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Polyhydroyxalkanoate synthase fusions as a strategy for oriented enzyme immobilisation.
Hooks, David O; Venning-Slater, Mark; Du, Jinping; Rehm, Bernd H A.
Afiliación
  • Hooks DO; Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand. d.o.hooks@massey.ac.nz.
  • Venning-Slater M; Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand. m.venningslater@massey.ac.nz.
  • Du J; Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand. j.du@massey.ac.nz.
  • Rehm BH; Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand. b.rehm@massey.ac.nz.
Molecules ; 19(6): 8629-43, 2014 Jun 24.
Article en En | MEDLINE | ID: mdl-24962396
Polyhydroxyalkanoate (PHA) is a carbon storage polymer produced by certain bacteria in unbalanced nutrient conditions. The PHA forms spherical inclusions surrounded by granule associate proteins including the PHA synthase (PhaC). Recently, the intracellular formation of PHA granules with covalently attached synthase from Ralstonia eutropha has been exploited as a novel strategy for oriented enzyme immobilisation. Fusing the enzyme of interest to PHA synthase results in a bifunctional protein able to produce PHA granules and immobilise the active enzyme of choice to the granule surface. Functionalised PHA granules can be isolated from the bacterial hosts, such as Escherichia coli, and maintain enzymatic activity in a wide variety of assay conditions. This approach to oriented enzyme immobilisation has produced higher enzyme activities and product levels than non-oriented immobilisation techniques such as protein inclusion based particles. Here, enzyme immobilisation via PHA synthase fusion is reviewed in terms of the genetic designs, the choices of enzymes, the control of enzyme orientations, as well as their current and potential applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aciltransferasas / Enzimas Inmovilizadas / Complejos Multienzimáticos Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aciltransferasas / Enzimas Inmovilizadas / Complejos Multienzimáticos Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Nueva Zelanda