Zobrazeno 1 - 7
of 7
pro vyhledávání: '"D C, La Grange"'
Autor:
Takahiro Bamba, Akihiko Kondo, Shaunita H. Rose, M J Mert, Tomohisa Hasunuma, D C la Grange, W.H. van Zyl
Publikováno v:
Journal of Industrial Microbiology and Biotechnology. 44:1459-1470
The yeast Saccharomyces cerevisiae cannot utilize xylose, but the introduction of a xylose isomerase that functions well in yeast will help overcome the limitations of the fungal oxido-reductive pathway. In this study, a diploid S. cerevisiae S288c[2
Publikováno v:
Journal of Biotechnology. 125:447-461
Commercial polysaccharase preparations are applied to winemaking to improve wine processing and quality. Expression of polysaccharase-encoding genes in Saccharomyces cerevisiae allows for the recombinant strains to degrade polysaccharides that tradit
Autor:
P. Van Rensburg, R.R. Cordero Otero, D. C. La Grange, S. B. Gundllapalli Moses, Isak S. Pretorius
Publikováno v:
Biotechnology Letters. 24:651-656
A haploid laboratory strain and four industrial (baking, brewing, wine, ATCC) strains of Saccharomyces cerevisiae were transformed with the Lipomyces kononenkoae α-amylase-encoding gene (LKA1). These transformants displayed significant differences i
Publikováno v:
Applied and environmental microbiology. 67(12)
The beta-xylosidase-encoding xlnD gene of Aspergillus niger 90196 was amplified by the PCR technique from first-strand cDNA synthesized on mRNA isolated from the fungus. The nucleotide sequence of the cDNA fragment was verified to contain a 2,412-bp
Publikováno v:
Applied microbiology and biotechnology. 54(2)
The xynB gene encoding the Bacillus pumilus beta-xylosidase was expressed separately and jointly with the Trichoderma reesei beta-xylanase (xyn2) gene in the yeast Saccharomyces cerevisiae. Both genes were placed under the transcriptional control of
Publikováno v:
Applied microbiology and biotechnology. 47(3)
A genomic DNA library of the bacterium Bacillus pumilus PLS was constructed and the beta-xylosidase gene (xynB) was amplified from a 3-kb genomic DNA fragment with the aid of the polymerase chain reaction technique. The amplified xynB gene was insert
The 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 op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3369737d5eb965caccaccff77fc35608
https://europepmc.org/articles/PMC167867/
https://europepmc.org/articles/PMC167867/