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Chemical Compound Review

AGN-PC-007OHL     3-hydroxyoctanoic acid

Synonyms: AG-D-84960, CHEBI:37098, H3898_SIGMA, HMDB01954, AC1L1BIF, ...
 
 
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Disease relevance of Poly-3-hydroxyoctanoate

  • phaZPfi, the gene encoding the extracellular poly(3-hydroxyoctanoic acid) depolymerase of Pseudomonas fluorescens GK13, was cloned, sequenced, and characterized [1].
  • Moreover, the polymer accumulated in the recombinant E. coli consisted mainly of 3-hydroxyoctanoate monomers [2].
  • Twenty-five gram-negative bacteria and one gram-positive bacterium capable of growing on poly(3-hydroxyoctanoic acid) [P(3HO)] as the sole source of carbon and energy were isolated from various soils, lake water, and activated sludge [3].
  • This result also provided evidence for the presumption that the Burkholderia strain possesses not only polyhydroxybutyrate synthase genes, but also synthase for medium-chain-length polyhydroxyalkanoates consisting of 3HHx, 3HO and 3HD [4].
  • The kinetic DSC study of PHA granules, which contained mostly 3-hydroxyoctanoate units (PHO), in Pseudomonas putida BM01 cells showed that the polymer within the granules existed in an amorphous state, but it crystallized after dehydration of the cells under freeze-drying condition (below -50 degrees C) followed by annealing at ambient temperature [5].
 

High impact information on Poly-3-hydroxyoctanoate

 

Associations of Poly-3-hydroxyoctanoate with other chemical compounds

 

Gene context of Poly-3-hydroxyoctanoate

  • These included 24% poly-3-hydroxybutyrate (PHB), 41% poly-3-hydroxyvalerate (PHV), 18% poly-3-hydroxyhexanoate (PHH), 10% poly-3-hydroxyoctanoate (PHO), 5% poly-3-hydroxydecanoate (PHD). and 2% poly-3-hydroxydodecanoate (PHDD), indicating that microorganisms could store various PHAs through the different metabolic pathways [10].
 

Analytical, diagnostic and therapeutic context of Poly-3-hydroxyoctanoate

References

  1. Molecular characterization of the extracellular poly(3-hydroxyoctanoic acid) [P(3HO)] depolymerase gene of Pseudomonas fluorescens GK13 and of its gene product. Schirmer, A., Jendrossek, D. J. Bacteriol. (1994) [Pubmed]
  2. Production of medium-chain-length poly(3-hydroxyalkanoates) from gluconate by recombinant Escherichia coli. Klinke, S., Ren, Q., Witholt, B., Kessler, B. Appl. Environ. Microbiol. (1999) [Pubmed]
  3. Degradation of poly(3-hydroxyoctanoic acid) [P(3HO)] by bacteria: purification and properties of a P(3HO) depolymerase from Pseudomonas fluorescens GK13. Schirmer, A., Jendrossek, D., Schlegel, H.G. Appl. Environ. Microbiol. (1993) [Pubmed]
  4. PCR cloning of polyhydroxyalkanoate biosynthesis genes from Burkholderia caryophylli and their functional expression in recombinant Escherichia coli. Hang, X., Zhang, G., Wang, G., Zhao, X., Chen, G.Q. FEMS Microbiol. Lett. (2002) [Pubmed]
  5. Differential scanning calorimetric study of poly(3-hydroxyoctanoate) inclusions in bacterial cells. Song, J.J., Yoon, S.C., Yu, S.M., Lenz, R.W. Int. J. Biol. Macromol. (1998) [Pubmed]
  6. Bacterial poly(hydroxyalkanoates) as a source of chiral hydroxyalkanoic acids. Ren, Q., Grubelnik, A., Hoerler, M., Ruth, K., Hartmann, R., Felber, H., Zinn, M. Biomacromolecules (2005) [Pubmed]
  7. Metabolic engineering of Escherichia coli for the production of medium-chain-length polyhydroxyalkanoates rich in specific monomers. Park, S.J., Park, J.P., Lee, S.Y. FEMS Microbiol. Lett. (2002) [Pubmed]
  8. Substrate specificities of poly(hydroxyalkanoate)-degrading bacteria and active site studies on the extracellular poly(3-hydroxyoctanoic acid) depolymerase of Pseudomonas fluorescens GK13. Schirmer, A., Matz, C., Jendrossek, D. Can. J. Microbiol. (1995) [Pubmed]
  9. 3-Hydroxyoctanoic aciduria: identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemia. Kelley, R.I., Morton, D.H. Clin. Chim. Acta (1988) [Pubmed]
  10. Behaviors of intercellular materials and nutrients in biological nutrient removal process supplied with domestic wastewater and food waste. Chae, S.R., Jeong, H.S., Lim, J.L., Kang, S.T., Shin, H.S., Paik, B.C., Youn, J.H. Water Environ. Res. (2004) [Pubmed]
  11. Production of chiral R-3-hydroxyalkanoic acids and R-3-hydroxyalkanoic acid methylesters via hydrolytic degradation of polyhydroxyalkanoate synthesized by pseudomonads. de Roo, G., Kellerhals, M.B., Ren, Q., Witholt, B., Kessler, B. Biotechnol. Bioeng. (2002) [Pubmed]
 
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