4.7 Article

Detoxification of 5-hydroxymethylfurfural by the Pleurotus ostreatus lignolytic enzymes aryl alcohol oxidase and dehydrogenase

期刊

BIOTECHNOLOGY FOR BIOFUELS
卷 8, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s13068-015-0244-9

关键词

Pleurotus ostreatus; 5-hydroxymethylfurfural (HMF); Aryl-alcohol oxidase; Aryl-alcohol dehydrogenase

资金

  1. US-Israel Binational Fund (BSF)
  2. Israel Science Foundation (ISF)
  3. Estates Committee

向作者/读者索取更多资源

Background: Current large-scale pretreatment processes for lignocellulosic biomass are generally accompanied by the formation of toxic degradation products, such as 5-hydroxymethylfurfural (HMF), which inhibit cellulolytic enzymes and fermentation by ethanol-producing yeast. Overcoming these toxic effects is a key technical barrier in the biochemical conversion of plant biomass to biofuels. Pleurotus ostreatus, a white-rot fungus, can efficiently degrade lignocellulose. In this study, we analyzed the ability of Pleurotus ostreatus to tolerate and metabolize HMF and investigated relevant molecular pathways associated with these processes. Results: Pleurotus ostreatus was capable to metabolize and detoxify HMF 30 mM within 48 h, converting it into 2,5-bis-hydroxymethylfuran (HMF alcohol) and 2,5-furandicarboxylic acid (FDCA), which subsequently allowed the normal yeast growth in amended media. We show that two enzymes groups, which belong to the ligninolytic system, aryl-alcohol oxidases and a dehydrogenase, are involved in this process. HMF induced the transcription and production of these enzymes and was accompanied by an increase in activity levels. We also demonstrate that following the induction of these enzymes, HMF could be metabolized in vitro. Conclusions: Aryl-alcohol oxidase and dehydrogenase gene family members are part of the transcriptional and subsequent translational response to HMF exposure in Pleurotus ostreatus and are involved in HMF transformation. Based on our data, we propose that these enzymatic capacities of Pleurotus ostreatus either be integrated in biomass pretreatment or the genes encoding these enzymes may function to detoxify HMF via heterologous expression in fermentation organisms, such as Saccharomyces cerevisiae.

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