TY - JOUR
T1 - Production of heteropolymeric polyhydroxyalkanoate in Eschericha coli from a single carbon source
AU - Eschenlauer, Arthur C.
AU - Stoup, Sandra K.
AU - Srienc, Friedrich
AU - Somers, David A.
PY - 1996/8
Y1 - 1996/8
N2 - Poly[β-hydroxybutyrate-co-β-hydroxyvalerate] co-polymer, PHBV, is a polyhydroxyalkanoate (PHA) that has greater utility as a biodegradable thermoplastic polyester than poly-β-hydroxybutyrate, PHB. In order to produce PHBV, a system of pathways is required to produce both hydroxybutyrate (HE) and hydroxyvalerate (HV) monomers from the sources of carbon. A working model for conversion of glucose to PHBV via acetyl- and propionyl-coenzyme A was constructed by expressing the PHA biosynthesis genes from Alcaligenes eutrophus in Escherichia coil strain K-12 under novel growth conditions. When 1 mM valine was added to 1% glucose medium, growth ceased and up to 2.5% of the incorporated monomers were HV; up to 4% were HV when 1 mM threonine was added as well. Threonine dehydratase (TD) converts threonine to α-ketobutyrate; TD is required for HV to be incorporated into PHA unless its transaminated reaction product, α-aminobutyrate, is added to the medium. Intracellular α-ketobutyrate accumulates when valine is added to the medium because valine, which cannot be metabolized to HV by E. coli strain K-12, stimulates TD and inhibits acetolactate synthase. In turn, α-ketobutyrate is converted to propionyl-CoA by the E. coil pyruvate dehydrogenase complex. This constitutes a defined system of pathways for synthesis of a heteropolymeric PHA from a single carbon source, which in the future could be transferred to other organisms including plants.
AB - Poly[β-hydroxybutyrate-co-β-hydroxyvalerate] co-polymer, PHBV, is a polyhydroxyalkanoate (PHA) that has greater utility as a biodegradable thermoplastic polyester than poly-β-hydroxybutyrate, PHB. In order to produce PHBV, a system of pathways is required to produce both hydroxybutyrate (HE) and hydroxyvalerate (HV) monomers from the sources of carbon. A working model for conversion of glucose to PHBV via acetyl- and propionyl-coenzyme A was constructed by expressing the PHA biosynthesis genes from Alcaligenes eutrophus in Escherichia coil strain K-12 under novel growth conditions. When 1 mM valine was added to 1% glucose medium, growth ceased and up to 2.5% of the incorporated monomers were HV; up to 4% were HV when 1 mM threonine was added as well. Threonine dehydratase (TD) converts threonine to α-ketobutyrate; TD is required for HV to be incorporated into PHA unless its transaminated reaction product, α-aminobutyrate, is added to the medium. Intracellular α-ketobutyrate accumulates when valine is added to the medium because valine, which cannot be metabolized to HV by E. coli strain K-12, stimulates TD and inhibits acetolactate synthase. In turn, α-ketobutyrate is converted to propionyl-CoA by the E. coil pyruvate dehydrogenase complex. This constitutes a defined system of pathways for synthesis of a heteropolymeric PHA from a single carbon source, which in the future could be transferred to other organisms including plants.
KW - Poly-β-hydroxyalkanoic acids
KW - Poly[β-hydroxybutyrate-co-β-hydroxyvalerate] co-polymer
KW - Propionyl co-enzyme A
KW - Pyruvate dehydrogenase
KW - Threonine
KW - Threonine dehydratase
KW - α-ketobutyrate
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U2 - 10.1016/0141-8130(96)01114-2
DO - 10.1016/0141-8130(96)01114-2
M3 - Article
C2 - 8842775
AN - SCOPUS:0030221651
VL - 19
SP - 121
EP - 130
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
SN - 0141-8130
IS - 2
ER -