The presence of lignocellulose-derived microbial inhibitory compounds (LDMICs) in lignocellulosic biomass (LB) hydrolysates is a barrier to efficient conversion of LB hydrolysates to fuels and chemicals by fermenting microorganisms. Results from this study provide convincing evidence regarding the effectiveness of metabolically engineered NCIMB 8052 for the fermentation of LB-derived hydrolysates to acetone-butanol-ethanol (ABE). The engineered microbial strain (_SDR) was produced by the integration of an additional copy of a short-chain dehydrogenase/reductase (SDR) gene (3904) into the chromosome of NCIMB 8052 wildtype, where it is controlled by the constitutive thiolase promoter.
View Article and Find Full Text PDFCarbon catabolite repression (CCR) limits microbial utilization of lignocellulose-derived pentoses. To relieve CCR in NCIMB 8052, we sought to downregulate catabolite control protein A (CcpA) using the M1GS ribozyme technology. A CcpA-specific ribozyme was constructed by tethering the catalytic subunit of RNase P (M1 RNA) to a guide sequence (GS) targeting CcpA mRNA (M1GS).
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