E-GEOD-48864 - Expression analysis of Aspergillus oryzae grown on different carbon sources
Released on 15 July 2013, last updated on 3 June 2014
Aspergillus oryzae RIB40
In this study, we focused on chemically defined inducers or substrates to drive expression of cellulases, hemicellulases and accessory enzymes in the model filamentous fungus Aspergillus oryzae. Cellohexaose (O-CHE), mannohexaose (O-MHE), xylopentaose (O-XPE), arabinoheptaose (O-AHP), 1,3:1,4-β-glucohexaose (O-BGHEXA), 63-α-D-glucosyl-maltotriosyl-maltotriose (O-GMH), 61-α-D-galactosyl-mannotriose (O-GM3), xyloglucan (X3Glc4-borohydride reduced; O-X3G4R), turanose (TYR) and sophorose (SOP) were used to induce the plant polysaccharide degradation machinery of A. oryzae. The strain used in this study was the A. oryzae sequenced strain RIB40, obtained from IBT culture collection at Technical University of Denmark. To obtain a global view of the A. oryzae transcriptome activated for plant biomass conversion, mRNA from growth after 2 h on 10 different carbohydrate active enzyme inducers (di- and –oligo saccharides) was subjected to custom-designed Agilent microarray analysis.
transcription profiling by array
D.B.R.K. Gupta Udatha <email@example.com>, D G Udatha, Evangelos Topakas, John A Smith, Lisbeth Olsson, Margarita Salazar, Melanie Z Khodaie, Mikael R Andersen