A novel NADPH-dependent aldehyde reductase gene from Saccharomyces cerevisiae NRRL Y-12632 involved in the detoxification of aldehyde inhibitors derived from lignocellulosic biomass conversion

• Published in: Gene Vol. 446; no. 1; pp. 1 - 10
• Main Authors: Liu, Z. Lewis, Moon, Jaewoong
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.10.2009
• Subjects: Aldehyde Reductase - chemistry; Aldehyde Reductase - genetics; Aldehyde Reductase - metabolism; Aldehydes - metabolism; Amino Acid Sequence; Base Sequence; Biomass; Cloning, Molecular; DNA Primers - genetics; DNA, Fungal - genetics; Ethanol - metabolism; Furaldehyde - analogs & derivatives; Furaldehyde - metabolism; Furaldehyde - pharmacology; Furfural; Gene expression; Genes, Fungal - drug effects; Inactivation, Metabolic; Lignin - metabolism; Molecular Sequence Data; NADP - metabolism; Phylogeny; Protein expression; Saccharomyces cerevisiae; Saccharomyces cerevisiae - enzymology; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - chemistry; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Sequence Homology, Amino Acid; Sequence Homology, Nucleic Acid; Sequence motif; Short-chain dehydrogenase/reductase; Stress tolerance; Substrate Specificity; HMF; NADPH; SDR; ORF; Furfural; RNA; qRT-PCR; AKR; Gene expression; Short-chain dehydrogenase/reductase; SDS-PAGE; SGD; Sequence motif; DNA; Stress tolerance; Protein expression; MDR
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2009.06.018

Aldehyde inhibitors such as furfural, 5-hydroxymethylfurfural, anisaldehyde, benzaldehyde, cinnamaldehyde, and phenylaldehyde are commonly generated during lignocellulosic biomass conversion process for low-cost cellulosic ethanol production that interferes with subsequent microbial growth and fermentation. In situ detoxification of the aldehyde inhibitors is possible by the tolerant ethanologenic yeast that involves multiple genes including numerous functional reductases. In this study, we report a novel aldehyde reductase gene clone Y63 from ethanologenic yeast Saccharomyces cerevisiae NRRL Y12632, representing the uncharacterized ORF YGL157W, which demonstrated NADPH-dependent reduction activities toward at least 14 aldehyde substrates. The identity of gene clone Y63 is the same with YGL157W of SGD since a variation of only 35 nucleotides in genomic sequence and three amino acid residues were observed between the two that share the same length of 347 residues in size. As one among the highly induced genes, YGL157W of Y-12632 showed significantly high levels of transcript abundance in response to furfural and HMF challenges. Based on the deduced amino acid sequence and the most conserved functional motif analyses including closely related reductases from five other yeast species to this date, YGL157W was identified as a member of the subclass ‘intermediate’ of the SDR (short-chain dehydrogenase/reductase) superfamily with the following typical characteristics: the most conserved catalytic site to lie at Tyr 169-X-X-X-Lys 173; an indispensable reduction catalytic triad at Ser 131, Tyr 169, and Lys 173, and an approved cofactor-binding motif at Gly 11-X-X-Gly 14-X-X-Ala 17 near the N-terminus. YGL039W, YDR541C, and YOL151W (GRE2) appeared to be the similar type of enzymes falling into the same category of the intermediate subfamily.