Cyanobacterial hydrogenases: diversity, regulation and applications
2007 (English)In: FEMS Microbiology Reviews, ISSN 0168-6445, E-ISSN 1574-6976, Vol. 31, no 6, 692-720 p.Article, review/survey (Refereed) Published
Cyanobacteria may possess two distinct nickel-iron (NiFe)-hydrogenases: an uptake enzyme found in N2-fixing strains, and a bidirectional one present in both non-N2-fixing and N2-fixing strains. The uptake hydrogenase (encoded by hupSL) catalyzes the consumption of the H2 produced during N2 fixation, while the bidirectional enzyme (hoxEFUYH) probably plays a role in fermn. and/or acts as an electron valve during photosynthesis. HupSL constitute a transcriptional unit, and are essentially transcribed under N2-fixing conditions. The bidirectional hydrogenase consists of a hydrogenase and a diaphorase part, and the corresponding five hox genes are not always clustered or cotranscribed. The biosynthesis/maturation of NiFe-hydrogenases is highly complex, requiring several core proteins. In cyanobacteria, the genes that are thought to affect hydrogenases pleiotropically (hyp), as well as the genes presumably encoding the hydrogenase-specific endopeptidases (hupW and hoxW) have been identified and characterized. Furthermore, NtcA and LexA have been implicated in the transcriptional regulation of the uptake and the bidirectional enzyme resp. Recently, the phylogenetic origin of cyanobacterial and algal hydrogenases was analyzed, and it was proposed that the current distribution in cyanobacteria reflects a differential loss of genes according to their ecol. needs or constraints. In addn., the possibilities and challenges of cyanobacterial-based H2 prodn. are addressed.
Place, publisher, year, edition, pages
2007. Vol. 31, no 6, 692-720 p.
cyanobacteria, hydrogenase, hup, hox, hyp, transcriptional regulator
IdentifiersURN: urn:nbn:se:uu:diva-12242DOI: 10.1111/j.1574-6976.2007.00085.xISI: 000250297800004PubMedID: 17903205OAI: oai:DiVA.org:uu-12242DiVA: diva2:40011