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The turnover of medium-chain-length polyhydroxyalkanoates in Pseudomonas putida KT2442 and the fundamental role of PhaZ depolymerase for the metabolic balance.

Abstract
Polyhydroxyalkanoates (PHAs) are biodegradable polymers produced by a wide range of bacteria, including Pseudomonads. These polymers are accumulated in the cytoplasm as carbon and energy storage materials when culture conditions are unbalanced and hence, they have been classically considered to act as sinks for carbon and reducing equivalents when nutrients are limited. Bacteria facing carbon excess and nutrient limitation store the extra carbon as PHAs through the PHA polymerase (PhaC). Thereafter, under starvation conditions, PHA depolymerase (PhaZ) degrades PHA and releases R-hydroxyalkanoic acids, which can be used as carbon and energy sources. To study the influence of a deficient PHA metabolism in the growth of Pseudomonas putida KT2442 we have constructed two mutant strains defective in PHA polymerase (phaC1)- and PHA depolymerase (phaZ)-coding genes respectively. By using these mutants we have demonstrated that PHAs play a fundamental role in balancing the stored carbon/biomass/number of cells as function of carbon availability, suggesting that PHA metabolism allows P. putida to adapt the carbon flux of hydroxyacyl-CoAs to cellular demand. Furthermore, we have established that the coordination of PHA synthesis and mobilization pathways configures a functional PHA turnover cycle in P. putida KT2442. Finally, a new strain able to secrete enantiomerically pure R-hydroxyalkanoic acids to the culture medium during cell growth has been engineering by redirecting the PHA cycle to biopolymer hydrolysis.
AuthorsLaura Isabel de Eugenio, Isabel F Escapa, Valle Morales, Nina Dinjaski, Beatriz Galán, José Luis García, María A Prieto
JournalEnvironmental microbiology (Environ Microbiol) Vol. 12 Issue 1 Pg. 207-21 (Jan 2010) ISSN: 1462-2920 [Electronic] England
PMID19788655 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Bacterial Proteins
  • Polyhydroxyalkanoates
  • Carbon
  • Acyltransferases
  • poly(3-hydroxyalkenoate)polymerase
  • Carboxylic Ester Hydrolases
  • poly(3-hydroxyalkanoic acid) depolymerase
  • Nitrogen
Topics
  • Acyltransferases (genetics, metabolism)
  • Bacterial Proteins (genetics, metabolism)
  • Carbon (metabolism)
  • Carboxylic Ester Hydrolases (genetics, metabolism)
  • Gene Deletion
  • Gene Expression Regulation, Bacterial
  • Microbial Viability
  • Nitrogen (metabolism)
  • Polyhydroxyalkanoates (metabolism)
  • Pseudomonas putida (genetics, growth & development, metabolism)
  • Substrate Specificity

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