Thursday, September 2, 2010

Article Alert from Biotechnology for Biofuels

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From: BioMed Central <info@biomedcentral.com>
Date: September 2, 2010 1:27:44 AM EDT

Article alert


The following new article has just been published in Biotechnology for Biofuels

For articles which have only just been published, you will see a 'provisional PDF' corresponding to the accepted manuscript. A fully formatted PDF and full text (HTML) version will be made available soon.

Research
Cross-reactions between engineered xylose and galactose pathways in recombinant Saccharomyces cerevisiae
Garcia Sanchez R, Hahn-Hagerdal B, Gorwa-Grauslund MF
Biotechnology for Biofuels 2010, 3:19 (1 September 2010)
[Abstract] [Provisional PDF]





Cross-reactions between engineered xylose and galactose pathways in recombinant Saccharomyces cerevisiae

Rosa Garcia Sanchez email, Barbel Hahn-Hagerdal email and Marie F Gorwa-Grauslund email

Biotechnology for Biofuels 2010, 3:19doi:10.1186/1754-6834-3-19


Published: 1 September 2010

Abstract (provisional)

Background

Overexpression of the PGM2 gene encoding phosphoglucomutase (Pgm2p) has been shown to improve galactose utilization both under aerobic and under anaerobic conditions. Similarly, xylose utilization has been improved by overexpression of genes encoding xylulokinase (XK), enzymes from the non-oxidative pentose phosphate pathway (non-ox PPP) and deletion of the endogenous aldose reductase GRE3 gene in engineered S. cerevisiae strains carrying either fungal or bacterial xylose pathways. In the present study, we investigated how the combination of these traits affect xylose and galactose utilization, in the presence or absence of glucose in S. cerevisiae strains engineered with the xylose reductase (XR)-xylitol dehydrogenase (XDH) pathway.

Results

In the absence of PGM2 overexpression, the combined overexpression of XK, the non-ox PPP and deletion of the GRE3 gene, significantly delayed aerobic growth on galactose, whereas no difference was observed between the control strain and the xylose-engineered strain when the PGM2 gene was overexpressed. Under anaerobic conditions, the overexpression of the PGM2 gene increased the ethanol yield and the xylose consumption rate in medium containing xylose as the only carbon source. The possibility of Pgm2p acting as a xylose isomerase (XI) could be excluded by measuring the XI activity in both strains. The additional copy of the PGM2 gene also resulted in a shorter fermentation time during the co-consumption of galactose and xylose. However, the effect was lost upon addition of glucose to the growth medium.

Conclusions

PGM2 overexpression was shown to benefit xylose and galactose fermentation, alone and in combination. In contrast, galactose fermentation was impaired in the engineered xylose-utilizing strain harbouring extra copies of the non-ox PPP genes and a deletion of the GRE3 gene, unless PGM2 was overexpressed. These cross-reactions are of particular relevance for the fermentation of mixed sugars from lignocellulosic feedstock.

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