Literature DB >> 23423895

Use of Sulfolobus solfataricus PCNA subunit proteins to direct the assembly of multimeric enzyme complexes.

Hidehiko Hirakawa1, Teruyuki Nagamune.   

Abstract

In nature, enzymes often form multienzyme complexes to enhance their catalytic efficiencies and, -moreover, evolve into genetically fused multidomain enzymes. Inspired by a natural fusion cytochrome P450 (P450) containing a monooxygenase domain and a reductase domain, we have developed a heterotrimeric protein-utilized method to form a multienzyme complex composed of a bacterial P450 and its catalytically essential two redox proteins. Three distinct proliferating cell nuclear antigens (PCNAs) from Sulfolobus solfataricus, each of which can be separately expressed, spontaneously form a heterotrimer. Fusion to the PCNAs enables complex formation of a bacterial P450 and two redox proteins through the self-assembling of the PCNAs and enhances the activity due to efficient electron transfer in the complex. This PCNA-mediated multienzyme complex formation will be available for other multienzyme reactions.

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Year:  2013        PMID: 23423895     DOI: 10.1007/978-1-62703-293-3_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Design and improvement of artificial redox modules by molecular fusion of flavodoxin and flavodoxin reductase from Escherichia coli.

Authors:  Patrick J Bakkes; Stefan Biemann; Ansgar Bokel; Marc Eickholt; Marco Girhard; Vlada B Urlacher
Journal:  Sci Rep       Date:  2015-07-16       Impact factor: 4.379

2.  Engineering of versatile redox partner fusions that support monooxygenase activity of functionally diverse cytochrome P450s.

Authors:  Patrick J Bakkes; Jan L Riehm; Tanja Sagadin; Ansgar Rühlmann; Peter Schubert; Stefan Biemann; Marco Girhard; Michael C Hutter; Rita Bernhardt; Vlada B Urlacher
Journal:  Sci Rep       Date:  2017-08-29       Impact factor: 4.379

  2 in total

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