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Reaction kinetic analysis of the 3-hydroxypropionate/4-hydroxybutyrate CO2 fixation cycle in extremely thermoacidophilic archaea.
Loder, Andrew J; Han, Yejun; Hawkins, Aaron B; Lian, Hong; Lipscomb, Gina L; Schut, Gerrit J; Keller, Matthew W; Adams, Michael W W; Kelly, Robert M.
Afiliación
  • Loder AJ; Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, United States.
  • Han Y; Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, United States.
  • Hawkins AB; Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, United States.
  • Lian H; Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, United States.
  • Lipscomb GL; Dept. of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, United States.
  • Schut GJ; Dept. of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, United States.
  • Keller MW; Dept. of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, United States.
  • Adams MWW; Dept. of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, United States.
  • Kelly RM; Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, United States. Electronic address: rmkelly@ncsu.edu.
Metab Eng ; 38: 446-463, 2016 11.
Article en En | MEDLINE | ID: mdl-27771364
The 3-hydroxypropionate/4-hydroxybutyrate (3HP/4HB) cycle fixes CO2 in extremely thermoacidophilic archaea and holds promise for metabolic engineering because of its thermostability and potentially rapid pathway kinetics. A reaction kinetics model was developed to examine the biological and biotechnological attributes of the 3HP/4HB cycle as it operates in Metallosphaera sedula, based on previous information as well as on kinetic parameters determined here for recombinant versions of five of the cycle enzymes (malonyl-CoA/succinyl-CoA reductase, 3-hydroxypropionyl-CoA synthetase, 3-hydroxypropionyl-CoA dehydratase, acryloyl-CoA reductase, and succinic semialdehyde reductase). The model correctly predicted previously observed features of the cycle: the 35-65% split of carbon flux through the acetyl-CoA and succinate branches, the high abundance and relative ratio of acetyl-CoA/propionyl-CoA carboxylase (ACC) and MCR, and the significance of ACC and hydroxybutyryl-CoA synthetase (HBCS) as regulated control points for the cycle. The model was then used to assess metabolic engineering strategies for incorporating CO2 into chemical intermediates and products of biotechnological importance: acetyl-CoA, succinate, and 3-hydroxypropionate.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dióxido de Carbono / Sulfolobaceae / Ácido Láctico / Redes y Vías Metabólicas / Análisis de Flujos Metabólicos / Hidroxibutiratos / Modelos Biológicos Tipo de estudio: Prognostic_studies Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dióxido de Carbono / Sulfolobaceae / Ácido Láctico / Redes y Vías Metabólicas / Análisis de Flujos Metabólicos / Hidroxibutiratos / Modelos Biológicos Tipo de estudio: Prognostic_studies Idioma: En Revista: Metab Eng Asunto de la revista: ENGENHARIA BIOMEDICA / METABOLISMO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
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