Bioreactor operation shows haloplasticity of a synthetic nitrifying community, enabling urine treatment in space

Additional file 4: Figure S2. Detection of aabgl1 copy numbers in the transformants by qPCR analysis. Tef1Îą gene was used as a single copy control

MOESM3 of Optimization of cellulolytic enzyme components through engineering Trichoderma reesei and on-site fermentation using the soluble inducer for cellulosic ethanol production from corn stover

Additional file 3: Figure S1. Construction of the aabgl1 overexpression T. reesei strains. A: Map of aabgl1 expression vector pCBHYGB-PB; B: Comparison of β-glucosidase production of the recombinant transformants and the host strain T. reesei Rut-C30; C: Detection of aabgl1 copy numbers in the transformants by qPCR analysis. Tef1ι gene was used as a single copy control

MOESM2 of Optimization of cellulolytic enzyme components through engineering Trichoderma reesei and on-site fermentation using the soluble inducer for cellulosic ethanol production from corn stover

Additional file 2: Table S2. Identified secreted proteins induced by MGD and CS

MOESM4 of Optimization of cellulolytic enzyme components through engineering Trichoderma reesei and on-site fermentation using the soluble inducer for cellulosic ethanol production from corn stover

Additional file 4: Figure S2. Detection of aabgl1 copy numbers in the transformants by qPCR analysis. Tef1Îą gene was used as a single copy control