
pmid: 21821073
Levulinic acid or 4-ketovaleric acid is a potential renewable substrate for production of polyhydroxyalkanoates. In this work, the initial reactions of LA metabolism by Cupriavidus necator were examined in vitro. The organic acid was converted by membrane-bound crude enzymes obtained from the cells pre-grown on LA, while no LA activity was detected from cells pre-grown on acetic acid. Acetyl-CoA and propionyl-CoA were two major intermediates in the initial reactions of LA conversion. A mass balance on propionyl-CoA accounts for 84 mol% of LA added in vitro. It explains an interesting phenomenon that 3-hydroxbutyrate and 3-hydroxyvalerate are two major monomers of the biopolyester formed from LA, instead of 4-hydroxvalerate that has the similar chemical structure of LA as the precursor. A Monod model was used to describe the kinetics of LA utilization as a sole carbon source or a co-substrate of glucose and fructose. The μ(max) and K(m) of LA alone were 0.26 h⁻¹ and 0.01 g/L, respectively. The content and composition of PHA are also dependent on the culture conditions such as carbon to nitrogen ratio. The in vitro observation is supported by the high utilization rate of LA and the high molar percentage of 3HB and 3HV in the PHA derived from LA.
3-Hydroxybutyric Acid, Polyhydroxyalkanoates, Cell Membrane, Cell Fractionation, Levulinic Acids, Kinetics, Acetyl Coenzyme A, Cupriavidus necator, Acyl Coenzyme A, Pentanoic Acids
3-Hydroxybutyric Acid, Polyhydroxyalkanoates, Cell Membrane, Cell Fractionation, Levulinic Acids, Kinetics, Acetyl Coenzyme A, Cupriavidus necator, Acyl Coenzyme A, Pentanoic Acids
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