| Literature DB >> 27771305 |
Mary E Walter1, Alicia Ortiz1, Casey Sondgeroth1, Nathan M Sindt1, Nikolas Duszenko1, Jennie L Catlett1, You Zhou2, Shah Valloppilly3, Christopher Anderson4, Samodha Fernando5, Nicole R Buan6.
Abstract
Bacterial and archaeal genomes can contain 30% or more hypothetical genes with no predicted function. Phylogenetically deep-branching microbes, such as methane-producing archaea (methanogens), contain up to 50% genes with unknown function. In order to formulate hypotheses about the function of hypothetical gene functions in the strict anaerobe, Methanosarcina acetivorans, we have developed high-throughput anaerobic techniques to UV mutagenize, screen, and select for mutant strains in 96-well plates. Using these approaches we have isolated 10 mutant strains that exhibit a variety of physiological changes including increased or decreased growth rate relative to the parent strain when cells use methanol and/or acetate as carbon and energy sources. This method provides an avenue for the first step in identifying new gene functions: associating a genetic mutation with a reproducible phenotype. Mutations in bona fide methanogenesis genes such as corrinoid methyltransferases and proton-translocating F420H2:methanophenazine oxidoreductase (Fpo) were also generated, opening the door to in vivo functional complementation experiments. Irradiation-based mutagenesis such as from ultraviolet (UV) light, combined with modern genome sequencing, is a useful procedure to discern systems-level gene function in prokaryote taxa that can be axenically cultured but which may be resistant to chemical mutagens. Copyright ÂEntities:
Keywords: Archaea; Methane; Methanogen; Methanosarcina; Struvite
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Year: 2016 PMID: 27771305 DOI: 10.1016/j.mimet.2016.10.010
Source DB: PubMed Journal: J Microbiol Methods ISSN: 0167-7012 Impact factor: 2.363