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pubmed-article:8021224pubmed:abstractTextNucleotide sequence analysis revealed a 1,791-bp open reading frame in the hox gene cluster of the gram-negative chemolithotroph Alcaligenes eutrophus H16. In order to investigate the biological role of this open reading frame, we generated an in-frame deletion allele via a gene replacement strategy. The resulting mutant grew significantly more slowly than the wild type under lithoautotrophic conditions (6.1 versus 4.2 h doubling time). A reduction in the level of the soluble NAD-reducing hydrogenase (60% of the wild-type activity) was shown to be the cause of the slow lithoautotrophic growth. We used plasmid-borne gene fusions to monitor the expression of the operons encoding the soluble and membrane-bound hydrogenases. The expression of both operons was lower in the mutant than in the wild-type strain. These results suggest that the newly identified gene, designated hoxX, encodes a regulatory component which, in conjunction with the transcriptional activator HoxA, controls hydrogenase synthesis.lld:pubmed
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pubmed-article:8021224pubmed:articleTitleThe Alcaligenes eutrophus H16 hoxX gene participates in hydrogenase regulation.lld:pubmed
pubmed-article:8021224pubmed:affiliationInstitut für Pflanzenphysiologie und Mikrobiologie, Freien Universität Berlin, Germany.lld:pubmed
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