Abstract
Bioethanol production from lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in the world, because Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose. The aim of this study was to obtain a novel yeast capable of stably producing ethanol from biomass containing xylose by protoplast fusion between S. cerevisiae and xylose-utilizing yeast. We describe a novel xylose-fermenting yeast strain, FSC1, developed for ethanol production by intergeneric hybridization between S. cerevisiae and Candida intermedia mutants by using a protoplast fusion technique. The characteristics of the FSC1 strain are reported with respect to xylose fermentation, morphology, gene, and protein expression. Mutation of the parental strains prior to protoplast fusion endowed the FSC1 strain with the ability to convert xylose to ethanol. Microscopic analysis confirmed that the parental and FSC1 strains produced spores in the potassium acetate medium. The FSC1 strain is uninucleate diploid, has a stable metabolism, and expresses proteins at a higher level than the parental strains. We found that FSC1 strain could stably achieve an ethanol yield of 0.38 g/g-substrate in fermentation of a mixture of glucose and xylose. In addition, the fermentation ability of FSC1was improved by successive chemical mutation, resulting in a higher ethanol yield of 0.42 g/g-substrate, corresponding to 82% theoretical yield. The mutation-fusion technique we have described here is very useful for the development of intergeneric hybrids capable of xylose fermentation, and the FSC strains generated using this technique have the potential for industrial use in ethanol production from lignocellulosic biomass.
Highlights
Bioethanol production from lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in the world, because Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose
Since the M2 strain lacks the xylitol dehydrogenase (XDH) activity, C. intermedia was used as a donor of xdh gene in cell fusion of this study
Hybridization between S. cerevisiae M2 and C. intermedia m11 by protoplast fusion Before protoplast fusion, we investigated the sporulation of C. intermedia m11 using the potassium acetate (KAc) medium
Summary
Bioethanol production from lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in the world, because Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose. Bioethanol production through the fermentation of lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this. The metabolic alteration of the yeast for ethanol production has been attempted through mutation, fusion, and recombination. Several attempts have been made to transfer specific genes for xylose utilization to S. cerevisiae by construction of recombinant strains (reviewed by Matsushika et al, ref [12]). The recombinants are expected to be practically applied for ethanol production from lignocellulose by overcoming such problems as redox imbalance in the initial step of xylose fermentation and reverse flux in glycolysis [13]
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