Enhanced H2 gas production from bagasse using adhE inactivated Klebsiella oxytoca HP1 by sequential dark-photo fermentations.

Sequential dark-photo fermentations (SDPF) was used for hydrogen production from bagasse, an acetaldehyde dehydrogenase (adhE) gene inactivated Klebsiella oxytoca HP1 (ΔadhE HP1) mutant was used to reduce the alcohol content in dark fermentation (DF) broths and to further enhance the hydrogen yield during the photo fermentation (PF) stage. Compared with that of the wild strain, the ethanol concentration in DF broths of ΔadhE HP1 decreased 69.4%, which resulted in a hydrogen yield in the PF stage and the total hydrogen yield over the two steps increased by 54.7% and 23.5%, respectively. The culture conditions for hydrogen production from acid pretreated bagasse by SDPF were optimized as culture temperature 37.5°C, initial pH 7.0, and cellulase loading 20FPA/g in the DF stage, with initial pH 6.5, temperature 30°C and photo intensity 5000lux in the PF stage. Under optimum conditions, by using ΔadhE HP1 and wild type strain, the H2 yields were 107.8±5.3mL H2/g-bagasse, 96.2±4.4mL H2/g-bagasse in DF and 54.3±2.2mL H2/g-bagasse, 35.1±2.0mL H2/g-bagasse in PF, respectively. The special hydrogen production rate (SHPR) were 5.51±0.34mL H2/g-bagasseh, 4.95±0.22mL H2/g-bagasseh in DF and 0.93±0.12mL H2/g-bagasseh, 0.59±0.07mL H2/g-bagasseh in PF, respectively. The total hydrogen yield from bagasse over two steps was 162.1±7.5mL H2/g-bagasse by using ΔadhE HP1, which was 50.4% higher than that from dark fermentation only. These results indicate that reducing ethanol content during dark fermentation by using an adhE inactivated strain can significantly enhance hydrogen production from bagasse in the SDPF system. This work also proved that SDPF was an effective way to improve hydrogen production from bagasse.