The mycobacterial binuclear iron monooxygenases require a specific chaperonin-like protein for functional expression in a heterologous host

Toshiki Furuya, Mika Hayashi, Hisashi Semba, Kuniki Kino

    Research output: Contribution to journalArticle

    8 Citations (Scopus)

    Abstract

    The mimABCD gene clusters in Mycobacterium smegmatis strain mc 2155 and Mycobacterium goodii strain 12523 encode binuclear iron monooxygenases that oxidize propane and phenol. In this study, we attempted to express each mimABCD gene cluster in a heterologous host. The actinomycetous strain Rhodococcus opacus B-4, which is phylogenetically close to Mycobacterium, was selected as the host. Each mimABCD gene cluster was cloned into the Rhodococcus-Escherichia coli shuttle vector, pTip-QC2, and then introduced into R. opacus cells. Although whole-cell assays were performed with phenol as a substrate, the transformed R. opacus cells did not oxidize this substrate. SDS/PAGE analysis revealed that the oxygenase large subunit MimA was expressed in the insoluble fraction of R. opacus cells. We found that a gene designated mimG, which lies downstream of mimABCD, exhibits similarity in the amino acid sequence of its product with the products of genes encoding the chaperonin GroEL. When the mimG gene was cloned and coexpressed with each mimABCD gene cluster in R. opacus strain B-4, this host successfully acquired oxidation activity towards phenol. SDS/PAGE and western blotting analyses demonstrated that MimA was clearly soluble when in the presence of MimG. These results indicated that MimG played essential roles in the productive folding of MimA, and that the resulting soluble MimA protein led to the active expression of MimABCD. The active expression of mycobacterial binuclear iron monooxygenases (MimABCD) in a heterologous host was dependent on the co-expression of a specific chaperonin-like protein (MimG). SDS/PAGE and western blotting analyses demonstrated that MimG played essential roles in productive folding of MimA and that the resulting soluble MimA protein led to the active expression of MimABCD.

    Original languageEnglish
    Pages (from-to)817-826
    Number of pages10
    JournalFEBS Journal
    Volume280
    Issue number3
    DOIs
    Publication statusPublished - 2013 Feb

    Fingerprint

    Chaperonins
    Acinetobacter
    Mixed Function Oxygenases
    Iron
    Genes
    Multigene Family
    Phenol
    Rhodococcus
    Polyacrylamide Gel Electrophoresis
    Proteins
    Mycobacterium
    Western Blotting
    Mycobacterium smegmatis
    Genetic Vectors
    Propane
    Oxygenases
    Gene encoding
    Substrates
    Escherichia coli
    Amino Acid Sequence

    Keywords

    • binuclear iron monooxygenase
    • chaperonin
    • GroEL
    • heterologous expression
    • Mycobacterium

    ASJC Scopus subject areas

    • Biochemistry
    • Cell Biology
    • Molecular Biology

    Cite this

    The mycobacterial binuclear iron monooxygenases require a specific chaperonin-like protein for functional expression in a heterologous host. / Furuya, Toshiki; Hayashi, Mika; Semba, Hisashi; Kino, Kuniki.

    In: FEBS Journal, Vol. 280, No. 3, 02.2013, p. 817-826.

    Research output: Contribution to journalArticle

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