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ARS Home » Midwest Area » Peoria, Illinois » National Center for Agricultural Utilization Research » Crop Bioprotection Research » Research » Publications at this Location » Publication #179834
Title: INDUCTION OF PLEIOTROPIC DRUG RESISTANCE GENE EXPRESSION INDICATES IMPORTANT ROLES OF PDR TO COPE WITH FURFURAL AND 5-HYDROXYMETHYLFURFURAL STRESS IN ETHANOLOGENIC YEAST

Author
item Liu, Zonglin
item Slininger, Patricia - Pat
item ANDERSH, BRAD - BRADLEY UNIV, PEORIA, IL

Submitted to: Biotechnology for Fuels and Chemicals Symposium Proceedings
Publication Type: Abstract Only
Publication Acceptance Date: 5/4/2005
Publication Date: 5/4/2005
Citation: Liu, Z., Slininger, P.J. 2005. Induction of pleiotropic drug resistance gene expression indicates important roles of pdr to cope with furfural and 5-hydroxymethylfurfural stress in ethanologenic yeast [abstract]. Biotechnology for Fuels and Chemicals Symposium Proceedings. Abstract No. 169.

Interpretive Summary:

Technical Abstract: Furfural and 5-hydroxymethylfurfural (HMF) derived from dehydration of pentose and hexoses by dilute acid hydrolysis of lignocellulosic biomass are major inhibitive compounds for enzymatic saccharification and microbial fermentation in ethanol conversion. Mechanisms of tolerance to furfural and HMF stress are unknown. Our interest lies on identification of relevant target genes and understanding of molecular mechanisms involved in the inhibitive stress tolerance in ethanologenic yeast. By means of functional analysis and comparative gene expression using microarray and quantitative real-time RT-PCR, we identified genes significantly enhanced in expression during the initial exposure to furfural and HMF stress. These genes belong to the pleiotropic drug resistance (PDR) gene family. Many PDR genes function as transporter of ATP-binding cassette proteins and are encoded for plasma membrane proteins. These genes mediate membrane translocation of ions and a wide range of substrates. This presentation will cover methods of our well-established quality-controlled microarray and qRT-PCR technologies and convincing evidence of yeast gene expression in the earlier stage to cope with the furfural and HMF stress.