Xylitol production by Debaryomyces hansenii and Candida guilliermondii from rapeseed straw hemicellulosic hydrolysate

•Rapeseed straw hemicellulosic hydrolysate was used for xylitol production.•Different strategies were evaluated for the hydrolysate detoxification.•C. guilliermondii exhibited higher tolerance to the toxic compounds than D. hansenii.•Toxic compounds and glucose concentration affected the yeast’s per...

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Veröffentlicht in:Bioresource technology 2018-01, Vol.247, p.736-743
Hauptverfasser: López-Linares, Juan Carlos, Romero, Inmaculada, Cara, Cristobal, Castro, Eulogio, Mussatto, Solange I.
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Sprache:eng
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Zusammenfassung:•Rapeseed straw hemicellulosic hydrolysate was used for xylitol production.•Different strategies were evaluated for the hydrolysate detoxification.•C. guilliermondii exhibited higher tolerance to the toxic compounds than D. hansenii.•Toxic compounds and glucose concentration affected the yeast’s performance.•Partial removal of toxic compounds was enough to achieve an efficient bioconversion. This study evaluated the possibility of using rapeseed straw hemicellulosic hydrolysate as a fermentation medium for xylitol production. Two yeast strains, namely Debaryomyces hansenii and Candida guilliermondii, were used for this bioconversion process and their performance to convert xylose into xylitol was compared. Additionally, different strategies were evaluated for the hydrolysate detoxification before its use as a fermentation medium. Assays in semi-defined media were also performed to verify the influence of hexose sugars on xylose metabolism by the yeasts. C. guilliermondii exhibited higher tolerance to toxic compounds than D. hansenii. Not only the toxic compounds present in the hydrolysate affected the yeast’s performance, but glucose also had a negative impact on their performance. It was not necessary to completely eliminate the toxic compounds to obtain an efficient conversion of xylose into xylitol, mainly by C. guilliermondii (YP/S=0.55g/g and 0.45g/g for C. guilliermondii and D. hansenii, respectively).
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2017.09.139