Abstract

Purple non-sulfur (PNS) bacteria produce hydrogen under photoheterotrophic conditions. The produced hydrogen, which is catalyzed by Mo-nitrogenase, is re-oxidized by a membrane-bound uptake hydrogenase. To improve hydrogen-producing efficiency, the hupSL gene that encodes the uptake hydrogenase, and its positive regulator gene hupR were knocked out in Rhodobacter sphaeroides 6016. Compared to the wild-type strain, the hydrogen yields of the hupSL − and hupR − mutants each increased by 11%. When the nifA gene, which encodes a specific transcriptional activator for all other nif genes was overexpressed in the hupR − mutant, the hydrogen yield increased by 20%. In addition, hydrogen production was detected in the nifA/hupR − mutant in the presence of 14 mM NH 4 +, whereas the wild-type strain produced no hydrogen under the same conditions.

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