record

dc.contributor.authorLa Grange, Daniel C.
dc.contributor.authorPretorius, Isak S.
dc.contributor.authorVan Zyl, Willem H.
dc.date.accessioned2011-04-07T08:27:35Z
dc.date.available2011-04-07T08:27:35Z
dc.date.issued1995-04
dc.identifier.citationLa Grange, Daniel C., Pretorius, Isak S., Van Zyl, Willem H. 1996. Expression of a Trichoderma reesei beta-xylanase gene (XYN2) in Saccharomyces cerevisiae. Applied and Environmental Microbiology, 62(3):1036-1044, http://aem.asm.org.ez.sun.ac.za/content/vol62/issue3/index.dtlen_ZA
dc.identifier.issn1098-5336 (Online Version)
dc.identifier.issn0099-2240 (Print Version)
dc.identifier.urihttp://hdl.handle.net/10019.1/8489
dc.descriptionIncludes bibliography
dc.description.abstractThe XYN2 gene encoding the main Trichoderma reesei QM 6a endo-beta-1,4-xylanase was amplified by PCR from first-strand cDNA synthesized on mRNA isolated from the fungus. The nucleotide sequence of the cDNA fragment was verified to contain a 699-bp open reading frame that encodes a 223-amino-acid propeptide. The XYN2 gene, located on URA3-based multicopy shuttle vectors, was successfully expressed in the yeast Saccharomyces cerevisiae under the control of the alcohol dehydrogenase II (ADH2) and phosphoglycerate kinase (PGK1) gene promoters and terminators, respectively. The 33-amino-acid leader peptide of the Xyn2 beta-xylanase was recognized and cleaved at the Kex2-like Lys-Arg residues, enabling the efficient secretion and glycosylation of the heterologous beta-xylanase. The molecular mass of the recombinant beta-xylanase was estimated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis to be 27 kDa. The construction of fur1 ura3 S. cerevisiae strains allowed for the autoselection of the URA3-based XYN2 shuttle vectors in nonselective complex medium. These autoselective S. cerevisiae strains produced 1,200 and 160 nkat of beta-xylanase activity per ml under the control of the ADH2 and PGK1 promoters in rich medium, respectively. The recombinant enzyme showed highest activity at pH 6 and 60 degrees C and retained more than 90% of its activity after 60 min at 50 degrees C.en_ZA
dc.format.extentp. 1036–1044 : ill.
dc.language.isoen_USen_ZA
dc.publisherAmerican Society for Microbiologyen_ZA
dc.subjectGene expressionen_ZA
dc.subjectSaccharomyces cerevisiae -- Geneticsen_ZA
dc.subjectXylanasesen_ZA
dc.subjectRecombinanten_ZA
dc.subjectTrichoderma reeseien_ZA
dc.subjectXylanen_ZA
dc.subjectBreakdownen_ZA
dc.titleExpression of a Trichoderma reesei beta-xylanase gene (XYN2) in Saccharomyces cerevisiaeen_ZA
dc.typeArticleen_ZA
dc.rights.holderAmerican Society for Microbiologyen_ZA


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record