TY - JOUR
T1 - Expression of an alcohol dehydrogenase gene in a heterotrophic bacterium induces carbon dioxide-dependent high-yield growth under oligotrophic conditions
AU - Inaba, Shinnosuke
AU - Sakai, Hironori
AU - Kato, Hiromi
AU - Horiuchi, Takayuki
AU - Yano, Hirokazu
AU - Ohtsubo, Yoshiyuki
AU - Tsuda, Masataka
AU - Nagata, Yuji
N1 - Funding Information:
This work was supported by Grants-in-Aid for Challenging Exploratory Research from the Japan Society for the Promotion of Science (JSPS) (nos 24658068, 26660054 and 16K14877), Grants-in-Aid for Scientific Research (B) from JSPS (nos 17H03781 and 19H02865) and the Institute for Fermentation, Osaka (IFO).
Funding Information:
information This work was supported by Grants- in- Aid for Challenging Exploratory Research from the Japan Society for the Promotion of Science (JSPS) (nos 24658068, 26660054 and 16K14877), Grants- in- Aid for Scientific Research (B) from JSPS (nos 17H03781 and 19H02865) and the Institute for Fermentation, Osaka (IFO). Acknowledgements We thank J. Hirano and H. Ui (Tohoku University) and R. Kugimiya (Chitose Laboratory Corp.) for technical support and for valuable discussions, respectively.
Publisher Copyright:
© 2020 The Authors.
PY - 2020
Y1 - 2020
N2 - 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 oligo-trophic 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.
AB - 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 oligo-trophic 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.
KW - Alcohol dehydrogenase
KW - CO fixation
KW - Poligotroph
KW - Sphingomonads
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UR - http://www.scopus.com/inward/citedby.url?scp=85087435046&partnerID=8YFLogxK
U2 - 10.1099/mic.0.000908
DO - 10.1099/mic.0.000908
M3 - Article
C2 - 32310743
AN - SCOPUS:85087435046
SN - 1350-0872
VL - 166
SP - 531
EP - 545
JO - Microbiology (United Kingdom)
JF - Microbiology (United Kingdom)
IS - 6
M1 - 000908
ER -