Expression of an alcohol dehydrogenase gene in a heterotrophic bacterium induces carbon dioxide-dependent high-yield growth under oligotrophic conditions. Issue 6 (20th June 2020)

• Record Type: Journal Article
• Authors: Inaba, Shinnosuke; Sakai, Hironori; Kato, Hiromi; Horiuchi, Takayuki; Yano, Hirokazu; Ohtsubo, Yoshiyuki; Tsuda, Masataka; Nagata, Yuji
• Is Part Of: Microbiology. Volume 166:Issue 6(2020)
• Page Start: 531
• Page End: 545
• Publication Date: 2020-06-20
• Subjects: sphingomonads -- poligotroph -- CO2 fixation -- alcohol dehydrogenase; Microbiology -- Periodicals; 579
• DOI: 10.1099/mic.0.000908
• Languages: English
• ISSNs: 1350-0872

Abstract

Abstract : Sphingobium japonicum strain UT26, whose γ-hexachlorocyclohexane-degrading ability has been studied in detail, is a typical aerobic and heterotrophic bacterium that needs organic carbon sources for its growth, and cannot grow on a minimal salt agar medium prepared without adding any organic carbon sources. Here, we isolated a mutant of UT26 with the ability to grow to visible state on such an oligotrophic medium from a transposon-induced mutant library. This high-yield growth under oligotrophic conditions (HYGO) phenotype was CO2 -dependent and accompanied with CO2 incorporation. In the HYGO mutant, a transposon was inserted just upstream of the putative Zn-dependent alcohol dehydrogenase (ADH) gene ( adhX ) so that the adhX gene was constitutively expressed, probably by the transposon-derived promoter. The adhX -deletion mutant (UT26DAX) harbouring a plasmid carrying the adhX gene under the control of a constitutive promoter exhibited the HYGO phenotype. Moreover, the HYGO mutants spontaneously emerged among the UT26-derived hypermutator strain cells, and adhX was highly expressed in these HYGO mutants, while no HYGO mutant appeared among UT26DAX-derived hypermutator strain cells, indicating the necessity of adhX for the HYGO phenotype. His-tagged AdhX that was expressed in Escherichia coli and purified to homogeneity showed ADH activity towards methanol and other alcohols. Mutagenesis analysis of the adhX gene indicated a correlation between the ADH activity and the HYGO phenotype. These results demonstrated that the constitutive expression of an adhX -encoding protein with ADH activity in UT26 leads to the CO2 -dependent HYGO phenotype. Identical or nearly identical adhX orthologues were found in other sphingomonad strains, and most of them were located on plasmids, suggesting that the adhX -mediated HYGO phenotype may be an important adaptation strategy to oligotrophic environments among sphingomonads.